Pentacyclic Triterpenoids Isolated from Celastraceae: A Focus in the 13C-NMR Data
Abstract
:1. Introduction
2. Pentacyclic Triterpenoids (PCTTs)
2.1. Friedelanes
2.2. Quinonemethides and Aromatics
2.3. Dimers
2.4. Lupanes
2.5. Oleananes
2.6. Ursanes
2.7. Other Triterpenoid Skeletons Isolated from Celastraceae
3. 13C-NMR Data of Pentacyclic Triterpenoids Isolated from Celastraceae Species (2001–2021)
4. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- Bukhari, S.; Jantan, I.; Seyed, M. Effects of plants and isolates of Celastraceae family on cancer pathways. Anticancer. Agents Med. Chem. 2015, 15, 681–693. [Google Scholar] [CrossRef] [PubMed]
- Christenhusz, M.J.M.; Byng, J.W. The number of known plants species in the world and its annual increase. Phytotaxa 2016, 216, 201–217. [Google Scholar] [CrossRef] [Green Version]
- Caneschi, C.; Muniyappa, M.; Duarte, L.; Silva, G.; Santos, O.; Spillane, C.; Filho, S. Effect of constituents from samaras of Austroplenckia populnea (Celastraceae) on human cancer cells. J. Intercult. Ethnopharmacol. 2015, 4, 6–11. [Google Scholar] [CrossRef] [PubMed]
- Rodrigues, A.C.B.C.; Oliveira, F.P.; Dias, R.B.; Sales, C.B.S.; Rocha, C.A.G.; Soares, M.B.P.; Costa, E.V.; Silva, F.M.A.; Rocha, W.C.; Koolen, H.H.F.; et al. In vitro and in vivo anti-leukemia activity of the stem bark of Salacia impressifolia (Miers) A. C. Smith (Celastraceae). J. Ethnopharmacol. 2019, 231, 516–524. [Google Scholar] [CrossRef]
- Menezes, L.D.; Gomes, G.O.; Antônio, J.; Da, P.; Neto, S.; Laundry, M.M.; Ferreira, V.M.; Valero, S.M. Evaluation of anti-inflammatory and antinociceptive activities of the Austroplenckia populnea extract in topical formulations. Afr. J. Pharm. Pharmacol. 2014, 8, 1180–1185. [Google Scholar] [CrossRef]
- Rodrigues, V.G.; Duarte, L.P.; Silva, R.R.; Silva, G.D.F.; Mercadante-Simões, M.O.; Takahashi, J.A.; Matildes, B.L.G.; Fonseca, T.H.S.; Gomes, M.A.; Vieira Filho, S.A. Salacia crassifolia (Celastraceae): Chemical constituents and antimicrobial activity. Quim. Nova 2015, 38, 237–242. [Google Scholar] [CrossRef]
- Cruz, W.; Ferraz, A.; Lima, W.; Silva, M.T.; Ferreira, F.; Siqueira, F.J.; De Brito, M.C.; Duarte, L.; Vieira Filho, S.; De Magalhães, J. Evaluation of the activity of Tontelea micrantha extracts against bacteria, candida and Mayaro virus. J. Pharm. Negat. Results 2018, 9, 21–26. [Google Scholar] [CrossRef] [Green Version]
- Magalhães, C.G.; De Fátima, S.G.D.; Duarte, L.P.; Takahashi, J.A.; Santos, V.R.; Figueiredo, R.C.; Filho, S.A.V. Maytenus salicifolia Reissek (Celastraceae): Evaluation of the activity of extracts and constituents against Helicobacter pylori and oral pathogenic microorganisms. Rev. Virtual Quim. 2016, 8, 1524–1536. [Google Scholar] [CrossRef]
- Magalhães, C.G.; Ferrari, F.C.; Guimarâes, D.A.S.; Silva, G.D.F.; Duarte, L.P.; Figueiredo, R.C.; Filho, S.A.V. Maytenus salicifolia: Triterpenes isolated from stems and antioxidant property of extracts from aerial parts. Rev. Bras. Farmacogn. 2011, 21, 415–419. [Google Scholar] [CrossRef] [Green Version]
- Ferreira, P.G.; Ferraz, A.C.; Figueiredo, J.E.; Lima, C.F.; Rodrigues, V.G.; Taranto, A.G.; Ferreira, J.M.S.; Brandão, G.C.; Vieira-Filho, S.A.; Duarte, L.P.; et al. Detection of the antiviral activity of epicatechin isolated from Salacia crassifolia (Celastraceae) against Mayaro virus based on protein C homology modelling and virtual screening. Arch. Virol. 2018, 163, 1567–1576. [Google Scholar] [CrossRef]
- Veloso, C.C.; Rodrigues, V.G.; Azevendo, A.O.; Oliveira, C.C.; Gomides, L.F.; Duarte, L.P.; Duarte, I.D.; Klein, A.; Perez, A.C. Antinociceptive effects of Maytenus imbricata Mart. Ex. Reissek (Celastraceae) root extract and its tingenone constituent. J. Med. Plants Res. 2014, 8, 68–76. [Google Scholar] [CrossRef] [Green Version]
- Zhang, L.; Ji, M.Y.; Qiu, B.; Li, Q.Y.; Zhang, K.Y.; Liu, J.C.; Dang, L.S.; Li, M.H. Phytochemicals and biological activities of species from the genus Maytenus. Med. Chem. Res. 2020, 29, 575–606. [Google Scholar] [CrossRef]
- Alvarenga, N.; Ferro, E.A. Bioactive triterpenes and related compounds from Celastraceae. Stud. Nat. Prod. Chem. 2006, 33, 239–307. [Google Scholar] [CrossRef]
- Truc, D.T.T.; Vy, C.T.H.; Phu, D.H.; Hoang, N.M.; Nhan, N.T. Lupan-Type Triterpenoids from the stems of Salacia chinensis L. (Celastraceae) and their α-glucosidase inhibitory activities. Vietnam J. Chem. 2019, 57, 433–437. [Google Scholar] [CrossRef]
- Renda, G.; Gökkaya, İ.; Şöhretoğlu, D. Immunomodulatory properties of triterpenes. Phytochem. Rev. 2021, 1–27. [Google Scholar] [CrossRef] [PubMed]
- Zhou, M.; Zhang, R.H.; Wang, M.; Xu, G.B.; Liao, S.G. Prodrugs of triterpenoids and their derivatives. Eur. J. Med. Chem. 2017, 131, 222–236. [Google Scholar] [CrossRef] [PubMed]
- Ríos, J.L.; Máñez, S. New pharmacological opportunities for betulinic acid. Planta Med. 2018, 84, 8–19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Xu, F.; Huang, X.; Wu, H.; Wang, X. Beneficial health effects of lupenone triterpene: A review. Biomed. Pharmacother. 2018, 103, 198–203. [Google Scholar] [CrossRef] [PubMed]
- Shen, Y.; Chen, B.L.; Zhang, Q.X.; Zheng, Y.Z.; Fu, Q. Traditional uses, secondary metabolites, and pharmacology of Celastrus species—A Review. J. Ethnopharmacol. 2019, 241, 111934. [Google Scholar] [CrossRef]
- Silva, F.C.O.; Ferreira, M.K.A.; Da Silva, A.W.; Matos, M.G.C.; Magalhães, F.E.A.; Da Silva, P.T.; Bandeira, P.N.; De Menezes, J.E.S.A.; Santos, H.S. Bioativities of plant-isolated triterpenes: A brief review. Rev. Virtual Quim. 2020, 12, 234–247. [Google Scholar] [CrossRef]
- Ghiulai, R.; Roşca, O.J.; Antal, D.S.; Mioc, M.; Mioc, A.; Racoviceanu, R.; Macaşoi, I.; Olariu, T.; Dehelean, C.; Creţu, O.M.; et al. Tetracyclic and pentacyclic triterpenes with high therapeutic efficiency in wound healing approaches. Molecules 2020, 25, 5557. [Google Scholar] [CrossRef] [PubMed]
- Huang, Y.Y.; Chen, L.; Ma, G.X.; Xu, X.D.; Jia, X.G.; Deng, F.S.; Li, X.J.; Yuan, J.Q. A review on phytochemicals of the genus Maytenus and their bioactive studies. Molecules 2021, 26, 4563. [Google Scholar] [CrossRef]
- Duarte, L.P. Núcleo de Estudo de Plantas Medicinais—Departamento de Química ICEX. Available online: http://zeus.qui.ufmg.br/~neplam/principal.htm. (accessed on 22 December 2021).
- Chung, P.Y. Novel targets of pentacyclic triterpenoids in Staphylococcus aureus: A Systematic Review. Phytomedicine 2020, 73, 152933. [Google Scholar] [CrossRef] [PubMed]
- Silva, F.C.; Duarte, L.P.; Vieira Filho, S.A. Celastraceae family: Source of pentacyclic triterpenes with potential biological activity. Rev. Virtual Quim. 2014, 6, 1205–1220. [Google Scholar] [CrossRef]
- Thimmappa, R.; Geisler, K.; Louveau, T.; O’Maille, P.; Osbourn, A. Triterpene biosynthesis in plants. Annu. Rev. Plant Biol. 2014, 65, 225–257. [Google Scholar] [CrossRef]
- Mahato, S.B.; Kundu, A.P. 13C NMR spectra of pentacyclic triterpenoids-A compilation and some salient features. Phytochemistry 1994, 37, 1517–1575. [Google Scholar] [CrossRef]
- Dewick, P.M. Medicinal Natural Products: A Biosynthetic Approach, 3rd ed.; John Wiley & Sons: Hoboken, NJ, USA, 2009; ISBN 9780470741689. [Google Scholar]
- Shan, W.G.; Zhang, L.W.; Xiang, J.G.; Zhan, Z.J. Natural friedelanes. Chem. Biodivers. 2013, 10, 1392–1434. [Google Scholar] [CrossRef]
- Pavia, D.L.; Lampman, G.M.; Kriz, G.S.; Vyvyan, J.R. Introdução á Espectroscopia; Cengage Learning: Bellingham, WA, USA, 2010; ISBN 9788522123384. [Google Scholar]
- Bazzocchi, I.L.; Núñez, M.J.; Reyes, C.P. Diels–alder adducts from Celastraceae species. Phytochem. Rev. 2018, 17, 669–690. [Google Scholar] [CrossRef]
- Corsino, J.; De Carvalho, P.R.F.; Kato, M.J.; Latorre, L.R.; Oliveira, O.M.M.F.; Araújo, A.R.; Bolzani, V.D.S.; França, S.C.; Pereira, A.M.S.; Furlan, M. Biosynthesis of friedelane and quinonemethide triterpenoids is compartmentalized in Maytenus aquifolium and Salacia campestris. Phytochemistry 2000, 55, 741–748. [Google Scholar] [CrossRef]
- González, A.G.; Bazzocchi, I.L.; Moujir, L.; Jiménez, I.A. Ethnobotanical uses of Celastraceae. bioactive metabolites. Stud. Nat. Prod. Chem. 2000, 23, 649–738. [Google Scholar] [CrossRef]
- Oliveira, F.F. Estudo Químico de Vismia parviflora e Síntese e Derivados Antroquinônicos. Ph.D. Thesis, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil, 1997. [Google Scholar]
- Chen, M.X.; Wang, D.Y.; Guo, J. 3-Oxo-11β-hydroxyfriedelane from the roots of Celastrus monospermus. J. Chem. Res. 2010, 34, 114–117. [Google Scholar] [CrossRef]
- Silva, F.C.; Duarte, L.P.; Silva, G.D.F.; Filho, S.A.V.; Ivana, S.L.; Takahashi, J.A.; Tm, W.S. Chemical constituents from branches of Maytenus gonoclada (Celastraceae) and evaluation of antimicrobial activity. J. Braz. Chem. Soc. 2011, 22, 943–949. [Google Scholar] [CrossRef] [Green Version]
- Silva, F.C.; Rodrigues, V.G.; Duarte, L.P.; Silva, G.D.F.; Miranda, R.R.S.; Filho, S.A.V. A new friedelane triterpenoid from the branches of Maytenus gonoclada (Celastraceae). J. Chem. Res. 2011, 35, 555–557. [Google Scholar] [CrossRef]
- Oliveira, M.L.G.; Duarte, L.P.; Silva, G.D.F.; Filho, S.A.V.; Knupp, V.F.; Alves, F.G.P. 3-Oxo-12α-hydroxyfriedelane from Maytenus gonoclada: Structure elucidation by 1H and 13C chemical shift assignments and 2D-NMR spectroscopy. Magn. Reson. Chem. 2007, 45, 895–898. [Google Scholar] [CrossRef] [PubMed]
- Kishi, A.; Morikawa, T.; Matsuda, H.; Yoshikawa, M. Structures of new friedelane and norfriedelane-type triterpenes and polyacylated eudesmane-type sesquiterpene from Salacia chinensis Linn. (S. Prinoides DC., Hippocrateaceae) and radical scavenging activities of principal constituents. Chem. Pharm. Bull. 2003, 51, 1051–1055. [Google Scholar] [CrossRef] [Green Version]
- Hisham, A.; Kumar, G.J.; Fujimoto, Y.; Hara, N. Salacianone and salacianol, two triterpenes from Salacia beddomei. Phytochemistry 1995, 40, 1227–1231. [Google Scholar] [CrossRef]
- Matsuda, H.; Murakami, T.; Yashiro, K.; Yamahara, J.; Yoshikawa, M. Antidiabetic principles of natural medicines. IV. Aldose reductase and α-glucosidase inhibitors from the Roots of Salacia oblonga WALL. (Celastraceae): Structure of a new friedelane-type triterpene, kotalagenin 16-acetate. Chem. Pharm. Bull. 1999, 47, 1725–1729. [Google Scholar] [CrossRef] [Green Version]
- Kuo, Y.H.; Kuo, L.M.Y. Antitumour and anti-aids triterpenes from Celastrus hindsii. Phytochemistry 1997, 44, 1275–1281. [Google Scholar] [CrossRef] [PubMed]
- Duarte, L.P.; Figueiredo, R.C.; Sousa, G.F.; Soares, D.B.D.S.; Rodrigues, S.B.V.; Silva, F.C.; De Fátima Silva, G.D.; Vieira Filho, S.A. Chemical constituents of Salacia elliptica (Celastraceae). Quim. Nova 2010, 33, 900–903. [Google Scholar] [CrossRef]
- Duarte, L.P.; Silva De Miranda, R.R.; Rodrigues, S.B.V.; De Fátima Silva, G.D.; Filho, S.A.V.; Knupp, V.F. Stereochemistry of 16α-hydroxyfriedelin and 3-oxo-16-methylfriedel- 16-ene established by 2D NMR spectroscopy. Molecules 2009, 14, 598–607. [Google Scholar] [CrossRef]
- Sousa, G.F.; Aguilar, M.G.; Dias, D.F.; Takahashi, J.A.; Moreira, M.E.C.; Vieira Filho, S.A.; Silva, G.D.F.; Rodrigues, S.B.V.; Messias, M.C.T.B.; Duarte, L.P. Anti-Inflammatory, antimicrobial and acetylcholinesterase inhibitory activities of friedelanes from Maytenus robusta branches and isolation of further triterpenoids. Phytochem. Lett. 2017, 21, 61–65. [Google Scholar] [CrossRef]
- Sousa, G.F.; Soares, D.C.F.; Mussel, W.D.N.; Pompeu, N.F.E.; Silva, G.D.; de, F.; Filho, S.A.V.; Duarte, L.P. Pentacyclic triterpenes from branches of Maytenus robusta and in vitro cytotoxic property against 4t1 cancer cells. J. Braz. Chem. Soc. 2014, 25, 1338–1345. [Google Scholar] [CrossRef]
- Rodríguez, F.M.; Perestelo, N.R.; Jiménez, I.A.; Bazzocchi, I.L. Friedelanes from Crossopetalum lobatum. A new example of a triterpene anhydride. Helv. Chim. Acta 2009, 92, 188–194. [Google Scholar] [CrossRef]
- Ardiles, A.E.; González-Rodríguez, Á.; Núñez, M.J.; Perestelo, N.R.; Pardo, V.; Jiménez, I.A.; Valverde, Á.M.; Bazzocchi, I.L. Studies of naturally occurring friedelane triterpenoids as insulin sensitizers in the treatment type 2 diabetes mellitus. Phytochemistry 2012, 84, 116–124. [Google Scholar] [CrossRef]
- Somwong, P.; Suttisri, R.; Buakeaw, A. A new 1,3-diketofriedelane triterpene from Salacia verrucosa. Fitoterapia 2011, 82, 1047–1051. [Google Scholar] [CrossRef]
- Setzer, W.N.; Setzer, M.C.; Lynton Peppers, R.; McFerrin, M.B.; Meehan, E.J.; Chen, L.; Bates, R.B.; Nakkiew, P.; Jackes, B.R. Triterpenoid constituents in the bark of Balanops australiana. Aust. J. Chem. 2000, 53, 809–812. [Google Scholar] [CrossRef]
- Niero, R.; Mafra, A.P.; Lenzi, A.C.; Cechinel-Filho, V.; Tischer, C.; Malheiros, A.; De Souza, M.M.; Yunes, R.A.; Delle Monache, F. A new triterpene with antinociceptive activity from Maytenus robusta. Nat. Prod. Res. 2006, 20, 1315–1320. [Google Scholar] [CrossRef]
- Ferreira, F.L.; Hauck, M.S.; Duarte, L.P.; de Magalhães, J.C.; da Silva, L.S.M.; Pimenta, L.P.S.; Lopes, J.C.D.; Mercadante-Simões, M.O.; Vieira Filho, S.A. Zika virus activity of the leaf and branch extracts of Tontelea micrantha and its hexane extracts phytochemical study. J. Braz. Chem. Soc. 2019, 30, 793–803. [Google Scholar] [CrossRef]
- Tamboli, A.R.; Namdeo, A.G. Isolation and characterization of Salacia chinensis and its evaluation of antioxidant activity. Int. J. Pharmacogn. 2020, 7, 126–132. [Google Scholar] [CrossRef]
- Kaweetripob, W.; Mahidol, C.; Prawat, H.; Ruchirawat, S. Lupane, friedelane, oleanane, and ursane triterpenes from the stem of Siphonodon celastrineus Griff. Phytochemistry 2013, 96, 404–417. [Google Scholar] [CrossRef]
- Giner, R.M.; Gray, A.I.; Gibbons, S.; Waterman, P.G. Friedelane triterpenes from the stem bark of Caloncoba glauca. Phytochemistry 1993, 33, 237–239. [Google Scholar] [CrossRef]
- Nozaki, H.; Matsuura, Y.; Hirono, S.; Kasai, R.; Chang, J.J.; Lee, K.H. Antitumor agents, 116.1 cytotoxic triterpenes from Maytenus diversifolia. J. Nat. Prod. 1990, 53, 1039–1041. [Google Scholar] [CrossRef] [PubMed]
- Patra, A.; Chaudhuri, S.K. Assignment of Carbon-13 nuclear magnetic resonance spectra of some friedelanes. Magn. Reson. Chem. 1987, 25, 95–100. [Google Scholar] [CrossRef]
- Chavez, H.; Estevez-Braun, A.; Ravelo, A.G.; Gonzalez, A.G. Friedelane triterpenoids from Maytenus macrocarpa. J. Nat. Prod. 1998, 61, 82–85. [Google Scholar] [CrossRef] [PubMed]
- Itokawa, H.; Shirota, O.; Ikuta, H.; Morita, H.; Takeya, K.; Iitaka, Y. Triterpenes from Maytenus ilicifolia. Phytochemistry 1991, 30, 3713–3716. [Google Scholar] [CrossRef]
- Moiteiro, C.; Justino, F.; Tavares, R.; Marcelo-Curto, M.J.; Florêncio, M.H.; Nascimento, M.S.J.; Pedro, M.; Cerqueira, F.; Pinto, M.M.M. Synthetic secofriedelane and friedelane derivatives as inhibitors of human lymphocyte proliferation and growth of human cancer cell lines in vitro. J. Nat. Prod. 2001, 64, 1273–1277. [Google Scholar] [CrossRef]
- Duan, H.; Takaishi, Y.; Momota, H.; Ohmoto, Y.; Taki, T.; Tori, M.; Takaoka, S.; Jia, Y.; Li, D. Immunosuppressive terpenoids from extracts of Tripterygium wilfordii. Tetrahedron 2001, 57, 8413–8424. [Google Scholar] [CrossRef]
- Wang, K.W.; Zhang, H.; Pan, Y.J. Novel triterpenoids from Microtropis triflora with antitumor activities. Helv. Chim. Acta 2007, 90, 277–281. [Google Scholar] [CrossRef]
- Maregesi, S.M.; Hermans, N.; Dhooghe, L.; Cimanga, K.; Ferreira, D.; Pannecouque, C.; Berghe, D.A.V.; Cos, P.; Maes, L.; Vlietinck, A.J.; et al. Phytochemical and biological investigations of Elaeodendron schlechteranum. J. Ethnopharmacol. 2010, 129, 319–326. [Google Scholar] [CrossRef]
- Setzer, W.N.; Holland, M.T.; Bozeman, C.A.; Rozmus, G.F.; Setzer, M.C.; Moriarity, D.M.; Reeb, S.; Vogler, B.; Bates, R.B.; Haber, W.A. Isolation and frontier molecular orbital investigation of bioactive quinone-methide triterpenoids from the bark of Salacia petenensis. Planta Med. 2001, 67, 65–69. [Google Scholar] [CrossRef]
- Li, Y.Z.; Li, Z.L.; Yin, S.L.; Shi, G.; Liu, M.S.; Jing, Y.K.; Hua, H.M. Triterpenoids from Calophyllum inophyllum and their growth inhibitory effects on human leukemia HL-60 cells. Fitoterapia 2010, 81, 586–589. [Google Scholar] [CrossRef]
- Ramaiah, P.A.; Devi, P.U.; Frolow, F.; Lavie, D. 3-Oxo-friedelan-20α-oic acid from Gymnosporia emarginata. Phytochemistry 1984, 23, 2251–2255. [Google Scholar] [CrossRef]
- Gottlieb, H.E.; Ramaiah, P.A.; Lavie, D. 13C NMR signal assignment of friedelin and 3a-hydroxyfriedelan-2-one. Magn. Reson. Chem. 1985, 23, 616–620. [Google Scholar] [CrossRef]
- Reyes, C.P.; Jiménez, I.A.; Bazzocchi, I.L. Pentacyclic triterpenoids from Maytenus cuzcoina. Nat. Prod. Commun. 2017, 12, 675–678. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Pereira, R.C.G.; Soares, D.C.F.; Oliveira, D.C.P.; de Sousa, G.F.; Vieira-Filho, S.A.; Mercadante-Simões, M.O.; Lula, I.; Silva-Cunha, A.; Duarte, L.P. Triterpenes from leaves of Cheiloclinium cognatum and their in vivo antiangiogenic activity. Magn. Reson. Chem. 2018, 56, 360–366. [Google Scholar] [CrossRef]
- Chang, C.W.; Wu, T.S.; Hsieh, Y.S.; Kuo, S.C.; Lee Chao, P.D. Terpenoids of Syzygium formosanum. J. Nat. Prod. 1999, 62, 327–328. [Google Scholar] [CrossRef]
- Yang, G.Z.; Li, Y.C. Cyclopeptide and Terpenoids from Tripterygium wilfordii HOOK. F. Helv. Chim. Acta 2002, 85, 168–174. [Google Scholar] [CrossRef]
- Duarte, M.C.; Tavares, J.F.; Madeiro, S.A.L.; Costa, V.C.O.; Filho, J.M.B.; De Fátima Agra, M.; Filho, R.B.; Da Silva, M.S. Maytensifolone, a new triterpene from Maytenus distichophylla Mart. Ex Reissek. J. Braz. Chem. Soc. 2013, 24, 1697–1700. [Google Scholar] [CrossRef]
- Gao, H.Y.; Guo, Z.H.; Cheng, P.; Xu, X.M.; Wu, L.J. New Triterpenes from Salacia hainanensis Chun et How with α-glucosidase inhibitory activity. J. Asian Nat. Prod. Res. 2010, 12, 834–842. [Google Scholar] [CrossRef]
- Fujita, R.; Duan, H.; Takaishi, Y. Terpenoids from Tripterigyum hypoglaucum. Phytochemistry 2000, 53, 715–722. [Google Scholar] [CrossRef]
- Santos, J.P.; Rodrigues, B.L.; Oliveira, W.X.C.; Silva, F.C.; De Sousa, G.F.; Vieira Filho, S.A.; Duarte, L.P.; Silva, R.R. Caryopristimerin, the first example of a sesquiterpene-triterpene homo diels-alder adduct, and a new 29-nor-friedelane from roots of Salacia crassifolia. J. Braz. Chem. Soc. 2019, 30, 1558–1565. [Google Scholar] [CrossRef]
- Li, K.; Duan, H.; Kawazoe, K.; Takaishi, Y. Terpenoids from Tripterygium wilfordii. Phytochemistry 1997, 45, 791–796. [Google Scholar] [CrossRef]
- Gonzalez, A.G.; Alvarenga, N.L.; Ravelo, A.G.; Jimenez, I.A.; Bazzocchi, I.L. Two triterpenes from Maytenus canariensis. J. Nat. Prod. 1995, 58, 570–573. [Google Scholar] [CrossRef]
- Addae-Mensah, I.; Adu-Kumi, S.; Waibel, R.; Oppong, I.V. A Novel D:A-friedooleanane triterpenoid and other constituents of the stem bark of Dichapetalum barteri Engl. Arkivoc 2007, 2007, 71–79. [Google Scholar] [CrossRef] [Green Version]
- Wu, X.Y.; Qin, G.W.; Fan, D.J.; Xu, R.S. 1-Hydroxy-2,5,8-trimethyl-9-fluorenone from Tripterygium wilfordii. Phytochemistry 1994, 36, 477–479. [Google Scholar] [CrossRef]
- Yeboah, E.M.O.; Majinda, R.R.T.; Kadziola, A.; Muller, A. Dihydro-β-agarofuran sesquiterpenes and pentacyclic triterpenoids from the root bark of Osyris lanceolata. J. Nat. Prod. 2010, 73, 1151–1155. [Google Scholar] [CrossRef]
- Lu, C.H.; Zhang, J.X.; Gan, F.Y.; Shen, Y.M. Chemical constituents of the suspension cell cultures of Maytenus hookeri. Acta Bot. Sin. 2002, 44, 603–610. [Google Scholar]
- Orabi, K.Y.; Al-Qasoumi, S.I.; El-Olemy, M.M.; Mossa, J.S.; Muhammad, I. Dihydroagarofuran alkaloid and triterpenes from Maytenus heterophylla and Maytenus arbutifolia. Phytochemistry 2001, 58, 475–480. [Google Scholar] [CrossRef]
- Ngassapa, O.; Soejarto, D.D.; Pezzuto, J.M.; Farnsworth, N.R. Quinone-methide triterpenes and salaspermic acid from Kokoona ochracea. J. Nat. Prod. 1994, 57, 1–8. [Google Scholar] [CrossRef]
- Zhang, X.W.; Wang, K.W.; Zhou, M.Q. Cytotoxic triterpenoids from the stalks of Microtropis triflora. Chem. Biodivers. 2017, 14, e1700066. [Google Scholar] [CrossRef]
- Klass, J.; Tinto, W.F.; Mclean, S.; Reynolds, W.F. Friedelane triterpenoids from Peritassa compta: Complete 1H and 13C assignments by 2D NMR spectroscopy. J. Nat. Prod. 1992, 55, 1626–1630. [Google Scholar] [CrossRef]
- Wandji, J.; Wansi, J.D.; Fuendjiep, V.; Dagne, E.; Mulholland, D.A.; Tillequin, F.; Fomum, Z.T.; Sondengam, B.L.; Nkeh, B.C.; Njamen, D. Sesquiterpene lactone and friedelane derivative from Drypetes molunduana. Phytochemistry 2000, 54, 811–815. [Google Scholar] [CrossRef]
- Sousa, G.F.; Ferreira, F.L.; Duarte, L.P.; Silva, G.D.F.; Messias, M.C.T.B.; Vieira Filho, S.A. Structural determination of 3β,11β-dihydroxyfriedelane from Maytenus robusta (Celastraceae) by 1D and 2D NMR. J. Chem. Res. 2012, 36, 203–205. [Google Scholar] [CrossRef]
- Costa, P.M.; Carvalho, M.G. New triterpene isolated from Eschweilera longipes (Lecythidaceae). An. Acad. Bras. Cienc. 2003, 75, 21–25. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Salazar, G.C.M.; Silva, G.D.F.; Duarte, L.P.; Vieira Filho, S.A.; Lula, I.S. Two epimeric friedelane triterpenes isolated from Maytenus truncata Reiss: 1H and 13C chemical shift assignments. Magn. Reson. Chem. 2000, 38, 977–980. [Google Scholar] [CrossRef]
- Gunatilaka, A.A.L.; Nanayakkara, N.P.D.; Sultanbawa, M.U.S.; Wazeer, M.I.M. 13C nuclear magnetic resonance spectra of some naturally occurring friedelanones. Org. Magn. Reson. 1980, 14, 415–417. [Google Scholar] [CrossRef]
- Dhanabalasingham, B.; Karunaratne, V.; Tezuka, Y.; Kikuchi, T.; Gunatilaka, A.A.L. Biogenetically important quinonemethides and other triterpenoid constituents of Salacia reticulata. Phytochemistry 1996, 42, 1377–1385. [Google Scholar] [CrossRef]
- Yang, J.H.; Luo, S.D.; Wang, Y.S.; Zhao, J.F.; Zhang, H.B.; Li, L. Triterpenes from Tripterygium wilfordii Hook. J. Asian Nat. Prod. Res. 2006, 8, 425–429. [Google Scholar] [CrossRef]
- Nakano, K.; Oose, Y.; Takaishi, Y. A novel epoxy-triterpene and nortriterpene from callus cultures of Tripterygium wilfordii. Phytochemistry 1997, 46, 1179–1182. [Google Scholar] [CrossRef]
- Sousa, G.F.; Duarte, L.P.; Alcântara, A.F.C.; Silva, G.D.F.; Vieira-Filho, S.A.; Silva, R.R.; Oliveira, D.M.; Takahashi, J.A. New Triterpenes from Maytenus robusta: Structural elucidation based on NMR experimental data and theoretical Calculations. Molecules 2012, 17, 13439–13456. [Google Scholar] [CrossRef]
- Vieira Filho, S.A.; Duarte, L.P.; Suva, G.D.F.; Lula, I.S.; Dos Santos, M.H. Total assignment of 1H And 13C NMR spectra of two 3, 4-secofriedelanes from Austroplenckia populnea. Magn. Reson. Chem. 2001, 39, 746–748. [Google Scholar] [CrossRef]
- Mena-Rejón, G.J.; Pérez-Espadas, A.R.; Moo-Puc, R.E.; Cedillo-Rivera, R.; Bazzocchi, I.L.; Jiménez-Diaz, I.A.; Quijano, L. Antigiardial activity of triterpenoids from Root Bark of Hippocratea excelsa. J. Nat. Prod. 2007, 70, 863–865. [Google Scholar] [CrossRef] [PubMed]
- Zhang, K.; Liu, J.; Wang, Y.; Huang, H.; Chen, Y. Constituents of triterpenes from Celastrus monospermus Roxb. Zhongshan Da Xue Xue Bao. Zi Ran Ke Xue Ban = Acta Sci. Nat. Univ. Sunyatseni 1998, 37, 85–88. [Google Scholar]
- Nogueiras, C.; Spengler, I.; Ravelo, A.G.; Jiménez, I.A. Triterpenes from the roots of Maytenus buxifolia. Rev. Latinoam. Química 2001, 29, 32–39. [Google Scholar]
- Martínez, V.M.; Corona, M.M.; Vélez, C.S.; Rodríguez-Hahn, L.; Joseph-Nathan, P. Terpenoids from Mortonia diffusa. J. Nat. Prod. 1988, 51, 793–796. [Google Scholar] [CrossRef]
- Betancor, C.; Freire, R.; Gonzalez, A.G.; Salazar, J.A.; Pascard, C.; Prange, T. Three Triterpenes And Other Terpenoids from Catha cassinoides. Phytochemistry 1980, 19, 1989–1993. [Google Scholar] [CrossRef]
- Joshi, B.S.; Kamat, V.N.; Viswanathan, N. Triterpenes of Salacia prinoides DC. Tetrahedron 1973, 29, 1365–1374. [Google Scholar] [CrossRef]
- Sousa, J.R.; Silva, G.D.F.; Pedersoli, J.L.; Alves, R.J. Friedelane and oleanane triterpenoids from bark wood of Austroplenckia populnea. Phytochemistry 1990, 29, 3259–3261. [Google Scholar] [CrossRef]
- Espindola, L.S.; Dusi, R.G.; Demarque, D.P.; Braz-Filho, R.; Yan, P.; Bokesch, H.R.; Gustafson, K.R.; Beutler, J.A. Cytotoxic Triterpenes from Salacia crassifolia and metabolite profiling of Celastraceae species. Molecules 2018, 23, 1494. [Google Scholar] [CrossRef] [Green Version]
- Almeida, M.T.R.; Ríos-Luci, C.; Padrón, J.M.; Palermo, J.A. Antiproliferative terpenoids and alkaloids from the roots of Maytenus vitis-idaea and Maytenus spinosa. Phytochemistry 2010, 71, 1741–1748. [Google Scholar] [CrossRef]
- Magalhães, C.G.; De Fátima Silva, G.D.; Duarte, L.P.; Bazzocchi, I.L.; Diaz, A.J.; Moujir, L.; López, M.R.; Figueiredo, R.C.; Vieira Filho, S.A. Salicassin, an unprecedented chalcone-diterpene adduct and a quinone methide triterpenoid from Maytenus salicifolia. Helv. Chim. Acta 2013, 96, 1046–1054. [Google Scholar] [CrossRef]
- Thiem, D.A.; Sneden, A.T.; Khan, S.I.; Tekwani, B.L. Bisnortriterpenes from Salacia madagascariensis. J. Nat. Prod. 2005, 68, 251–254. [Google Scholar] [CrossRef] [PubMed]
- Likhitwitayawuid, K.; Bavovada, R.; Lin, L.Z.; Cordell, G.A. Revised structure of 20-hydroxytingenone and 13C NMR assignments of 22β-hydroxytingenone. Phytochemistry 1993, 34, 759–763. [Google Scholar] [CrossRef]
- Gunatilaka, A.A.L.; Fernando, H.C.; Kikuchi, T.; Tezuka, Y. 1H and 13C NMR Analysis of three quinone-methide triterpenoids. Magn. Reson. Chem. 1989, 27, 803–807. [Google Scholar] [CrossRef]
- Jeller, A.H.; Silva, D.H.S.; Lião, L.M.; Bolzani, V.D.S.; Furlan, M. Antioxidant phenolic and quinonemethide triterpenes from Cheiloclinium cognatum. Phytochemistry 2004, 65, 1977–1982. [Google Scholar] [CrossRef]
- Sneden, A.T. Isoiguesterin, a new antileukemic bisnortriterpene from Salacia madagascariensis. J. Nat. Prod. 1981, 44, 503–507. [Google Scholar] [CrossRef]
- Santos, J.P. Estudo fitoquímico e da atividade biológica de constituintes das raízes e galhos de Salacia crassifolia (Celastraceae). Ph.D. Thesis, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil, 2019. [Google Scholar]
- González, A.G.; Alvarenga, N.L.; Ravelo, A.G.; Bazzocchi, I.L.; Ferro, E.A.; Navarro, A.G.; Moujir, L.M. Scutione, a New bioactive norquinonemethide triterpene from Maytenus scutioides (Celastraceae). Bioorganic Med. Chem. 1996, 4, 815–820. [Google Scholar] [CrossRef]
- Tezuka, Y.; Kikuchi, T.; Dhanabalasingham, B.; Karunaratne, V.; Gunatilaka, A.A.L. Studies on terpenoids and steroids, 25. complete 1H- and 13C-NMR spectral assignments of salaciquinone, a new 7-oxo-quinonemethide dinortriterpenoid. J. Nat. Prod. 1994, 57, 270–276. [Google Scholar] [CrossRef]
- Khalid, S.A.; Friedrichsen, G.M.; Christensen, S.B.; El Tahir, A.; Satti, G.M. Isolation and characterization of pristimerin as the antiplasmodial and antileishmanial agent of Maytenus senegalensis (Lam.) Exell. Arkivoc 2007, 2007, 129–134. [Google Scholar] [CrossRef] [Green Version]
- Lião, L.M.; Silva, G.A.; Monteiro, M.R.; Albuquerque, S. Trypanocidal activity of quinonemethide triterpenoids from Cheiloclinium cognatum (Hippocrateaceae). Z. Nat. C 2008, 63, 207–210. [Google Scholar] [CrossRef]
- Sotanaphun, U.; Suttisri, R.; Lipipun, V.; Bavovada, R. Quinone-methide triterpenoids from Glyptopetalum sclerocarpum. Phytochemistry 1998, 49, 1749–1755. [Google Scholar] [CrossRef]
- Ochieng, C.O.; Opiyo, S.A.; Mureka, E.W.; Ishola, I.O. Cyclooxygenase inhibitory compounds from Gymnosporia heterophylla Aerial Parts. Fitoterapia 2017, 119, 168–174. [Google Scholar] [CrossRef] [PubMed]
- Kennedy, M.L.; Llanos, G.G.; Castanys, S.; Gamarro, F.; Bazzocchi, I.L.; Jiménez, I.A. Terpenoids from Maytenus species and assessment of their reversal activity against a multidrug-resistant Leishmania tropica Line. Chem. Biodivers. 2011, 8, 2291–2298. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Rodríguez, F.M.; López, M.R.; Jiménez, I.A.; Moujir, L.; Ravelo, A.G.; Bazzocchi, I.L. New phenolic triterpenes from Maytenus blepharodes. Semisynthesis of 6-deoxoblepharodol from pristimerin. Tetrahedron 2005, 61, 2513–2519. [Google Scholar] [CrossRef]
- Sotanaphun, U.; Lipipun, V.; Bavovada, R. Constituents of the pericarp of Glyptopetalum sclerocarpum. Fitoterapia 2004, 75, 606–608. [Google Scholar] [CrossRef]
- González, A.G.; Alvarenga, N.L.; Ravelo, A.G.; Jiménez, I.A.; Bazzocchi, I.L.; Canela, N.J.; Moujir, L.M. Antibiotic phenol nor-triterpenes from Maytenus canariensis. Phytochemistry 1996, 43, 129–132. [Google Scholar] [CrossRef]
- Shirota, O.; Morita, H.; Takeya, K.; Itokawa, H.; Iitaka, Y. Cytotoxic aromatic triterpenes from Maytenus ilicifolia and Maytenus chuchuhuasca. J. Nat. Prod. 1994, 57, 1675–1681. [Google Scholar] [CrossRef]
- Rodrigues, V.G.; Duarte, L.P.; Silva, G.D.F.; Silva, F.C.; Góes, J.V.; Takahashi, J.A.; Pimenta, L.P.S.; Filho, S.A.V. Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata. Quim. Nova 2012, 35, 1375–1380. [Google Scholar] [CrossRef] [Green Version]
- Gupta, M.; Alvarenga, N.; Rodriguez, F.; Ravelo, A.; Ignacio, J.; Bazzocchi, I. New phenolic and quinone-methide triterpenes from Maytenus species (Celastraceae). Nat. Prod. Lett. 1995, 7, 209–218. [Google Scholar] [CrossRef]
- Ankli, A.; Heilmann, J.; Heinrich, M.; Sticher, O. Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri. Phytochemistry 2000, 54, 531–537. [Google Scholar] [CrossRef]
- Núñez, M.J.; Kennedy, M.L.; Jiménez, I.A.; Bazzocchi, I.L. Uragogin and blepharodin, unprecedented hetero-diels-alder adducts from Celastraceae species. Tetrahedron 2011, 67, 3030–3033. [Google Scholar] [CrossRef]
- Morota, T.; Yang, C.X.; Ogino, T.; Qin, W.Z.; Katsuhara, T.; Xu, L.H.; Komatsu, Y.; Miao, K.L.; Maruno, M.; Yang, B.H. D:A-friedo-24-noroleanane triterpenoids from Tripterigium wilfordii. Phytochemistry 1995, 39, 1159–1163. [Google Scholar] [CrossRef]
- Gutiérrez, F.; Estévez-Braun, A.; Ravelo, Á.G.; Astudillo, L.; Zárate, R. Terpenoids from the medicinal plant Maytenus ilicifolia. J. Nat. Prod. 2007, 70, 1049–1052. [Google Scholar] [CrossRef] [PubMed]
- Takaishi, Y.; Wariishi, N.; Tateishi, H.; Kawazoe, K.; Nakano, K.; Ono, Y.; Tokuda, H.; Nishino, H.; Iwashima, A. Triterpenoid inhibitors of interleukin-1 secretion and tumour-promotion from Tripterygium wilfordii Var. Regelii. Phytochemistry 1997, 45, 969–974. [Google Scholar] [CrossRef]
- Yang, G.Z.; Xi, M.L.; Li, Y.C. Two novel phenolic triterpenes from Tripterygium wilfordii. J. Asian Nat. Prod. Res. 2001, 3, 83–88. [Google Scholar] [CrossRef]
- Gamlath, C.B.; Gunaherath, K.B.; Leslie Gunatilaka, A.A. Studies on terpenoids and steroids. Part 10.1 Structures of four new natural phenolic D:A-friedo-24-noroleanane triterpenoids. J. Chem. Soc. Perkin Trans. 1 1987, 2849–2854. [Google Scholar] [CrossRef]
- Sotanaphun, U.; Lipipun, V.; Suttisri, R.; Bavovada, R. Antimicrobial activity and stability of tingenone derivatives. Planta Med. 1999, 65, 450–452. [Google Scholar] [CrossRef]
- González, A.G.; Kennedy, M.L.; Rodríguez, F.M.; Bazzocchi, I.L.; Jiménez, I.A.; Ravelo, A.G.; Moujir, L. Absolute configuration of triterpene dimers from Maytenus species (Celastraceae). Tetrahedron 2001, 57, 1283–1287. [Google Scholar] [CrossRef]
- Shirota, O.; Morita, H.; Takeya, K.; Itokawa, H. Revised structures of cangorosins, triterpene dimers from Maytenus ilicifolia. J. Nat. Prod. 1997, 60, 111–115. [Google Scholar] [CrossRef]
- Shirota, O.; Morita, H.; Takeya, K.; Itokawa, H. New geometric and stereoisomeric triterpene dimers from Maytenus chuchuhuasca. Chem. Pharm. Bull. 1998, 46, 102–106. [Google Scholar] [CrossRef] [Green Version]
- Shirota, O.; Sekita, S.; Satake, M.; Morita, H.; Takeya, K.; Itokawa, H. Nine regioisomeric and stereoisomeric triterpene dimers from Maytenus chuchuhuasca. Chem. Pharm. Bull. 2004, 52, 739–746. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Shirota, O.; Sekita, S.; Satake, M.; Morita, H.; Takeya, K.; Itokawa, H. Nine triterpene dimers from Maytenus chuchuhuasca. Helv. Chim. Acta 2004, 87, 1536–1544. [Google Scholar] [CrossRef]
- Mesa-Siverio, D.; Chávez, H.; Estévez-Braun, A.; Ravelo, Á.G. Cheiloclines A-I. First examples of octacyclic sesquiterpene-triterpene hetero-diels-alder adducts. Tetrahedron 2005, 61, 429–436. [Google Scholar] [CrossRef]
- Wu, J.; Zhou, Y.; Wang, L.; Zuo, J.; Zhao, W. Terpenoids from root bark of Celastrus orbiculatus. Phytochemistry 2012, 75, 159–168. [Google Scholar] [CrossRef] [PubMed]
- Shirota, O.; Morita, H.; Takeya, K.; Itokawa, H. Five new triterpene dimers from Maytenus chuchuhuasca. J. Nat. Prod. 1997, 60, 1100–1104. [Google Scholar] [CrossRef]
- Shirota, O.; Sekita, S.; Satake, M.; Morita, H.; Takeya, K.; Itokawa, H. Two cangorosin a type triterpene dimers from Maytenus chuchuhuasca. Chem. Pharm. Bull. 2004, 52, 1148–1150. [Google Scholar] [CrossRef] [Green Version]
- Salazar, G.D.C.M.; de Sousa, G.F.; Duarte, L.P.; Silva, R.R.; Vieira-Filho, S.A.; de Fátima Silva, G.D. Truncatin: A triterpene dimer isolated from Maytenus truncata Reissek (Celastraceae). WORLD J. Pharm. Pharm. Sci. 2021, 10, 60–71. [Google Scholar]
- González, A.G.; Alvarenga, N.L.; Estévez-Braun, A.; Ravelo, A.G.; Bazzocchi, I.L.; Mouijir, L. Structure and absolute configuration of triterpene dimers from Maytenus scutioides. Tetrahedron 1996, 52, 9597–9608. [Google Scholar] [CrossRef]
- Corbett, R.E.; Cong, A.N.T.; Wilkins, A.L.; Thomson, R.A. Lichens and fungi. Part 17. The synthesis and absolute configuration at C-20 of the (R)- and (S)-Epimers of some 29-substituted lupane derivatives and of some 30-norlupan-20-ol derivatives and the crystal tructure of (20R)-3β-Acetoxylupan-29-ol. J. Chem. Soc. Perkin Trans. 1985, 2051–2056. [Google Scholar] [CrossRef]
- Yamashita, H.; Matsuzaki, M.; Kurokawa, Y.; Nakane, T.; Goto, M.; Lee, K.H.; Shibata, T.; Bando, H.; Wada, K. Four new triterpenoids from the bark of Euonymus alatus Forma Ciliato-Dentatus. Phytochem. Lett. 2019, 31, 140–146. [Google Scholar] [CrossRef]
- Callies, O.; Bedoya, L.M.; Beltrán, M.; Muñoz, A.; Calderón, P.O.; Osorio, A.A.; Jiménez, I.A.; Alcamí, J.; Bazzocchi, I.L. Isolation, structural modification, and HIV inhibition of pentacyclic lupane-type triterpenoids from Cassine xylocarpa and Maytenus cuzcoina. J. Nat. Prod. 2015, 78, 1045–1055. [Google Scholar] [CrossRef] [PubMed]
- Reyes, C.P.; Núñez, M.J.; Jiménez, I.A.; Busserolles, J.; Alcaraz, M.J.; Bazzocchi, I.L. Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2. Bioorganic Med. Chem. 2006, 14, 1573–1579. [Google Scholar] [CrossRef] [PubMed]
- Silva, S.R.D.; Silva, G.D.S.; Barbosa, L.C.A.; Duarte, L.P.; Vieira Filho, S.A. Lupane pentacyclic triterpenes isolated from stems and branches of Maytenus imbricata (Celastraceae). Helv. Chim. Acta 2005, 88, 1102–1109. [Google Scholar] [CrossRef]
- Fern, A.; Hern, A.; Garc, T.H.; Spengler-salabarr, I.; Naturales, P.; Habana, L. Triterpenes with anti-inflammatory activity isolated from the bark of the endemic species Maytenus elaeodendroides, Griseb. Rev. Cuba. Química 2020, 32, 61–73. [Google Scholar]
- Carpenter, R.C.; Sotheeswaran, S.; Sultanbawa, M.U.S.; Ternai, B. 13C NMR studies of some lupane and taraxerane triterpenes. Org. Magn. Reson. 1980, 14, 462–465. [Google Scholar] [CrossRef]
- Núñez, M.J.; Reyes, C.P.; Jiménez, I.A.; Moujir, L.; Bazzocchi, I.L. Lupane triterpenoids from Maytenus species. J. Nat. Prod. 2005, 68, 1018–1021. [Google Scholar] [CrossRef]
- Satiraphan, M.; Pamonsinlapatham, P.; Sotanaphun, U.; Sittisombut, C.; Raynaud, F.; Garbay, C.; Michel, S.; Cachet, X. Lupane triterpenes from the leaves of the tropical rain forest tree Hopea odorata Roxb. and their cytotoxic activities. Biochem. Syst. Ecol. 2012, 44, 407–412. [Google Scholar] [CrossRef]
- Chen, I.H.; Du, Y.C.; Lu, M.C.; Lin, A.S.; Hsieh, P.W.; Wu, C.C.; Chen, S.L.; Yen, H.F.; Chang, F.R.; Wu, Y.C. Lupane-type triterpenoids from Microtropis fokienensis and Perrottetia arisanensis and the apoptotic effect of 28-hydroxy-3-oxo-lup-20(29)-en-30-al. J. Nat. Prod. 2008, 71, 1352–1357. [Google Scholar] [CrossRef]
- Zhou, J.; Wei, X.H.; Chen, F.Y.; Li, C.J.; Yang, J.Z.; Ma, J.; Bao, X.Q.; Zhang, D.; Zhang, D.M. Anti-inflammatory pentacyclic triterpenes from the stems of Euonymus carnosus. Fitoterapia 2017, 118, 21–26. [Google Scholar] [CrossRef]
- Monaco, P.; Previtera, L. Isoprenoids from the leaves of Quercus suber. J. Nat. Prod. 1984, 47, 673–676. [Google Scholar] [CrossRef]
- Rashid, M.A.; Gray, A.I.; Waterman, P.G.; Armstrong, J.A. Coumarins from Phebalium tuberculosum Ssp. Megaphyllum and Phebalium filifolium. J. Nat. Prod. 1992, 55, 851–858. [Google Scholar] [CrossRef] [PubMed]
- Kang, H.R.; Eom, H.J.; Lee, S.R.; Choi, S.U.; Sung Kang, K.; Lee, K.R.; Kim, K.H. Bioassay-guided isolation of antiproliferative triterpenoids from Euonymus alatus Twigs. Nat. Prod. Commun. 2015, 10, 1929–1932. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Yu, M.H.; Shi, Z.F.; Yu, B.W.; Pi, E.H.; Wang, H.Y.; Hou, A.J.; Lei, C. Triterpenoids and α-Glucosidase Inhibitory Constituents from Salacia hainanensis. Fitoterapia 2014, 98, 143–148. [Google Scholar] [CrossRef] [PubMed]
- Fuchino, H.; Satoh, T.; Tanaka, N. Chemical evaluation of betula species in japan. I. Constituents of Betula ermanii. Chem. Pharm. Bull. 1995, 43, 1937–1942. [Google Scholar] [CrossRef] [Green Version]
- Delgado-Méndez, P.; Herrera, N.; Chávez, H.; Estévez-Braun, A.; Ravelo, Á.G.; Cortes, F.; Castanys, S.; Gamarro, F. New terpenoids from Maytenus apurimacensis as MDR reversal agents in the parasite leishmania. Bioorganic Med. Chem. 2008, 16, 1425–1430. [Google Scholar] [CrossRef] [PubMed]
- Miranda, R.R.S.; Silva, G.D.D.F.; Duarte, L.P.; Vieira Filho, S.A. Triterpene esters isolated from leaves of Maytenus salicifolia REISSEK. Helv. Chim. Acta 2007, 90, 652–658. [Google Scholar] [CrossRef]
- Lai, Y.C.; Chen, C.K.; Tsai, S.F.; Lee, S.S. Triterpenes as α-glucosidase inhibitors from Fagus hayatae. Phytochemistry 2012, 74, 206–211. [Google Scholar] [CrossRef]
- Burns, D.; Reynolds, W.F.; Buchanan, G.; Reese, P.B.; Enriquez, R.G. Assignment of 1H and 13C spectra and investigation of hindered side-chain rotation in lupeol derivatives. Magn. Reson. Chem. 2000, 38, 488–493. [Google Scholar] [CrossRef]
- Dantanarayana, A.P.; Kumar, N.S.; Muthukuda, P.M.; I, M.; Wazeer, M. A lupane derivative and the 13C NMR chemical shifts of some lupanols from Pleurostylia opposita. Phytochemistry 1982, 21, 2065–2068. [Google Scholar] [CrossRef]
- Menezes-De-Oliveira, D.; Aguilar, M.I.; King-Díaz, B.; Vieira-Filho, S.A.; Pains-Duarte, L.; De Fátima Silva, G.D.; Lotina-Hennsen, B. The triterpenes 3β-lup-20(29)-en-3-ol and 3β-lup-20(29)-en-3-yl acetate and the carbohydrate 1,2,3,4,5,6-hexa-o-acetyl-dulcitol as photosynthesis light reactions inhibitors. Molecules 2011, 16, 9939–9956. [Google Scholar] [CrossRef]
- Li, J.J.; Yang, J.; Lü, F.; Qi, Y.T.; Liu, Y.Q.; Sun, Y.; Wang, Q. Chemical constituents from the stems of Celastrus orbiculatus. Chin. J. Nat. Med. 2012, 10, 279–283. [Google Scholar] [CrossRef]
- Kuroyanagi, M.; Shiotsu, M.; Ebihara, T.; Kawai, H.; Ueno, A.; Fukushima, S. Chemical studies on Viburnum awabuki K. KOCH. Chem. Pharm. Bull. 1986, 34, 4012–4017. [Google Scholar] [CrossRef] [Green Version]
- Pieroni, L.G.; De Rezende, F.M.; Ximenes, V.F.; Dokkedal, A.L. Antioxidant activity and total phenols from the methanolic extract of Miconia albicans (Sw.) Triana Leaves. Molecules 2011, 16, 9439–9450. [Google Scholar] [CrossRef]
- Choi, C.I.; Lee, S.R.; Kim, K.H. Antioxidant and α-glucosidase inhibitory activities of constituents from Euonymus alatus Twigs. Ind. Crops Prod. 2015, 76, 1055–1060. [Google Scholar] [CrossRef]
- Aguiar, R.M.; David, J.P.; David, J.M. Unusual naphthoquinones, catechin and triterpene from Byrsonima microphylla. Phytochemistry 2005, 66, 2388–2392. [Google Scholar] [CrossRef] [PubMed]
- Savona, G.; Bruno, M.; Rodríguez, B.L.; Marco, J. Triterpenoids from Salvia deserta. Phytochemistry 1987, 26, 3305–3308. [Google Scholar] [CrossRef]
- Huang, J.; Guo, Z.H.; Cheng, P.; Sun, B.H.; Gao, H.Y. Three new triterpenoids from Salacia hainanensis Chun et How showed effective anti-α-glucosidase activity. Phytochem. Lett. 2012, 5, 432–437. [Google Scholar] [CrossRef]
- Pistelli, L.; Noccioli, C.; Giachi, I.; Dimitrova, B.; Gevrenova, R.; Morelli, I.; Potenza, D. Lupane-triterpenes from Bupleurum flavum. Nat. Prod. Res. 2005, 19, 783–788. [Google Scholar] [CrossRef]
- Souza, A.D.L.; Rocha, A.F.I.; Pinheiro, M.L.B.; Andrade, C.H.D.S.; Galotta, A.L.D.A.Q.; Santos, M.D.P.S.S.D. Constituintes químicos de Gustavia augusta L. (Lecythidaceae). Quim. Nova 2001, 24, 439–442. [Google Scholar] [CrossRef]
- Ahmad, V.U.; Bano, S.; Voelter, W.; Fuchs, W. Chemical Examination of Nepeta hindostana (Roth) Haines the structure of nepeticin. Tetrahedron Lett. 1981, 22, 1714–1718. [Google Scholar] [CrossRef]
- Tanaka, R.; Masuda, K.; Matsunaga, S. Lup-20(29)-en-3β,15α-diol and ocotillol-II from the stem bark of Phyllanthus flexuosus. Phytochemistry 1993, 32, 472–474. [Google Scholar] [CrossRef]
- Ulubelen, A.; Topcu, G.; Lotter, H.; Wagner, H.; Eriş, C. Triterpenoids from the aerial parts of Salvia montbretii. Phytochemistry 1994, 36, 413–415. [Google Scholar] [CrossRef]
- Chaturvedula, V.S.P.; Schilling, J.K.; Johnson, R.K.; Kingston, D.G.I. New cytotoxic lupane triterpenoids from the twigs of Coussarea paniculata. J. Nat. Prod. 2003, 66, 419–422. [Google Scholar] [CrossRef]
- Hisham, A.; Kumar, G.J.; Fujimoto, Y.; Hara, N. 20,29-Epoxysalacianone and 6β-hydroxysalacianone, two lupane triterepenes from Salacia beddomei. Phytochemistry 1996, 42, 789–794. [Google Scholar] [CrossRef]
- Razdan, T.K.; Harkar, S.; Qadri, B.; Qurishi, M.A.; Khuroo, M.A. Lupene derivatives from Skimmia laureola. Phytochemistry 1988, 27, 1890–1892. [Google Scholar] [CrossRef]
- Ngassapa, O.D.; Soejarto, D.D.; Che, C.T.; Pezzuto, J.M.; Farnsworth, N.R. New cytotoxic lupane lactones from Kokoona ochracea. J. Nat. Prod. 1991, 54, 1353–1359. [Google Scholar] [CrossRef] [PubMed]
- Djerassi, C.; Farkas, E.; Liu, H.L.; Thomas, G.H. Terpenoids. XVII. The cactus triterpenes thurberogenin and stellatogenin. J. Am. Chem. Soc. 1955, 77, 5330–5336. [Google Scholar] [CrossRef]
- Djerassi, C.; Hodges, R. Terpenoids. XXIII. Interconversion of thurberogenin and betulinic acid. J. Am. Chem. Soc. 1956, 78, 3534–3538. [Google Scholar] [CrossRef]
- Castellanos, L.; De Correa, R.S.; Martínez, E.; Calderon, J.S. Oleanane triterpenoids from Cedrela montana (Meliaceae). Z. Naturforsch.—Sect. C J. Biosci. 2002, 57, 575–578. [Google Scholar] [CrossRef]
- Anoda, N.; Matsunaga, M.; Kubo, M.; Harada, K.; Fukuyama, Y. Six new triterpenoids from the aerial parts of Maytenus diversifolia. Nat. Prod. Commun. 2016, 11, 1085–1088. [Google Scholar] [CrossRef] [Green Version]
- Xiao, Y.; Gou-liang, W.; Fu-Jun, G. Studies on triterpenoid constituents isolated from the roots of Sabia schumanniana. J. Integr. Plant Biol. 1994, 36, 154–158. [Google Scholar]
- Cáceres-Castillo, D.; Mena-Rejón, G.J.; Cedillo-Rivera, R.; Quijano, L. 21β-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa. Phytochemistry 2008, 69, 1057–1064. [Google Scholar] [CrossRef] [PubMed]
- Mathias, L.; Vieira, I.J.C.; Braz-Filho, R.; Rodrigues Filho, E. A New pentacyclic triterpene isolated from Myroxylon balsamum (Syn. Myroxylon peruiferum). J. Braz. Chem. Soc. 2000, 11, 195–198. [Google Scholar] [CrossRef] [Green Version]
- Chen, I.H.; Chang, F.R.; Wu, C.C.; Chen, S.L.; Hsieh, P.W.; Yen, H.F.; Du, Y.C.; Wu, Y.C. Cytotoxic triterpenoids from the leaves of Microtropis fokienensis. J. Nat. Prod. 2006, 69, 1543–1546. [Google Scholar] [CrossRef]
- Chen, I.H.; Du, Y.C.; Hwang, T.L.; Chen, I.F.; Lan, Y.H.; Yen, H.F.; Chang, F.R.; Wu, Y.C. Anti-inflammatory triterpenoids from the stems of Microtropis fokienensis. Molecules 2014, 19, 4608–4623. [Google Scholar] [CrossRef] [Green Version]
- Osorio, A.A.; Muñóz, A.; Torres-Romero, D.; Bedoya, L.M.; Perestelo, N.R.; Jiménez, I.A.; Alcamí, J.; Bazzocchi, I.L. Olean-18-ene triterpenoids from Celastraceae species inhibit HIV replication targeting NF-KB and Sp1 dependent transcription. Eur. J. Med. Chem. 2012, 52, 295–303. [Google Scholar] [CrossRef]
- Shirota, O.; Tamemura, T.; Morita, H.; Takeya, K.; Itokawa, H. Triterpenes from brazilian medicinal plant “Chuchuhuasi” (Maytenus krukovii). J. Nat. Prod. 1996, 59, 1072–1075. [Google Scholar] [CrossRef]
- Kaweetripob, W.; Mahidol, C.; Thongnest, S.; Prawat, H.; Ruchirawat, S. Polyoxygenated ursane and oleanane triterpenes from Siphonodon celastrineus. Phytochemistry 2016, 129, 58–67. [Google Scholar] [CrossRef]
- Gao, L.; Duan, L.K.; Feng, J.E.; Jiang, Y.T.; Gao, J.; Fan, J.T.; Dai, R.; Jiang, Z.Y. Four new triterpene glucosides from Salacia cochinchinensis Lour. Nat. Prod. Res. 2020, 12, 1–8. [Google Scholar] [CrossRef]
- Wang, K.W.; Wang, S.W. Chemical constituents of Euonymus bockii. Chem. Nat. Compd. 2014, 50, 948–949. [Google Scholar] [CrossRef]
- Núñez, M.J.; Ardiles, A.E.; Martínez, M.L.; Torres-Romero, D.; Jiménez, I.A.; Bazzocchi, I.L. Triterpenoids from Cassine xylocarpa and Celastrus vulcanicola (Celastraceae). Phytochem. Lett. 2013, 6, 148–151. [Google Scholar] [CrossRef]
- Niampoka, C.; Suttisri, R.; Bavovada, R.; Takayama, H.; Aimi, N. Potentially cytotoxic triterpenoids from the root bark of Siphonodon celastrineus Griff. Arch. Pharm. Res. 2005, 28, 546–549. [Google Scholar] [CrossRef]
- Wang, H.; Tian, X.; Chen, Y.Z. Chemical constituents of the aerial part of Celastrus hypoleucus. J. Chin. Chem. Soc. 2002, 49, 433–436. [Google Scholar] [CrossRef]
- Vieira Filho, S.A.; Duarte, L.P.; Silva, G.D.F.; Howarth, O.W.; Lula, L.S. 3β-(Stearyloxy)olean-12-ene from Austroplenckia populnea: Structure elucidation by 2D-NMR and quantitative 13C-NMR spectroscopy. Helv. Chim. Acta 2003, 86, 3445–3449. [Google Scholar] [CrossRef]
- Martins, L.R.; Takahashi, J.A. Rearrangement and oxidation of β-amyrin promoted by growing cells of Lecanicillium muscarinium. Nat. Prod. Res. 2010, 24, 767–774. [Google Scholar] [CrossRef] [PubMed]
- Knight, S.A. Carbon-13 NMR spectra of some tetra- and pentacyclic triterpenoids. Org. Magn. Reson. 1974, 6, 603–611. [Google Scholar] [CrossRef]
- Wang, K.W. A new fatty acid ester of triterpenoid from Celastrus rosthornianus with anti-tumor activitives. Nat. Prod. Res. 2007, 21, 669–674. [Google Scholar] [CrossRef]
- Muhammad, I.; El Sayed, K.A.; Mossa, J.S.; Al-Said, M.S.; El-Feraly, F.S.; Clark, A.M.; Hufford, C.D.; Oh, S.; Mayer, A.M.S. Bioactive 12-oleanene triterpene and secotriterpene acids from Maytenus undata. J. Nat. Prod. 2000, 63, 605–610. [Google Scholar] [CrossRef]
- Piacente, S.; Dos Santos, L.C.; Mahmood, N.; Pizza, C. Triterpenes from Maytenus macrocarpa and evaluation of their anti-HIV activity. Nat. Prod. Commun. 2006, 1, 1073–1078. [Google Scholar] [CrossRef]
- Mokoka, T.A. Isolation and Characterization of Compounds Active against Cryptococcus neoformans from Maytenus undata (Thunb.) Blakelock (Celastraceae) Leaves. Master’s Thesis, Universiteit van Pretoria, Pretoria, South Africa, 2007. [Google Scholar]
- Ye, Y.; Kinoshita, K.; Koyama, K.; Takahashi, K.; Kondo, N.; Yuasa, H. New triterpenes from Machaerocereus eruca. J. Nat. Prod. 1998, 61, 456–460. [Google Scholar] [CrossRef]
- Culioli, G.; Mathe, C.; Archier, P.; Vieillescazes, C. A lupane triterpene from Frankincense (Boswellia Sp., Burseraceae). Phytochemistry 2003, 62, 537–541. [Google Scholar] [CrossRef]
- Sati, S.C.; Sati, D.; Sharma, A.; Pandey, L.P. Chemical constituents from bark of Euonymus tingen (Celastraceae). J. Emerg. Technol. Innov. Res. 2012, 7, 1494–1497. [Google Scholar]
- Din, A.U.; Uddin, G.; Hussain, N.; Choudary, M.I. Ficusonic Acid: A new cytotoxic triterpene isolated from Maytenus royleanus (Wall. Ex M. A. Lawson) Cufodontis. J. Braz. Chem. Soc. 2013, 24, 663–668. [Google Scholar] [CrossRef]
- Luo, Y.; Xu, Q.L.; Dong, L.M.; Zhou, Z.Y.; Chen, Y.C.; Zhang, W.M.; Tan, J.W. A new ursane and a new oleanane triterpene acids from the whole plant of Spermacoce latifolia. Phytochem. Lett. 2015, 11, 127–131. [Google Scholar] [CrossRef]
- Kolak, U.; Topçu, G.; Birteksöz, S.; Ötük, G.; Ulubelen, A. Terpenoids and steroids from the roots of Salvia blepharochlaena. Turkish J. Chem. 2005, 29, 177–186. [Google Scholar]
- Ikuta, A.; Kamiya, K.; Satake, T.; Saiki, Y. Triterpenoids from callus tissue cultures of Paeonia species. Phytochemistry 1995, 38, 1203–1207. [Google Scholar] [CrossRef]
- Aguilar-Gonzalez, A.R.; Mena-Rejón, G.J.; Padilla-Montaño, N.; Toscano, A.; Quijano, L. Triterpenoids from Hippocratea excelsa. The crystal structure of 29-hydroxytaraxerol. Z. Nat. B 2005, 60, 577–584. [Google Scholar] [CrossRef] [Green Version]
- Liu, S.J.; Liao, Z.X.; Liu, C.; Yao, G.Y.; Wang, H.S. A new triterpenoid and eremophilanolide from Ligularia przewalskii. Phytochem. Lett. 2014, 9, 11–16. [Google Scholar] [CrossRef]
- Ikuta, A.; Morikawa, A. Triterpenes from Stauntonia hexaphylla Callus tissues. J. Nat. Prod. 1992, 55, 1230–1233. [Google Scholar] [CrossRef]
- Kinjc, J.E.; Miyamotc, I.; Nohara, T.; Murakamj, K.; Kids, K.; Tomimatsu, T.; Yamasaki, M. Oleanene-sapogenols from Puerariae radix. Chem. Pharm. Bull. 1985, 33, 1293–1296. [Google Scholar] [CrossRef]
- Hui-Zheng, X.; Zhi-Zhen, L.; Chohachi, K.; Soejarto, D.D.; Cordell, G.A.; Fong, H.H.S.; Hodgson, W. 3β-(3,4-Dihydroxycinnamoyl)-erythrodiol and 3β-(4-hydroxycinnamoyl)-erythrodiol from Larrea tridentata. Phytochemistry 1988, 27, 233–235. [Google Scholar] [CrossRef]
- Ragasa, C.Y.; De Luna, R.D.; Hofilena, J.G. Antimicrobial terpenoids from Pterocarpus indicus. Nat. Prod. Res. 2005, 19, 305–309. [Google Scholar] [CrossRef] [PubMed]
- Choi, S.Z.; Sang, U.C.; Kang, R.L. Pytochemical constituents of the aerial parts from solidago Virga-aurea Var. Gigantea. Arch. Pharm. Res. 2004, 27, 164–168. [Google Scholar] [CrossRef] [PubMed]
- Gonzalez, A.G.; Fraga, B.M.; Gonzalez, P.; Hernandez, M.G.; Ravelo, A.G. 13C NMR spectra of olean-18-ene derivatives. Phytochemistry 1981, 20, 1919–1921. [Google Scholar] [CrossRef]
- Mba’ning, B.M.; Lenta, B.N.; Ngouela, S.; Noungoué, D.T.; Tantangmo, F.; Talontsi, F.M.; Tsamo, E.; Laatsch, H. Salacetal, an Oleanane-type triterpene from Salacia longipes Var. Camerunensis. Z. Naturforsch.—Sect. B J. Chem. Sci. 2011, 66, 1270–1274. [Google Scholar] [CrossRef]
- Djerassi, C.; Henry, J.A.; Lemin, A.J.; Rios, T.; Thomas, G.H. Terpenoids. XXIV.1 The Structure Of The Cactus Triterpene Queretaroic Acid. J. Am. Chem. Soc. 1956, 78, 3783–3787. [Google Scholar] [CrossRef]
- Shibata, S.; Takahashi, K.; Yano, S.; Harada, M.; Saito, H.; Tamura, Y.; Kumagai, A.; Hirabayashi, K.; Yamamoto, M.; Nagata, N. Chemical modification of glycyrrhetinic acid in relation to the biological activities. Chem. Pharm. Bull. 1987, 35, 1910–1918. [Google Scholar] [CrossRef] [Green Version]
- Bandaranayake, W.M. Terpenoids of Canarium zeylanicum. Phytochemistry 1980, 19, 255–257. [Google Scholar] [CrossRef]
- El-Seedia, H.R.; Hazella, A.C.; Torssell, K.B.G. Triterpenes, lichexanthone and an acetylenic acid from Minquartia guianensis. Phytochemistry 1994, 35, 1297–1299. [Google Scholar] [CrossRef]
- Kutney, J.P.; Hewitt, G.M.; Lee, G.; Piotrowska, K.; Roberts, M.; Rettig, S.J. Studies with tissue cultures of the chinese herbal plant, Tripterygium wilfordii. isolation of metabolites of interest in rheumatoid arthritis, immunosuppression, and male contraceptive activity. Can. J. Chem. 1992, 70, 1455–1480. [Google Scholar] [CrossRef]
- Nozaki, H.; Suzuki, H.; Hirayama, T.; Kasai, R.; Wu, R.W.; Lee, K.H. Antitumour triterpenes of Maytenus diversifolia. Phytochemistry 1986, 25, 479–485. [Google Scholar] [CrossRef]
- Luis, J.G.; Andrés, L.S. New ursane type triterpenes from Salvia mellifera Greene. Nat. Prod. Lett. 1999, 13, 187–194. [Google Scholar] [CrossRef]
- Lima, F.V.; Malheiros, A.; Otuki, M.F.; Calixto, J.B.; Yunes, R.A.; Cechinel Filho, V.; Delle Monache, F. Three new triterpenes from the resinous bark of Protium kleinii and their antinociceptive activity. J. Braz. Chem. Soc. 2005, 16, 578–582. [Google Scholar] [CrossRef]
- Terazawa, S.; Uemura, Y.; Koyama, Y.; Kawakami, S.; Sugimoto, S.; Matsunami, K.; Otsuka, H.; Shinzato, T.; Kawahata, M.; Yamaguchi, K. Microtropins Q–W, Ent-Labdane Glucosides: Microtropiosides G–I, ursane-type triterpene diglucoside and flavonol glycoside from the leaves of Microtropis japonica. Chem. Pharm. Bull. 2017, 65, 930–939. [Google Scholar] [CrossRef] [Green Version]
- Nakagawa, H.; Takaishi, Y.; Fujimoto, Y.; Duque, C.; Garzon, C.; Sato, M.; Okamoto, M.; Oshikawa, T.; Ahmed, S.U. Chemical constituents from the colombian medicinal plant Maytenus laevis. J. Nat. Prod. 2004, 67, 1919–1924. [Google Scholar] [CrossRef]
- Odak, J.A.; Manguro, L.O.A.; Wong, K.C. New compounds with antimicrobial activities from Elaeodendron buchananii Stem Bark. J. Asian Nat. Prod. Res. 2018, 20, 510–524. [Google Scholar] [CrossRef]
- Tanaka, N.; Duan, H.; Takaishi, Y.; Kawazoe, K.; Goto, S. Terpenoids from Tripterygium doianum (Celastraceae). Phytochemistry 2002, 61, 93–98. [Google Scholar] [CrossRef]
- Okoye, N.N.; Ajaghaku, D.L.; Okeke, H.N.; Ilodigwe, E.E.; Nworu, C.S.; Okoye, F.B.C. b-Amyrin and a-amyrin acetate isolated from the stem bark of Alstonia boonei Display Profound Anti-Inflammatory Activity. Pharm. Biol. 2014, 2014. 52, 1478–1486. [Google Scholar] [CrossRef] [Green Version]
- Miranda, R.R.S.; Silva, G.D.F.; Duarte, L.P.; Fortes, I.C.P.; Vieira Filho, S.A. Structural determination of 3β-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy. Magn. Reson. Chem. 2006, 44, 127–131. [Google Scholar] [CrossRef]
- Tkachev, A.V.; Denisov, A.Y.; Gatilov, Y.V.; Bagryanskaya, I.Y.; Shevtsov, S.A.; Rybalova, T.V. Stereochemistry of hydrogen peroxide - acetic acid oxidation of ursolic acid and related compounds. Tetrahedron 1994, 50, 11459–11488. [Google Scholar] [CrossRef]
- Zhang, D.M.; Yu, D.Q. Structure of tripterygic acid A: A New triterpene of Tripterygium wilfordii. Planta Med. 1990, 56, 98–100. [Google Scholar] [CrossRef] [PubMed]
- Mazumder, K.; Siwu, E.R.O.; Nozaki, S.; Watanabe, Y.; Tanaka, K.; Fukase, K. Ursolic acid derivatives from bangladeshi medicinal plant, Saurauja roxburghii: Isolation and cytotoxic activity against A431 and C6 glioma cell lines. Phytochem. Lett. 2011, 4, 287–291. [Google Scholar] [CrossRef]
- Talapatra, S.K.; Sarkar, A.C.; Talapatra, B. Two pentacyclic triterpenes from Rubia cordifolia. Phytochemistry 1981, 20, 1923–1927. [Google Scholar] [CrossRef]
- Gnoatto, S.C.B.; Dassonville-Klimpt, A.; Da Nascimento, S.; Galéra, P.; Boumediene, K.; Gosmann, G.; Sonnet, P.; Moslemi, S. Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition. Eur. J. Med. Chem. 2008, 43, 1865–1877. [Google Scholar] [CrossRef] [PubMed]
- Zhang, Y.; Adelakun, T.A.; Qu, L.; Li, X.; Li, J.; Han, L.; Wang, T. New terpenoid glycosides obtained from Rosmarinus officinalis L. aerial parts. Fitoterapia 2014, 99, 78–85. [Google Scholar] [CrossRef]
- González, A.G.; Andres, L.S.; Ravelo, A.G.; Luis, J.G.; Bazzocchi, I.L.; West, J. Terpenoids from Salvia mellifera. Phytochemistry 1990, 29, 1691–1693. [Google Scholar] [CrossRef]
- Santos, J.P.; Oliveira, W.X.C.; Vieira-Filho, S.A.; Pereira, R.C.G.; Souza, G.F.; Gouveia, V.A.; de Paula Sabino, A.; Evangelista, F.C.G.; Takahashi, J.A.; Moura, M.A.F.; et al. Phytochemical and biological studies of constituents from roots of Salacia crassifolia (CELASTRACEAE). Quim. Nova 2020, 43, 558–567. [Google Scholar] [CrossRef]
- Siddiqui, S.; Hafeez, F.; Begum, S.; Siddiqui, B.S. Kaneric Acid, A new triterpene from the leaves of Nerium oleander. J. Nat. Prod. 1986, 49, 1086–1090. [Google Scholar] [CrossRef]
- Shan, H.; Wilson, W.K.; Castillo, D.A.; Matsuda, S.P.T. Are isoursenol and γ-amyrin rare triterpenes in nature or simply overlooked by usual analytical methods? Org. Lett. 2015, 17, 3986–3989. [Google Scholar] [CrossRef]
- Maia, R.M.; Barbosa, P.R.; Cruz, F.G.; Roque, N.F.; Fascio, M. Triterpenes from the resin of protium Heptaphyllum march (Burseraceae): Characterization in binary mixtures. Quim. Nova 2000, 23, 623–626. [Google Scholar] [CrossRef]
- Ding, P.; Zhou, M.Q.; Wang, K.W. A new cytotoxic triterpenoid from Microtropis triflora Merr. et Freem. Chin. Pharm. J. 2016, 24, 1557–1561. [Google Scholar]
- Tsichritzis, F.; Jakupovic, J.F. Diterpenes and other constituents from Relhania Species. Phytochemistry 1990, 29, 3173–3187. [Google Scholar] [CrossRef]
- Lai, J.; Ito, K. Studies on the constituents of Marsdenia formosana Masamune. V. Isolation and structure of a new triterpenoid, marsformosanone. Chem. Pharm. Bull. 1979, 27, 2248–2251. [Google Scholar] [CrossRef] [Green Version]
- Rodriguez Perez, F.M. Estudio fitoquímico de especies de la familia Celastraceae (flora Panameña): Maytenus blepharodes y Crossopetalum lobatuum. Ph.D. Thesis, Univesity of La Laguna, San Cristobal de La Laguna, Spain, 2000. [Google Scholar]
- Akihisa, T.; Yamamoto, K.; Tamura, T.; Nambara, T.; Iida, T.; Kimura, Y.; Chang, F.C. Triterpenoid ketones from Lingnania chungii Mcclure: Arborinone, friedelin and glutinone. Chem. Pharm. Bull. 1992, 40, 789–791. [Google Scholar] [CrossRef] [Green Version]
- Lião, L.M.; Vieira, P.C.; Rodrigues-Filho, E.; Fernandes, J.B.; Silva, M.F.G.F. Isomeric triterpenoids from Peritassa campestris. Z. Naturforsch.—Sect. C J. Biosci. 2002, 57, 403–406. [Google Scholar] [CrossRef] [PubMed]
- Sun, X.B.; Zhao, P.H.; Xu, Y.J.; Sun, L.M.; Cao, M.A.; Yuan, C.S. Chemical constituents from the roots of Polygonum bistorta. Chem. Nat. Compd. 2007, 43, 563–566. [Google Scholar] [CrossRef]
- Sakurai, N.; Yaguchi, Y.; Inoue, T. Triterpenoids from Myrica rubra. Phytochemistry 1986, 26, 217–219. [Google Scholar] [CrossRef]
- Hussein Ayoub, S.M.; Babiker, A.I. Monechmol, A. New pentacyclic triterpene from Monechma debile. Planta Med. 1984, 50, 520–521. [Google Scholar] [CrossRef] [PubMed]
- Weeratunga, G.; Kumar, V. D:B-Friedoolean-5-ene-3β,29-diol, an angular methyl oxygenated d: B-friedooleanene from Elaeodendron balae. Phytochemistry 1985, 24, 2369–2372. [Google Scholar] [CrossRef]
- Oliveira, M.L.G.; Assenco, R.A.G.; Silva, G.D.F.; Lopes, J.C.D.; Silva, F.C.; Lanna, M.C.S.; de Magalhães, J.C.; Duarte, L.P.; Vieira Filho, S.A. Cytotoxicity, anti-poliovirus activity and in silico biological evaluation of constituents from Maytenus gonoclada (Celastraceae). Int. J. Pharm. Pharm. Sci. 2014, 6, 130–137. [Google Scholar]
- Zhang, Y.; Nakamura, S.; Wang, T.; Matsuda, H.; Yoshikawa, M. The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis. Tetrahedron 2008, 64, 7347–7352. [Google Scholar] [CrossRef]
- Wang, Y.; Chen, W.S.; Wu, Z.J.; Xi, Z.X.; Chen, W.; Zhao, G.J.; Li, X.; Sun, L.N. Chemical constituents from Salacia amplifolia. Biochem. Syst. Ecol. 2011, 39, 205–208. [Google Scholar] [CrossRef]
- Yoshikawa, M.; Shimoda, H.; Nishida, N.; Takada, M.; Matsuda, H. Salacia reticulata and its polyphenolic constituents with lipase inhibitory and lipolytic activities have mild antiobesity effects in rats. J. Nutr. 2002, 132, 1819–1824. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Facundo, V.A.; Oliveira Meneguetti, D.U.; Militão, J.S.L.T.; Lima, R.A.; Hurtado, F.B.; Casseb, A.A.; Teixeira, L.F.; da Silva, I.; do, C.; da Silva, G.V.J.; et al. Chemical constituents from Maytenus guianensis Klotzsch Ex Reissek (Celastraceae) amazon rainforest. Biochem. Syst. Ecol. 2015, 58, 270–273. [Google Scholar] [CrossRef]
- Lima, R.A.; Bay-Hurtado, F.; Meneguetti, D.U.O.; Facundo, J.B.; Militão, J.S.L.T.; Matos, N.B.; Facundo, V.A. Microbiological evaluation of isolated compounds from the bark of Maytenus guianensis Klotzsch Ex Reissek (Celastraceae). Rev. Eletrônica Gestão Educ. Tecnol. Ambient. 2016, 20, 592. [Google Scholar] [CrossRef]
- Mba’ning, B.M.; Ateba, J.E.T.; Awantu, A.F.; Amaral, L.S.; Happi, G.M.; Neumann, B.; Stammler, G.; Lenta, B.N.; Ngouela, S.A.; Malavazi, I.; et al. Chemical constituents from the leaves and liana of Salacia nitida (Benth.) N.E.Br. (Celastraceae) and their antimicrobial activities. Trends Phytochem. Res. Trends Phytochem. Res 2019, 3, 2019–2083. [Google Scholar]
- Andrade, S.F.; Comunello, E.; Noldin, V.F.; Delle Monache, F.; Filho, V.C.; Niero, R. Antiulcerogenic activity of fractions and 3,15-dioxo-21α-hydroxy friedelane isolated from Maytenus robusta (Celastraceae). Arch. Pharm. Res. 2008, 31, 41–46. [Google Scholar] [CrossRef]
- Ferreira, F.L.; Rodrigues, V.G.; Silva, F.C.; Matildes, B.L.G.; Takahashi, J.A.; Silva, G.D.F.; Duarte, L.P.; Oliveira, D.M.; Filho, S.A.V. Maytenus distichophylla and Salacia crassifolia: Source of products with potential acetylcholinesterase inhibition. Rev. Bras. Farmacogn. 2017, 27, 471–474. [Google Scholar] [CrossRef]
- Vieira Filho, S.A.; Duarte, L.P.; Silva, G.D.; de, F.; Mazaro, R.; Di Stasi, L.C. Constituintes químicos e atividade antiespermatogênica em folhas de Austroplenckia populnea (Celastraceae). Rev. Bras. Farmacogn. 2002, 12, 123–124. [Google Scholar] [CrossRef] [Green Version]
- Torres-Romero, D.; King-Díaz, B.; Strasser, R.J.; Jiménez, I.A.; Lotina-Hennsen, B.; Bazzocchi, I.L. Friedelane triterpenes from Celastrus vulcanicola as photosynthetic inhibitors. J. Agric. Food Chem. 2010, 58, 10847–10854. [Google Scholar] [CrossRef]
- Pereira, R.C.G.; Evangelista, F.C.G.; dos Santos Júnior, V.S.; de Paula Sabino, A.; Maltarollo, V.G.; de Freitas, R.P.; Duarte, L.P. Cytotoxic activity of triterpenoids from Cheiloclinium cognatum branches against chronic and acute leukemia cell Lines. Chem. Biodivers. 2020, 17, e2000773. [Google Scholar] [CrossRef]
- Tu, G.H.; Shi, X.W.; Zhao, Y.; Zheng, C.D.; Gao, J.M. Triterpenes of Euonymus alatus and their cytotoxic activity; Chem. Nat. Compound. 2011, 47, 656–657. [Google Scholar] [CrossRef]
- Wang, K.W.; Ju, X.Y.; Zhang, C.C.; Zhang, J.Y. Phytochemical and chemotaxonomic study on Microtropis triflora. Biochem. Syst. Ecol. 2014, 52, 1–3. [Google Scholar] [CrossRef]
- Arciniegas, A.; Ramírez Apan, M.T.; Pérez-Castorena, A.L.; De Vivar, A.R. Anti-inflammatory constituents of Mortonia greggii Gray. Zeitschrift fur Naturforsch. - Sect. C J. Biosci. 2004, 59, 237–243. [Google Scholar] [CrossRef] [PubMed]
- He, M.F.; Liu, L.; Ge, W.; Shaw, P.C.; Jiang, R.; Wu, L.W.; But, P.P.H. Antiangiogenic activity of Tripterygium wilfordii and its terpenoids. J. Ethnopharmacol. 2009, 121, 61–68. [Google Scholar] [CrossRef]
- de Figueiredo, P.T.R.; Silva, E.W.R.; Cordeiro, L.V.; Barros, R.P.C.; Lima, E.; Scotti, M.T.; da Silva, M.S.; Tavares, J.F.; de, O.; Costa, V.C. Lupanes and friedelanes, the first chemical constituents of the aerial parts of Maytenus erythroxylon Reissek. Phytochem. Lett. 2021, 45, 19–24. [Google Scholar] [CrossRef]
- Andrade, S.F.; Silva Filho, A.A.; Resende, D.D.O.; Silva, M.L.A.; Cunha, W.R.; Nanayakkara, N.P.D.; Bastos, J.K. Antileishmanial, antimalarial and antimicrobial activities of the extract and isolated compounds from Austroplenckia populnea (Celastraceae). Z. Nat. C 2008, 63, 497–502. [Google Scholar] [CrossRef]
- Duarte, L.P.; Vieira Filho, S.A.; Silva, G.D.D.F.; De Sousa, J.R.; Pinto, A.D.S. Anti-trypanosomal activity of pentacyclic triterpenes isolated from Austroplenckia populnea (Celastraceae). Rev. Inst. Med. Trop. Sao Paulo 2002, 44, 109–112. [Google Scholar] [CrossRef] [Green Version]
- Sousa, J.R.; Silva, G.D.F.; Miyakoshi, T.; Chen, C.L. Constituents of the root wood of Austroplenckia populnea Var. Ovata. J. Nat. Prod. 2006, 69, 1225–1227. [Google Scholar] [CrossRef]
- Lindsey, K.L.; Budesinsky, M.; Kohout, L.; van Staden, J. Antibacterial activity of maytenonic acid isolated from the root-bark of Maytenus senegalensis. S. Afr. J. Bot. 2006, 2006. 72, 473–477. [Google Scholar] [CrossRef] [Green Version]
- Kamtcha, D.W.; Tene, M.; Bedane, K.G.; Knauer, L.; Strohmann, C.; Tane, P.; Kusari, S.; Spiteller, M. Cardenolides from the stem bark of Salacia staudtiana. Fitoterapia 2018, 127, 402–409. [Google Scholar] [CrossRef] [PubMed]
- Aguilar, M.G.; Sousa, G.F.; Evangelista, F.C.G.; Sabino, A.P.; Vieira Filho, S.A.; Duarte, L.P. Imines and lactones derived from friedelanes and their cytotoxic activity. Nat. Prod. Res. 2020, 34, 810–815. [Google Scholar] [CrossRef] [PubMed]
- Morales, S.A.T.; Aguilar, M.G.; Pereira, R.C.G.; Duarte, L.P.; Sousa, G.F.; de Oliveira, D.M.; Evangelista, F.C.G.; Sabino, A.P.; Viana, R.O.; Alves, V.S.; et al. Constituents from roots of Maytenus distichophylla, antimicrobial activity and toxicity for cells and Caenorhabditis elegans. Quim. Nova 2020, 43, 1066–1073. [Google Scholar] [CrossRef]
- El Deeb, K.S.; Al-Haidari, R.A.; Mossa, J.S.; Ateya, A.M. Phytochemical and pharmacological studies of Maytenus forsskaoliana. Saudi Pharm. J. 2003, 11, 184–191. [Google Scholar]
- Martucciello, S.; Balestrieri, M.L.; Felice, F.; Estevam, C.; dos, S.; Sant’Ana, A.E.G.; Pizza, C.; Piacente, S. Effects of triterpene derivatives from Maytenus rigida on VEGF-induced kaposi’s sarcoma cell proliferation. Chem. Biol. Interact. 2010, 183, 450–454. [Google Scholar] [CrossRef] [PubMed]
- Valladao, F.N.; De Miranda, R.R.S.; De Oliveira, G.S.; Silva, G.D.F.; Duarte, L.P.; Filho, S.A.V. Constituents of fruit pulp of Maytenus salicifolia and complete 1D/2D NMR data of 3β-hydroxy-D:B-friedo-olean-5-ene. Chem. Nat. Compd. 2010, 46, 686–691. [Google Scholar] [CrossRef]
- Mokoka, T.A.; McGaw, L.J.; Mdee, L.K.; Bagla, V.P.; Iwalewa, E.O.; Eloff, J.N. Antimicrobial activity and cytotoxicity oftriterpenes isolated from leaves of Maytenus undata (Celastraceae). BMC Complement. Altern. Med. 2013, 13, 1–9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Silva, F.M.A.; Paz, W.H.P.; Vasconcelos, L.S.F.; da Silva, A.L.B.; da Silva-Filho, F.A.; de Almeida, R.A.; de Souza, A.D.L.; Pinheiro, M.L.B.; Koolen, H.H.F. Chemical constituents from Salacia impressifolia (Miers) A. C. Smith collected at the amazon rainforest. Biochem. Syst. Ecol. 2016, 68, 77–80. [Google Scholar] [CrossRef]
- de Souza e Silva, S.R.; de Fátima Silva, G.D.; de Almeida Barbosa, L.C.; Duarte, L.P.; King-Diaz, B.; Archundia-Camacho, F.; Lotina-Hennsen, B. Uncoupling and inhibition properties of 3,4-seco-friedelan-3-oic acid isolated from Maytenus imbricata. Pestic. Biochem. Physiol. 2007, 87, 109–114. [Google Scholar] [CrossRef]
- Yelani, T.; Hussein, A.A.; Meyer, J.J.M. Isolation and identification of poisonous triterpenoids from Elaeodendron croceum. Nat. Prod. Res. 2010, 24, 1418–1425. [Google Scholar] [CrossRef]
- Oliveira, D.M.; Silva, G.D.F.; Duarte, L.P.; Vieira Filho, S.A. Chemical constituents isolated from roots of Maytenus acanthophylla Reissek (Celastraceae). Biochem. Syst. Ecol. 2006, 34, 661–665. [Google Scholar] [CrossRef]
- Silva, T.M.; Carvalho, C.M.; Lima, R.A.; Facundo, V.A.; da Cunha, R.M.; Meneguetti, D.U.; de, O. Antibacterial activity of fractions and isolates of Maytenus guianensis Klotzsch Ex Reissek (Celastraceae) chichuá amazon. Rev. Soc. Bras. Med. Trop. 2018, 51, 533–536. [Google Scholar] [CrossRef] [PubMed]
- Pina, E.S.; Silva, D.B.; Teixeira, S.P.; Coppede, J.S.; Furlan, M.; França, S.C.; Lopes, N.P.; Pereira, A.M.S.; Lopes, A.A. Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging. Sci. Rep. 2016, 6, 22627. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Mohamad, T.A.S.T.; Naz, H.; Jalal, R.S.; Hussin, K.; Rahman, M.R.A.; Adam, A.; Weber, J.F.F. Chemical and pharmacognostical characterization of two malaysian plants both known as ajisamat. Rev. Bras. Farmacogn. 2013, 23, 724–730. [Google Scholar] [CrossRef] [Green Version]
- Furukawa, M.; Furukawa, M.; Makino, M.; Uchiyama, T.; Fujimoto, Y.; Matsuzaki, K. New sesquiterpene pyridine alkaloids from Hippocratea excelsa. Nat. Prod. Commun. 2018, 13, 957–960. [Google Scholar] [CrossRef] [Green Version]
- Taddeo, V.; Castillo, U.; Martínez, M.; Menjivar, J.; Jiménez, I.; Núñez, M.; Bazzocchi, I. Development and validation of an HPLC-PDA method for biologically active quinonemethide triterpenoids isolated from Maytenus chiapensis. Medicines 2019, 6, 36. [Google Scholar] [CrossRef] [Green Version]
- Santos, V.A.F.F.M.; Leite, K.M.; Da Costa Siqueira, M.; Regasini, L.O.; Martinez, I.; Nogueira, C.T.; Galuppo, M.K.; Stolf, B.S.; Pereira, A.M.S.; Cicarelli, R.M.B.; et al. Antiprotozoal activity of quinonemethide triterpenes from Maytenus ilicifolia (Celastraceae). Molecules 2013, 18, 1053–1062. [Google Scholar] [CrossRef]
- Mejía-Manzano, L.A.; Barba-Dávila, B.A.; Gutierrez-Uribe, J.A.; Escalante-Vázquez, E.J.; Serna-Saldívar, S.O. Extraction and isolation of antineoplastic pristimerin from Mortonia greggii (Celastraceae). Nat. Prod. Commun. 2015, 10, 1923–1928. [Google Scholar] [CrossRef] [Green Version]
- Nizer, W.S.C.; Ferraz, A.C.; Moraes, T.; de, F.S.; Lima, W.G.; dos Santos, J.P.; Duarte, L.P.; Ferreira, J.M.S.; de Brito Magalhães, C.L.; Vieira-Filho, S.A.; et al. Pristimerin isolated from Salacia crassifolia (Mart. Ex. Schult.) G. Don. (Celastraceae) roots as a potential antibacterial agent against Staphylococcus aureus. J. Ethnopharmacol. [CrossRef]
- Ruphin, F.P.; Baholy, R.; Emmanue, A.; Amelie, R.; Martin, M.T.; Koto-te-Nyiwa, N. Antiplasmodial, cytotoxic activities and characterization of a new naturally occurring quinone methide pentacyclic triterpenoid derivative isolated from Salacia leptoclada Tul. (Celastraceae) originated from madagascar. Asian Pac. J. Trop. Biomed. 2013, 3, 780–784. [Google Scholar] [CrossRef] [Green Version]
- Rodrigues-Filho, E.; Barros, F.A.P.; Fernandes, J.B.; Braz-Filho, R. Detection and identification of quinonemethide triterpenes in Peritassa campestris by Mass Spectrometry. Rapid Commun. Mass Spectrom. 2002, 16, 627–633. [Google Scholar] [CrossRef] [PubMed]
- Silva, F.C.; Guedes, F.A.F.; Franco, M.W.; Barbosa, F.A.R.; Marra, C.A.; Duarte, L.P.; Silva, G.D.F.; Vieira-Filho, S.A. Algistatic effect of a quinonamethide triterpene on Microcystis novacekii. J. Appl. Phycol. 2013, 25, 1723–1728. [Google Scholar] [CrossRef]
- Meneguetti, D.U.O.; Lima, R.A.; Hurtado, F.B.; Passarini, G.M.; Macedo, S.R.A.; de Barros, N.B.; Oliveira, F.A.D.S.; de Medeiros, P.S.D.M.; Militão, J.S.L.T.; Nicolete, R.; et al. Screening of the in vitro antileishmanial activities of compounds and secondary metabolites isolated from Maytenus guianensis Klotzsch Ex Reissek (Celastraceae) chichuá amazon. Rev. Soc. Bras. Med. Trop. 2016, 49, 579–585. [Google Scholar] [CrossRef] [Green Version]
- Moujir, L.; López, M.R.; Reyes, C.P.; Jiménez, I.A.; Bazzocchi, I.L. Structural requirements for antimicrobial activity of phenolic nor-triterpenes from Celastraceae species. Appl. Sci. 2019, 9, 2957. [Google Scholar] [CrossRef] [Green Version]
- León, L.; Beltrán, B.; Moujir, L. Antimicrobial activity of 6-oxophenolic triterpenoids. Mode of action against Bacillus subtilis. Planta Med. 2005, 71, 313–319. [Google Scholar] [CrossRef] [PubMed]
- An, H.; Zhu, Y.; Xu, W.; Liu, Y.; Zhang, J.; Lin, Z. Evaluation of immunosuppressive activity of demethylzeylasteral in a beagle dog kidney transplantation model. Cell Biochem. Biophys. 2015, 73, 673–679. [Google Scholar] [CrossRef] [PubMed]
- Mthethwa, N.S.; Oyedeji, B.A.O.; Obi, L.C.; Aiyegoro, O.A. Anti-Staphylococcal, anti-HIV and cytotoxicity studies of four south african medicinal plants and isolation of bioactive compounds from Cassine transvaalensis (Burtt. Davy) codd. BMC Complement. Altern. Med. 2014, 14, 1–9. [Google Scholar] [CrossRef] [Green Version]
- Jeong, S.Y.; Zhao, B.T.; Kim, Y.H.; Min, B.S.; Woo, M.H. Cytotoxic and antioxidant compounds isolated from the cork Of Euonymus alatus Sieb. Nat. Prod. Sci. 2013, 19, 366–371. [Google Scholar]
- Li, C.; Li, B.; Ye, J.; Zhang, W.; Shen, Y.; Yin, J. A new norditerpenoid from Euonymus grandiflorus Wall. Nat. Prod. Res. 2013, 27, 1716–1721. [Google Scholar] [CrossRef] [PubMed]
- Pimenta, A.A.; De Souza, S.S.R.; De Fátima Silva, G.D.; De Almeida Barbosa, L.C.; Ellena, J.; Doriguetto, A.C. A Pentacyclic triterpene from Maytenus imbricata: Structure elucidation by X-ray crystallography. Struct. Chem. 2006, 17, 149–153. [Google Scholar] [CrossRef]
- Chander, M.P.; Kumar, K.V.; Shriram, A.N.; Vijayachari, P. Anti-leptospiral activities of an endemic plant Glyptopetalum calocarpum (Kurz.) prain used as a medicinal plant by nicobarese of andaman and nicobar islands. Nat. Prod. Res. 2015, 29, 1575–1577. [Google Scholar] [CrossRef] [PubMed]
- Bhavita, D.; Lakshmi, B.; Zaveri, M. Phytochemical investigation, isolation and characterization of betulin from leaf of Gymnosporia montana. Int. J. Pharm. Sci. Res. 2021, 12, 1752–1756. [Google Scholar] [CrossRef]
- Alarcon, J.; Cespedes, C.L. Triterpenes and β-agarofurane sesquiterpenes from tissue culture of Maytenus boaria. Bol. Latinoam. Caribe Plantas Med. Aromat. 2016, 15, 206–214. [Google Scholar]
- Moo-Puc, J.A.; Martín-Quintal, Z.; Mirón-López, G.; Moo-Puc, R.E.; Quijano, L.; Mena-Rejón, G.J. Isolation and antitrichomonal activity of the chemical constituents of the leaves of Maytenus phyllanthoides Benth. (Celastraceae). Quim. Nova 2014, 37, 85–88. [Google Scholar] [CrossRef] [Green Version]
- Herrera-España, A.D.; Mena-Rejón, G.J.; Hernández-Ortega, S.; Quijano, L.; Mirón-Lópeza, G. Crystal structure of ochraceolide a isolated from Elaeodendron trichotomum (Turcz.) Lundell. Acta Crystallogr. Sect. E Crystallogr. Commun. 2017, 73, 1475–1478. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Zhao, Q.; Li, H.M.; Chen, X.Q.; Li, R.T.; Liu, D. Terpenoids from Tripterygium hypoglaucum and their anti-inflammatory activity. Chem. Nat. Compd. 2018, 54, 471–474. [Google Scholar] [CrossRef]
- Chen, X.Q.; Zan, K.; Wang, Q. Olean-type triterpenes of Celastrus orbiculatus. Biochem. Syst. Ecol. 2012, 44, 338–340. [Google Scholar] [CrossRef]
- Doriguetto, A.C.; Duarte, L.P.; Ellena, J.A.; Silva, G.D.F.; Mascarenhas, Y.P.; Cota, A.B. 3-Oxoolean-12-en-20-yl α-methylcarboxylate. Acta Crystallogr. Sect. E Struct. Rep. Online 2003, 59, 164–166. [Google Scholar] [CrossRef]
- Khan, H.; Khan, I.; Shah, M.; Shahidullah, A.; Khalil, N.; Aziz, A.; Wajid, A.; Jan, H.; Rahman, I. Antibacterial and antifungal activities of compounds isolated from Gymnosporia royleana (Celastraceae). West Indian Med. J. 2017, 68, 136–141. [Google Scholar] [CrossRef]
- Singha, S.; Yotmanee, P.; Yahuafai, J.; Siripong, P.; Prabpai, S.; Sutthivaiyakit, S. Siphonagarofurans A-J: Poly-o-acylated β-dihydroagarofuran sesquiterpenoids from the fruits of Siphonodon celastrineus. Phytochemistry 2020, 174, 112345. [Google Scholar] [CrossRef]
- Chang, X.; Wang, Z.Y.; Chen, X.; Ma, Y.N.; Zhang, H.Y.; Zhao, T.Z. Two new sesquiterpene pyridine alkaloids from root barks of Celastrus angulatus. J. Asian Nat. Prod. Res. 2019, 21, 1043–1051. [Google Scholar] [CrossRef] [PubMed]
- Núñez, M.J.; Ardiles, A.E.; Martínez, M.L.; Torres-Romero, D.; Jiménez, I.A.; Bazzocchi, I.L. Unusual D:B-Friedobaccharane and oxygenated friedelane-type triterpenoids from Salvadorean Celastraceae Species. Phytochem. Lett. 2012, 5, 244–248. [Google Scholar] [CrossRef]
- Yan, L.H.; Liu, X.Q.; Zhu, H.; Xu, Q.R.; Wang, W.M.; Zhang, S.M.; Zhang, Q.W.; Zhang, S.S.; Wang, Z.M. Chemical Constituents of Euonymus fortunei. J. Asian Nat. Prod. Res. 2015, 17, 952–958. [Google Scholar] [CrossRef] [PubMed]
C | F1 | F2 | F3 | F4 a | F6 b | F7 | F8 b | F9 | F10 | F11 |
---|---|---|---|---|---|---|---|---|---|---|
1 | 25.0 | 22.3 | 22.3 | 22.3 | 22.8 | 22.3 | 202.8 | 22.2 | 202.4 | 22.8 |
2 | 41.6 | 41.4 | 41.2 | 41.4 | 42.7 | 41.5 | 60.6 | 41.4 | 60.4 | 41.9 |
3 | 213.3 | 212.7 | 212.3 | 212.7 | 211.9 | 213.0 | 204.0 | 213.0 | 203.8 | 212.1 |
4 | 52.1 | 58.1 | 58.0 | 58.1 | 57.8 | 58.2 | 58.9 | 58.1 | 58.6 | 58.3 |
5 | 43.1 | 41.8 | 41.8 | 41.9 | 42.4 | 42.0 | 38.1 | 42.0 | 37.4 | 42.4 |
6 | 42.2 | 41.1 | 40.8 | 41.2 | 41.7 | 41.3 | 41.5 | 41.1 | 40.2 | 41.5 |
7 | 17.9 | 18.3 | 18.4 | 18.1 | 22.7 | 20.0 | 20.4 | 18.3 | 17.9 | 18.9 |
8 | 52.8 | 51.3 | 52.0 | 52.9 | 54.4 | 53.5 | 52.4 | 49.9 | 48.8 | 50.8 |
9 | 44.1 | 38.3 | 38.1 | 38.2 | 38.0 | 37.8 | 37.1 | 37.4 | 36.6 | 38.0 |
10 | 60.1 | 59.3 | 59.1 | 59.4 | 59.8 | 59.4 | 72.3 | 59.5 | 71.5 | 59.8 |
11 | 76.9 | 47.0 | 47.3 | 47.4 | 37.1 | 35.6 | 34.9 | 34.9 | 33.7 | 35.6 |
12 | 42.0 | 72.1 | 71.2 | 72.7 | 31.6 | 31.2 | 29.9 | 29.3 | 29.1 | 30.4 |
13 | 41.1 | 44.8 | 45.7 | 45.3 | 41.0 | 40.6 | 39.7 | 39.9 | 39.3 | 39.9 |
14 | 38.2 | 41.1 | 40.8 | 40.4 | 46.8 | 44.1 | 42.9 | 39.2 | 38.8 | 40.2 |
15 | 32.4 | 31.6 | 50.3 | 33.4 | 75.5 | 74.6 | 31.3 | 36.8 | 38.7 | 40.2 |
16 | 35.9 | 35.9 | 218.3 | 36.1 | 48.4 | 48.4 | 78.1 | 74.3 | 75.5 | 75.7 |
17 | 30.0 | 31.3 | 45.7 | 30.8 | 30.9 | 30.2 | 35.0 | 41.0 | 37.0 | 37.7 |
18 | 42.5 | 44.3 | 45.4 | 44.2 | 42.6 | 41.6 | 45.5 | 41.7 | 45.6 | 46.66 |
19 | 35.4 | 31.7 | 38.5 | 38.4 | 32.2 | 35.6 | 35.7 | 33.7 | 33.8 | 34.3 |
20 | 28.1 | 33.3 | 27.8 | 28.4 | 28.4 | 28.1 | 28.1 | 28.0 | 27.7 | 28.6 |
21 | 32.7 | 29.9 | 31.5 | 32.7 | 36.2 | 31.9 | 31.8 | 33.8 | 33.2 | 35.0 |
22 | 39.2 | 38.1 | 30.7 | 39.6 | 39.5 | 38.7 | 34.9 | 19.8 | 26.2 | 27.8 |
23 | 6.9 | 6.8 | 6.8 | 6.8 | 7.2 | 6.8 | 7.3 | 6.7 | 7.0 | 7.5 |
24 | 14.8 | 14.6 | 14.6 | 14.6 | 14.4 | 14.5 | 15.8 | 14.7 | 15.7 | 15.1 |
25 | 12.9 | 19.2 | 18.7 | 19.3 | 16.9 | 17.9 | 18.2 | 19.2 | 18.8 | 19.4 |
26 | 20.1 | 18.7 | 20.5 | 20.5 | 65.8 | 14.0 | 63.2 | 16.5 | 16.8 | 17.7 |
27 | 19.5 | 11.6 | 9.0 | 11.6 | 19.7 | 18.7 | 20.9 | 19.7 | 19.1 | 20.0 |
28 | 32.0 | 31.7 | 27.3 | 31.8 | 32.7 | 32.6 | 25.9 | 71.3 | 29.9 | 31.0 |
29 | 31.7 | 71.6 | 31.3 | 34.9 | 35.7 | 30.9 | 37.8 | 37.0 | 31.8 | 32.7 |
30 | 35.0 | 29.2 | 35.0 | 31.9 | 31.0 | 35.6 | 30.4 | 31.8 | 36.2 | 36.9 |
C=O | 171.3 | |||||||||
OCH3 | 21.3 | |||||||||
Ref | [35] | [36] | [37] | [38] | [39] | [40] | [41] | [42] | [43] | [44] |
C | F12 a | F13 | F14 b | F15 a | F16 | F17 | F18 | F19 | F20 | F21 |
1 | 21.7 | 22.2 | 22.3 | 68.8 | 75.8 | 74.0 | 71.4 | 202.7 | 22.3 | 22.3 |
2 | 40.9 | 41.4 | 41.6 | 51.9 | 35.0 | 30.1 | 52.7 | 60.6 | 41.5 | 41.3 |
3 | 211.1 | 212.8 | 212.5 | 210.4 | 212.3 | 213.2 | 211.3 | 204.1 | 213.2 | 212.7 |
4 | 57.4 | 58.0 | 58.3 | 57.5 | 55.9 | 53.3 | 59.1 | 59.1 | 58.2 | 58.1 |
5 | 41.5 | 42.1 | 42.3 | 39.4 | 43.3 | 42.7 | 43.9 | 37.8 | 42.0 | 41.8 |
6 | 40.5 | 41.1 | 41.4 | 41.8 | 41.8 | 41.2 | 34.3 | 40.6 | 41.2 | 40.2 |
7 | 18.0 | 18.4 | 18.6 | 17.8 | 17.9 | 18.2 | 18.8 | 18.1 | 18.0 | 21.2 |
8 | 53.0 | 53.3 | 53.5 | 53.4 | 53.8 | 53.0 | 53.9 | 50.6 | 51.2 | 44.7 |
9 | 36.9 | 37.4 | 37.6 | 36.6 | 42.0 | 36.9 | 38.6 | 37.3 | 37.5 | 37.9 |
10 | 58.7 | 59.3 | 59.7 | 64.8 | 57.4 | 52.4 | 62.6 | 71.9 | 59.5 | 59.0 |
11 | 35.1 | 35.6 | 35.8 | 37.0 | 30.2 | 35.9 | 35.7 | 34.2 | 35.3 | 36.8 |
12 | 30.0 | 30.7 | 30.8 | 29.9 | 31.0 | 30.5 | 30.4 | 29.8 | 30.2 | 33.9 |
13 | 39.6 | 40.1 | 39.3 | 39.4 | 39.8 | 39.8 | 39.8 | 38.8 | 39.0 | 47.5 |
14 | 38.8 | 39.1 | 40.1 | 39.3 | 37.5 | 38.4 | 38.5 | 38.7 | 38.8 | 56.3 |
15 | 44.7 | 44.3 | 44.4 | 33.2 | 32.7 | 32.1 | 32.7 | 30.5 | 30.4 | 213.3 |
16 | 75.7 | 74.4 | 75.6 | 36.0 | 36.0 | 35.4 | 36.2 | 35.9 | 36.1 | 53.8 |
17 | 40.5 | 36.4 | 32.1 | 30.4 | 29.9 | 30.0 | 30.2 | 32.5 | 32.5 | 34.0 |
18 | 39.9 | 44.1 | 44.8 | 41.9 | 42.7 | 42.7 | 43.0 | 44.2 | 44.3 | 45.3 |
19 | 29.3 | 30.4 | 35.8 | 30.8 | 35.3 | 28.9 | 35.5 | 36.0 | 35.9 | 38.9 |
20 | 32.7 | 33.1 | 28.0 | 33.2 | 28.1 | 33.4 | 28.2 | 34.3 | 34.4 | 28.0 |
21 | 27.7 | 27.5 | 32.1 | 27.8 | 32.7 | 28.2 | 33.0 | 74.3 | 74.3 | 71.7 |
22 | 29.5 | 36.4 | 36.0 | 39.7 | 39.3 | 28.1 | 39.3 | 47.0 | 47.0 | 46.3 |
23 | 6.4 | 6.9 | 6.8 | 7.1 | 6.7 | 6.9 | 6.9 | 7.3 | 6.8 | 6.8 |
24 | 14.0 | 14.6 | 14.7 | 16.0 | 14.7 | 14.3 | 17.4 | 16.0 | 14.6 | 14.9 |
25 | 17.5 | 18.1 | 18.2 | 18.4 | 63.0 | 17.9 | 19.2 | 18.2 | 17.7 | 18.9 |
26 | 21.1 | 20.1 | 20.1 | 18.6 | 20.1 | 20.0 | 20.2 | 17.8 | 18.2 | 15.4 |
27 | 19.3 | 21.4 | 21.5 | 21.0 | 18.6 | 18.7 | 18.7 | 19.3 | 19.3 | 12.1 |
28 | 66.7 | 25.4 | 24.9 | 32.1 | 32.2 | 32.2 | 32.2 | 33.1 | 33.2 | 31.5 |
29 | 74.0 | 74.4 | 30.8 | 74.5 | 35.0 | 28.9 | 31.8 | 24.9 | 31.9 | 31.4 |
30 | 25.4 | 25.7 | 35.5 | 25.9 | 31.7 | 72.0 | 34.9 | 31.8 | 24.9 | 33.8 |
Ref | [45] | [46] | [27] | [45] | [47] | [48] | [48] | [49] | [50] | [51] |
C | F22 | F23 | F24 | F25 | F26 | F27 | F28 b | F29 | F30 | F31 |
1 | 22.4 | 202.8 | 24.7 | 24.6 | 202.8 | 22.5 | 22.4 | 22.3 | 202.7 | 22.1 |
2 | 41.6 | 60.5 | 42.6 | 42.5 | 60.6 | 41.6 | 41.6 | 41.5 | 60.6 | 41.3 |
3 | 213.2 | 230.7 | 212.9 | 212.8 | 204.1 | 213.3 | 211.7 | 212.9 | 204.1 | 213.6 |
4 | 58.4 | 59.7 | 58.5 | 58.5 | 58.9 | 58.4 | 57.9 | 58.3 | 59.0 | 57.8 |
5 | 42.4 | 37.5 | 42.4 | 42.4 | 38.1 | 42.3 | 42.1 | 42.1 | 37.2 | 41.9 |
6 | 41.4 | 38.5 | 41.8 | 41.7 | 41.7 | 41.5 | 41.2 | 41.4 | 40.6 | 41.0 |
7 | 18.4 | 17.0 | 17.9 | 18.0 | 20.4 | 18.6 | 18.4 | 18.3 | 18.0 | 18.1 |
8 | 53.4 | 45.2 | 53.7 | 53.9 | 52.0 | 53.8 | 53.2 | 53.5 | 51.5 | 52.2 |
9 | 37.6 | 37.1 | 42.0 | 42.0 | 37.1 | 37.6 | 37.5 | 37.5 | 37.8 | 37.3 |
10 | 59.6 | 69.0 | 60.7 | 60.7 | 72.4 | 59.7 | 59.2 | 59.6 | 71.9 | 59.1 |
11 | 35.8 | 35.8 | 29.9 | 30.0 | 35.0 | 37.8 | 35.7 | 35.5 | 33.4 | 35.3 |
12 | 30.8 | 26.5 | 31.2 | 31.4 | 29.9 | 24.1 | 30.5 | 30.0 | 29.7 | 29.9 |
13 | 39.8 | 38.1 | 39.7 | 39.9 | 39.7 | 45.4 | 40.1 | 39.6 | 39.2 | 39.1 |
14 | 38.4 | 40.0 | 37.7 | 37.9 | 42.0 | 38.4 | 38.2 | 38.4 | 39.1 | 38.0 |
15 | 32.5 | 34.7 | 32.7 | 33.0 | 20.1 | 32.2 | 29.5 | 31.1 | 31.2 | 31.3 * |
16 | 38.8 | 36.8 | 36.0 | 35.0 | 35.3 | 36.2 | 32.6 | 29.2 | 29.0 | 29.0 |
17 | 30.0 | 30.8 | 30.1 | 33.1 | 30.4 | 30.3 | 36.6 | 35.1 | 35.1 | 35.1 |
18 | 42.8 | 44.0 | 42.7 | 41.9 | 43.5 | 43.3 | 39.0 | 38.9 | 39.3 | 39.2 |
19 | 36.0 | 35.4 | 35.3 | 37.0 | 35.4 | 37.1 | 29.8 | 31.5 | 34.4 | 34.4 |
20 | 33.9 | 28.3 | 28.1 | 42.7 | 28.3 | 28.5 | 33.6 | 33.3 | 28.1 | 27.9 |
21 | 75.8 | 32.5 | 32.7 | 218.7 | 32.9 | 32.6 | 29.2 | 30.2 | 31.4 | 31.4 * |
22 | 48.6 | 38.9 | 39.2 | 55.0 | 39.1 | 40.1 | 33.0 | 28.3 | 34.3 | 33.2 |
23 | 6.9 | 7.5 | 7.0 | 7.0 | 7.3 | 7.1 | 7.2 | 6.8 | 7.3 | 6.7 |
24 | 14.8 | 15.7 | 14.7 | 14.7 | 15.7 | 14.9 | 14.7 | 14.7 | 15.9 | 14.5 |
25 | 18.0 | 67.1 | 63.0 | 62.7 | 17.8 | 18.2 | 18.0 | 18.2 | 18.1 | 18.0 |
26 | 20.8 | 69.9 | 20.1 | 20.9 | 64.0 | 22.3 | 20.1 | 18.6 | 19.1 | 18.9 |
27 | 18.9 | 19.3 | 18.5 | 18.4 | 19.7 | 63.4 | 19.0 | 19.1 | 19.2 | 19.1 |
28 | 34.5 | 30.0 | 32.1 | 33.6 | 31.7 | 32.8 | 67.1 | 69.0 | 68.0 | 67.0 |
29 | 34.9 | 31.4 | 35.0 | 28.8 | 34.5 | 35.8 | 73.6 | 28.6 | 34.2 | 32.9 |
30 | 24.1 | 35.1 | 31.7 | 25.0 | 32.0 | 30.6 | 27.5 | 73.4 | 32.8 | 34.2 |
Ref | [52] | [53] | [48] | [54] | [41] | [55] | [56] | [57] | [58] | [57] |
C | F32 | F34 | F35 | F36 | F37 | F38 | F39c | F40 | F41 | F42 |
1 | 22.7 | 22.2 | 22.5 | 25.9 | 32.4 | 31.7 | 28.2 | 24.8 | 202.7 | 22.3 |
2 | 41.4 | 41.3 | 41.6 | 75.4 | 76.9 | 74.4 | 71.0 | 42.6 | 60.6 | 41.5 |
3 | 213.4 | 212.2 | 212.8 | 105.6 | 212.0 | 209.7 | 199.6 | 212.3 | 204.1 | 212.9 |
4 | 58.6 | 57.9 | 58.6 | 47.4 | 52.7 | 52.4 | 127.1 | 58.6 | 59.1 | 58.3 |
5 | 42.3 | 42.0 | 42.4 | 46.8 | 42.7 | 54.2 | 158.8 | 42.3 | 37.8 | 42.1 |
6 | 41.9 | 40.8 | 41.7 | 33.3 | 40.8 | 36.7 | 30.4 | 41.6 | 40.6 | 41.4 |
7 | 18.4 | 18.5 | 18.5 | 19.2 | 17.5 | 19.4 | 20.3 | 18.2 | 18.0 | 18.3 |
8 | 53.2 | 52.3 | 53.7 | 49.8 | 52.7 | 49.6 | 47.3 | 54.0 | 52.0 | 53.1 |
9 | 38.0 | 37.5 | 37.8 | 37.1 | 38.0 | 37.5 | 37.2 | 41.1 | 37.2 | 37.5 |
10 | 59.6 | 59.0 | 59.9 | 53.2 | 52.7 | 55.7 | 51.8 | 60.3 | 71.9 | 59.6 |
11 | 35.7 | 35.2 | 36.0 | 34.3 | 35.6 | 34.5 | 32.4 | 30.1 | 34.5 | 35.7 |
12 | 31.0 | 28.9 | 30.8 | 29.0 | 30.2 | 29.4 | 28.9 | 30.7 | 30.1 | 29.4 |
13 | 37.6 | 39.0 | 38.6 | 39.2 | 39.4 | 40.2 | 39.2 | 39.9 | 39.6 | 39.9 |
14 | 39.3 | 40.6 | 40.3 | 39.1 | 38.9 | 39.4 | 39.5 | 37.9 | 38.3 | 38.2 |
15 | 28.6 | 50.2 | 33.0 | 29.1 | 32.7 | 28.3 | 27.9 | 33.1 | 32.1 | 32.2 |
16 | 32.8 | 218.4 | 36.2 | 36.2 | 36.5 | 29.6 | 35.1 | 34.9 | 35.8 | 29.7 |
17 | 48.6 | 45.7 | 30.8 | 30.1 | 29.8 | 44.8 | 37.7 | 33.0 | 30.0 | 30.0 |
18 | 35.9 | 43.2 | 42.3 | 44.5 | 42.4 | 45.4 | 43.4 | 41.8 | 42.6 | 42.9 |
19 | 29.8 | 30.1 | 39.8 | 30.4 | 35.0 | 31.6 | 31.3 | 36.9 | 29.4 | 30.6 |
20 | 33.7 | 32.7 | 33.4 | 40.6 | 27.8 | 41.4 | 41.9 | 42.7 | 33.4 | 33.4 |
21 | 28.0 | 27.0 | 30.0 | 30.0 | 32.0 | 214.2 | 213.7 | 218.7 | 28.1 | 28.3 |
22 | 33.7 | 31.1 | 28.1 | 36.6 | 40.8 | 77.5 | 53.3 | 55.0 | 38.1 | 39.9 |
23 | 7.2 | 6.9 | 7.0 | 7.1 | 6.3 | 7.9 | 10.7 | 7.0 | 7.3 | 6.8 |
24 | 15.0 | 14.6 | 14.9 | 72.4 | 13.8 | 174.2 | 14.8 | 16.0 | 14.7 | |
25 | 17.5 | 17.2 | 18.1 | 16.7 | 17.9 | 16.8 | 17.0 | 65.1 | 18.1 | 18.0 |
26 | 20.5 | 20.3 | 18.6 | 16.2 | 18.4 | 15.5 | 15.0 | 21.5 | 20.0 | 18.6 |
27 | 19.2 | 15.9 | 20.9 | 17.5 | 19.9 | 19.4 | 17.9 | 18.6 | 18.6 | 19.9 |
28 | 208.9 | 27.4 | 32.3 | 31.9 | 32.1 | 25.4 | 32.3 | 33.8 | 32.1 | 32.2 |
29 | 24.4 | 74.1 | 75.0 | 179.4 | 31.7 | 28.8 | 28.9 | 29.0 | ||
30 | 74.7 | 25.8 | 26.1 | 32.1 | 34.7 | 15.0 | 14.7 | 25.0 | 72.0 | 72.1 |
OCH3 | 51.7 | |||||||||
C=O | 166.8 | |||||||||
Iso | 130.2 | |||||||||
Orto | 129.5 | |||||||||
Meta | 128.6 | |||||||||
Para | 133.1 | |||||||||
Ref | [48] | [46] | [59] | [48] | [60] | [61] | [62] | [54] | [49] | [57] |
C | F43 | F44 | F45 | F47 | F49 | F50 | F51 | F52 | F53 | F54 |
1 | 31.3 | 200.5 | 27.6 | 22.2 | 22.3 | 39.0 | 36.1 | 26.7 | 26.7 | 210.9 |
2 | 193.1 | 102.6 | 41.2 | 41.5 | 41.5 | 211.4 | 211.7 | 72.7 | 73.2 | 53.9 |
3 | 146.5 | 175.5 | 213.0 | 213.0 | 213.0 | 77.2 | 77.0 | 106.3 | 106.8 | 75.4 |
4 | 126.9 | 49.9 | 57.9 | 58.2 | 58.2 | 54.8 | 54.6 | 45.6 | 45.7 | 50.0 |
5 | 54.7 | 41.6 | 41.7 | 42.1 | 42.1 | 38.0 | 38.1 | 52.8 | 47.0 | 44.5 |
6 | 30.7 | 41.1 | 40.7 | 41.2 | 41.3 | 41.1 | 40.7 | 72.8 | 33.6 | 42.7 |
7 | 18.4 | 17.6 | 17.8 | 18.0 | 18.2 | 17.3 | 17.6 | 30.4 | 19.2 | 18.2 |
8 | 49.4 | 52.3 | 51.5 | 52.8 | 50.4 | 53.8 | 53.2 | 46.5 | 49.7 | 53.2 |
9 | 37.0 | 37.1 | 37.4 | 37.1 | 37.5 | 41.8 | 37.7 | 37.0 | 37.0 | 37.2 |
10 | 55.8 | 68.7 | 59.0 | 59.2 | 59.6 | 60.8 | 60.5 | 52.7 | 52.6 | 71.8 |
11 | 33.1 | 35.3 | 34.8 | 35.4 | 35.2 | 29.5 | 35.1 | 34.0 | 34.1 | 35.2 |
12 | 29.2 | 30.4 | 30.4 | 30.6 | 30.5 | 30.5 | 20.3 | 29.7 | 29.0 | 30.9 |
13 | 39.2 | 39.4 | 37.5 | 38.7 | 39.3 * | 39.7 | 39.7 | 39.2 | 39.1 | 40.6 |
14 | 39.1 | 38.3 | 38.4 | 37.6 | 39.4 * | 38.2 | 38.4 | 38.9 | 49.1 | 38.8 |
15 | 28.9 | 32.5 | 32.6 | 32.4 | 30.0 | 32.7 | 32.4 | 29.1 | 29.0 | 33.3 |
16 | 36.0 | 36.0 | 29.3 | 34.9 | 36.2 | 35.9 | 36.0 | 36.1 | 36.2 | 36.6 |
17 | 30.1 | 29.9 | 42.4 | 47.7 | 30.2 | 30.0 | 30.0 | 30.5 | 30.1 | 31.1 |
18 | 44.4 | 42.7 | 38.5 | 36.4 | 44.6 | 42.6 | 42.9 | 44.5 | 44.5 | 42.6 |
19 | 30.4 | 35.1 | 34.1 | 35.4 | 29.2 | 35.3 | 35.4 | 30.1 | 30.4 | 30.7 |
20 | 40.5 | 28.2 | 32.8 | 28.3 | 40.6 | 28.1 | 28.2 | 40.5 | 40.5 | 34.0 |
21 | 29.9 | 32.8 | 31.0 | 32.4 | 29.6 | 32.7 | 32.8 | 30.0 | 30.0 | 28.7 |
22 | 36.5 | 39.3 | 22.0 | 28.0 | 36.6 | 39.2 | 39.3 | 36.5 | 36.4 | 40.5 |
23 | 10.6 | 8.5 | 6.6 | 6.8 | 6.8 | 10.9 | 10.8 | 9.9 | 6.9 | 12.4 |
24 | 194.9 | 15.1 | 14.3 | 14.6 | 14.6 | 14.0 | 14.2 | 64.6 | 72.2 | 18.4 |
25 | 17.4 | 18.1 | 17.0 | 17.2 | 17.5 | 63.7 | 17.4 | 16.5 | 16.7 | 19.0 |
26 | 15.9 | 20.4 | 19.0 | 20.0 | 18.5 | 20.3 | 20.2 | 16.1 | 16.1 | 21.3 |
27 | 17.2 | 18.7 | 16.1 | 18.8 | 16.1 | 18.5 | 18.5 | 1.4 | 17.4 | 19.1 |
28 | 31.8 | 32.0 | 177.0 | 209.1 | 31.9 | 32.2 | 31.1 | 31.8 | 31.8 | 32.7 |
29 | 179.1 | 35.0 | 26.7 | 34.5 | 179.3 | 35.0 | 31.8 | 179.1 | 179.1 | 74.7 |
30 | 31.9 | 31.7 | 79.7 | 29.4 | 31.9 | 31.7 | 35.0 | 32.0 | 32.0 | 26.9 |
OCH3 | 51.5 | 55.6 | 51.5 | |||||||
Ref | [63] | [64] | [48] | [65] | [66] | [47] | [67] | [68] | [48] | [69] |
C | F55 | F56 | F57 | F59 b | F60 | F61 | F62 | F63 | F64 b | F65 c |
1 | 21.7 | 29.6 | 146.3 | 35.6 | 21.9 | 22.3 | 22.4 | 74.0 | 28.7 | 26.6 |
2 | 37.1 | 72.4 | 130.1 | 41.1 | 41.2 | 41.7 | 41.7 | 29.7 | 74.2 | 68.5 |
3 | 216.6 | 202.3 | 200.9 | 212.4 | 212.4 | 212.8 | 212.7 | 231.2 | 108.1 | 71.2 |
4 | 58.7 | 129.5 | 57.7 | 58.1 | 58.2 | 58.8 | 58.8 | 53.3 | 46.8 | 42.8 |
5 | 39.9 | 157.8 | 49.1 | 42.5 | 42.6 | 41.3 | 41.3 | 42.7 | 47.5 | 49.0 |
6 | 37.4 | 65.4 | 77.2 | 50.4 | 52.2 | 49.0 | 48.9 | 41.2 | 34.0 | 37.2 |
7 | 17.7 | 29.9 | 28.7 | 69.2 | 68.6 | 68.4 | 68.3 | 18.1 | 19.7 | 19.0 |
8 | 53.5 | 40.9 | 48.2 | 58.2 | 58.6 | 52.9 | 52.6 | 53.1 | 50.4 | 49.2 |
9 | 37.0 | 38.5 | 36.7 | 38.8 | 39.0 | 37.2 | 37.6 | 36.9 | 37.5 | 44.0 |
10 | 49.4 | 48.9 | 60.3 | 59.3 | 58.9 | 60.0 | 59.8 | 52.4 | 53.3 | 50.0 |
11 | 35.7 | 33.4 | 45.4 | 36.0 | 35.9 | 37.6 | 31.2 | 32.7 | 34.7 | 33.8 |
12 | 30.5 | 29.5 | 69.3 | 29.9 | 29.6 | 30.5 | 37.5 | 29.5 | 29.5 | 28.8 |
13 | 39.7 | 39.3 | 40.0 | 40.3 | 40.3 | 40.4 | 39.5 | 39.7 | 39.6 | 39.6 |
14 | 38.3 | 40.6 | 45.6 | 44.2 | 40.0 | 39.1 | 44.9 | 38.0 | 39.3 | 38.8 |
15 | 32.4 | 28.3 | 49.6 | 27.0 | 29.5 | 32.4 | 32.8 | 30.2 | 29.7 | 27.8 |
16 | 36.0 | 29.8 | 214.2 | 35.5 | 38.3 | 35.8 | 29.1 | 35.3 | 36.7 | 28.9 |
17 | 30.0 | 45.2 | 47.1 | 30.1 | 30.4 | 30.5 | 38.3 | 30.0 | 30.5 | 36.4 |
18 | 42.7 | 45.8 | 44.7 | 43.3 | 42.3 | 41.6 | 38.0 | 42.4 | 44.8 | 45.0 |
19 | 35.3 | 32.0 | 39.6 | 21.9 | 35.3 | 29.6 | 35.1 | 31.3 | 30.9 | 30.9 |
20 | 28.1 | 41.7 | 42.3 | 28.3 | 33.5 | 33.1 | 28.5 | 40.2 | 40.7 | 40.8 |
21 | 32.7 | 214.1 | 218.1 | 32.4 | 27.9 | 27.9 | 35.9 | 28.2 | 30.5 | 213.2 |
22 | 39.2 | 78.1 | 47.2 | 39.2 | 36.1 | 39.4 | 32.5 | 38.2 | 37.4 | 76.7 |
23 | 13.5 | 11.1 | 9.8 | 6.9 | 6.9 | 6.9 | 6.9 | 6.8 | 8.4 | 11.3 |
24 | 23.1 | 8.7 | 15.9 | 15.9 | 16.1 | 16.1 | 14.4 | 72.1 | 176.5 | |
25 | 18.0 | 17.0 | 19.6 | 18.8 | 18.9 | 19.0 | 18.8 | 17.5 | 16.9 | 15.2 |
26 | 20.4 | 15.8 | 19.9 | 64.2 | 13.1 | 21.8 | 21.4 | 20.9 | 16.8 | 17.3 |
27 | 18.7 | 19.3 | 8.7 | 20.1 | 20.8 | 18.3 | 18.5 | 17.7 | 18.1 | 18.6 |
28 | 32.1 | 25.9 | 29.1 | 31.2 | 31.8 | 32.1 | 179.2 | 32.0 | 32.1 | 25.5 |
29 | 35.0 | 28.4 | 34.7 | 29.1 | 74.5 | 34.4 | 31.8 | 181.3 | ||
30 | 31.7 | 15.4 | 24.4 | 31.1 | 71.3 | 26.0 | 29.6 | 183.1 | 32.3 | 14.9 |
Ref | [70] | [71] | [72] | [39] | [73] | [48] | [48] | [48] | [74] | [75] |
C | F66 | F67 + | F68 | F69 b | F70 b | F71 | F72 | F73 | F74 | F75 b |
1 | 30.8 | 28.2 | 32.6 | 30.9 | 39.0 | 22.3 | 22.2 | 22.3 | 36.5 | 20.3 |
2 | 74.1 | 76.5 | 75.0 | 193.5 | 194.6 | 41.5 | 42.0 | 41.5 | 212.3 | 38.9 |
3 | 213.3 | 208.1 | 212.4 | 149.0 | 144.2 | 213.2 | 213.3 | 213.3 | 77.3 | 105.9 |
4 | 52.7 | 54.3 | 55.6 | 125.8 | 139.9 | 58.2 | 58.2 | 58.3 | 54.8 | 53.7 |
5 | 43.1 | 43.1 | 43.1 | 54.9 | 40.0 | 42.1 | 44.7 | 42.0 | 39.6 | 47.0 |
6 | 41.3 | 41.0 | 41.2 | 32.7 | 33.6 | 41.2 | 41.5 | 41.3 | 40.9 | 33.9 |
7 | 18.5 | 18.2 | 18.1 | 18.9 | 18.2 | 18.2 | 18.4 | 18.2 | 17.9 | 19.4 |
8 | 50.9 | 50.4 | 53.2 | 49.5 | 50.8 | 53.1 | 52.9 | 50.7 | 51.0 | 50.0 |
9 | 37.2 | 36.6 | 37.4 | 37.1 | 37.8 | 37.5 | 37.7 | 37.4 | 38.3 | 37.3 |
10 | 52.6 | 53.3 | 56.5 | 55.5 | 56.1 | 59.4 | 59.2 | 59.8 | 60.9 | 57.1 |
11 | 35.4 | 35.1 | 35.3 | 33.3 | 35.0 | 35.6 | 35.9 | 36.1 | 35.0 | 34.6 |
12 | 30.5 | 30.1 | 30.2 | 30.9 | 30.7 | 30.3 | 31.0 | 29.5 | 29.7 | 29.4 |
13 | 39.5 | 39.2 | 39.7 | 39.4 | 39.7 | 39.7 | 41.0 | 39.2 | 38.0 | 39.4 |
14 | 39.7 | 39.3 | 38.1 | 39.6 | 39.8 | 38.0 | 38.8 | 39.1 | 39.5 | 39.2 |
15 | 29.8 | 30.4 | 32.8 | 30.5 | 30.6 | 32.8 | 29.3 | 29.4 | 30.1 | 29.3 |
16 | 37.8 | 36.2 | 35.4 | 36.6 | 36.8 | 35.4 | 32.6 | 36.6 | 36.5 | 36.5 |
17 | 30.4 | 29.1 | 29.6 | 30.5 | 31.2 | 29.5 | 37.6 | 30.1 | 30.5 | 30.3 |
18 | 44.8 | 44.5 | 42.5 | 44.8 | 45.0 | 42.5 | 37.6 | 44.2 | 44.7 | 44.6 |
19 | 30.8 | 36.9 | 31.3 | 29.5 | 29.9 | 31.2 | 35.4 | 29.3 | 30.6 | 30.7 |
20 | 40.7 | 40.6 | 40.3 | 40.7 | 40.9 | 40.3 | 28.4 | 40.4 | 40.6 | 40.5 |
21 | 29.7 | 29.9 | 28.2 | 29.4 | 30.1 | 28.2 | 34.8 | 30.2 | 29.7 | 30.3 |
22 | 36.7 | 29.4 | 38.2 | 37.4 | 37.2 | 38.2 | 32.6 | 35.2 | 37.1 | 37.2 |
23 | 6.8 | 6.5 | 6.5 | 10.7 | 10.5 | 6.8 | 6.8 | 6.9 | 11.2 | 8.4 |
24 | 14.2 | 14.1 | 14.7 | 195.8 | 19.1 | 14.6 | 14.6 | 14.6 | 14.6 | 72.9 |
25 | 18.0 | 18.3 | 17.8 | 17.2 | 18.2 | 17.7 | 17.5 | 18.4 | 18.1 | 16.7 |
26 | 18.5 | 16.1 | 20.9 | 17.9 | 18.5 | 20.9 | 20.7 | 16.3 | 18.2 | 17.9 |
27 | 16.1 | 17.5 | 17.7 | 16.2 | 17.0 | 17.7 | 18.5 | 18.0 | 16.6 | 16.5 |
28 | 32.1 | 31.8 | 31.8 | 32.3 | 32.0 | 32.0 | 185.0 | 31.8 | 32.2 | 31.9 |
29 | 181.2 | 31.9 | 183.3 | 181.5 | 181.2 | 31.9 | 29.7 | 184.8 | 32.1 | 181.2 |
30 | 32.1 | 179.4 | 32.0 | 32.1 | 32.3 | 184.7 | 34.5 | 31.5 | 182.4 | 32.2 |
COOCH3 | 179.4 | |||||||||
COOCH3 | 51.6 | |||||||||
COOCH3 | 169.8 | |||||||||
COOCH3 | 21.2 | |||||||||
Ref | [76] | [77] | [78] | [59] | [79] | [80] | [56] | [81] | [82] | [83] |
C | F76 | F77 c | F79 | F80 | F81 | F82 | F83 | F84 | F85 | F86 |
1 | 19.3 | 26.6 | 22.4 | 16.0 | 148.2 | 202.7 | 202.8 | 22.2 | 22.3 | 22.3 |
2 | 36.3 | 67.6 | 41.7 | 35.4 | 130.4 | 60.6 | 60.6 | 40.8 | 41.1 | 41.4 |
3 | 71.9 | 83.1 | 212.7 | 73.0 | 201.5 | 204.0 | 204.2 | 212.1 | 212.1 | 213.1 |
4 | 52.9 | 43.3 | 58.8 | 49.4 | 57.6 | 59.0 | 59.1 | 57.9 | 58.1 | 58.2 |
5 | 37.4 | 48.6 | 41.3 | 38.0 | 43.7 | 37.8 | 37.8 | 42.2 | 42.2 | 42.0 |
6 | 40.9 | 33.3 | 48.9 | 41.9 | 39.5 | 40.5 | 40.6 | 41.0 | 41.0 | 40.5 |
7 | 17.4 | 18.7 | 68.3 | 17.7 | 18.1 | 18.1 | 18.1 | 18.4 | 18.6 | 21.3 |
8 | 52.6 | 49.6 | 52.9 | 53.7 | 51.5 | 52.4 | 52.2 | 53.0* | 53.1 | 45.3 |
9 | 37.0 | 36.8 | 37.6 | 37.3 | 36.8 | 37.2 | 37.2 | 55.5 | 43.8 | 37.2 |
10 | 59.6 | 52.2 | 59.8 | 61.5 | 61.9 | 71.8 | 71.9 | 53.1* | 59.3 | 59.3 |
11 | 35.6 | 33.7 | 31.1 | 35.8 | 34.4 | 34.5 | 34.6 | 214.2 | 51.4 | 34.4 |
12 | 30.9 | 28.7 | 37.8 | 30.9 | 28.8 | 30.3 | 30.2 | 51.2 | 214.2 | 29.4 |
13 | 37.8 | 38.6 | 39.5 | 40.1 | 39.0 | 39.7 | 39.5 | 44.0 | 55.5 | 42.4 |
14 | 38.6 | 38.6 | 44.6 | 38.5 | 40.5 | 38.1 | 38.2 | 43.8 | 44.0 | 54.2 |
15 | 32.3 | 29.4 | 32.8 | 32.8 | 49.8 | 32.7 | 32.4 | 31.6 | 35.6 | 214.9 |
16 | 29.2 | 35.9 | 29.2 | 36.1 | 218.7 | 35.0 | 35.9 | 36.1 | 36.2 | 54.0 |
17 | 44.5 | 29.7 | 38.4 | 30.7 | 45.3 | 33.2 | 30.0 | 29.6 | 29.7 | 33.5 |
18 | 37.6 | 44.0 | 38.4 | 42.0 | 43.9 | 41.8 | 42.7 | 36.4 | 36.6 | 44.0 |
19 | 34.5 | 29.7 | 35.1 | 29.9 | 35.4 | 37.0 | 35.3 | 35.4 | 31.7 | 34.9 |
20 | 28.2 | 40.6 | 28.5 | 33.3 | 27.6 | 42.8 | 28.2 | 28.3 | 28.4 | 27.9 |
21 | 35.1 | 29.4 | 35.8 | 28.0 | 31.6 | 218.8 | 32.8 | 33.0 | 33.1 | 33.8 |
22 | 32.2 | 36.3 | 32.4 | 39.7 | 30.7 | 55.0 | 39.3 | 38.9 | 39.1 | 38.6 |
23 | 9.6 | 14.3 | 6.9 | 11.8 | 6.7 | 7.3 | 7.3 | 6.8 | 6.9 | 6.8 |
24 | 14.3 | 96.5 | 16.1 | 16.6 | 13.7 | 16.0 | 16.0 | 14.5 | 14.6 | 15.0 |
25 | 17.4 | 16.3 | 18.8 | 18.4 | 19.1 | 17.8 | 18.0 | 18.1 | 18.2 | 17.4 |
26 | 20.3 | 16.1 | 21.7 | 20.8 | 19.8 | 21.3 | 20.3 | 19.0 | 19.9 | 14.7 |
27 | 18.3 | 17.2 | 18.5 | 18.7 | 16.2 | 18.5 | 18.7 | 19.8 | 19.1 | 18.9 |
28 | 183.7 | 31.7 | 183.3 | 32.3 | 27.4 | 33.5 | 32.0 | 31.8 | 31.9 | 32.2 |
29 | 29.5 | 179.6 | 34.3 | 75.0 | 35.2 | 28.8 | 31.8 | 31.7 | 31.8 | 33.3 |
30 | 34.2 | 31.6 | 29.7 | 26.0 | 31.1 | 25.0 | 35.0 | 34.2 | 34.3 | 33.4 |
Ref | [48] | [84] | [48] | [69] | [45] | [52] | [85] | [86] | [35] | [51] |
C | F87 | F88 | F89 | F90 | F91 b | F92 | F93 a | F94 | F95 | F96 |
1 | 22.2 | 21.6 | 22.2 | 18.6 | 17.0 | 16.0 | 16.2 | 41.3 | 27.8 | 31.4 |
2 | 41.4 | 40.8 | 41.4 | 35.4 | 40.3 | 35.5 | 36.1 | 41.6 | 170.4 | 193.2 |
3 | 212.5 | 210.6 | 212.8 | 72.0 | 74.7 | 72.0 | 71.6 | 213.0 | 177.0 | 146.5 |
4 | 58.2 | 57.8 | 58.1 | 49.4 | 491 | 49.4 | 49.6 | 59.5 | 47.3 | 127.0 |
5 | 42.1 | 47.0 | 42.0 | 38.3 | 41.4 | 37.9 | 38.1 | 42.2 | 38.9 | 54.7 |
6 | 41.0 | 56.9 | 41.2 | 41.9 | 36.0 | 41.8 | 42.0 | 35.6 | 34.5 | 30.6 |
7 | 18.6 | 210.2 | 18.1 | 17.5 | 19.3 | 17.7 | 17.7 | 30.7 | 17.1 | 18.3 |
8 | 52.4 | 63.4 | 53.0 | 52.9 | 53.8 | 53.2 | 53.3 | 53.4 | 52.0 | 48.7 |
9 | 37.7 | 42.4 | 37.4 | 43.9 | 36.8 | 37.1 | 37.2 | 37.5 | 35.3 | 37.0 |
10 | 59.4 | 59.0 | 59.4 | 62.3 | 61.6 | 61.5 | 61.6 | 58.2 | 46.1 | 56.0 |
11 | 35.4 | 35.5 | 35.5 | 76.6 | 36.5 | 35.5 | 35.7 | 22.4 * | 32.0 | 33.3 |
12 | 29.1 | 29.8 | 30.4 | 42.0 | 31.4 | 30.3 | 30.7 | 32.9 | 30.1 | 28.8 |
13 | 39.2 | 39.4 | 39.6 | 38.5 | 37.6 | 39.7 | 38.4 | 38.3 | 39.6 | 40.7 |
14 | 40.5 | 37.5 | 38.2 | 40.9 | 39.9 | 38.0 | 39.7 | 40.0 | 38.0 | 39.5 |
15 | 50.2 | 31.6 | 32.2 | 32.3 | 32.5 | 32.3 | 32.3 | 18.4 * | 32.3 | 28.2 |
16 | 218.8 | 36.3 | 35.9 | 36.0 | 35.6 | 32.0 | 35.9 | 37.1 | 35.7 | 35.9 |
17 | 45.3 | 30.1 | 29.9 | 30.0 | 30.7 | 36.1 | 30.0 | 42.8 | 30.0 | 31.4 |
18 | 44.0 | 41.8 | 42.8 | 42.6 | 43.6 | 38.5 | 42.9 | 42.0 | 42.6 | 45.3 |
19 | 35.5 | 34.9 | 35.2 | 35.7 | 35.6 | 29.3 | 35.4 | 35.1 | 35.2 | 29.8 |
20 | 27.6 | 28.0 | 28.0 | 28.1 | 28.8 | 33.1 | 28.2 | 33.3 | 28.1 | 149.1 |
21 | 31.7 | 32.8 | 32.7 | 32.8 | 32.9 | 28.4 | 32.9 | 218.8 | 32.6 | 30.7 |
22 | 30.8 | 38.6 | 39.2 | 39.2 | 39.0 | 28.7 | 39.3 | 55.1 | 39.1 | 38.0 |
23 | 6.8 | 6.8 | 6.7 | 12.1 | 14.8 | 11.9 | 12.1 | 6.9 | 12.5 | 10.7 |
24 | 14.7 | 15.1 | 14.5 | 16.7 | 65.8 | 16.5 | 16.6 | 17.9 | 20.6 | 194.9 |
25 | 17.3 | 18.2 | 17.8 | 13.5 | 18.4 | 18.3 | 18.3 | 14.8 | 72.6 | 18.1 |
26 | 20.3 | 19.2 | 18.5 | 19.9 | 18.9 | 20.0 | 20.1 | 33.6 | 20.2 | 15.1 |
27 | 16.2 | 19.4 | 20.1 | 19.5 | 20.8 | 18.8 | 18.7 | 21.4 | 18.5 | 17.9 |
28 | 27.4 | 32.1 | 32.0 | 32.0 | 33.6 | 66.7 | 32.1 | 18.6 | 32.1 | 31.4 |
29 | 31.1 | 31.8 | 31.7 | 35.0 | 35.6 | 73.8 | 35.0 | 25.1 | 35.0 | |
30 | 35.2 | 34.6 | 34.9 | 31.7 | 32.7 | 26.5 | 31.8 | 28.9 | 31.6 | 107.6 |
Ref | [57] | [57] | [57] | [87] | [88] | [69] | [89] | [90] | [47] | [91] |
C | F97C | F98 | F99 | F100 | F101 | F102 | F103 | |||
1 | 26.9 | 22.0 | 28.7 | 19.1 | 21.3 | 21.1 | 116.0 | |||
2 | 105.0 | 41.2 | 71.5 | 34.5 | 38.0 | 37.2 | 166.1 | |||
3 | 77.1 | 212.8 | 200.1 | 175.6 | 176.2 | 177.8 | ||||
4 | 47.7 | 57.9 | 127.7 | 36.1 | 35.8 | 36.2 | 197.9 | |||
5 | 44.6 | 41.9 | 159.2 | 36.8 | 37.5 | 37.9 | 135.5 | |||
6 | 30.1 | 41.0 | 30.9 | 38.8 | 38.7 | 39.0 | 136.0 | |||
7 | 18.6 | 18.0 | 20.8 | 18.0 | 17.9 | 18.2 | 118.6 | |||
8 | 48.1 | 53.1 | 47.7 | 52.6 | 52.1 | 53.1 | 163.3 | |||
9 | 37.5 | 37.2 | 37.6 | 42.9 | 38.8 | 39.1 | 39.2 | |||
10 | 52.1 | 59.2 | 52.3 | 58.2 | 59.6 | 59.9 | 165.9 | |||
11 | 33.3 | 35.3 | 33.1 | 84.1 | 34.7 | 35.3 | 31.2 | |||
12 | 28.8 | 29.8 | 29.5 | 37.6 | 29.5 | 30.3 | 29.2 | |||
13 | 40.2 | 38.0 | 39.5 | 40.7 | 39.0 | 39.7 | 38.3 | |||
14 | 39.1 | 39.6 | 40.0 | 37.9 | 37.9 | 38.4 | 47.6 | |||
15 | 28.3 | 32.3 | 28.1 | 32.1 | 31.1 | 32.4 | 28.5 | |||
16 | 29.6 | 35.5 | 29.7 | 35.9 | 29.0 | 36.1 | 36.6 | |||
17 | 44.8 | 30.1 | 44.9 | 30.0 | 35.0 | 30.1 | 30.4 | |||
18 | 45.6 | 41.6 | 45.3 | 42.6 | 39.3 | 43.0 | 44.6 | |||
19 | 31.7 | 30.3 | 31.7 | 35.3 | 34.3 | 35.4 | 31.1 | |||
20 | 41.5 | 31.4 | 41.3 | 28.1 | 27.8 | 28.2 | 40.4 | |||
21 | 213.9 | 27.7 | 214.0 | 32.7 | 33.2 | 32.9 | 29.7 | |||
22 | 77.4 | 38.8 | 77.2 | 39.2 | 31.3 | 39.3 | 34.4 | |||
23 | 16.1 | 6.6 | 11.2 | 7.7 | 7.3 | 7.6 | 18.1 | |||
24 | 175.3 | 14.4 | 22.1 | 19.2 | 19.5 | |||||
25 | 16.6 | 17.6 | 15.6 | 13.6 | 17.8 | 18.0 | 25.6 | |||
26 | 15.8 | 18.2 | 19.1 | 19.9 | 18.6 | 20.2 | 24.0 | |||
27 | 19.3 | 20.7 | 17.5 | 19.3 | 19.0 | 18.7 | 20.3 | |||
28 | 26.1 | 31.8 | 25.2 | 32.0 | 67.3 | 32.2 | 31.5 | |||
29 | 74.3 | 34.9 | 32.6 | 35.0 | 179.1 | |||||
30 | 15.6 | 25.9 | 14.8 | 31.7 | 33.9 | 31.9 | 32.8 | |||
C=O | 161.2 | |||||||||
OCH3 | 51.8 | |||||||||
OCH3 | 51.8 | |||||||||
Ref | [62] | [92] | [93] | [94] | [95] | [95] | [96] |
C | Q1 | Q2 | Q3 | Q4 | Q5 | Q6 b | Q7 | Q8 | Q9 | Q10 |
---|---|---|---|---|---|---|---|---|---|---|
1 | 121.6 | 119.8 | 119.8 | 164.7 | 119.5 | 119.7 | 119.8 | 120.0 | 119.5 | 119.8 |
2 | 178.8 | 178.4 | 178.3 | 178.3 | 178.1 | 178.4 | 178.4 | 178.1 | 178.3 | 178.4 |
3 | 145.9 | 146.0 | 146.2 | 146.0 | 145.9 | 146.1 | 146.2 | 146.3 | 146.0 | 146.1 |
4 | 118.0 | 117.0 | 117.5 | 118.2 | 118.0 | 117.2 | 117.1 | 116.8 | 117.2 | 117.2 |
5 | 128.6 | 127.5 | 128.5 | 127.5 | 127.3 | 127.9 | 127.9 | 127.9 | 127.3 | 127.8 |
6 | 132.2 | 133.8 | 132.1 | 134.0 | 134.0 | 133.3 | 133.3 | 134.4 | 134.0 | 133.6 |
7 | 118.8 | 117.9 | 118.6 | 117.2 | 118.0 | 118.3 | 118.3 | 121.9 | 118.0 | 118.2 |
8 | 167.2 | 165.7 | 164.9 | 169.7 | 170.1 | 168.7 | 168.7 | 18.6 | 169.7 | 168.4 |
9 | 48.1 | 43.0 | 43.0 | 47.8 | 43.0 | 42.9 | 42.9 | 44.6 | 42.4 | 42.6 |
10 | 161.6 | 164.4 | 164.2 | 164.0 | 164.8 | 164.2 | 164.2 | 159.7 | 164.6 | 164.7 |
11 | 65.3 | 34.3 | 32.5 | 33.7 | 33.0 | 33.2 | 33.2 | 37.3 | 33.5 | 34.0 |
12 | 43.4 | 27.5 | 31.1 | 30.2 | 30.0 | 29.9 | 29.9 | 35.9 | 29.5 | 30.0 |
13 | 40.6 | 40.3 | 39.0 | 42.6 | 40.7 | 40.0 | 40.0 | 42.4 | 39.2 | 40.6 |
14 | 44.9 | 47.3 | 49.6 | 44.6 | 45.0 | 44.2 | 44.2 | 136.9 | 44.5 | 44.3 |
15 | 28.7 | 129.4 | 73.0 | 28.4 | 28.6 | 29.4 | 29.4 | 128.6 | 28.2 | 28.3 |
16 | 36.2 | 135.6 | 41.4 | 68.2 | 36.5 * | 35.7 | 35.7 | 40.5 | 36.1 | 29.5 |
17 | 30.87 | 33.7 | 37.6 | 30.2 | 31.6 | 35.9 | 35.9 | 39.8 | 38.1 | 44.8 |
18 | 43.9 | 42.6 | 43.7 | 46.9 | 43.2 | 43.3 | 43.3 | 43.7 | 46.1 | 45.1 |
19 | 30.81 | 30.7 | 31.9 | 29.6 | 24.8 ** | 36.9 | 36.9 | 40.7 | 30.8 | 32.0 |
20 | 40.4 | 41.0 | 41.8 | 39.4 | 35.7 | 73.7 | 73.7 | 75.0 | 42.6 | 40.9 |
21 | 29.7 | 29.4 | 213.7 | 28.4 | 24.8 ** | 214.9 | 214.9 | 213.0 | 38.1 | 213.5 |
22 | 34.3 | 32.3 | 54.2 | 38.3 | 36.5 * | 50.5 | 50.5 | 50.5 | 67.9 | 76.4 |
23 | 10.4 | 10.3 | 10.3 | 10.3 | 10.4 | 10.3 | 10.3 | 10.4 | 10.1 | 10.3 |
24 | ||||||||||
25 | 34.4 | 37.4 | 41.0 | 38.3 | 38.9 | 38.5 | 38.5 | 29.6 | 38.1 | 39.2 |
26 | 21.4 | 28.8 | 23.6 | 21.7 | 21.6 | 23.3 | 23.3 | 22.1 | 21.6 | 21.6 |
27 | 18.5 | 18.0 | 23.5 | 19.7 | 21.4 | 19.4 | 19.4 | 23.7 | 19.0 | 20.5 |
28 | 31.4 | 27.4 | 32.9 | 24.2 | 31.4 | 33.2 | 33.2 | 30.4 | 24.0 | 25.0 |
29 | 178.7 | 178.3 | 178.2 | 29.0 | 178.2 | |||||
30 | 32.7 | 31.3 | 15.0 | 32.4 | 69.6 | 29.0 | 24.8 | 32.2 | 14.7 | |
OCH3 | 51.8 | 51.6 | 51.8 | 51.6 | ||||||
Ref | [103] | [104] | [104] | [105] | [106] | [107] | [108] | [104] | [109] | [63] |
C | Q11 | Q12 | Q13 | Q14 | Q15 | Q16 | Q17 | Q18 | Q19 | Q20 c |
1 | 119.4 | 120.6 | 119.7 | 120.0 | 119.6 | 119.4 | 119.9 | 120.0 | 119.4 | 119.8 |
2 | 178.4 | 178.3 | 181.1 | 178.1 | 178.3 | 178.4 | 178.0 | 178.1 | 178.8 | 178.6 |
3 | 146.0 | 147.0 | 161.9 | 146.3 | 146.0 | 146.0 | 146.2 | 146.2 | 146.1 | 146.3 |
4 | 117.1 | 127.5 | 140.9 | 116.8 | 117.1 | 117.2 | 116.7 | 116.7 | 118.6 | 117.4 |
5 | 127.5 | 120.4 | 117.2 | 128.1 | 127.4 | 127.4 | 127.5 | 127.7 | 127.6 | 127.6 |
6 | 133.9 | 135.4 | 131.7 | 134.4 | 133.9 | 134.2 | 134.9 | 134.5 | 137.8 | 134.4 |
7 | 118.2 | 118.3 | 200.4 | 122.1 | 117.9 | 118.2 | 121.6 | 121.5 | 122.2 | 118.3 |
8 | 169.8 | 165.3 | 41.9 | 158.6 | 170.1 | 170.7 | 159.7 | 159.0 | 160.2 | 170.4 |
9 | 42.9 | 39.3 | 58.4 | 44.2 | 42.9 | 43.3 | 44.5 | 44.5 | 45.5 | 43.0 |
10 | 164.7 | 172.6 | 146.6 | 159.7 | 165.0 | 164.4 | 159.7 | 159.9 | 163.5 | 165.1 |
11 | 33.6 | 28.7 | 32.1 | 36.0 | 33.9 | 33.1 | 37.5 | 37.4 | 37.3 | 33.6 |
12 | 29.8 | 29.3 | 30.2 | 31.8 | 29.7 | 29.4 | 35.6 | 34.8 | 35.2 | 29.7 |
13 | 39.4 | 39.9 | 39.6 | 42.1 | 41.3 | 40.0 | 43.1 | 42.4 | 43.3 | 39.5 |
14 | 45.0 | 43.1 | 29.2 | 135.6 | 44.8 | 44.0 | 135.3 | 136.0 | 135.5 | 45.1 |
15 | 28.6 | 29.5 | 27.9 | 127.9 | 28.4 | 29.7 | 128.3 | 126.6 | 129.8 | 28.7 |
16 | 36.4 | 32.4 | 35.9 | 45.6 | 36.0 | 36.5 | 37.8 | 37.9 | 39.0 | 36.4 |
17 | 30.8 | 45.3 | 31.0 | 36.3 | 31.6 | 30.2 | 33.7 | 38.9 | 35.6 | 30.9 |
18 | 43.6 | 44.2 | 44.2 | 47.8 | 44.9 | 43.7 | 43.9 | 38.7 | 43.6 | 44.4 |
19 | 25.5 | 33.8 | 28.8 | 37.8 | 30.4 | 25.2 | 33.9 | 33.9 | 34.2 | 30.9 |
20 | 46.2 | 31.0 | 40.5 | 41.7 | 147.9 | 33.0 | 42.6 | 47.4 | 48.0 | 40.5 |
21 | 25.1 | 34.5 | 29.8 | 213.8 | 30.5 | 22.5 | 28.6 | 69.2 | 68.0 | 29.9 |
22 | 34.0 | 36.3 | 36.5 | 49.8 | 36.9 | 35.2 | 36.1 | 79.4 | 39.0 | 34.8 |
23 | 10.3 | 10.5 | 10.2 | 10.4 | 10.2 | 10.3 | 10.3 | 10.3 | 10.5 | 10.3 |
24 | ||||||||||
25 | 38.4 | 38.4 | 38.2 | 28.5 | 38.9 | 37.7 | 29.4 | 29.5 | 29.4 | 38.3 |
26 | 21.7 | 21.5 | 21.5 | 21.3 | 21.3 | 23.4 | 21.9 | 21.8 | 21.9 | 21.7 |
27 | 18.4 | 18.7 | 18.3 | 23.1 | 19.7 | 17.9 | 24.0 | 24.5 | 24.3 | 18.4 |
28 | 31.5 | 31.5 | 31.5 | 30.2 | 31.1 | 36.2 | 31.5 | 27.0 | 31.1 | 31.7 |
29 | 177.4 | 182.5 | 178.8 | 69.3 | 179.3 | 179.0 | 178.8 | 179.1 | ||
30 | 74.1 | 30.7 | 30.8 | 16.0 | 108.2 | 19.8 | 13.7 | 17.5 | 32.7 | |
OCH3 | 51.9 | 51.4 | 51.8 | 52.7 | 52.3 | 51.7 | ||||
Ref | [91] | [110] | [111] | [112] | [113] | [91] | [104] | [109] | [109] | [114] |
C | Q21 | Q22 | ||||||||
1 | 119.8 | 119.8 | ||||||||
2 | 178.6 | 178.4 | ||||||||
3 | 146.3 | 146.0 | ||||||||
4 | 117.4 | 117.1 | ||||||||
5 | 127.8 | 127.7 | ||||||||
6 | 134.1 | 133.6 | ||||||||
7 | 118.3 | 118.1 | ||||||||
8 | 170.3 | 168.7 | ||||||||
9 | 43.2 | 42.7 | ||||||||
10 | 165.1 | 164.7 | ||||||||
11 | 34.0 | 33.8 | ||||||||
12 | 30.2 | 29.9 | ||||||||
13 | 40.7 | 40.6 | ||||||||
14 | 45.2 | 44.6 | ||||||||
15 | 28.9 | 28.5 | ||||||||
16 | 37.4 | 35.5 | ||||||||
17 | 30.6 | 38.2 | ||||||||
18 | 44.3 | 43.5 | ||||||||
19 | 25.0 | 32.0 | ||||||||
20 | 31.4 | 41.8 | ||||||||
21 | 71.2 | 213.6 | ||||||||
22 | 44.4 | 52.5 | ||||||||
23 | 10.4 | 10.2 | ||||||||
24 | ||||||||||
25 | 38.9 | 39.0 | ||||||||
26 | 21.8 | 21.5 | ||||||||
27 | 21.4 | 19.7 | ||||||||
28 | 35.4 | 32.5 | ||||||||
29 | ||||||||||
30 | 18.6 | 15.1 | ||||||||
Ref | [115] | [116] |
C | A1 | A3 | A5 | A6 | A7 | A8 + | A9 a | A10 b | A11 | A12 c |
---|---|---|---|---|---|---|---|---|---|---|
1 | 109.5 | 109.1 | 108.4 | 108.6 | 125.6 | 105.9 | 110.0 | 108.4 | 106.8 | 109.0 |
2 | 150.8 | 144.2 | 140.9 | 148.0 | 147.7 | 156.0 | 144.0 | 148.8 | 150.0 | 151.7 |
3 | 152.8 | 132.9 | 139.7 | 140.6 | 140.3 | 146.2 | 126.8 | 141.4 | 143.0 | 143.5 |
4 | 113.2 | 132.0 | 122.0 | 125.4 | 125.1 | 134.1 | 122.7 | 126.1 | 128.0 | 127.9 |
5 | 141.9 | 154.9 | 126.6 | 122.5 | 122.6 | 123.7 | 151.4 | 122.3 | 119.0 | 119.9 |
6 | 201.2 | 187.2 | 28.3 | 187.6 | 187.7 | 187.7 | 187.3 | 187.9 | 201.2 | 182.8 |
7 | 43.8 | 126.1 | 18.5 | 126.1 | 108.8 | 126.1 | 126.8 | 126.0 | 74.5 | 147.4 |
8 | 35.4 | 151.9 | 44.1 | 171.2 | 172.1 | 171.4 | 150.7 | 170.8 | 50.3 | 139.1 |
9 | 38.6 | 40.4 | 36.8 | 40.1 | 44.4 | 40.6 | 40.6 | 40.3 | 38.11 | 40.7 |
10 | 123.5 | 171.2 | 143.8 | 151.2 | 151.9 | 154.9 | 170.7 | 151.2 | 152.8 | 152.8 |
11 | 32.4 | 34.0 | 34.1 | 33.8 | 34.4 | 35.6 | 34.6 | 35.6 | 36.3 | 34.2 |
12 | 29.9 | 29.8 | 30.2 | 30.0 | 29.9 | 30.2 | 30.2 | 30.3 | 30.6 | 30.5 |
13 | 36.8 | 38.9 | 38.9 | 39.6 | 40.8 | 40.6 | 39.3 | 40.0 | 40.5 | 40.0 |
14 | 35.9 | 44.7 | 39.4 | 43.8 | 40.1 | 44.8 | 44.6 | 44.3 | 39.1 | 47.2 |
15 | 30.3 | 28.5 | 29.0 | 29.0 | 28.2 | 28.8 | 28.9 | 28.4 | 29.7 | 29.6 |
16 | NR | 36.4 | 36.5 | 35.5 | 36.8 ** | 37.5 | 36.6 | 32.1 | 36.2 | 37.8 |
17 | 35.7 | 30.8 | 30.3 | 36.2 | 31.6 | 30.8 | 30.6 | 38.4 | 29.8 | 31.1 |
18 | 40.4 | 44.3 | 44.5 | 43.3 | 44.8 | 42.7 | 44.4 | 43.5 | 44.1 | 45.4 |
19 | 29.5 | 30.5 | 30.6 | 36.8 | 30.5 * | 27.9 | 31.1 | 34.3 | 29.8 | 31.9 |
20 | 39.1 | 40.3 | 40.6 | 73.8 | 148.2 | 132.4 | 44.4 | 42.0 | 41.0 | 41.7 |
21 | 29.6 | 29.7 | 30.0 | 215.0 | 30.5 * | 119.9 | 30.1 | 214.7 | 29.9 | 30.9 |
22 | 28.2 | 34.8 | 36.2 | 50.2 | 36.8 ** | 35.2 | 35.1 | 52.7 | 34.0 | 36.2 |
23 | 14.7 | 11.3 | 13.6 | 13.6 | 14.4 | 14.8 | 13.7 | 14.0 | 14.0 | |
24 | ||||||||||
25 | 31.9 | 37.6 | 27.4 | 37.9 | 38.4 | 39.2 | 37.8 | 38.6 | 27.5 | 41.6 |
26 | 25.3 | 20.8 | 15.9 | 22.1 | 20.4 | 21.4 | 20.9 | 20.8 | 15.9 | 19.6 |
27 | 16.7 | 18.3 | 17.3 | 19.4 | 19.6 | 15.7 | 18.5 | 19.7 | 15.9 | 20.6 |
28 | 15.2 | 31.6 | 31.8 | 33.1 | 31.1 | 33.1 | 31.6 | 32.6 | 31.7 | 32.1 |
29 | 179.4 | 178.8 | 179.3 | 28.9 | 106.5 | 24.0 | 178.7 | 179.8 | 180.7 | |
30 | 31.5 | 32.7 | 31.9 | 32.6 | 15.1 | 31.9 | 32.9 | |||
OCH3 | 55.7 | 51.5 | 56.0 | |||||||
OCH3 | 55.1 | 61.1 | 51.5 | 60.7 | 51.5 | 51.4 | 52.2 | |||
Ref | [117] | [118] | [119] | [120] | [106] | [121] | [122] | [123] | [124] | [125] |
C | A13 | A14 | A15 | A16 | A17 + | A18 | A19 d | A20 | A21 | A22 |
1 | 107.9 | 107.5 | 109.2 | 107.9 | 104.1 | 110.1 | 116.6 | 112.4 | 107.8 | 108.8 |
2 | 150.0 | 148.4 | 146.6 | 150.0 | 156.3 | 151.7 | 150.7 | 152.6 * | 141.7 | 148.2 |
3 | 141.4 | 140.9 | 139.5 | 141.4 | 146.1 | 144.7 | 150.0 | 143.5 | 140.4 | 140.7 |
4 | 129.1 | 127.0 | 130.0 | 129.1 | 135.1 | 134.0 | 117.0 | 120.4 | 122.0 | 125.6 |
5 | 122.8 | 124.5 | 125.0 | 122.8 | 125.1 | 122.4 | 122.3 | 121.8 | 123.9 | 122.5 |
6 | 182.0 | 201.9 | 200.7 | 182.0 | 201.0 | 185.8 | 186.3 | 185.8 | 43.9 | 187.7 |
7 | 197.0 | 37.9 | 37.7 | 197.0 | 37.7 | 129.3 | 125.2 | 124.8 | 209.8 | 125.9 |
8 | 60.3 | 42.9 | 42.6 | 60.3 | 42.5 | 160.1 | 174.4 | 177.4 ** | 58.3 | 171.3 |
9 | 38.7 | 37.6 | 37.2 | 38.7 | 38.0 | 42.2 | 40.5 | 41.7 | 38.8 | 40.3 |
10 | 153.6 | 153.2 | 152.2 | 153.6 | 156.2 | 151.2 | 150.4 | 151.7 * | 142.4 | 151.7 |
11 | 33.5 | 36.6 | 33.2 | 33.5 | 33.8 | 37.1 | 33.7 | 35.0 | 33.7 | 34.3 |
12 | 27.8 | 30.15 | 29.9 | 27.8 | 29.6 | 35.8 | 29.6 | 30.8 | 29.4 | 30.2 |
13 | 39.5 | 39.7 | 38.8 | 39.5 | 40.2 | 40.7 | 39.4 | 40.7 | 39.1 | 40.1 |
14 | 39.2 | 39.2 | 39.4 | 39.2 | 40.3 | 134.7 | 45.1 | 46.4 | 38.7 | 44.4 |
15 | 38.7 | 28.8 | 28.5 | 38.7 | 28.2 | 125.9 | 28.7 | 30.0 | 28.4 | 28.4 |
16 | 35.8 | 36.4 | 36.2 | 35.8 | 38.5 | 38.0 | 26.4 | 37.6 | 36.1 | 35.5 |
17 | 30.2 | 30.7 | 30.3 | 30.2 | 30.7 | 48.8 | 30.5 | 31.6 | 30.3 | 38.2 |
18 | 43.6 | 45.1 | 44.7 | 43.6 | 42.9 | 46.2 | 44.3 | 45.7 | 43.6 | 43.5 |
19 | 30.6 | 31.1 | 30.5 | 30.6 | 27.6 | 34.2 | 30.8 | 31.9 | 30.6 | 32.0 |
20 | 40.7 | 41.1 | 40.1 | 40.7 | 133.0 | 50.3 | 40.1 | 41.3 | 40.6 | 41.9 |
21 | 30.3 | 30.1 | 29.8 | 30.3 | 120.2 | 74.3 | 29.8 | 30.9 | 29.8 | 214.0 |
22 | 35.8 | 33.5 | 36.1 | 35.8 | 35.4 | 214.0 | 34.8 | 36.0 | 35.9 | 52.6 |
23 | 13.8 | 14.0 | 13.2 | 14.3 | 15.1 | 200.2 | 173.1 ** | 11.5 | 13.7 | |
24 | ||||||||||
25 | 31.5 | 26.0 | 25.6 | 31.5 | 27.0 | 21.6 | 36.3 | 37.4 | 27.9 | 38.5 |
26 | 14.7 | 15.7 | 15.4 | 14.7 | 15.4 | 21.7 | 20.5 | 21.3 | 15.1 | 20.7 |
27 | 16.9 | 15.7 | 16.9 | 16.9 | 15.4 | 23.9 | 18.7 | 19.4 | 16.8 | 19.7 |
28 | 31.5 | 32.1 | 31.7 | 31.5 | 33.0 | 22.5 | 31.6 | 32.1 | 31.5 | 32.6 |
29 | 180.0 | 180.1 | 179.1 | 180.0 | 24.0 | 175.2 | 181.2 | 182.5 ** | 179.4 | |
30 | 32.5 | 32.9 | 32.2 | 32.5 | 13.7 | 32.6 | 33.2 | 32.3 | 15.1 | |
OCH3 | 56.0 | 52.7 | ||||||||
OCH3 | 51.8 | 52.2 | 51.4 | 51.8 | 60.6 | 61.7 | 51.6 | |||
1′ | 126.5 | 170.0 | ||||||||
2′ | 104.2 | 121.3 | ||||||||
3′ | 147.4 | 112.2 | ||||||||
4′ | 135.8 | 146.2 | ||||||||
5′ | 147.4 | 150.8 | ||||||||
6′ | 104.2 | 125.2 | ||||||||
7′ | 77.2 | 114.2 | ||||||||
8′ | 75.5 | |||||||||
9′ | 62.8 | |||||||||
OCH3 | 56.4 | 56.1 | ||||||||
OCH3 | 51.4 | |||||||||
OCH3 | 20.6 | |||||||||
C=O | 170.3 | |||||||||
Ref | [119] | [124] | [126] | [119] | [124] | [109] | [127] | [127] | [119] | [128] |
C | A23 | A24 | A25 a | A26 a | A27 d | A28 | A29 | |||
1 | 108.3 | 107.7 | 110.7 | 110.6 | 108.5 | 116.5 | 113.8 | |||
2 | 141.4 | 141.6 | 143.4 | 141.3 | 142.9 | 150.5 | 173.7 | |||
3 | 139.8 | 139.5 | 145.2 | 143.1 | 141.9 | 149.7 | 155.5 | |||
4 | 122.5 | 120.9 | 121.4 | 122.5 | 119.6 | 116.3 | 111.3 | |||
5 | 126.3 | 125.7 | 126.7 | 126.0 | 122.8 | 117.1 | 119.4 | |||
6 | 28.0 | 27.8 | 45.4 | 46.1 | 120.9 | 186.0 | 188.0 | |||
7 | 18.3 | 126.0 | 119.6 | 120.9 | 137.3 | 122.8 | 124.4 | |||
8 | 43.3 | 139.0 | 151.1 | NR | 43.3 | 149.1 | 153.4 | |||
9 | 36.7 | 36.2 | 38.3 | 38.1 | 144.1 | 45.3 | 45.6 | |||
10 | 143.8 | 140.0 | 142.6 | 145.1 | 128.5 | 125.3 | 152.8 | |||
11 | 34.2 | 33.0 | 37.6 | 37.7 | 119.4 | 36.4 | 36.6 | |||
12 | 30.0 | 29.4 | 31.4 | 30.6 | 32.6 | 28.6 | 28.6 | |||
13 | 40.0 | 43.5 | 38.8 | 38.7 | 39.4 | 39.7 | 39.7 | |||
14 | 39.3 | 58.0 | 44.7 | 44.5 | 40.1 | 40.5 | 40.5 | |||
15 | 27.9 | 211.4 | 29.9 | 29.7 | 23.3 | 31.0 | 30.9 | |||
16 | 29.6 | 47.5 | 37.6 | 37.4 | 36.7 | 34.8 | 34.8 | |||
17 | 44.9 | 49.4 | 31.1 | 30.9 | 31.1 | 44.1 | 43.0 | |||
18 | 45.4 | 44.3 | 45.1 | 44.9 | 46.3 | 44.1 | 44.2 | |||
19 | 31.7 | 30.7 | 31.3 | 31.1 | 30.7 | 29.8 | 29.8 | |||
20 | 41.3 | 40.0 | 40.8 | 40.6 | 38.3 | 30.7 | 30.5 | |||
21 | 214.2 | 212.4 | 31.4 | 31.2 | 29.2 | 29.8 | 29.8 | |||
22 | 77.6 | 77.8 | 35.9 | 35.7 | 37.2 | 33.5 | 34.4 | |||
23 | 11.5 | 11.6 | 13.4 | 13.8 | 11.1 | 200.3 | 178.7 | |||
24 | ||||||||||
25 | 28.2 | 33.4 | 36.5 | 35.7 | 22.4 | 36.4 | 36.8 | |||
26 | 15.3 | 25.6 | 22.7 | 22.4 | 19.1 | 20.6 | 20.2 | |||
27 | 19.2 | 21.4 | 18.9 | 18.8 | 18.7 | 32.8 | 32.7 | |||
28 | 25.2 | 24.6 | 32.0 | 31.9 | 32.7 | 18.3 | 18.3 | |||
29 | 181.3 | 181.0 | 179.7 | 178.9 | 179.8 | |||||
30 | 14.8 | 14.8 | 33.5 | 33.3 | 30.4 | 31.8 | 31.6 | |||
CH3 | 22.7 | 21.4 | 51.6 | 51.6 | ||||||
CHOH | 70.8 | 72.1 | ||||||||
Ref | [129] | [39] | [130] | [130] | [127] | [131] | [131] |
C | D1 | D2 | D3 | D6 | D7 | D8 | D9 | D10 | D11 | D12 |
---|---|---|---|---|---|---|---|---|---|---|
1 | 115.5 | 108.2 | 115.5 | 113.0 | 113.0 | 113.1 | 113.0 | 113.1 | 115.5 | 115.0 |
2 | 191.2 | 144.3 | 191.0 | 191.5 | 191.5 | 191.5 | 191.6 | 191.4 | 190.2 | 189.4 |
3 | 91.7 | 140.6 | 91.8 | 91.3 | 91.3 | 91.2 | 91.3 | 91.3 | 92.0 | 91.1 |
4 | 79.9 | 123.2 | 79.0 | 79.5 | 79.5 | 79.5 | 79.4 | 79.5 | 79.4 | 76.9 |
5 | 130.8 | 124.6 | 130.8 | 134.1 | 134.3 | 134.1 | 134.3 | 134.1 | 130.2 | 132.2 |
6 | 126.1 | 71.4 | 125.9 | 134.1 | 133.9 | 133.9 | 134.1 | 133.8 | 126.6 | 128.5 |
7 | 116.2 | 73.7 | 116.1 | 24.2 | 24.2 | 24.2 | 24.2 | 24.2 | 116.3 | 117.2 |
8 | 160.6 | 44.7 | 160.6 | 41.6 | 41.2 | 41.6 | 41.1 | 41.6 | 160.4 | 163.3 |
9 | 41.7 | 40.2 | 41.7 | 37.4 | 37.4 | 37.4 | 37.3 | 37.4 | 41.7 | 43.4 |
10 | 173.8 | 143.7 | 173.5 | 170.2 | 169.8 | 170.0 | 169.8 | 170.0 | 173.8 | 172.9 |
11 | 32.7 | 34.7 | 32.7 | 30.7 | 30.5 | 30.6 | 30.7 | 32.0 | 33.2 | 33.1 |
12 | 29.5 | 30.7 | 29.5 | 29.4 | 29.4 | 29.4 | 29.7 | 29.4 | 29.8 1 | 29.8 |
13 | 38.1 | 39.6 | 38.1 | 38.9 | 40.11 | 38.9 | 40.0 1 | 40.1 | 39.5 2 | 39.9 |
14 | 44.5 | 40.00 | 44.5 | 40.1 | 40.21 | 40.1 | 39.9 1 | 38.9 | 44.3 | 44.0 |
15 | 28.4 | 31.4 | 28.4 | 28.3 | 27.9 | 28.41 | 27.7 | 28.3 | 28.3 | 28.5 |
16 | 36.5 | 36.1 | 36.4 | 36.0 | 35.3 | 36.0 | 29.3 | 36.0 | 35.4 3 | 35.4 |
17 | 30.5 | 29.8 | 30.2 | 30.2 | 38.1 | 30.2 | 44.7 2 | 30.1 | 38.3 4 | 38.2 |
18 | 44.6 | 43.6 | 44.1 | 44.6 | 43.9 | 44.6 | 45.4 | 44.6 | 43.4 | 43.6 |
19 | 30.9 | 29.9 | 30.9 | 30.5 | 31.8 | 30.5 | 31.7 | 30.5 | 32.1 | 31.9 |
20 | 40.5 | 40.6 | 40.5 | 40.5 | 42.3 | 40.5 | 41.2 | 40.5 | 42.3 | 41.9 |
21 | 29.9 | 30.7 | 29.9 | 29.9 | 213.8 | 29.9 | 213.8 | 29.7 | 213.6 | 213.6 |
22 | 34.8 | 37.0 | 34.7 | 36.0 | 53.5 | 36.0 | 77.2 | 36.0 | 52.5 | 52.4 |
23 | 22.4 | 11.1 | 22.5 | 22.7 | 22.7 | 22.7 | 22.8 | 22.7 | 22.3 | 24.6 |
24 | ||||||||||
25 | 34.8 | 28.0 | 34.8 | 22.1 | 22.9 | 22.1 | 23.0 | 22.1 | 35.6 | 39.7 |
26 | 22.5 | 17.6 | 22.5 | 16.0 | 15.7 | 16.0 | 15.8 | 16.0 | 22.3 | 22.4 |
27 | 18.6 | 18.3 | 18.6 | 16.9 | 18.1 | 16.9 | 18.9 | 16.8 | 20.1 | 19.7 |
28 | 31.6 | 31.9 | 31.7 | 31.7 | 32.7 | 31.7 | 25.1 | 31.7 | 32.8 5 | 32.5 |
29 | 179.11 | 179.4 | 179.0 1 | 179.0 | 179.0 | 179.0 | ||||
30 | 32.9 | 31.7 | 31.9 | 32.3 | 15.2 | 32.3 | 14.9 | 32.3 | 15.2 6 | 15.1 |
OCH3 | 51.72 | 51.3 | 51.5 2 | 51.7 | 51.7 | 51.7 | ||||
1′ | 110.4 | 109.5 | 110.4 | 110.5 | 110.6 | 110.4 | 110.6 | 110.4 | 109.6 | 108.8 |
2′ | 139.1 | 140.1 | 141.3 | 144.5 | 144.5 | 144.5 | 144.5 | 144.5 | 145.0 | 145.3 |
3′ | 136.2 | 138.9 | 137.0 | 138.3 | 138.3 | 138.4 | 138.2 | 138.4 | 137.6 | 137.4 |
4′ | 122.9 | 125.6 | 125.5 | 129.4 | 129.4 | 129.5 | 129.3 | 129.6 | 129.0 | 129.7 |
5′ | 127.9 | 123.6 | 127.2 | 123.3 | 123.3 | 123.4 | 123.7 | 123.4 | 126.0 | 125.3 |
6′ | 26.4 | 28.0 | 75.2 | 187.2 | 187.2 | 187.1 | 187.2 | 187.0 | 201.1 | 200.0 |
7′ | 18.5 | 18.5 | 21.8 | 126.3 | 126.3 | 126.3 | 126.3 | 126.3 | 37.6 | 37.4 |
8′ | 43.9 | 44.1 | 38.5 | 171.0 | 171.0 | 170.0 | 171.1 | 169.7 | 41.9 | 41.8 |
9′ | 36.8 | 36.9 | 37.6 | 40.1 | 40.1 1 | 39.9 | 40.1 | 39.7 | 37.1 | 37.0 |
10′ | 144.4 | 145.1 | 144.7 | 151.8 | 151.8 | 151.7 | 151.8 | 151.7 | 151.7 | 152.2 |
11′ | 33.9 | 34.3 | 33.8 | 34.2 | 34.3 | 34.4 | 34.3 | 34.6 | 32.9 | 33.2 |
12′ | 30.0 | 30.3 | 29.8 | 29.7 | 29.9 | 30.2 | 29.9 | 29.8 | 29.7 1 | 29.5 |
13′ | 38.9 | 39.0 | 38.9 | 39.0 | 39.0 | 40.2 | 39.0 | 40.1 | 39.4 2 | 39.2 |
14′ | 39.4 | 39.4 | 39.1 | 44.7 | 44.7 | 44.3 | 44.8 2 | 44.0 | 40.0 | 39.8 |
15′ | 28.9 | 29.1 | 29.0 | 28.5 | 28.6 | 28.3 1 | 28.6 | 28.2 | 28.0 | 27.7 |
16′ | 36.4 | 36.3 | 36.1 | 36.4 | 36.4 | 35.5 | 36.4 | 29.6 | 35.3 3 | 29.3 |
17′ | 30.6 | 30.2 | 29.3 | 30.5 | 30.5 | 38.2 | 30.5 | 44.91 | 38.2 4 | 45.0 |
18′ | 44.1 | 44.4 | 44.4 | 44.3 | 44.3 | 43.5 | 44.3 | 45.01 | 44.0 | 45.3 |
19′ | 30.4 | 29.5 | 30.5 | 31.0 | 31.0 | 32.0 | 31.1 | 30.1 | 31.8 | 31.7 |
20′ | 40.4 | 40.6 | 40.4 | 40.6 | 40.6 | 41.9 | 40.6 | 40.9 | 41.9 | 41.3 |
21′ | 30.3 | 30.7 | 30.3 | 29.9 | 29.7 | 213.7 | 29.7 | 213.6 | 214.1 | 214.0 |
22′ | 36.3 | 36.6 | 36.6 | 35.0 | 35.0 | 52.7 | 35.0 | 76.1 | 53.6 | 77.2 |
23′ | 10.9 | 10.9 | 10.6 | 13.4 | 13.4 | 13.4 | 13.4 | 13.4 | 13.0 | 13.3 |
24′ | ||||||||||
25′ | 27.2 | 27.2 | 31.5 | 37.7 | 37.7 | 38.7 | 37.6 | 38.9 | 26.2 | 26.5 |
26′ | 15.8 | 16.1 | 16.3 | 20.9 | 20.9 | 20.8 | 20.8 | 20.9 | 15.0 | 15.1 |
27′ | 17.2 | 17.3 | 17.4 | 18.6 | 18.5 | 20.0 | 18.6 | 20.8 | 18.2 | 19.0 |
28′ | 31.8 | 31.9 | 26.4 | 31.6 | 31.6 | 32.6 | 31.6 | 25.0 | 32.6 5 | 25.1 |
29′ | 178.7 1 | 179.8 | 178.7 1 | 179.2 | 179.3 | 179.4 | ||||
30′ | 32.7 | 30.8 | 32.7 | 32.9 | 32.9 | 15.1 | 33.0 | 14.8 | 15.1 6 | 14.8 |
OCH3 | 51.5 2 | 51.6 | 51.7 2 | 51.6 | 51.6 | 51.7 | ||||
OCH3 | 55.4 | |||||||||
Ref | [133] | [134] | [133] | [135] | [136] | [136] | [137] | [137] | [136] | [136] |
C | D13 | D14 | D15 | D16 | D17 | D18 | D19 | D20 | D21 | D22 |
1 | 114.0 | 108.3 | 49.1 | 108.6 | 107.8 | 107.6 | 109.1 | 108.8 | 111.4 | 108.9 |
2 | 191.2 | 144.4 | 193.1 | 146.5 | 142.0 | 141.4 | 144.9 | 141.1 | 149.6 | 137.9 |
3 | 91.3 | 140.7 | 192.1 | 141.7 | 137.7 | 141.4 | 142.7 | 141.7 | 143.2 | 142.2 |
4 | 79.1 | 123.2 | 60.5 | 123.0 | 121.4 | 120.8 | 122.3 | 121.3 | 126.0 | 121.1 |
5 | 134.7 | 124.7 | 131.7 | 125.4 | 124.3 | 124.4 | 125.7 | 126.0 | 124.1 | 125.0 |
6 | 135.9 | 71.5 | 28.2 | 124.3 | 124.4 | 123.6 | 124.3 | 124.2 | 187.7 | 124.3 |
7 | 68.5 | 74.5 | 18.3 | 128.6 | 128.4 | 127.7 | 128.7 | 129.2 | 126.1 | 128.8 |
8 | 51.7 | 45.1 | 45.7 | 45.4 | 45.6 | 44.8 | 44.4 | 45.6 | 171.2 | 45.5 |
9 | 41.1 | 40.3 | 37.4 | 37.5 | 37.2 | 36.3 | 37.2 | 37.2 | 40.05 | 37.0 |
10 | 168.7 | 143.7 | 148.8 | 143.6 | 142.2 | 141.3 | 143.3 | 142.8 | 151.7 | 141.8 |
11 | 31.2 | 34.8 | 31.0 | 31.0 | 31.1 | 30.4 | 30.5 | 31.2 | 34.12 | 31.9 |
12 | 29.4 | 30.4 | 29.7 | 30.0 | 30.4 | 29.2 | 38.2 | 30.5 | 28.5 | 30.5 |
13 | 39.4 | 39.7 | 39.6 | 38.9 | 39.3 | 38.1 | 38.8 | 38.9 | 39.0 | 38.8 |
14 | 41.8 | 40.0 | 39.3 | 39.0 | 39.2 | 38.2 | 45.4 | 39.0 | 44.6 | 39.0 |
15 | 31.0 | 31.7 | 28.9 | 28.1 | 28.1 | 27.3 | 28.1 | 28.2 | 29.8 | 28.1 |
16 | 36.2 | 36.2 | 36.4 | 35.5 | 36.0 | 35.6 | 35.4 | 36.0 | 35.4 | 36.2 |
17 | 30.0 | 29.8 | 30.3 | 30.3 | 30.6 | 29.6 | 30.3 | 30.4 | 30.5 | 30.4 |
18 | 44.8 | 43.6 | 44.5 | 44.4 | 44.5 | 43.7 | 43.6 | 44.5 | 44.3 | 44.4 |
19 | 30.6 | 30.0 | 30.4 | 30.6 | 30.0 | 29.2 | 30.0 | 30.1 | 30.8 | 31.0 |
20 | 40.61 | 40.7 | 40.7 | 40.6 | 40.5 | 39.7 | 40.5 | 40.5 | 40.4 | 40.5 |
21 | 29.8 | 31.6 | 30.0 | 29.7 | 29.9 | 29.8 | 29.9 | 29.9 | 29.9 | 29.4 |
22 | 35.8 | 37.1 | 36.7 | 36.5 | 36.4 | 36.1 | 35.9 | 36.4 | 36.4 | 36.3 |
23 | 22.4 | 11.1 | 9.0 | 10.8 | 10.8 | 9.9 | 10.7 | 10.7 | 13.1 | 10.9 |
24 | ||||||||||
25 | 24.0 | 28.0 | 22.3 | 22.2 | 16.8 | 21.6 | 22.1 | 22.3 | 37.7 | 22.3 |
26 | 16.5 | 17.8 | 16.0 | 17.0 | 22.2 | 16.0 | 16.8 | 16.9 | 20.8 | 16.8 |
27 | 17.4 | 18.3 | 17.2 | 17.5 | 17.4 | 16.6 | 17.3 | 17.4 | 18.3 | 17.4 |
28 | 31.7 | 32.00 | 31.9 | 31.8 | 31.8 | 31.0 | 31.7 | 31.8 | 31.6 | 31.8 |
29 | 179.0 | 179.4 | 179.2 | 179.3 | 179.1 | 178.3 | 179.1 | 179.1 | 178.8 | 179.1 |
30 | 32.4 | 32.00 | 31.9 | 32.2 | 32.1 | 31.3 | 32.1 | 32.1 | 32.7 | 32.1 |
OCH3 | 51.7 | 51.6 | 51.6 | 51.6 | 51.5 | 50.7 | 51.6 | 51.5 | 51.5 | 51.5 |
1′ | 110.6 | 107.9 | 60.8 | 92.7 | 87.1 | 90.3 | 92.2 | 90.5 | 92.7 | 139.9 |
2′ | 144.2 | 141.6 | 24.4 | 38.6 | 41.8 | 44.6 | 36.3 | 45.8 | 38.4 | 36.0 |
3′ | 138.0 | 139.1 | 41.3 | 128.7 | 124.2 | 124.4 | 128.2 | 128.2 | 128.1 | 74.2 |
4′ | 129.3 | 122.0 | 39.8 | 140.5 | 151.2 | 141.2 | 140.6 | 140.6 | 140.6 | 90.1 |
5′ | 123.5 | 124.1 | 44.4 | 97.1 | 84.3 | 89.4 | 96.8 | 89.7 | 96.8 | 134.6 |
6′ | 187.2 | 124.3 | 25.1 | 38.1 | 35.2 | 35.2 | 38.9 | 84.6 | 39.1 | 30.0 |
7′ | 126.2 | 128.6 | 36.1 | 43.7 | 45.3 | 39.9 | 45.5 | 41.4 | 43.3 | 49.4 |
8′ | 171.0 | 45.8 | 151.4 | 36.0 | 38.9 | 35.8 | 32.7 | 29.7 | 34.8 | 29.9 |
9′ | 40.2 | 37.5 | 42.5 | 32.7 | 39.0 | 29.7 | 31.1 | 29.6 | 33.0 | 39.8 |
10′ | 151.9 | 143.8 | 36.2 | 40.1 | 32.9 | 43.0 | 39.4 | 43.2 | 39.3 | 42.6 |
11′ | 34.2 | 31.7 | 34.8 | 151.0 | 151.9 | 150.6 | 151.1 | 140.1 | 150.8 | 150.7 |
12′ | 29.9 | 30.0 | 21.9 | 108.7 | 108.4 | 108.0 | 108.6 | 119.1 | 108.8 | 108.6 |
13′ | 39.0 | 38.9 | 30.0 | 19.9 | 19.4 | 20.1 | 19.9 | 169.7 | 20.0 | 20.5 |
14′ | 44.7 | 39.1 | 16.7 | 19.1 | 20.3 | 17.8 | 19.1 | 19.0 | 19.1 | 17.1 |
15′ | 28.6 | 30.4 | 111.8 | 12.6 | 22.9 | 10.7 | 12.5 | 14.4 | 12.4 | 13.9 |
16′ | 36.4 | 36.1 | ||||||||
17′ | 30.5 | 30.5 | ||||||||
18′ | 44.3 | 44.5 | ||||||||
19′ | 30.9 | 29.4 | ||||||||
20′ | 40.5 1 | 40.6 | ||||||||
21′ | 29.8 | 31.6 | ||||||||
22′ | 35.0 | 36.6 | ||||||||
23′ | 13.4 | 10.8 | ||||||||
24′ | ||||||||||
25′ | 37.6 | 22.3 | ||||||||
26′ | 20.9 | 17.2 | ||||||||
27′ | 18.4 | 17.3 | ||||||||
28′ | 31.6 | 31.8 | ||||||||
29′ | 179.0 | 179.6 | ||||||||
30′ | 32.8 | 31.6 | ||||||||
OCH3 | 51.7 | 51.4 | ||||||||
Ref | [136] | [134] | [75] | [138] | [138] | [138] | [138] | [138] | [138] | [138] |
C | D23 | D24 | D25 | D26 | D27 | D28 | D30 | D31 | D32 | D33 |
1 | 107.6 | 108.2 | 116.0 | 114.8 | 116.5 | 114.6 | 115.4 | 108.2 | 115.9 | 114.9 |
2 | 145.8 | 142.4 | 187.8 | 187.3 | 193.3 | 189.6 | 191.0 | 144.4 | 190.8 | 189.6 |
3 | 136.2 | 138.6 | 92.2 | 90.8 | 93.1 | 91.3 | 91.8 | 140.6 | 92.0 | 90.7 |
4 | 122.7 | 121.6 | 79.1 | 76.9 | 79.2 | 77.2 | 79.1 | 123.0 | 79.4 | 77.2 11 |
5 | 124.0 | 124.6 | 130.3 | 131.7 | 130.7 | 131.3 | 130.6 | 124.7 | 130.5 | 132.1 |
6 | 124.2 | 124.2 | 126.6 | 128.8 | 126.7 | 129.8 | 126.1 | 71.3 | 125.9 | 128.7 |
7 | 128.3 | 128.6 | 116.0 | 117.3 | 115.7 | 117.2 | 116.2 | 74.2 | 116.2 | 116.9 |
8 | 45.6 | 45.6 | 161.8 | 164.4 | 162.4 | 164.8 | 160.8 | 45.0 | 161.2 | 164.5 |
9 | 37.3 | 37.3 | 41.9 | 43.8 | 42.0 | 43.9 | 41.8 | 40.3 | 41.6 | 44.1 |
10 | 143.0 | 142.7 | 174.4 | 173.4 | 174.8 | 173.8 | 173.8 | 143.9 | 173.4 | 173.3 |
11 | 31.1 | 31.1 | 32.8 | 32.9 | 33.4 | 32.88 | 32.8 | 34.6 | 32.8 | 32.9 |
12 | 30.1 | 30.0 | 29.2 | 29.4 | 29.3 | 29.3 | 29.5 | 30.3 | 29.2 | 29.9 1 |
13 | 39.0 | 38.9 | 38.1 | 38.9 | 38.0 | 38.5 | 38.2 | 39.6 | 37.9 | 38.7 |
14 | 38.9 | 39.0 | 44.6 | 44.3 | 44.6 | 44.4 | 44.5 | 39.9 | 44.6 | 44.4 |
15 | 28.2 | 28.2 | 28.3 | 28.6 | 28.4 | 28.6 | 28.3 | 28.5 | 28.5 | 28.6 2 |
16 | 36.4 | 36.0 | 36.3 | 36.2 | 36.2 | 36.2 | 36.4 | 36.1 | 36.3 | 36.4 |
17 | 30.4 | 30.4 | 30.5 | 30.4 | 30.4 | 30.4 | 30.4 | 29.9 | 30.5 | 30.6 |
18 | 44.5 | 44.5 | 44.0 | 44.1 | 44.1 | 44.1 | 44.2 | 43.9 | 44.2 | 44.4 3 |
19 | 30.6 | 30.6 | 30.9 | 30.6 | 31.0 | 30.7 | 30.9 | 30.7 | 30.6 | 30.9 4 |
20 | 40.5 | 40.5 | 40.0 | 40.3 | 39.7 | 40.1 | 40.5 | 40.7 | 40.3 | 40.5 5 |
21 | 30.0 | 29.8 | 29.6 | 29.8 | 29.7 | 29.4 | 29.8 | 29.7 | 29.4 | 29.9 6 |
22 | 36.0 | 36.4 | 34.6 | 34.8 | 34.3 | 34.4 | 34.8 | 36.9 | 34.7 | 34.8 7 |
23 | 11.0 | 10.9 | 22.2 | 24.5 | 22.2 | 24.4 | 22.0 | 11.1 | 22.4 | 24.2 |
24 | ||||||||||
25 | 22.3 | 22.2 | 34.8 | 39.2 | 35.2 | 39.1 | 34.8 | 28.2 | 37.5 | 39.3 |
26 | 16.9 | 16.9 | 22.4 | 22.5 | 18.4 | 18.6 | 22.3 | 17.1 | 22.0 | 22.4 |
27 | 17.5 | 17.4 | 18.8 | 18.5 | 22.2 | 22.2 | 18.7 | 18.4 | 18.9 | 18.3 8 |
28 | 31.8 | 31.8 | 31.6 | 31.5 | 31.4 | 31.4 | 31.6 | 31.8 | 31.6 | 31.6 9 |
29 | 179.1 | 179.1 | 184.5 | 184.3 | 182.4 | 183.5 | 178.7 | 179.4 | 184.4 | 178.9 10 |
30 | 32.1 | 32.1 | 32.6 | 32.4 | 31.8 | 32.4 | 32.7 | 31.3 | 32.7 | 32.8 |
OCH3 | 51.5 | 51.5 | 51.7 | 51.6 | 51.6 | |||||
1′ | 135.4 | 142.7 | 111.2 | 110.8 | 36.2 | 37.9 | 108.8 | 108.2 | 110.4 | 110.7 |
2′ | 36.5 | 34.5 | 144.4 | 145.0 | 18.7 | 18.8 | 140.8 | 142.1 | 144.7 | 144.2 |
3′ | 74.2 | 78.8 | 137.5 | 137.4 | 40.4 | 41.3 | 136.5 | 138.0 | 138.2 | 138.5 |
4′ | 89.9 | 86.1 | 127.2 | 128.3 | 33.0 | 33.1 | 121.3 | 121.0 | 129.5 | 128.2 |
5′ | 137.7 | 138.0 | 124.4 | 123.6 | 49.8 | 49.2 | 126.0 | 125.7 | 23.0 | 124.0 |
6′ | 32.1 | 35.0 | 192.0 | 189.9 | 35.7 | 35.9 | 124.0 | 124.4 | 187.5 | 187.8 |
7′ | 49.6 | 46.3 | 126.0 | 126.1 | 197.1 | 198.4 | 129.4 | 128.9 | 126.0 | 126.2 |
8′ | 29.7 | 30.0 | 171.4 | 171.0 | 126.0 | 125.9 | 45.5 | 45.9 | 171.4 | 171.5 |
9′ | 39.6 | 38.5 | 40.3 | 40.0 | 150.3 | 151.3 | 37.4 | 37.6 | 40.0 | 39.9 |
10′ | 42.6 | 34.7 | 150.1 | 151.1 | 37.7 | 37.7 | 142.8 | 141.9 | 151.9 | 151.1 |
11′ | 150.7 | 151.2 | 34.0 | 33.8 | 112.6 | 112.1 | 30.6 | 31.1 | 34.2 | 34.2 |
12′ | 108.7 | 108.5 | 29.3 | 29.1 | 147.2 | 147.0 | 30.0 | 30.0 | 29.9 | 29.6 1 |
13′ | 20.4 | 20.4 | 38.9 | 38.5 | 139.8 | 139.4 | 38.9 | 39.0 | 39.0 | 39.0 |
14′ | 17.1 | 19.3 | 44.7 | 44.6 | 114.9 | 115.8 | 39.0 | 39.1 | 44.6 | 44.7 |
15′ | 14.0 | 22.3 | 28.3 | 28.4 | 32.8 | 32.5 | 28.4 | 29.9 | 28.5 | 28.5 2 |
16′ | 36.2 | 36.2 | 21.3 | 21.3 | 36.0 | 36.1 | 36.3 | 36.4 | ||
17′ | 30.4 | 30.3 | 23.3 | 23.2 | 30.6 | 30.5 | 30.4 | 30.6 | ||
18′ | 44.1 | 44.1 | 44.5 | 44.5 | 44.0 | 44.3 3 | ||||
19′ | 30.5 | 30.7 | 31.0 | 30.7 | 31.1 | 30.8 4 | ||||
20′ | 39.7 | 40.1 | 40.4 | 40.6 | 40.2 | 40.4 5 | ||||
21′ | 29.5 | 29.7 | 29.7 | 30.0 | 29.3 | 29.7 6 | ||||
22′ | 34.4 | 34.5 | 36.4 | 36.7 | 34.4 | 34.7 7 | ||||
23′ | 12.9 | 13.2 | 10.8 | 11.0 | 13.2 | 12.8 | ||||
24′ | ||||||||||
25′ | 36.8 | 37.5 | 22.5 | 22.2 | 34.7 | 38.0 | ||||
26′ | 20.7 | 20.9 | 16.9 | 17.1 | 20.9 | 20.9 | ||||
27′ | 18.6 | 18.8 | 17.4 | 17.6 | 18.8 | 18.2 8 | ||||
28′ | 31.3 | 31.5 | 31.8 | 31.8 | 32.5 | 31.6 9 | ||||
29′ | 183.6 | 184.3 | 178.7 | 179.5 | 183.6 | 178.7 10 | ||||
30′ | 32.4 | 32.2 | 32.1 | 32.1 | 32.8 | |||||
OCH3 | 51.6 | 51.5 | 32.4 | 51.6 | ||||||
Ref | [138] | [138] | [139] | [139] | [139] | [139] | [133] | [134] | [139] | [136] |
C | D34 | D35 | D36 | D37 | D38 | D39 | D40 | D41 | D42 | D43 |
1 | 116.0 | 114.9 | 116.0 | 109.0 | 111.4 | 115.8 | 114.7 | 115.5 | 115.5 | 115.0 |
2 | 190.4 | 189.5 | 190.4 | 145.1 | 149.7 | 191.1 | 189.4 | 190.2 | 190.3 | 189.5 |
3 | 91.8 | 90.6 | 91.8 | 142.8 | 143.3 | 91.9 | 91.0 | 92.0 | 92.0 | 91.0 |
4 | 79.4 | 76.9 | 79.3 | 122.5 | 125.2 | 78.8 | 77.3 | 79.3 | 79.4 | 76.8 |
5 | 130.9 | 132.0 | 130.9 | 125.7 | 122.4 | 131.1 | 131.8 | 130.3 | 130.3 | 132.1 |
6 | 126.1 | 128.7 | 126.2 | 124.6 | 187.5 | 126.1 | 128.8 | 126.6 | 126.6 | 128.7 |
7 | 116.2 | 116.8 | 116.4 | 128.3 | 126.2 | 116.4 | 117.2 | 116.3 | 116.3 | 117.3 |
8 | 160.2 | 164.6 | 159.9 | 44.9 | 170.2 | 159.5 | 164.4 | 160.3 | 160.1 | 163.0 |
9 | 41.5 | 44.2 | 41.4 | 39.4 | 39.3 | 41.3 | 43.9 | 41.7 | 41.6 | 43.7 1 |
10 | 173.2 | 173.4 | 173.2 | 143.3 | 151.7 | 173.4 | 173.2 | 173.7 | 173.8 | 173.0 |
11 | 33.3 | 32.8 | 33.5 | 31.7 | 34.3 | 33.5 | 32.8 | 33.2 | 33.4 | 33.3 |
12 | 29.8 1 | 29.5 | 29.9 1 | 29.9 | 30.2 | 30.0 | 29.8 | 29.9 1 | 29.9 1 | 29.9 |
13 | 39.5 | 38.6 | 39.5 | 38.3 | 39.9 | 39.5 | 38.6 | 39.4 | 39.4 | 39.8 |
14 | 44.2 | 44.4 1 | 43.9 | 32.8 | 44.3 | 44.1 | 44.4 | 44.3 | 44.0 | 43.61 |
15 | 28.3 | 28.6 | 28.1 | 27.5 | 28.4 | 28.3 | 28.6 | 28.3 | 28.0 | 28.2 |
16 | 35.5 | 36.4 | 29.5 2 | 35.3 | 35.6 | 29.7 | 36.4 | 35.4 | 29.5 | 29.5 |
17 | 38.2 | 30.5 | 44.7 | 35.4 | 38.2 | 39.0 | 30.5 | 38.2 | 44.7 | 45.0 |
18 | 43.4 | 44.1 | 44.9 | 43.5 | 43.5 | 43.8 | 44.2 | 43.4 | 44.9 | 44.8 |
19 | 32.2 | 30.8 | 32.1 | 31.0 | 32.0 | 32.1 | 30.9 | 32.1 | 32.1 | 31.9 |
20 | 41.9 | 40.4 | 40.8 | 40.1 | 41.9 | 41.8 | 40.5 | 41.9 | 40.8 | 40.9 |
21 | 213.6 | 29.9 | 213.5 | 214.3 | 213.7 | 213.6 | 29.8 | 213.6 | 213.6 | 213.5 |
22 | 52.5 | 34.7 | 76.5 | 53.9 | 52.6 | 52.5 | 35.0 | 52.5 | 76.5 | 76.4 |
23 | 22.1 | 24.2 | 22.2 | 10.8 | 13.2 | 22.1 | 24.6 | 22.3 | 22.2 | 24.6 |
24 | ||||||||||
25 | 35.7 | 39.3 | 35.8 | 32.8 | 38.7 | 35.6 | 39.2 | 35.6 | 35.6 | 40.1 |
26 | 22.3 | 22.4 | 22.4 | 18.6 | 20.8 | 22.3 | 22.3 | 22.3 | 22.4 | 22.3 |
27 | 20.1 | 18.2 | 20.9 | 16.1 | 19.7 | 15.0 | 18.2 | 20.0 | 20.9 | 20.4 |
28 | 32.5 | 31.5 | 25.0 | 22.7 | 32.6 | 32.5 | 31.6 | 32.6 | 25.0 | 25.0 |
29 | 178.8 | 179.1 | ||||||||
30 | 15.1 | 32.7 | 14.7 | 15.1 | 15.1 | 20.0 | 32.9 | 15.1 | 14.8 | 14.8 |
OCH3 | 51.6 | 51.6 | ||||||||
1′ | 110.5 | 110.7 | 110.6 | 92.9 | 92.8 | 108.1 | 110.6 | 111.4 | 111.3 | 110.6 |
2′ | 144.4 | 144.3 | 144.4 | 38.4 | 38.8 | 141.6 | 145.2 | 144.6 | 144.6 | 145.1 |
3′ | 138.3 | 138.5 | 138.3 | 128.2 | 128.1 | 137.6 | 137.5 | 137.6 | 137.6 | 137.5 |
4′ | 129.3 | 128.3 | 129.3 | 140.6 | 140.7 | 122.5 | 128.3 | 127.6 | 127.7 | 128.4 |
5′ | 123.3 | 123.9 | 123.4 | 96.8 | 96.8 | 125.0 | 123.8 | 124.5 | 124.5 | 123.9 |
6′ | 187.2 | 187.6 | 187.2 | 38.2 | 38.4 | 124.0 | 187.4 | 187.9 | 187.8 | 187.3 |
7′ | 126.3 | 126.1 | 126.2 | 43.6 | 43.3 | 129.2 | 126.1 | 126.1 | 126.2 | 126.1 |
8′ | 171.0 | 170.4 | 171.1 | 35.7 | 35.4 | 45.5 | 171.2 | 171.7 | 171.6 | 171.7 |
9′ | 40.1 | 39.7 | 40.8 | 32.7 | 33.0 | 38.2 | 40.0 | 40.0 | 39.9 | 40.0 |
10′ | 151.8 | 151.0 | 151.8 | 42.2 | 39.3 | 143.8 | 151.1 | 150.5 | 150.5 | 151.2 |
11′ | 34.3 | 34.3 | 34.3 | 151.2 | 150.9 | 36.6 | 34.0 | 34.2 | 34.2 | 34.0 |
12′ | 30.0 | 30.2 | 29.8 1 | 108.6 | 108.8 | 36.4 | 29.8 | 29.9 1 | 29.91 | 29.9 |
13′ | 39.0 | 40.2 | 39.0 | 19.9 | 20.0 | 37.5 | 39.0 | 39.0 | 39.0 | 39.0 |
14′ | 44.7 | 44.31 | 44.9 | 19.0 | 19.1 | 38.2 | 44.7 | 44.7 | 44.9 | 44.7 |
15′ | 28.6 | 28.4 | 28.6 | 12.5 | 12.4 | 28.3 | 28.5 | 28.5 | 28.5 | 28.5 |
16′ | 36.4 | 35.5 | 36.4 | 35.4 | 36.4 | 36.4 | 36.4 | 36.4 | ||
17′ | 30.5 | 38.2 | 30.5 | 30.4 | 30.5 | 30.5 | 30.5 | 30.5 | ||
18′ | 44.3 | 43.5 | 44.3 | 44.4 | 44.2 | 44.3 | 44.3 | 44.2 | ||
19′ | 31.1 | 32.0 | 31.1 | 29.8 | 30.8 | 30.9 | 30.8 | 30.9 | ||
20′ | 40.6 | 41.9 | 40.7 | 40.6 | 40.4 | 40.4 | 40.4 | 40.5 | ||
21′ | 29.7 1 | 214.7 | 29.7 2 | 29.8 | 29.5 | 29.9 1 | 29.8 | 29.7 | ||
22′ | 35.0 | 52.6 | 35.0 | 35.8 | 34.7 | 34.7 | 34.8 | 35.0 | ||
23′ | 13.3 | 12.8 | 13.3 | 10.8 | 13.2 | 13.0 | 13.0 | 13.2 | ||
24′ | ||||||||||
25′ | 37.6 | 38.9 | 37.7 | 22.3 | 37.7 | 37.6 | 37.6 | 37.7 | ||
26′ | 20.9 | 20.8 | 20.8 | 17.5 | 20.9 | 20.8 | 20.8 | 20.9 | ||
27′ | 18.5 | 19.7 | 18.6 | 17.0 | 18.4 | 18.3 | 18.3 | 18.5 | ||
28′ | 31.6 | 32.6 | 31.6 | 31.8 | 31.5 | 31.6 | 31.6 | 31.6 | ||
29′ | 179.3 | 179.4 | 179.3 | 178.8 | 178.7 | 178.8 | 179.1 | |||
30′ | 32.9 | 15.1 | 33.0 | 31.8 | 32.7 | 32.7 | 32.7 | 32.9 | ||
OCH3 | 51.6 | 51.8 | 51.5 | 51.4 | 51.6 | 51.6 | 51.4 | |||
Ref | [136] | [136] | [137] | [128] | [128] | [128] | [140] | [136] | [137] | [137] |
C | D44 | D45 | D46 | D47 | D48 | D49 | D50 | |||
1 | 115.2 | 114.6 | 115.5 | 115.5 | 108.2 | 108.2 | 128.3 | |||
2 | 190.2 | 189.4 | 190.2 | 189.5 | 144.5 | 144.5 | 183.6 | |||
3 | 92.0 | 91.1 | 92.0 | 92.0 | 140.7 | 140.7 | 96.9 | |||
4 | 79.4 | 77.2 | 79.4 | 79.4 | 122.8 | 122.9 | 92.3 | |||
5 | 129.8 | 131.8 | 130.3 | 130.2 | 124.7 | 124.7 | 39.5 | |||
6 | 126.8 | 128.9 | 126.6 | 126.5 | 71.4 | 71.4 | 28.1 | |||
7 | 116.1 | 117.2 | 116.2 | 116.3 | 74.1 | 74.1 | 32.8 | |||
8 | 161.5 | 164.4 | 160.4 | 160.5 | 43.6 | 43.6 | 30.4 | |||
9 | 42.0 | 44.0 | 41.7 | 41.8 | 40.4 1 | 40.4 1 | 43.7 | |||
10 | 174.3 | 173.2 | 173.7 | 173.6 | 143.7 | 143.7 | 140.7 | |||
11 | 32.9 | 32.8 | 33.2 | 32.8 | 34.5 | 34.5 | 35.4 | |||
12 | 29.5 | 29.61 | 29.8 | 29.5 | 30.2 | 30.2 | 30.6 | |||
13 | 38.1 | 38.6 | 39.4 | 38.5 | 40.6 1 | 40.6 1 | 44.5 | |||
14 | 44.7 | 44.4 | 44.3 | 44.2 | 40.4 1 | 40.4 1 | 40.5 | |||
15 | 28.4 | 28.6 | 28.3 | 28.4 | 29.3 | 29.3 | 30.0 | |||
16 | 36.3 | 36.4 | 35.4 | 35.5 | 35.5 | 35.5 | 36.4 | |||
17 | 30.5 | 30.5 | 38.2 | 37.1 | 37.9 | 37.9 | 40.5 | |||
18 | 44.1 | 44.3 | 43.4 | 43.6 | 43.8 | 43.7 | 43.7 | |||
19 | 30.9 | 30.8 | 32.1 | 34.2 1 | 31.9 | 31.9 | 43.7 | |||
20 | 40.4 | 40.4 | 41.9 | 53.6 | 42.2 | 42.2 | 151.2 | |||
21 | 29.8 | 30.1 2 | 213.6 | 209.4 | 214.7 | 214.6 2 | 39.0 | |||
22 | 34.7 | 34.7 | 52.5 | 51.9 | 53.9 | 53.9 | 38.2 | |||
23 | 22.2 | 24.6 | 22.3 | 22.3 | 11.3 | 11.3 | 12.6 | |||
24 | ||||||||||
25 | 34.9 | 39.1 | 35.6 | 35.2 | 29.1 | 29.1 | ||||
26 | 22.5 | 22.4 | 22.3 | 22.8 | 15.7 | 15.7 | 19.1 | |||
27 | 18.7 | 18.2 | 20.0 | 18.2 | 19.3 | 19.2 | 32.1 | |||
28 | 31.6 | 31.6 | 32.6 | 32.6 | 33.1 | 33.1 | 20.5 | |||
29 | 178.9 | 178.8 | 175.1 | 108.7 | ||||||
30 | 32.7 | 32.8 | 15.1 | 25.1 | 15.2 | 15.2 | 19.9 | |||
OCH3 | 51.6 | 51.6 | 52.6 | |||||||
1′ | 111.4 | 110.5 | 111.4 | 111.4 | 109.7 | 109.7 | 109.2 | |||
2′ | 144.7 | 145.2 | 144.7 | 144.6 | 141.5 | 141.4 | 145.0 | |||
3′ | 137.7 | 137.6 | 137.7 | 137.6 | 140.3 | 140.3 | 142.8 | |||
4′ | 127.8 | 128.6 | 127.8 | 127.8 | 121.8 | 121.8 | 122.4 | |||
5′ | 124.5 | 123.9 | 124.5 | 124.5 | 124.3 | 124.3 | 125.7 | |||
6′ | 187.7 | 187.2 | 187.7 | 187.7 | 119.7 | 119.8 | 124.4 | |||
7′ | 126.1 | 126.2 | 126.2 | 126.1 | 138.2 | 138.1 | 128.7 | |||
8′ | 170.4 | 169.9 | 170.8 | 170.7 | 43.9 | 43.9 | 45.5 | |||
9′ | 39.7 | 39.7 | 39.8 | 39.8 | 142.8 | 143.0 | 37.3 | |||
10′ | 150.4 | 151.1 | 150.3 | 150.4 | 131.8 | 131.8 | 143.3 | |||
11′ | 34.5 | 34.3 | 34.1 | 34.3 1 | 122.7 | 122.6 | 31.2 | |||
12′ | 30.2 | 30.1 2 | 29.9 | 30.1 | 37.5 | 37.4 | 30.0 | |||
13′ | 40.1 | 40.1 | 39.2 | 40.2 | 40.1 | 40.1 | 38.9 | |||
14′ | 44.0 | 43.9 | 44.3 | 44.3 | 40.7 | 40.4 1 | 38.9 | |||
15′ | 28.2 | 28.2 | 28.6 | 28.4 | 24.0 | 23.6 | 28.1 | |||
16′ | 29.6 | 29.5 1 | 35.7 | 35.5 | 35.9 | 29.5 | 36.4 | |||
17′ | 44.9 | 44.9 | 37.1 | 38.2 | 39.2 | 45.3 | 30.4 | |||
18′ | 45.0 | 45.0 | 43.9 | 43.5 | 45.7 | 46.7 | 44.5 | |||
19′ | 32.0 | 31.9 | 34.2 | 32.0 | 32.5 | 32.1 | 30.6 | |||
20′ | 40.9 | 40.9 | 53.6 | 41.9 | 42.4 | 41.3 | 40.5 | |||
21′ | 213.7 | 213.6 | 209.4 | 213.7 | 214.9 | 214.5 2 | 30.0 | |||
22′ | 76.5 | 76.7 | 51.9 | 52.6 | 51.2 | 75.4 | 36.0 | |||
23′ | 13.0 | 13.2 | 13.0 | 13.0 | 10.7 | 10.7 | 10.8 | |||
24′ | ||||||||||
25′ | 38.7 | 38.9 | 38.2 | 38.4 | 22.4 | 22.4 | 22.1 | |||
26′ | 20.9 | 20.9 | 21.2 | 20.8 | 19.6 | 19.8 | 16.9 | |||
27′ | 20.6 | 20.7 | 17.8 | 19.7 | 20.6 | 21.4 | 17.4 | |||
28′ | 25.0 | 25.0 | 32.6 | 32.6 | 31.5 | 24.2 | 31.8 | |||
29′ | 175.0 | 179.2 | ||||||||
30′ | 14.8 | 14.7 | 25.1 | 15.1 | 15.4 | 15.0 | 32.1 | |||
OCH3 | 52.5 | 51.6 | ||||||||
Ref | [137] | [137] | [137] | [137] | [141] | [141] | [142] |
C | L1 + | L2 | L3 | L4 | L5 | L6 | L7 | L8 | L9 | L10 |
---|---|---|---|---|---|---|---|---|---|---|
1 | 38.4 | 38.7 | 41.8 | 123.6 | 42.1 | 39.6 | 39.6 | 79.5 | 39.8 | 39.3 |
2 | 23.7 | 27.4 | 34.0 | 165.1 | 34.2 | 34.1 | 34.1 | 42.9 | 34.3 | 34.3 |
3 | 80.9 | 79.0 | 218.3 | 205.3 | 218.8 | 218.0 | 217.7 | 216.1 | 218.2 | 221.4 |
4 | 37.9 | 38.9 | 47.5 | 45.0 | 47.6 | 47.3 | 47.2 | 47.1 | 47.5 | 50.7 |
5 | 55.4 | 55.2 | 54.6 | 52.9 | 54.8 | 54.9 | 54.9 | 51.2 | 55.1 | 55.3 |
6 | 18.2 | 18.3 | 19.4 | 18.9 | 19.6 | 19.6 | 19.6 | 19.6 | 19.8 | 19.2 |
7 | 34.3 | 34.3 | 33.9 | 34.5 | 34.3 | 33.5 | 33.6 | 32.9 | 33.7 | 33.6 |
8 | 40.9 | 40.8 | 42.2 | 42.9 | 42.4 | 40.8 | 40.6 | 41.0 | 41.0 | 40.7 |
9 | 49.9 | 50.0 | 54.5 | 48.9 | 54.9 | 49.3 | 49.8 | 50.6 | 50.0 | 49.5 |
10 | 37.1 | 37.1 | 38.0 | 40.6 | 38.2 | 36.8 | 36.9 | 45.1 | 37.0 | 36.6 |
11 | 20.9 | 20.8 | 70.1 | 70.6 | 70.5 | 21.4 | 21.5 | 22.9 | 21.6 | 21.7 |
12 | 27.6 * | 26.5 | 37.2 | 37.3 | 37.4 | 24.8 | 25.1 | 25.1 | 25.0 | 25.2 |
13 | 37.9 | 37.8 | 36.1 | 37.1 | 37.2 | 37.4 | 37.7 | 37.9 | 37.8 | 37.5 |
14 | 43.1 | 42.9 | 42.2 | 42.8 | 42.6 | 44.1 | 41.9 | 42.9 | 42.8 | 42.8 |
15 | 27.2 | 27.2 | 26.8 | 27.3 | 27.4 | 36.8 | 26.9 | 27.5 | 27.3 | 27.0 |
16 | 35.3 | 35.3 | 33.6 | 35.3 | 35.4 | 76.9 | 33.1 | 35.5 | 35.9 | 34.0 |
17 | 43.0 | 43.1 | 47.3 | 43.0 | 43.0 | 48.6 | 80.2 | 42.9 | 42.0 | 47.8 |
18 | 49.0 | 47.1 | 47.8 | 47.5 | 47.6 | 47.6 | 48.3 | 47.9 * | 48.2 | 48.6 |
19 | 42.8 | 37.4 | 47.4 | 47.7 | 47.7 | 47.5 | 48.0 | 48.2 * | 60.0 | 47.8 |
20 | 49.0 | 49.7 | 149.5 | 150.2 | 150.2 | 149.9 | 149.6 | 150.7 | 148.4 | 150.3 |
21 | 25.2 * | 23.6 | 29.4 | 29.7 | 29.8 | 29.8 | 29.4 | 29.8 | 77.9 | 29.7 |
22 | 40.0 | 40.5 | 28.8 | 39.8 | 39.8 | 37.7 | 38.5 | 40.0 | 49.6 | 29.1 |
23 | 28.0 | 28.0 | 27.2 | 21.4 | 27.5 | 26.6 | 26.6 | 28.0 | 26.8 | 22.1 |
24 | 16.6 | 15.4 | 20.5 | 28.2 | 20.8 | 21.0 | 21.0 | 19.8 | 21.2 | 65.3 |
25 | 16.1 ** | 16.0 | 16.5 | 19.9 | 16.7 | 16.0 | 16.0 | 11.9 | 16.1 | 17.0 |
26 | 16.0 ** | 15.9 | 16.6 | 17.4 | 16.9 | 15.8 | 15.9 | 15.9 | 16.0 | 15.6 |
27 | 14.4 | 14.3 | 14.4 | 14.4 | 14.4 | 16.1 | 13.8 | 14.4 | 14.6 | 14.7 |
28 | 18.0 | 17.9 | 60.3 | 18.0 | 18.1 | 11.7 | 18.1 | 19.8 | 60.5 | |
29 | 207.0 | 7.3 | 110.1 | 113.5 | 109.9 | 109.8 | 109.6 | 109.5 | 111.5 | 109.8 |
30 | 14.5 | 205.1 | 18.9 | 19.3 | 19.4 | 19.3 | 19.3 | 19.3 | 19.9 | 19.1 |
COOCH3 | 21.3 | |||||||||
COOCH3 | 171.0 | |||||||||
Ref | [144] | [145] | [146] | [147] | [148] | [149] | [145] | [150] | [14] | [151] |
C | L11 | L12 | L13 | L14 | L15 | L16 | L17 a | L18 | L20 | L21 |
1 | 39.6 | 39.6 | 125.2 | 39.8 | 40.2 | 39.7 | 34.1 | 42.4 | 39.7 | 53.5 |
2 | 34.1 | 34.1 | 159.2 | 34.0 | 35.7 | 34.3 | 26.6 | 34.3 | 34.2 | 211.4 |
3 | 218.2 | 218.0 | 205.0 | 218.0 | 216.5 | 218.3 | 75.1 | 218.6 | 217.9 | 82.5 |
4 | 47.3 | 47.4 | 44.6 | 47.3 | 47.7 | 47.5 | 38.1 | 47.6 | 47.4 | 45.6 |
5 | 54.9 | 55.0 | 53.5 | 54.8 | 55.4 | 55.1 | 49.2 | 54.9 | 55.1 | 54.6 |
6 | 19.6 | 19.6 | 19.0 | 19.0 | 20.4 | 19.8 | 18.5 | 19.5 | 19.7 | 18.5 |
7 | 33.5 | 33.5 | 33.7 | 33.5 | 34.2 | 33.8 | 34.5 | 34.2 | 33.7 | 34.0 |
8 | 40.9 | 42.7 | 41.8 | 40.9 | 41.5 | 41.0 | 41.1 | 42.1 | 40.8 | 41.3 |
9 | 49.7 | 49.6 | 44.5 | 49.7 | 49.8 | 50.0 | 50.8 | 54.7 | 49.7 | 50.4 |
10 | 36.8 | 36.9 | 39.5 | 36.8 | 37.7 | 37.0 | 37.7 | 38.2 | 36.9 | 43.9 |
11 | 21.4 | 21.4 | 21.2 | 21.3 | 22.2 | 21.7 | 20.8 | 70.1 | 21.5 | 21.0 |
12 | 26.8 | 27.6 | 25.2 | 25.2 | 28.2 | 26.8 | 26.1 | 37.6 | 27.6 | 25.1 |
13 | 37.3 | 37.1 | 37.5 | 37.4 | 38.0 | 38.3 | 35.2 | 37.6 | 37.9 | 37.2 |
14 | 42.7 | 40.8 | 43.0 | 42.8 | 43.5 | 43.0 | 41.4 | 42.3 | 42.8 | 42.8 |
15 | 27.0 | 26.9 | 27.0 | 27.0 | 28.2 | 27.6 | 28.2 | 28.8 | 27.4 | 27.1 |
16 | 33.8 | 29.1 | 29.1 | 29.1 | 34.5 | 35.6 | 22.9 | 28.9 | 35.4 | 29.3 |
17 | 47.8 | 48.0 | 47.7 | 47.7 | 37.6 | 43.2 | 54.0 | 59.3 | 43.3 | 47.8 |
18 | 49.3 | 52.3 | 48.6 | 48.6 | 50.4 | 49.0 | 55.5 | 59.3 | 47.7 | 48.7 |
19 | 43.5 | 36.5 | 47.8 | 47.3 | 52.8 | 43.9 | 92.2 | 47.2 | 47.7 | 47.8 |
20 | 154.4 | 157.0 | 150.3 | 150.0 | 211.5 | 154.9 | 141.4 | 149.1 | 157.2 | 150.2 |
21 | 29.1 | 32.8 | 29.7 | 29.7 | 27.8 | 31.9 | 34.4 | 29.8 | 32.7 | 29.7 |
22 | 31.7 | 33.9 | 33.9 | 33.9 | 40.4 | 40.0 | 29.3 | 32.9 | 40.0 | 33.8 |
23 | 26.7 | 26.6 | 21.4 | 26.6 | 27.1 | 26.8 | 29.2 | 20.7 | 26.6 | 29.1 |
24 | 21.1 | 21.1 | 27.8 | 21.0 | 21.3 | 21.2 | 22.8 | 27.4 | 21.1 | 16.4 |
25 | 16.0 | 15.9 | 19.2 | 15.8 | 16.1 | 16.1 | 16.5 | 16.8 | 15.9 | 17.0 |
26 | 15.8 | 15.8 | 16.5 | 15.9 | 14.8 | 16.0 | 15.7 | 16.7 | 15.8 | 14.8 |
27 | 14.7 | 14.6 | 14.6 | 14.7 | 16.4 | 14.6 | 13.6 | 14.1 | 14.4 | 15.6 |
28 | 60.2 | 60.2 | 60.6 | 60.5 | 18.3 | 17.9 | 178.6 | 206.0 | 17.8 | 60.5 |
29 | 107.2 | 133.2 | 109.9 | 109.7 | 106.9 | 112.3 | 110.7 | 133.0 | 109.9 | |
30 | 65.0 | 194.9 | 19.0 | 19.6 | 29.3 | 65.2 | 19.3 | 19.0 | 195.0 | 19.1 |
Ref | [152] | [153] | [151] | [149] | [14] | [14] | [153] | [151] | [148] | [73] |
C | L22 | L23 b | L24 | L25 | L26 | L28 | L29 | L30 | L31 | L32 |
1 | 34.0 | 35.4 | 33.6 | 53.4 | 38.6 | 38.6 | 26.3 | 38.6 | 53.5 | 38.7 |
2 | 22.9 | 23.7 | 25.9 * | 211.5 | 24.0 | 27.4 | 23.1 | 27.3 | 211.4 | 26.9 |
3 | 78.2 | 80.3 | 76.4 | 82.9 | 81.0 | 78.9 | 76.0 | 78.8 | 82.9 | 78.9 |
4 | 36.7 | 37.7 | 37.5 | 45.6 | 38.3 | 38.9 | 36.4 | 38.8 | 45.6 | 38.8 |
5 | 50.3 | 51.6 | 49.9 ** | 54.6 | 55.6 | 55.3 | 52.4 | 55.1 | 54.6 | 55.3 |
6 | 18.0 | 19.2 | 18.4 | 18.5 | 18.4 | 18.3 | 20.9 | 18.2 | 18.5 | 18.2 |
7 | 34.4 | 35.3 | 34.4 | 33.8 | 34.2 | 34.3 | 33.0 | 34.1 | 33.8 | 34.3 |
8 | 40.9 | 42.2 | 41.0 | 41.2 | 41.2 | 40.6 | 43.1 | 40.7 | 43.9 | 40.8 |
9 | 50.7 | 51.5 | 50.5 ** | 50.4 | 50.5 | 50.4 | 45.7 | 50.2 | 50.4 | 50.4 |
10 | 37.2 | 38.3 | 37.3 | 44.0 | 37.3 | 37.2 | 39.8 | 37.1 | 41.3 | 37.1 |
11 | 20.8 | 21.9 | 20.8 | 21.1 | 21.1 | 21.0 | 23.6 | 20.8 | 21.0 | 20.8 |
12 | 27.2 | 28.8 | 25.6 * | 24.8 | 25.4 | 27.3 | 25.8 | 27.2 | 25.0 | 27.4 |
13 | 39.8 | 39.2 | 38.7 | 37.9 | 37.3 | 36.6 | 38.3 | 36.2 | 37.2 | 38.5 |
14 | 44.0 | 43.9 | 42.6 | 42.9 | 42.9 | 41.8 | 40.3 | 42.5 | 42.8 | 42.5 |
15 | 28.1 | 28.5 | 29.5 | 29.4 | 27.3 | 26.8 | 27.8 | 26.9 | 27.0 | 29.2 |
16 | 32.1 | 36.4 | 28.8 | 35.4 | 29.3 | 32.8 | 35.6 | 28.8 | 29.1 | 31.7 |
17 | 54.3 | 44.3 | 59.3 | 42.9 | 48.0 | 80.3 | 43.0 | 47.8 | 47.7 | 59.3 |
18 | 143.8 | 52.0 | 48.0 *** | 48.2 | 49.0 | 49.2 | 48.3 | 49.6 | 48.6 | 48.6 |
19 | 139.2 | 38.3 | 47.5 *** | 47.29 | 48.0 | 52.2 | 47.9 | 52.0 | 47.7 | 43.2 |
20 | 207.2 | 158.3 | 149.8 | 150.7 | 150.7 | 212.2 | 150.9 | 213.5 | 48.6 | 154.1 |
21 | 34.8 | 33.4 | 30.0 | 29.8 | 30.0 | 27.5 | 29.9 | 27.6 | 29.7 | 28.9 |
22 | 35.1 | 40.9 | 33.2 | 29.9 | 34.4 | 38.7 | 40.0 | 33.9 | 33.9 | 32.9 |
23 | 27.7 | 28.3 | 28.2 | 29.2 | 28.2 | 28.0 | 29.6 | 27.9 | 29.3 | 28.0 |
24 | 21.7 | 22.2 | 22.2 | 16.4 | 16.9 | 15.4 | 24.0 | 15.4 | 16.3 | 15.3 |
25 | 16.5 | 16.5 | 15.9 **** | 17.0 | 16.4 | 16.2 | 101.4 | 16.0 | 17.0 | 15.9 |
26 | 16.1 | 16.7 | 16.1 **** | 15.6 | 16.2 | 16.0 | 16.2 | 15.9 | 15.6 | 16.1 |
27 | 15.7 | 15.1 | 14.2 | 14.5 | 15.0 | 13.2 | 14.7 | 14.6 | 14.7 | 14.3 |
28 | 66.0 | 18.3 | 205.6 | 18.0 | 60.8 | 18.0 | 60.5 | 60.5 | 206.3 | |
29 | 134.8 | 110.1 | 109.5 | 109.9 | 109.3 | 109.9 | 107.4 | |||
30 | 30.7 | 197.3 | 19.0 | 19.3 | 19.3 | 29.9 | 19.3 | 29.4 | 19.1 | 65.0 |
OCH3 | 21.4 | 21.3 | 54.6 | |||||||
C=O | 170.8 | 173.4 | 167.7 | |||||||
1′ | 126.7 | |||||||||
2′ | 130.1 | |||||||||
3′ | 115.8 | |||||||||
4′ | 159.3 | |||||||||
5′ | 130.1 | |||||||||
6′ | 130.1 | |||||||||
7′ | 116.3 | |||||||||
8′ | 144.5 | |||||||||
Ref | [154] | [154] | [155] | [73] | [156] | [145] | [54] | [157] | [158] | [145] |
C | L33 a | L35 c | L36 | L37 | L38 | L39 | L40 | L41 | L42 | L43 |
1 | 39.3 | 38.4 | 78.7 | 38.4 | 38.4 | 38.6 | 38.6 | 53.5 | 38.7 | 38.7 |
2 | 28.3 | 23.8 | 4.2 | 23.9 | 23.8 | 27.3 | 27.4 | 211.5 | 27.3 | 27.4 |
3 | 78.0 | 81.3 | 77.6 | 55.4 | 80.6 | 78.9 | 78.9 | 82.9 | 78.9 | 79.0 |
4 | 39.3 | 38.1 | NR | 38.1 | 37.9 | 38.8 | 38.8 | 45.6 | 38.8 | 38.9 |
5 | 53.2 | 55.4 | 53.1 | 55.4 | 55.4 | 55.2 | 55.2 | 54.6 | 55.5 | 55.3 |
6 | 30.3 | 18.2 | 17.8 | 18.2 | 18.2 | 18.2 | 18.3 | 18.5 | 18.2 | 18.3 |
7 | 74.4 | 34.1 | 34.0 | 34.2 | 34.3 | 34.2 | 34.2 | 33.8 | 34.3 | 34.3 |
8 | 47.2 | 41.9 | 41.4 | 40.9 | 40.9 | 40.7 | 40.7 | 41.2 | 40.8 | 40.8 |
9 | 51.1 | 50.3 | 51.4 | 50.3 | 50.4 | 50.3 | 50.2 | 50.4 | 50.4 | 50.2 |
10 | 37.6 | 37.1 | 43.5 | 37.1 | 37.1 | 37.1 | 37.2 | 44.0 | 37.1 | 37.1 |
11 | 21.3 | 21.8 | 23.8 | 21.0 | 21.0 | 20.7 | 20.9 | 21.1 | 20.7 | 20.9 |
12 | 26.3 | 25.1 | 25.0 | 25.1 | 25.1 | 27.5 | 27.3 | 24.9 | 25.5 | 27.6 A |
13 | 39.3 | 37.3 | 38.1 | 38.1 | 38.1 | 37.2 | 37.0 | 37.9 | 38.7 | 37.7 |
14 | 44.0 | 42.7 | 37.6 | 43.0 * | 42.9 | 42.3 | 42.7 | 42.9 | 42.5 | 42.7 |
15 | 34.0 | 27.0 | 27.5 | 27.4 | 27.5 | 29.0 | 27.4 | 27.4 | 29.2 * | 27.3 |
16 | 32.8 | 29.2 | 35.6 | 35.6 | 35.6 | 28.7 | 35.0 | 35.5 | 28.8 * | 35.4 |
17 | 26.7 | 48.2 | 42.9 | 42.8 * | 43.0 | 59.3 | 43.0 | 43.0 | 59.3 | 43.3 |
18 | 49.7 | 48.8 | 48.3 | 48.3 | 48.3 | 48.0 | 49.7 | 48.2 | 48.0 ** | 51.2 B |
19 | 47.7 | 47.7 | 48.0 | 47.7 | 48.0 | 51.1 | 52.6 | 47.9 | 47.5 ** | 36.7 C |
20 | 151.1 | 150.4 | 150.8 | 151.0 | 151.0 | 211.8 | 212.9 | 150.8 | 149.7 | 157.0 B |
21 | 30.9 | 29.7 | 29.8 | 29.9 | 29.9 | 27.6 | 27.6 | 29.8 | 29.8 | 32.6 B |
22 | 37.2 | 34.0 | 40.0 | 40.0 | 40.0 | 32.4 | 39.8 | 39.9 | 33.2 | 39.9 |
23 | 28.5 | 28.0 | 27.8 | 28.0 | 28.0 | 28.0 | 28.0 | 29.3 | 27.9 | 28.0 |
24 | 16.4 | 16.7 | 16.2 | 16.7 | 16.6 | 15.4 | 15.4 | 16.4 | 15.4 | 15.4 |
25 | 16.3 | 16.2 | 12.0 | 16.2 ** | 16.2 | 16.1 | 16.1 | 17.0 | 15.9 *** | 16.1 |
26 | 10.9 | 16.0 | 16.2 | 16.0 ** | 16.0 | 15.8 | 15.9 | 15.6 | 16.1 *** | 15.9 |
27 | 15.1 | 14.8 | 14.4 | 14.5 | 14.5 | 14.2 | 14.5 | 14.5 | 14.2 | 14.4 |
28 | 176.6 | 60.6 | 17.9 | 18.0 | 18.0 | 206.1 | 18.0 | 18.0 | 205.6 | 17.8 |
29 | 110.0 | 109.8 | 109.4 | 109.4 | 109.4 | 30.2 | 29.2 | 109.5 | 110.1 | 132.9 B |
30 | 19.5 | 19.1 | 19.2 | 19.3 | 19.3 | 19.3 | 19.0 | 195.1 | ||
1′ | 127.3 | 167.6 | 127.1 | 173.7 | ||||||
2′ | 115.3 | 115.7 | 115.1 | 34.9 | ||||||
3′ | 144.2 | 145.1 | 144.9 | 25.2 | ||||||
4′ | 146.8 | 127.4 | 147.3 | 29.2 | ||||||
5′ | 114.2 | 114.4 | 113.9 | 29.3 | ||||||
6′ | 122.3 | 144.0 | 122.0 | 29.4 | ||||||
7′ | 144.9 | 146.6 | 144.9 | 29.6 | ||||||
8′ | 115.8 | 115.5 | 115.7 | 29.7 | ||||||
9′–14′ | 168.0 | 122.4 | 167.7 | 29.7 | ||||||
15′ | 29.5 | |||||||||
16′ | 31.9 | |||||||||
17′ | 22.7 | |||||||||
18′ | 14.1 | |||||||||
Ref | [153] | [159] | [160] | [159] | [161] | [145] | [145] | [162] | [155] | [163] |
C | L44 | L45 | L46 | L47 | L48 | L49 | L50a | L51 | L52 | L53 |
1 | 42.5 | 42.5 | 42.1 | 42.1 | 38.4 | 40.9 | 42.6 | 38.4 | 40.1 | 39.8 |
2 | 34.4 | 34.4 | 34.4 | 34.5 | 27.7 | 178.5 | 174.4 | 36.2 | 34.5 | 34.3 |
3 | 216.8 | 216.8 | 216.7 | 216.8 | 81.0 | 187.5 | 182.4 | 217.2 | 216.3 | 218.3 |
4 | 48.9 | 48.9 | 48.9 | 49.0 | 37.8 | 45.6 | 46.9 | 47.0 | 42.2 | 47.0 |
5 | 56.6 | 56.6 | 56.5 | 56.6 | 55.4 | 48.2 | 48.4 | 49.6 | 56.5 | 55.1 |
6 | 69.7 | 69.7 | 69.6 | 69.7 | 18.2 | 21.3 | 21.6 | 19.9 | 69.8 | 19.8 |
7 | 42.1 | 42.1 | 42.2 | 42.2 | 34.2 | 33.7 | 33.8 | 33.5 | 41.9 | 37.2 |
8 | 40.7 | 40.7 | 40.0 | 40.0 | 40.9 | 41.8 | 41.1 | 40.8 | 37.5 | 40.8 |
9 | 50.6 | 50.6 | 50.6 | 50.5 | 50.4 | 41.7 | 42.0 | 52.4 | 50.9 * | 50.0 |
10 | 36.8 | 36.8 | 36.7 | 36.7 | 37.1 | 40.7 | 42.3 | 36.6 | 34.5 | 37.1 |
11 | 21.8 | 21.8 | 21.3 | 21.3 | 21.0 | 19.2 | 22.2 | 21.7 | 21.3 | 21.5 |
12 | 28.7 | 28.7 | 26.7 | 29.7 | 25.1 | 24.9 | 27.3 | 26.0 | 25.2 | 25.7 |
13 | 36.8 | 36.8 | 37.1 | 36.8 | 38.1 | 37.9 | 38.6 | 38.6 | 37.5 | 38.6 |
14 | 43.9 | 43.9 | 42.9 | 43.2 | 42.8 | 43.2 | 43.5 | 42.7 | 42.9 | 42.6 |
15 | 27.7 | 27.7 | 27.4 | 27.4 | 27.5 | 27.5 | 27.9 | 31.1 | 29.9 | 29.8 |
16 | 35.6 | 35.6 | 35.3 | 35.3 | 35.6 | 35.5 | 35.6 | 32.6 | 32.2 | 32.2 |
17 | 44.6 | 44.6 | 43.1 | 43.0 | 43.0 | 43.2 | 43.2 | 56.4 | 56.9 | 56.5 |
18 | 48.5 | 48.5 | 48.9 | 50.6 | 48.3 | 48.4 | 48.9 | 47.5 | 49.5 * | 49.3 |
19 | 50.1 | 50.1 | 43.7 | 42.1 | 48.0 | 48.0 | 43.8 | 49.6 | 47.0 | 47.5 |
20 | 73.4 | 73.4 | 154.6 | 157.2 | 151.0 | 150.9 | 156.5 | 151.1 | 150.3 | 150.5 |
21 | 29.1 | 29.1 | 31.7 | 32.7 | 30.0 | 29.8 | 32.2 | 30.0 | 30.7 | 30.7 |
22 | 40.2 | 40.2 | 39.8 | 39.8 | 40.0 | 39.9 | 40.0 | 37.3 | 37.0 | 33.8 |
23 | 24.9 | 24.9 | 25.0 | 25.0 | 27.1 | 29.8 | 27.8 | 68.0 | 25.7 | 26.8 |
24 | 23.7 | 23.7 | 23.7 | 23.7 | 16.2 | 21.3 | 24.8 | 17.2 | 21.3 | 21.2 |
25 | 17.5 | 17.5 | 17.0 | 16.9 | 16.5 | 20.8 | 20.4 | 16.0 | 17.3 ** | 16.1 |
26 | 17.0 | 17.0 | 17.1 | 17.1 | 16.0 | 15.9 | 16.3 | 15.9 | 17.1 ** | 16.0 |
27 | 15.2 | 15.2 | 14.8 | 14.7 | 14.5 | 14.6 | 15.0 | 14.6 | 15.0 | 14.8 |
28 | 19.2 | 19.2 | 17.7 | 17.8 | 18.0 | 18.0 | 17.9 | 178.6 | 181.9 | 181.2 |
29 | 31.7 | 31.7 | 106.9 | 133.2 | 109.4 | 109.4 | 105.9 | 109.6 | 109.8 | 109.9 |
30 | 25.2 | 25.2 | 65.0 | 195.1 | 19.3 | 19.2 | 64.3 | 19.3 | 19.5 | 19.5 |
C=O | 171.0 | |||||||||
OCH3 | 21.3 | |||||||||
Ref | [164] | [164] | [146] | [146] | [165] | [73] | [153] | [166] | [167] | [14] |
C | L54 | L55 | L56 | L57 a | L58 d | L59 a | L61 | L62 | L63 | L64 |
1 | 39.6 | 33.9 | 34.0 | 34.0 | 34.0 | 38.7 | 159.9 | 38.7 | 75.9 | 75.9 |
2 | 34.1 | 28.1 | 26.2 | 26.7 | 25.1 | 28.4 | 125.1 | 27.4 | 36.4 | 36.4 |
3 | 218.2 | 179.1 | 75.0 | 75.3 | 76.9 | 78.2 | 205.6 | 79.0 | 76.6 | 76.9 |
4 | 47.3 | 147.5 | 38.1 | 38.2 | 38.5 | 39.4 | 44.6 | 38.8 | 37.4 | 37.5 |
5 | 54.9 | 50.4 | 46.4 | 49.3 | 54.9 | 56.0 | 53.4 | 55.3 | 47.8 | 47.9 |
6 | 19.6 | 24.5 | 26.1 | 18.7 | 18.0 | 18.9 | 19.0 | 18.3 | 18.4 | 18.5 |
7 | 33.6 | 32.8 | 76.7 | 34.7 | 33.9 | 34.9 | 33.7 | 34.3 | 34.0 | 34.1 |
8 | 40.7 | 40.9 | 46.3 | 41.2 | 41.2 | 41.2 | 41.7 | 40.8 | 42.9 | 41.7 |
9 | 49.6 | 40.4 | 51.2 | 50.5 | 49.9 | 51.0 | 44.4 | 50.4 | 51.2 | 51.3 |
10 | 36.8 | 39.2 | 37.8 | 37.7 | 36.7 | 37.6 | 39.5 | 37.1 | 37.4 | 43.7 |
11 | 21.5 | 21.4 | 20.8 | 21.2 | 20.5 | 21.3 | 21.2 | 21.0 | 23.7 | 23.9 |
12 | 29.7 | 25.4 | 26.5 | 28.2 | 27.1 | 26.2 | 25.1 | 26.7 | 25.2 | 25.2 |
13 | 37.8 | 38.3 | 39.1 | 38.2 | 37.6 | 39.6 | 38.2 | 38.0 | 36.9 | 37.7 |
14 | 42.8 | 42.8 | 44.4 | 43.1 | 42.6 | 42.9 | 43.0 | 43.0 | 41.7 | 42.9 * |
15 | 27.3 | 30.6 | 33.0 | 27.8 | 31.7 | 31.3 | 27.4 | 27.4 | 27.1 | 27.5 |
16 | 35.4 | 32.1 | 33.4 | 35.9 | 36.4 | 33.0 | 35.5 | 35.5 | 29.2 | 35.7 |
17 | 43.1 | 56.5 | 56.3 | 43.5 | 55.5 | 56.7 | 43.1 | 42.8 | 43.6 | 43.0 * |
18 | 50.9 | 49.4 | 49.6 | 51.3 | 46.7 | 47.9 | 48.1 | 48.9 | 48.8 | 48.1 ** |
19 | 40.7 | 46.9 | 48.0 | 41.4 | 48.7 | 49.9 | 47.3 | 43.8 | 47.8 | 48.4 ** |
20 | 146.3 | 150.4 | 151.4 | 149.2 | 150.4 | 151.4 | 150.8 | 154.8 | 150.3 | 150.8 |
21 | 32.9 | 29.7 | 31.2 | 33.5 | 30.1 | 30.4 | 29.8 | 31.8 | 29.7 | 29.8 |
22 | 39.7 | 36.9 | 37.7 | 40.2 | 38.3 | 37.7 | 40.0 | 39.8 | 34.0 | 40.0 |
23 | 26.6 | 113.4 | 29.0 | 29.4 | 28.1 | 28.8 | 27.8 | 28.0 | 27.7 | 27.6 |
24 | 21.0 | 23.2 | 22.4 | 22.7 | 15.8 | 16.4 | 21.4 | 16.1 | 21.9 | 22.0 |
25 | 15.9 | 20.1 | 16.1 | 16.3 | 15.9 | 16.5 | 19.2 | 16.0 | 11.7 | 11.5 |
26 | 15.8 | 15.9 | 12.1 | 16.4 | 16.0 | 16.5 | 16.4 | 15.4 | 16.2 | 16.1 |
27 | 14.4 | 14.6 | 15.1 | 14.8 | 14.4 | 15.0 | 14.4 | 14.5 | 14.8 | 14.6 |
28 | 17.9 | 176.6 | 179.0 | 18.2 | 177.3 | 178.9 | 18.0 | 17.7 | 60.6 | 18.1 |
29 | 124.9 | 109.7 | 109.9 | 122.4 | 109.6 | 110.0 | 109.5 | 107.6 | 109.8 | 109.5 |
30 | 171.2 | 19.3 | 19.5 | 170.3 | 19.0 | 19.6 | 19.3 | 65.0 | 19.0 | 19.3 |
OCH3 | 51.3 | 51.3 | ||||||||
1′ | 166.3 | |||||||||
2′ | 117.6 | |||||||||
3′ | 156.4 | |||||||||
4′ | 27.0 | |||||||||
5′ | 20.2 | |||||||||
Ref | [146] | [118] | [153] | [154] | [168] | [169] | [170] | [145] | [146] | [150] |
C | L65 | L66 | L67 | L68 | L69 | L70 | L71 | L72 | L73 | L74 |
1 | 79.0 | 44.5 | 39.5 | 39.6 | 35.5 | 35.4 | 33.5 | 32.5 | 39.0 | 38.9 |
2 | 37.5 | 71.3 | 34.1 | 34.2 | 25.6 | 25.6 | 28.2 | 25.3 | 27.5 | 27.4 |
3 | 75.7 | 78.5 | 217.8 | 218.1 | 75.9 | 75.9 | 76.0 | 76.4 | 78.6 | 78.9 |
4 | 38.9 | 38.2 | 47.3 | 47.3 | 37.8 | 37.8 | 38.8 | 37.6 | 39.4 | 38.8 |
5 | 53.1 | 55.2 | 54.9 | 54.9 | 48.9 | 48.9 | 48.5 | 48.2 | 55.6 | 54.9 |
6 | 18.0 | 18.1 | 19.6 | 19.7 | 18.0 | 18.3 | 21.1 | 18.4 | 18.1 | 18.5 |
7 | 34.1 | 34.2 | 33.2 | 33.6 | 35.1 | 35.1 | 34.2 | 34.4 | 35.3 | 37.8 |
8 | 41.3 | 40.9 | 40.9 | 40.8 | 42.6 | 42.7 | 40.9 | 41.1 | 41.1 | 42.5 |
9 | 51.4 | 50.9 | 49.6 | 49.8 | 55.6 | 55.6 | 50.4 | 50.5 | 55.7 | 51.0 |
10 | 43.5 | 36.9 | 36.8 | 36.9 | 39.1 | 39.1 | 37.3 | 37.3 | 37.7 | 37.4 |
11 | 23.8 | 21.1 | 21.2 | 21.5 | 70.5 | 70.6 | 20.8 | 21.2 | 70.5 | 21.0 |
12 | 25.0 | 25.2 | 25.3 | 25.2 | 37.6 | 37.6 | 25.2 | 25.3 | 27.7 | 25.2 |
13 | 38.0 | 38.0 | 37.3 | 38.2 | 36.3 | 37.1 | 37.1 | 38.0 | 37.7 | 37.6 |
14 | 42.8 | 42.9 | 42.7 | 42.9 | 42.9 | 42.7 | 42.7 | 43.0 | 42.6 | 47.9 |
15 | 27.4 | 27.3 | 26.9 | 27.4 | 27.0 | 27.3 | 27.1 | 27.6 | 27.5 | 69.7 |
16 | 35.5 | 35.6 | 34.8 | 35.5 | 33.8 | 35.4 | 29.2 | 35.8 | 35.5 | 46.5 |
17 | 42.9 | 43.0 | 37.8 | 43.0 | 47.8 | 43.0 | 48.1 | 43.2 | 43.0 | 43.0 |
18 | 48.3 | 48.3 | 47.0 | 48.3 | 48.2 | 47.7 | 47.8 | 48.2 | 47.7 | 48.1 |
19 | 47.9 | 48.0 | 59.0 | 48.0 | 47.6 | 47.7 | 48.0 | 48.2 | 47.4 | 47.4 |
20 | 150.8 | 151.0 | 143.4 | 150.6 | 149.8 | 150.2 | 150.4 | 151.2 | 150.2 | 150.4 |
21 | 29.7 | 29.9 | 217.7 | 29.9 | 29.1 | 29.8 | 29.8 | 29.9 | 29.9 | 30.1 |
22 | 39.9 | 40.0 | 55.4 | 40.0 | 29.3 | 39.8 | 34.0 | 40.2 | 39.9 | 39.7 |
23 | 27.8 | 29.6 | 26.6 | 26.7 | 22.3 | 22.3 | 28.1 | 28.2 | 28.3 | 27.9 |
24 | 14.9 | 17.1 | 21.0 | 21.0 | 28.7 | 28.7 | 16.0 | 22.4 | 15.6 | 15.4 |
25 | 11.9 | 17.1 | 15.9 | 16.0 | 16.3 | 16.2 | 16.1 | 16.4 | 16.1 | 16.1 |
26 | 16.2 | 16.0 | 15.7 | 15.8 | 17.2 | 17.2 | 16.1 | 16.2 | 17.3 | 16.6 |
27 | 14.4 | 14.5 | 14.5 | 14.5 | 14.1 | 14.6 | 14.8 | 14.7 | 14.5 | 8.0 |
28 | 18.0 | 18.0 | 18.7 | 18.0 | 60.2 | 18.0 | 60.1 | 18.2 | 18.1 | 19.2 |
29 | 109.4 | 109.3 | 115.0 | 109.4 | 110.2 | 109.8 | 109.6 | 109.6 | 109.8 | 109.7 |
30 | 19.2 | 19.3 | 20.8 | 19.3 | 19.1 | 19.3 | 18.9 | 19.5 | 19.4 | 19.4 |
Ref | [171] | [172] | [40] | [145] | [151] | [147] | [173] | [174] | [175] | [176] |
C | L75 | L76 c | L77 | L78c | L79 | L80 | L81 | L82 | L83 | L84 |
1 | 38.7 | 38.7 | 34.2 | 38.2 | 38.7 | 38.9 | 40.7 | 38.7 | 38.4 | 40.7 |
2 | 27.3 | 27.5 | 27.2 | 30.6 | 27.0 | 27.5 | 29.7 | 27.4 | 27.0 | 27.6 |
3 | 78.3 | 78.9 | 79.0 | 82.3 | 79.0 | 78.8 | 79.1 | 78.8 | 76.8 | 79.1 |
4 | 38.8 | 38.7 | 38.9 | 40.9 | 38.9 | 38.8 | 39.6 | 38.3 | 41.9 | 39.6 |
5 | 55.6 | 55.2 | 55.4 | 59.5 | 55.3 | 55.4 | 55.6 | 55.2 | 49.9 | 55.5 |
6 | 18.2 | 18.3 | 18.2 | 22.0 | 18.3 | 18.3 | 69.0 | 18.3 | 18.4 | 69.1 |
7 | 34.1 | 34.5 | 34.1 | 37.5 | 34.2 | 33.4 | 42.1 | 34.2 | 34.0 | 42.4 |
8 | 40.8 | 41.3 | 40.8 | 42.7 | 40.9 | 40.9 | 39.9 | 40.9 | 40.8 | 40.4 |
9 | 49.4 | 50.2 | 50.4 | 54.5 | 50.4 | 50.4 | 51.9 | 50.3 | 50.4 | 50.9 |
10 | 36.8 | 37.0 | 42.6 | 32.2 | 37.1 | 37.2 | 36.7 | 37.1 | 37.0 | 36.6 |
11 | 21.4 | 21.4 | 20.8 | 24.7 | 20.8 | 21.0 | 21.1 | 20.9 | 21.4 | 21.6 |
12 | 24.8 | 27.4 | 25.3 | 30.8 | 25.1 | 26.7 | 25.3 | 25.1 | 26.6 | 28.8 |
13 | 37.4 | 37.4 | 37.9 | 41.3 | 37.3 | 38.0 | 37.2 | 38.0 | 37.9 | 36.6 |
14 | 44.1 | 44.6 | 42.9 | 44.8 | 42.7 | 42.8 | 43.0 | 42.8 | 42.8 | 43.8 |
15 | 36.8 | 27.7 | 27.2 | 33.0 | 27.3 | 27.5 | 27.5 | 27.4 | 27.4 | 27.5 |
16 | 76.9 | 35.5 | 35.3 | 38.0 | 29.2 | 35.5 | 35.5 | 35.5 | 35.4 | 35.5 |
17 | 48.6 | 43.5 | 42.8 | 46.4 | 47.8 | 43.0 | 43.1 | 42.9 | 43.0 | 44.6 |
18 | 47.6 | 48.3 | 48.2 | 53.3 | 48.7 | 48.9 | 48.4 | 48.2 | 48.8 | 48.4 |
19 | 47.4 | 49.9 | 47.8 | 47.4 | 47.8 | 43.8 | 48.0 | 47.9 | 43.8 | 49.9 |
20 | 150.0 | 73.5 | 150.4 | 150.7 | 150.5 | 155.2 | 150.9 | 150.6 | 154.7 | 73.5 |
21 | 29.8 | 29.0 | 29.7 | 35.4 | 29.8 | 31.8 | 29.9 | 29.8 | 31.7 | 29.2 |
22 | 37.7 | 40.2 | 40.0 | 33.1 | 33.9 | 39.9 | 40.0 | 39.9 | 39.8 | 40.2 |
23 | 28.0 | 28.0 | 28.0 | 31.2 | 27.9 | 28.1 | 27.6 | 28.0 | 72.1 | 27.7 |
24 | 15.0 | 15.4 | 15.6 | 19.3 | 15.3 | 15.4 | 16.6 | 15.4 | 11.2 | 16.9 |
25 | 16.0 | 16.1 | 60.7 | 18.6 | 16.1 | 16.0 | 17.7 | 16.1 | 16.5 | 17.8 |
26 | 16.0 | 16.1 | 16.2 | 19.2 | 15.9 | 16.1 | 16.9 | 15.9 | 16.0 | 17.2 |
27 | 16.0 | 14.8 | 14.8 | 17.8 | 14.7 | 14.6 | 14.9 | 14.5 | 14.6 | 15.2 |
28 | 11.6 | 19.2 | 18.1 | 62.9 | 60.6 | 17.7 | 18.0 | 18.0 | 17.7 | 19.2 |
29 | 109.6 | 24.7 | 109.9 | 109.8 | 109.7 | 106.4 | 109.4 | 109.2 | 106.8 | 24.8 |
30 | 19.0 | 31.5 | 19.2 | 67.8 | 19.0 | 64.6 | 19.3 | 19.3 | 65.0 | 31.6 |
Ref | [149] | [177] | [178] | [157] | [179] | [148] | [151] | [180] | [145] | [146] |
C | L85 | L86 | ||||||||
1 | 40.7 | 39.5 | ||||||||
2 | 27.5 | 34.0 | ||||||||
3 | 79.1 | 217.8 | ||||||||
4 | 39.6 | 47.2 | ||||||||
5 | 55.6 | 54.7 | ||||||||
6 | 68.9 | 19.6 | ||||||||
7 | 42.0 | 33.4 | ||||||||
8 | 40.0 | 40.8 | ||||||||
9 | 51.0 | 49.2 | ||||||||
10 | 36.7 | 36.8 | ||||||||
11 | 21.0 | 21.2 | ||||||||
12 | 25.3 | 26.5 | ||||||||
13 | 36.4 | 37.7 | ||||||||
14 | 42.9 | 43.0 | ||||||||
15 | 27.1 | 27.7 | ||||||||
16 | 33.6 | 34.5 | ||||||||
17 | 47.7 | 43.8 | ||||||||
18 | 48.8 | 52.2 | ||||||||
19 | 47.7 | 45.0 | ||||||||
20 | 150.4 | 139.1 | ||||||||
21 | 29.7 | 82.2 | ||||||||
22 | 29.1 | 47.7 | ||||||||
23 | 27.6 | 26.7 | ||||||||
24 | 16.9 | 21.0 | ||||||||
25 | 17.7 | 15.9 | ||||||||
26 | 16.9 | 15.7 | ||||||||
27 | 15.1 | 14.1 | ||||||||
28 | 60.4 | 19.3 | ||||||||
29 | 109.7 | 124.7 | ||||||||
30 | 19.1 | 171.2 | ||||||||
Ref | [151] | [181] |
C | O1 | O2 | O3 | O4 | O5 | O6 | O7 | O8 | O9 a | O10 a |
---|---|---|---|---|---|---|---|---|---|---|
1 | 38.7 | 32.8 | 41.1 | 40.3 | 33.8 | 39.3 | 40.3 | 40.3 | 39.0 | 72.3 |
2 | 33.8 | 26.6 | 32.8 | 34.4 | 25.5 | 27.3 | 34.4 | 34.2 | 34.2 | 35.5 |
3 | 216.2 | 75.9 | 217.4 | 218.0 | 76.1 | 78.6 | 218.2 | 217.8 | 215.9 | 72.3 |
4 | 47.5 | 37.4 | 47.7 | 47.7 | 37.5 | 39.0 | 47.8 | 47.7 | 47.6 | 40.1 |
5 | 54.7 | 48.2 | 54.9 | 55.5 | 48.8 | 55.0 | 55.4 | 55.3 | 54.5 | 47.8 |
6 | 18.7 | 17.5 | 19.7 | 19.8 | 18.3 | 18.2 | 19.8 | 19.7 | 19.2 | 17.8 |
7 | 30.5 | 31.1 | 32.8 | 33.9 | 33.2 | 33.1 | 32.7 | 32.6 | 30.9 | 32.8 |
8 | 40.6 | 40.7 | 41.9 | 42.9 | 43.3 | 43.0 | 43.2 | 43.2 | 41.7 | 45.2 |
9 | 50.1 | 50.4 | 55.5 | 50.4 | 51.2 | 51.6 | 48.7 | 48.5 | 52.8 | 53.8 |
10 | 36.2 | 36.6 | 37.6 | 37.7 | 38.3 | 38.1 | 37.6 | 37.5 | 36.3 | 42.1 |
11 | 52.5 | 57.0 | 67.9 | 76.3 | 75.9 | 75.8 | 81.7 | 82.0 | 132.3 | 200.9 |
12 | 57.0 | 52.9 | 125.5 | 121.6 | 122.5 | 121.5 | 122.3 | 121.2 | 131.3 | 128.6 |
13 | 87.3 | 87.9 | 149.0 | 149.3 | 148.3 | 149.7 | 150.8 | 152.8 | 84.9 | 169.7 |
14 | 41.2 | 41.3 | 43.2 | 42.0 | 41.8 | 41.7 | 42.0 | 42.3 | 44.2 | 44.0 |
15 | 26.7 | 26.7 | 26.4 | 26.2 | 26.1 | 26.1 | 26.3 | 27.9 | 25.7 | 26.7 |
16 | 21.2 | 21.6 | 26.0 | 26.8 | 28.1 | 26.6 | 28.1 | 26.6 | 26.0 | 26.5 |
17 | 43.8 | 43.7 | 32.3 | 32.4 | 34.8 | 32.3 | 34.9 | 33.1 | 41.9 | 32.5 |
18 | 49.6 | 49.1 | 46.7 | 47.2 | 46.3 | 46.8 | 46.5 | 47.0 | 51.1 | 47.6 |
19 | 37.8 | 32.5 | 46.3 | 46.4 | 46.7 | 46.3 | 46.9 | 46.7 | 32.4 | 45.2 |
20 | 31.5 | 36.8 | 31.0 | 31.1 | 36.3 | 31.1 | 36.5 | 31.1 | 36.7 | 31.0 |
21 | 34.3 | 29.7 | 34.6 | 34.7 | 73.9 | 34.5 | 74.0 | 34.6 | 30.9 | 34.5 |
22 | 27.0 | 27.7 | 36.8 | 36.9 | 45.2 | 36.8 | 45.2 | 36.9 | 30.6 | 36.7 |
23 | 25.9 | 28.0 | 26.7 | 26.7 | 28.6 | 28.0 | 26.7 | 26.9 | 26.2 | 28.8 |
24 | 21.1 | 21.8 | 21.5 | 21.5 | 22.4 | 15.4 | 21.6 | 21.5 | 21.0 | 16.2 |
25 | 16.4 | 17.0 | 16.2 | 16.4 | 16.7 | 18.0 | 16.4 | 18.0 | 17.3 | 18.0 |
26 | 18.7 | 20.1 | 17.9 | 18.1 | 18.2 | 16.8 | 18.2 | 16.2 | 19.4 | 19.1 |
27 | 19.8 | 18.1 | 26.1 | 25.2 | 25.2 | 25.1 | 24.7 | 24.7 | 19.6 | 23.6 |
28 | 179.2 | 179.1 | 28.4 | 28.5 | 28.4 | 28.3 | 28.5 | 28.5 | 77.1 | 28.8 |
29 | 33.2 | 26.6 | 33.0 | 33.2 | 28.9 | 33.1 | 29.1 | 33.2 | 28.9 | 33.0 |
30 | 23.6 | 65.7 | 23.6 | 23.6 | 16.9 | 23.5 | 17.0 | 23.6 | 65.0 | 23.5 |
OCH3 | 53.7 | 53.7 | 53.7 | |||||||
Ref | [184] | [185] | [186] | [104] | [187] | [188] | [187] | [187] | [189] | [190] |
C | O11 | O12 | O13 | O14 | O15 | O16 | O17 | O18 b | O19 a | O20 |
1 | 39.6 | 39.4 | 39.3 | 40.0 | 38.1 | 39.8 | 48.6 | 47.6 | 47.7 | 46.6 |
2 | 33.8 | 34.2 | 34.2 | 34.5 | 24.0 | 34.0 | 69.1 | 69.6 | 68.7 | 69.0 |
3 | 218.1 | 217.7 | 217.8 | 217.5 | 80.3 | 218.3 | 83.1 | 85.9 | 85.7 | 84.0 |
4 | 47.0 | 47.5 | 47.5 | 48.1 | 37.5 | 47.2 | 39.3 | 44.3 | 43.9 | 39.3 |
5 | 54.6 | 55.4 | 55.3 | 55.7 | 55.0 | 54.8 | 55.5 | 57.3 | 56.5 | 55.4 |
6 | 19.4 | 19.7 | 19.6 | 19.1 | 18.8 | 19.6 | 17.7 | 19.8 | 19.2 | 18.4 |
7 | 33.7 | 32.2 | 32.1 | 32.3 | 32.2 | 33.7 | 34.0 | 34.3 | 33.5 | 33.1 |
8 | 40.6 | 39.9 | 39.7 | 45.2 | 39.6 | 40.6 | 43.5 | 40.9 | 40.0 | 39.4 |
9 | 50.1 | 46.9 | 46.8 | 61.3 | 47.2 | 50.4 | 56.8 | 49.2 | 48.3 | 47.6 |
10 | 36.7 | 36.7 | 36.7 | 37.0 | 38.0 | 36.8 | 40.1 | 39.2 | 38.3 | 38.3 |
11 | 21.3 | 23.8 | 23.7 | 199.3 | 23.3 | 21.5 | 72.3 | 25.1 | 24.2 | 23.6 |
12 | 25.7 | 123.6 | 122.4 | 128.2 | 123.1 | 26.0 | 211.1 | 124.6 | 122.4 | 124.5 |
13 | 37.6 | 142.5 | 143.8 | 168.9 | 142.6 | 38.9 | 82.4 | 144.4 | 144.4 | 140.5 |
14 | 43.6 | 41.9 | 41.8 | 43.8 | 41.8 | 43.2 | 45.3 | 42.5 | 42.1 | 42.6 |
15 | 27.3 | 25.6 | 26.0 | 26.1 | 25.2 | 27.3 | 22.6 | 30.3 | 29.1 | 24.4 |
16 | 36.3 | 23.6 | 28.2 | 30.9 | 18.0 | 36.8 | 30.5 | 27.9 | 23.1 | 25.3 |
17 | 36.9 | 39.6 | 35.0 | 37.3 | 31.7 | 34.5 | 33.6 | 47.0 | 47.0 | 35.3 |
18 | 142.9 | 48.0 | 46.7 | 43.0 | 46.1 | 147.5 | 49.0 | 45.0 | 41.8 | 43.5 |
19 | 127.7 | 41.4 | 47.0 | 45.5 | 40.0 | 124.7 | 38.5 | 82.3 | 46.2 | 33.9 |
20 | 40.0 | 151.6 | 36.3 | 31.3 | 42.6 | 28.0 | 31.4 | 35.9 | 30.8 | 39.6 |
21 | 73.1 | 69.1 | 74.0 | 34.1 | 36.6 | 27.9 | 34.1 | 29.4 | 34.0 | 39.9 |
22 | 43.5 | 45.9 | 45.3 | 21.8 | 75.2 | 37.3 | 39.0 | 33.1 | 32.2 | 83.2 |
23 | 26.6 | 26.6 | 26.5 | 21.7 | 23.8 | 26.8 | 28.7 | 23.8 | 24.2 | 28.7 |
24 | 20.7 | 21.6 | 21.5 | 26.7 | 16.5 | 20.9 | 16.6 | 66.1 | 65.7 | 16.9 |
25 | 16.3 | 15.3 | 15.2 | 16.0 | 15.3 | 16.5 | 17.2 | 17.5 | 17.3 | 17.0 |
26 | 15.7 | 16.8 | 16.7 | 18.7 | 16.5 | 15.9 | 20.7 | 17.7 | 17.4 | 17.1 |
27 | 13.9 | 25.8 | 25.8 | 23.7 | 25.9 | 14.5 | 18.5 | 25.1 | 26.1 | 24.1 |
28 | 26.7 | 68.8 | 28.3 | 69.6 | 24.9 | 25.5 | 31.3 | 178.6 | 176.6 | 25.0 |
29 | 28.5 | 29.1 | 23.6 | 177.9 | 70.5 | 25.1 | 28.6 | 33.2 | 182.5 | |
30 | 21.4 | 103.6 | 16.9 | 33.2 | 20.3 | 25.6 | 31.9 | 25.2 | 23.8 | 21.1 |
OCH3 | 51.7 | |||||||||
1′ | 173.5 | 93.9 | 93.7 | |||||||
2′ | 34.6 | 78.6 | 78.6 | |||||||
3′ | 23.3 | 78.0 | 79.0 | |||||||
4′–11′ | 28.9–29.4 | 70.8 | 70.6 | |||||||
5′ | 78.8 | 79.2 | ||||||||
6′ | 62.2 | 62.0 | ||||||||
1″ | 103.4 | 104.6 | ||||||||
2″ | 75.7 | 76.0 | ||||||||
3″ | 77.8 | 78.4 | ||||||||
4′’ | 72.5 | 72.7 | ||||||||
5″ | 77.9 | 78.4 | ||||||||
6″ | 63.7 | 63.8 | ||||||||
12′ | 31.7 | |||||||||
13′ | NR | |||||||||
14′ | 13.9 | |||||||||
Ref | [191] | [61] | [96] | [192] | [68] | [191] | [193] | [194] | [194] | [61] |
C | O21 | O22 a | O23 | O24 | O25 | O26 | O27 | O28 a | O29 | O30 |
1 | 79.6 | 40.0 | 39.5 | 34.7 | 33.4 | 34.1 | 39.1 | 212.9 | 40.3 | 38.7 |
2 | 44.5 | 34.4 | 34.3 | 29.4 | 25.4 | 22.7 | 27.3 | 45.4 | 23.9 | 23.8 |
3 | 172.4 | 215.9 | 218.1 | 98.0 | 75.8 | 78.0 | 78.7 | 79.0 | 80.2 | 81.2 |
4 | 56.0 | 47.8 | 47.6 | 40.0 | 37.5 | 36.7 | 39.2 | 40.1 | 38.3 | 37.1 |
5 | 85.0 | 55.1 | 55.3 | 50.2 | 48.4 | 49.7 | 55.0 | 54.9 | 55.2 | 56.0 |
6 | 33.2 | 19.0 | 19.9 | 19.4 | 17.4 | 17.7 | 17.5 | 18.1 | 17.7 | 18.2 |
7 | 27.6 | 32.1 | 32.8 | 30.8 | 32.6 | 32.5 | 32.9 | 34.4 | 34.0 | 35.1 |
8 | 43.2 | 45.3 | 40.0 | 38.5 | 43.5 | 43.5 | 46.3 | 40.7 | 44.1 | 40.3 |
9 | 55.2 | 61.2 | 46.9 | 41.6 | 61.6 | 61.6 | 60.4 | 42.8 | 54.2 | 50.5 |
10 | 44.5 | 37.0 | 36.9 | 35.0 | 37.1 | 37.0 | 37.4 | 53.5 | 39.3 | 37.1 |
11 | 67.3 | 198.9 | 23.9 | 23.6 | 200.3 | 200.1 | 195.3 | 24.4 | 75.3 | 24.8 |
12 | 133.5 | 128.4 | 124.7 | 122.3 | 128.3 | 128.2 | 142.8 | 26.7 | 202.2 | 124.2 |
13 | 139.8 | 170.6 | 140.5 | 143.4 | 169.4 | 169.3 | 138.3 | 39.6 | 83.2 | 144.1 |
14 | 42.6 | 43.7 | 42.9 | 41.6 | 45.6 | 45.6 | 41.5 | 43.7 | 44.8 | 42.1 |
15 | 19.8 | 26.7 | 25.4 | 25.8 | 25.7 | 25.8 | 26.5 | 27.8 | 22.9 | 27.2 |
16 | 34.1 | 26.9 | 24.5 | 28.0 | 22.0 | 21.5 | 26.7 | 31.3 | 39.1 | 27.5 |
17 | 51.4 | 32.5 | 35.5 | 36.0 | 37.0 | 37.0 | 31.3 | 32.5 | 33.5 | 32.0 |
18 | 37.8 | 47.3 | 43.7 | 47.0 | 42.7 | 42.7 | 38.7 | 140.7 | 49.1 | 47.4 |
19 | 40.5 | 40.8 | 40.0 | 46.5 | 44.9 | 45.0 | 41.3 | 132.6 | 38.3 | 46.9 |
20 | 47.7 | 36.0 | 39.7 | 36.0 | 31.0 | 31.0 | 30.9 | 32.5 | 31.5 | 31.1 |
21 | 215.9 | 29.9 | 39.7 | 73.8 | 33.9 | 33.8 | 34.7 | 33.4 | 34.5 | 34.8 |
22 | 40.4 | 36.4 | 83.3 | 45.0 | 30.6 | 30.6 | 36.9 | 31.1 | 30.0 | 37.2 |
23 | 21.0 | 21.5 | 27.0 | 27.0 | 28.4 | 28.0 | 28.0 | 28.6 | 28.2 | 28.0 |
24 | 20.3 | 26.5 | 21.7 | 18.0 | 22.3 | 21.9 | 15.5 | 16.6 | 16.4 | 16.6 |
25 | 13.8 | 15.9 | 15.2 | 67.7 | 16.3 | 16.3 | 16.5 | 16.1 | 16.4 | 15.5 |
26 | 19.1 | 18.5 | 16.7 | 17.0 | 18.6 | 18.6 | 18.7 | 17.0 | 20.9 | 16.5 |
27 | 22.6 | 23.4 | 25.3 | 25.1 | 23.6 | 23.5 | 23.2 | 15.1 | 18.9 | 25.7 |
28 | 26.8 | 28.7 | 24.2 | 28.1 | 69.7 | 69.7 | 29.2 | 63.6 | 31.4 | 28.7 |
29 | 28.4 | 28.2 | 182.7 | 16.6 | 32.9 | 32.9 | 33.1 | 31.4 | 32.3 | 33.2 |
30 | 21.3 | 65.3 | 21.2 | 28.8 | 23.4 | 23.4 | 23.4 | 29.7 | 24.5 | 23.7 |
OCH3 | 21.7 | 21.4 | ||||||||
C=O | 170.7 | 171.2 | ||||||||
1′ | 129.7 | 127.4 | ||||||||
2′ | 130.1 | 115.4 | ||||||||
3′ | 128.6 | 144.1 | ||||||||
4′ | 133.2 | 146.6 | ||||||||
5′ | 128.6 | 114.3 | ||||||||
6′ | 130.1 | 122.2 | ||||||||
7′ | 165.6 | 144.8 | ||||||||
8′ | 116.0 | |||||||||
9′ | 167.8 | |||||||||
Ref | [117] | [190] | [195] | [196] | [154] | [154] | [54] | [190] | [197] | [198] |
C | O31 | O32 | O33 | O34 | O36 | O37 | O38 | O39 | O40 | O41 |
1 | 38.1 | 38.6 | 38.4 | 53.5 | 39.2 | 38.6 | 38.7 | 38.5 | 42.2 | 42.0 |
2 | 24.4 | 23.7 | 23.7 | 211.1 | 26.4 | 27.2 | 27.3 | 22.5 | 34.4 | 34.1 |
3 | 80.7 | 80.6 | 80.6 | 83.1 | 78.3 | 78.9 | 79.0 | 80.8 | 216.7 | 216.5 |
4 | 37.6 | 80.6 | 37.8 | 45.9 | 39.3 | 38.7 | 38.8 | 37.8 | 49.0 | 48.7 |
5 | 51.3 | 55.6 | 55.4 | 54.8 | 55.0 | 55.2 | 55.3 | 55.5 | 56.4 | 56.2 |
6 | 18.2 | 18.2 | 18.3 | 18.8 | 17.5 | 18.3 | 18.5 | 18.5 | 69.7 | 69.4 |
7 | 32.1 | 34.9 | 32.7 | 33.0 | 32.8 | 33.1 | 32.8 | 32.8 | 42.2 | 42.0 |
8 | 38.0 | 40.8 | 39.9 | 40.1 | 43.4 | 39.3 | 38.8 | 39.7 | 39.9 | 39.6 |
9 | 153.9 | 51.1 | 47.7 | 47.7 | 61.8 | 47.5 | 47.7 | 47.8 | 51.3 | 51.1 |
10 | 40.7 | 37.2 | 36.9 | 43.8 | 37.1 | 37.0 | 37.6 | 37.1 | 36.8 | 36.6 |
11 | 115.9 | 21.1 | 23.6 | 23.7 | 200.2 | 23.5 | 23.6 | 23.9 | 21.4 | 21.2 |
12 | 120.7 | 26.2 | 121.8 | 124.1 | 128.3 | 124.6 | 121.8 | 121.9 | 26.1 | 26.0 |
13 | 147.2 | 38.4 | 145.2 | 140.7 | 170.4 | 140.2 | 145.1 | 145.4 | 38.1 | 37.4 |
14 | 42.8 | 43.3 | 41.8 | 42.9 | 45.4 | 39.5 | 41.8 | 41.9 | 43.5 | 43.3 |
15 | 25.6 | 27.5 | 26.2 | 24.5 | 26.4 | 25.2 | 26.2 | 26.4 | 27.5 | 27.4 |
16 | 27.2 | 37.7 | 27.0 | 25.4 | 27.3 | 24.3 | 27.0 | 26.0 | 36.9 | 37.3 |
17 | 32.0 | 34.3 | 32.5 | 35.5 | 32.3 | 35.2 | 32.5 | 32.7 | 34.5 | 34.2 |
18 | 45.6 | 142.7 | 47.4 | 43.6 | 47.6 | 43.4 | 47.4 | 47.4 | 147.6 | 142.4 |
19 | 46.8 | 129.8 | 46.9 | 40.0 | 45.2 | 39.8 | 46.9 | 47.0 | 124.9 | 129.8 |
20 | 31.1 | 32.3 | 31.1 | 39.7 | 31.0 | 42.5 | 31.1 | 31.3 | 37.4 | 32.1 |
21 | 34.6 | 33.4 | 34.8 | 34.0 | 34.4 | 33.8 | 34.8 | 23.9 | 28.0 | 33.0 |
22 | 37.1 | 37.4 | 37.2 | 83.2 | 36.5 | 83.1 | 37.2 | 121.9 | 37.4 | 37.1 |
23 | 28.7 | 28.0 | 28.1 | 29.6 | 28.7 | 28.1 | 28.2 | 145.4 | 25.1 | 23.4 |
24 | 16.9 | 16.6 | 16.8 | 16.8 | 16.4 | 15.6 | 15.5 | 41.9 | 23.6 | 24.8 |
25 | 20.0 | 16.7 | 15.6 | 16.7 | 15.7 | 15.6 | 15.6 | 26.4 | 17.3 | 16.9 |
26 | 21.0 | 16.1 | 16.9 | 16.9 | 18.7 | 17.0 | 16.9 | 26.0 | 17.7 | 17.6 |
27 | 25.3 | 14.5 | 26.0 | 24.3 | 23.4 | 25.0 | 26.0 | 32.7 | 14.9 | 14.5 |
28 | 28.2 | 25.3 | 28.4 | 25.2 | 28.2 | 24.0 | 28.4 | 47.4 | 25.5 | 25.0 |
29 | 33.2 | 31.3 | 33.3 | 182.5 | 33.0 | 182.4 | 33.3 | 47.0 | 70.5 | 31.2 |
30 | 23.7 | 29.2 | 23.7 | 21.2 | 23.5 | 21.0 | 23.7 | 31.3 | 25.7 | 29.0 |
1′ | 127.8 | 173.7 | 173.5 | 173.9 | ||||||
2′ | 115.5 | 34.5 | 34.9 | 35.0 | ||||||
3′ | 143.8 | 25.2 | 25.2 | 25.4 | ||||||
4′ | 146.2 | 29.2 | 29.2 | 29.4–29.9 | ||||||
5′ | 114.3 | 29.3 | 29.3 | 29.4–29.9 | ||||||
6′ | 122.4 | 29.3 | 29.4 | 29.4–29.9 | ||||||
7′ | 144.4 | 29.7 | 29.6 | 29.4–29.9 | ||||||
8′ | 116.4 | 29.7 | 29.7 | 29.4–29.9 | ||||||
9′–13′ | 167.4 | 29.7 | 29.7 | 29.4–29.9 | ||||||
14′ | 29.7 | 29.7 | 31.2 | |||||||
15′ | 29.7 | 29.5 | 23.0 | |||||||
16′ | 31.9 | 31.9 | 14.4 | |||||||
17′ | 22.7 | 22.7 | ||||||||
18′ | 14.1 | 14.1 | ||||||||
Ref | [198] | [161] | [199] | [166] | [200] | [111] | [201] | [202] | [191] | [191] |
C | O42 | O43 c | O44 | O45 | O47 d | O50 | O51 a | O52 c | O53 | O54 |
1 | 38.9 | 42.5 | 40.6 | 128.4 | 40.1 | 39.3 | 47.8 | 34.6 | 41.5 | 40.1 |
2 | 34.0 | 35.3 | 34.8 | 143.9 | 35.0 | 34.2 | 68.6 | 42.2 | 175.2 | 37.4 |
3 | 216.9 | 217.0 | 218.6 | 201.2 | 219.0 | 217.9 | 83.8 | 76.6 | 180.3 | 213.6 |
4 | 47.1 | 48.6 | 48.4 | 44.0 | 48.0 | 47.5 | 39.8 | 37.2 | 46.0 | 44.8 |
5 | 52.4 | 56.8 | 55.9 | 53.9 | 56.0 | 55.3 | 55.9 | 48.5 | 48.9 | 53.6 |
6 | 30.3 | 20.9 | 20.1 | 18.8 | 20.3 | 19.7 | 18.9 | 37.9 | 20.7 | 23.9 |
7 | 72.9 | 32.2 | 31.5 | 32.7 | 26.7 | 32.1 | 33.2 | 18.1 | 32.1 | 31.6 |
8 | 43.3 | 44.3 | 44.4 | 40.5 | 40.5 | 39.8 | 48.2 | 32.8 | 39.3 | 39.1 |
9 | 46.9 | 55.4 | 50.7 | 43.1 | 47.5 | 46.8 | 48.2 | 43.2 | 39.4 | 45.3 |
10 | 36.7 | 38.9 | 38.1 | 38.4 | 37.8 | 36.7 | 38.6 | 55.6 | 41.6 | 36.7 |
11 | 23.5 | 68.3 | 76.6 | 23.6 | 24.0 | 23.7 | 23.5 | 67.1 | 23.9 | 22.0 |
12 | 122.5 | 128.7 | 122.8 | 123.0 | 123.4 | 123.3 | 122.5 | 126.1 | 124.6 | 122.5 |
13 | 143.8 | 147.2 | 148.9 | 143.4 | 143.5 | 143.2 | 144.9 | 147.7 | 140.1 | 143.8 |
14 | 45.3 | 43.0 | 42.2 | 41.9 | 43.4 | 41.9 | 42.2 | 41.4 | 43.3 | 41.8 |
15 | 29.2 | 27.3 | 26.5 | 25.7 | 26.3 | 25.4 | 28.3 | 25.1 | 24.4 | 27.6 |
16 | 22.3 | 28.0 | 27.2 | 28.1 | 29.0 | 22.2 | 23.7 | 26.5 | 25.3 | 23.0 |
17 | 36.7 | 33.1 | 32.3 | 37.4 | 39.5 | 36.9 | 46.7 | 31.5 | 35.4 | 46.5 |
18 | 43.0 | 49.0 | 48.1 | 43.9 | 49.8 | 41.1 | 41.7 | 47.0 | 43.6 | 41.3 |
19 | 46.4 | 43.3 | 42.6 | 39.9 | 44.2 | 39.9 | 42.0 | 30.9 | 39.8 | 45.8 |
20 | 31.0 | 44.8 | 43.3 | 42.5 | 46.0 | 42.4 | 31.0 | 43.5 | 39.6 | 30.7 |
21 | 34.1 | 34.2 | 33.3 | 36.2 | 40.6 | 28.5 | 34.3 | 30.9 | 33.9 | 33.8 |
22 | 30.8 | 39.5 | 38.6 | 75.8 | 78.7 | 29.8 | 33.3 | 38.0 | 83.2 | 32.4 |
23 | 26.4 | 27.4 | 27.0 | 27.3 | 26.6 | 21.6 | 29.4 | 28.4 | 28.5 | 116.0 |
24 | 21.5 | 22.2 | 21.9 | 21.9 | 21.7 | 26.6 | 16.9 | 22.1 | 23.4 | |
25 | 15.0 | 17.0 | 16.7 | 20.0 | 15.5 | 15.3 | 17.5 | 16.4 | 19.2 | 13.1 |
26 | 9.7 | 18.9 | 18.4 | 17.5 | 17.2 | 16.7 | 17.7 | 17.8 | 17.2 | 17.0 |
27 | 25.9 | 26.3 | 25.5 | 25.4 | 26.2 | 25.4 | 26.2 | 26.5 | 23.7 | 25.8 |
28 | 69.6 | 29.3 | 29.0 | 19.9 | 25.8 | 69.0 | 180.2 | 28.4 | 25.2 | 180.4 |
29 | 33.1 | 29.3 | 29.3 | 184.0 | 34.3 | 184.5 | 33.3 | 28.0 | 182.4 | 33.0 |
30 | 23.8 | 178.9 | 183.3 | 23.8 | 181.0 | 19.2 | 23.8 | 179.2 | 20.7 | 23.5 |
OCH3 | 54.1 | 52.2 | ||||||||
Ref | [154] | [203] | [203] | [61] | [204] | [61] | [157] | [205] | [61] | [166] |
C | O55 | O56 | O58 a | O60 a | O61 | O62 a | O63 b | O65 b | O67 a | O68 |
1 | 36.8 | 39.6 | 33.6 | 38.9 | 33.6 | 37.9 | 38.2 | 38.9 | 38.9 | 38.5 |
2 | 32.4 | 34.4 | 26.2 | 28.1 | 26.2 | 25.1 | 26.6 | 28.2 | 27.6 | 26.7 |
3 | 217.7 | 217.8 | 75.2 | 78.0 | 70.8 | 81.9 | 79.7 | 79.6 | 73.7 | 78.7 |
4 | 39.1 | 47.7 | 37.8 | 39.7 * | 47.4 | 55.4 | 38.0 | 40.1 | 42.9 | 38.6 |
5 | 55.3 | 55.6 | 49.1 | 55.8 | 49.1 | 46.9 | 48.0 | 56.5 | 48.8 | 55.1 |
6 | 19.5 | 20.0 | 18.6 | 18.8 | 19.7 | 20.3 | 19.5 | 19.0 | 18.7 | 18.2 |
7 | 33.8 | 32.5 | 32.9 | 33.2 | 32.7 | 32.6 | 33.7 | 33.4 | 33.6 | 32.5 |
8 | 39.3 | 40.1 | 40.3 | 37.3 * | 39.8 | 39.9 | 39.6 | 41.2 | 39.8 | 39.7 |
9 | 47.4 | 47.1 | 47.7 | 48.1 | 46.7 | 47.1 | 49.6 | 48.9 | 48.2 | 47.5 |
10 | 46.9 | 37.0 | 37.3 | 37.9 | 37.6 | 37.9 | 39.9 | 37.8 | 37.3 | 36.8 |
11 | 23.6 | 24.0 | 23.8 | 23.8 | 23.5 | 23.5 | 20.2 | 24.4 | 23.8 | 23.4 |
12 | 122.4 | 123.0 | 123.2 | 122.7 | 121.7 | 120.9 | 124.3 | 123.5 | 122.7 | 123.1 |
13 | 143.6 | 144.3 | 144.4 | 144.7 | 145.1 | 143.0 | 144.7 | 144.5 | 145.0 | 143.2 |
14 | 41.7 | 42.1 | 42.0 | 42.2 | 41.9 | 42.0 | 43.2 | 43.5 | 42.2 | 41.5 |
15 | 32.2 | 27.3 | 25.9 | 28.3 | 26.0 | 35.9 | 24.7 | 26.5 | 28.4 | 25.2 |
16 | 21.4 | 26.3 | 23.0 | 24.0 | 26.9 | 73.1 | 27.9 | 29.0 | 23.8 | 21.8 |
17 | 46.6 | 32.7 | 37.6 | 46.6 | 32.5 | 48.6 | 41.2 | 39.5 | 46.7 | 36.7 |
18 | 41.0 | 46.4 | 41.7 | 41.6 | 47.3 | 41.2 | 56.6 | 49.9 | 42.0 | 41.1 |
19 | 45.8 | 40.5 | 41.4 | 42.0 | 46.7 | 47.5 | 40.0 | 44.3 | 46.5 | 40.1 |
20 | 30.7 | 42.8 | 42.8 | 35.9 | 31.1 | 30.9 | 43.9 | 46.2 | 31.0 | 42.1 |
21 | 32.4 | 29.2 | 29.5 | 29.6 | 34.7 | 35.8 | 76.0 | 40.7 | 34.3 | 28.4 |
22 | 26.4 | 36.1 | 30.8 | 32.9 | 37.1 | 32.8 | 41.5 | 78.8 | 33.3 | 29.7 |
23 | 27.7 | 26.8 | 29.2 | 28.4 | 183.2 | 206.4 | 28.7 | 28.3 | 68.2 | 27.9 |
24 | 15.0 | 21.7 | 22.7 | 16.5 | 24.2 | 10.2 | 17.4 | 16.1 | 13.1 | 15.4 |
25 | 15.0 | 15.5 | 15.7 | 15.3 | 13.1 | 15.4 | 16.1 | 15.7 | 16.0 | 15.3 |
26 | 17.0 | 17.0 | 17.0 | 17.4 | 16.7 | 17.2 | 16.3 | 17.3 | 17.5 | 16.5 |
27 | 25.8 | 26.1 | 26.0 | 26.2 | 25.9 | 27.1 | 26.7 | 26.3 | 26.2 | 25.7 |
28 | 183.9 | 28.4 | 68.3 | 180.2 | 28.4 | 174.8 | 21.0 | 25.8 | 180.4 | 68.6 |
29 | 33.0 | 185.1 | 181.5 | 28.2 | 33.3 | 33.2 | 182.3 | 34.1 | 33.3 | 181.7 |
30 | 23.5 | 19.4 | 20.1 | 65.5 | 23.7 | 24.5 | 25.2 | 181.1 | 23.8 | 19.1 |
Ref | [166] | [102] | [61] | [206] | [207] | [208] | [209] | [204] | [157] | [61] |
C | O69 b | O70 | O71 a | O72 a | O73 | O75 a | O76 | O77 | O81 | O82 |
1 | 42.0 | 38.1 | 213.0 | 38.5 | 38.5 | 49.6 | 38.3 | 78.7 | 34.9 | 32.5 |
2 | 28.0 | 23.4 | 45.4 | 28.0 | 27.4 | 170.6 | 23.5 | 172.2 | 25.2 | 26.0 |
3 | 80.0 | 81.0 | 78.4 | 78.1 | 78.7 | 182.0 | 80.8 | 110.9 | 76.0 | 76.1 |
4 | 39.7 | 37.7 | 40.0 | 39.5 | 38.7 | 45.4 | 37.9 | 36.4 | 37.4 | 37.3 |
5 | 57.1 | 55.4 | 54.7 | 55.3 | 55.2 | 55.2 | 55.2 | 48.8 | 48.7 | 47.3 |
6 | 68.7 | 18.2 | 18.2 | 18.8 | 18.3 | 20.7 | 18.3 | 17.6 | 18.3 | 18.3 |
7 | 41.6 | 32.6 | 33.2 | 32.9 | 32.6 | 33.4 | 32.6 | 34.5 | 33.0 | 32.5 |
8 | 40.7 | 39.4 | 39.7 | 41.1 | 39.3 | 41.1 | 39.8 | 41.1 | 43.6 | 37.0 |
9 | 49.4 | 47.6 | 39.7 | 54.8 | 47.6 | 45.9 | 47.5 | 41.0 | 56.4 | 48.9 |
10 | 37.6 | 37.0 | 52.7 | 37.1 | 37.0 | 38.5 | 36.8 | 40.1 | 38.2 | 33.0 |
11 | 24.5 | 23.4 | 25.7 | 126.0 | 23.1 | 74.5 | 23.7 | 22.1 | 67.6 | 23.4 |
12 | 124.0 | 122.6 | 123.2 | 127.0 | 122.1 | 121.4 | 121.6 | 24.2 | 126.1 | 122.6 |
13 | 144.4 | 143.6 | 144.1 | 136.6 | 143.4 | 149.8 | 145.2 | 133.5 | 148.0 | 143.7 |
14 | 43.3 | 41.6 | 42.5 | 42.5 | 41.6 | 43.1 | 41.7 | 45.2 | 41.8 | 41.7 |
15 | 28.8 | 27.7 | 28.3 | 33.3 | 27.7 | 25.8 | 26.1 | 26.4 | 26.0 | 26.0 |
16 | 24.1 | 22.9 | 23.7 | 25.6 | 23.4 | 27.5 | 26.9 | 39.3 | 28.0 | 32.5 |
17 | 47.9 | 46.6 | 46.8 | 48.7 | 46.6 | 32.9 | 32.5 | 34.6 | 34.7 | 25.2 |
18 | 41.9 | 41.0 | 42.3 | 133.8 | 41.3 | 47.2 | 47.2 | 133.9 | 45.8 | 35.0 |
19 | 41.4 | 45.7 | 46.2 | 41.0 | 45.8 | 41.6 | 46.7 | 38.7 | 46.7 | 46.6 |
20 | 36.8 | 30.7 | 31.0 | 32.8 | 30.6 | 36.1 | 31.1 | 33.3 | 36.3 | 50.0 |
21 | 29.3 | 33.6 | 34.3 | 37.5 | 33.8 | 30.0 | 34.7 | 35.4 | 73.9 | 74.0 |
22 | 33.1 | 32.5 | 33.2 | 36.3 | 32.3 | 36.6 | 37.1 | 36.4 | 45.1 | 36.3 |
23 | 28.4 | 28.1 | 29.0 | 28.5 | 28.1 | 28.2 | 28.1 | 19.3 | 28.3 | 45.4 |
24 | 17.6 | 17.2 | 16.8 | 16.0 | 15.6 | 23.3 | 16.8 | 24.3 | 22.3 | 28.2 |
25 | 17.3 | 15.2 | 15.0 | 18.4 | 15.3 | 17.7 | 15.6 | 15.0 | 16.7 | 22.3 |
26 | 18.8 | 16.7 | 18.1 | 17.1 | 16.8 | 17.1 | 16.9 | 18.1 | 18.1 | 16.8 |
27 | 26.5 | 25.9 | 26.0 | 20.1 | 26.0 | 25.5 | 26.0 | 21.3 | 26.3 | 15.2 |
28 | 181.8 | 184.0 | 180.1 | 178.9 | 181.0 | 28.4 | 28.4 | 23.8 | 28.5 | 26.0 |
29 | 74.4 | 33.1 | 33.3 | 32.4 | 33.1 | 28.2 | 33.3 | 32.3 | 28.9 | 28.3 |
30 | 19.5 | 23.6 | 23.8 | 24.4 | 23.6 | 65.6 | 23.7 | 24.0 | 16.9 | 29.0 |
1′ | 167.1 | |||||||||
2′ | 116.2 | |||||||||
3′ | 144.6 | |||||||||
4′ | 127.1 | |||||||||
5′ | 109.2 | |||||||||
6′ | 146.8 | |||||||||
7′ | 147.8 | |||||||||
8′ | 114.6 | |||||||||
9′ | 123.0 | |||||||||
OCH3 | 21.3 | 55.9 | ||||||||
C=O | 171.1 | |||||||||
Ref | [210] | [211] | [157] | [212] | [27] | [190] | [213] | [214] | [187] | [187] |
C | O84 | O85 | O86 | O88 | O89 | O90 | O91 | O92 | O93 | O94 |
1 | 39.5 | 39.2 | 38.6 | 38.6 | 38.2 | 39.6 | 39.9 | 41.3 | 41.4 | 38.6 |
2 | 27.4 | 28.2 | 27.2 | 19.0 | 23.7 | 33.8 | 34.0 | 27.6 | 27.7 | 27.1 |
3 | 78.7 | 78.1 | 79.0 | 79.0 | 80.9 | 218.0 | 217.8 | 78.5 | 78.5 | 78.7 |
4 | 39.0 | 39.4 | 38.8 | 38.8 | 37.8 | 47.0 | 47.2 | 39.5 | 39.1 | 38.6 |
5 | 55.1 | 55.9 | 55.2 | 55.2 | 55.2 | 54.6 | 55.0 | 55.7 | 55.9 | 55.2 |
6 | 18.4 | 18.9 | 18.4 | 18.4 | 18.3 | 19.4 | 19.7 | 17.9 | 18.0 | 18.0 |
7 | 32.9 | 33.3 | 32.6 | 32.6 | 32.6 | 33.4 | 34.0 | 35.5 | 35.6 | 34.5 |
8 | 43.3 | 40.1 | 39.8 | 39.8 | 39.8 | 40.3 | 40.7 | 42.8 | 42.9 | 40.7 |
9 | 49.7 | 48.1 | 47.6 | 47.6 | 47.7 | 50.2 | 50.6 | 56.3 | 56.5 | 50.8 |
10 | 37.9 | 37.3 | 36.9 | 36.2 | 36.9 | 33.7 | 37.0 | 39.4 | 39.5 | 36.9 |
11 | 81.7 | 23.9 | 23.6 | 23.5 | 23.5 | 21.3 | 21.7 | 70.9 | 71.1 | 20.7 |
12 | 121.2 | 122.5 | 122.3 | 122.2 | 121.7 | 25.9 | 26.3 | 38.3 | 38.6 | 25.7 |
13 | 153.2 | 144.9 | 144.2 | 144.8 | 145.2 | 38.7 | 38.6 | 37.7 | 37.3 | 37.5 |
14 | 41.8 | 42.5 | 41.7 | 41.7 | 41.7 | 42.5 | 43.4 | 42.8 | 43.0 | 43.5 |
15 | 26.4 | 26.5 | 25.6 | 26.1 | 28.3 | 27.2 | 27.6 | 27.3 | 27.5 | 27.1 |
16 | 27.4 | 28.7 | 22.0 | 27.2 | 26.2 | 33.9 | 37.7 | 31.5 | 37.6 | 36.4 |
17 | 32.3 | 38.0 | 36.9 | 32.9 | 32.5 | 40.6 | 34.4 | 39.0 | 34.3 | 37.0 |
18 | 46.9 | 45.4 | 42.3 | 46.3 | 47.3 | 143.4 | 142.6 | 137.5 | 141.6 | 143.1 |
19 | 46.9 | 46.9 | 46.5 | 29.0 | 46.8 | 127.8 | 130.0 | 134.5 | 129.9 | 127.5 |
20 | 31.2 | 30.9 | 31.0 | 41.0 | 31.2 | 45.1 | 32.4 | 32.2 | 32.4 | 37.0 |
21 | 34.7 | 42.3 | 34.1 | 36.2 | 34.7 | 215.2 | 33.4 | 33.2 | 33.4 | 73.1 |
22 | 37.0 | 75.6 | 31.0 | 36.9 | 37.1 | 52.3 | 37.4 | 31.1 | 37.3 | 43.7 |
23 | 28.2 | 28.8 | 15.5 | 15.6 | 28.0 | 24.5 | 26.9 | 28.2 | 28.2 | 27.7 |
24 | 15.5 | 15.9 | 28.1 | 28.1 | 16.7 | 20.7 | 21.0 | 15.5 | 15.6 | 15.8 |
25 | 18.3 | 16.6 | 15.5 | 15.5 | 15.6 | 13.3 | 16.0 | 16.8 | 17.4 | 16.4 |
26 | 16.8 | 17.3 | 16.7 | 16.8 | 16.8 | 15.6 | 16.0 | 17.4 | 16.9 | 15.8 |
27 | 24.7 | 25.8 | 25.9 | 26.0 | 25.9 | 14.7 | 14.5 | 14.4 | 14.3 | 13.9 |
28 | 28.5 | 28.8 | 69.7 | 16.8 | 26.9 | 25.6 | 25.3 | 65.4 | 25.3 | 26.7 |
29 | 33.3 | 33.3 | 33.2 | 26.9 | 33.3 | 28.8 | 31.3 | 29.7 | 31.3 | 28.5 |
30 | 23.7 | 21.2 | 23.6 | 74.8 | 23.7 | 26.3 | 29.2 | 30.5 | 29.2 | 21.4 |
OCH3 | 21.3 | |||||||||
C=O | 171.0 | |||||||||
Ref | [215] | [216] | [217] | [218] | [219] | [191] | [220] | [191] | [220] | [191] |
C | O95 | O96 | O97 | O98 | O99 | O100 | O101 | O102 | ||
1 | 38.9 | 40.8 | 38.5 | 38.8 | 31.6 | 38.8 | 34.8 | 38.3 | ||
2 | 27.4 | 27.5 | 27.4 | 27.9 | 25.9 | 27.9 | 33.0 | 22.7 | ||
3 | 78.9 | 79.1 | 79.0 | 78.6 | 75.7 | 78.6 | 217.0 | 80.9 | ||
4 | 38.9 | 39.7 | 39.0 | 38.9 | 37.7 | 38.9 | 47.2 | 37.9 | ||
5 | 55.4 | 55.6 | 55.7 | 51.2 | 44.9 | 51.2 | 48.1 | 55.3 | ||
6 | 18.2 | 69.0 | 18.3 | 18.4 | 18.2 | 18.4 | 19.7 | 18.3 | ||
7 | 34.6 | 42.2 | 34.7 | 32.2 | 31.9 | 32.2 | 30.4 | 32.5 | ||
8 | 40.7 | 39.7 | 40.8 | 37.0 | 40.7 | 37.0 | 46.6 | 39.8 | ||
9 | 51.1 | 51.8 | 51.3 | 154.3 | 154.9 | 154.3 | 53.7 | 47.5 | ||
10 | 37.2 | 36.8 | 37.3 | 40.7 | 38.8 | 40.7 | 37.8 | 36.9 | ||
11 | 21.0 | 21.2 | 21.2 | 115.8 | 115.3 | 115.8 | 72.1 | 23.5 | ||
12 | 26.1 | 26.2 | 26.2 | 120.8 | 121.4 | 120.8 | 120.5 | 121.6 | ||
13 | 38.8 | 37.6 | 39.0 | 147.1 | 145.2 | 147.1 | 152.8 | 145.2 | ||
14 | 43.2 | 43.5 | 43.4 | 42.8 | 42.8 | 42.8 | 41.7 | 41.7 | ||
15 | 27.4 | 27.6 | 27.6 | 25.7 | 25.5 | 25.7 | 26.7 | 26.1 | ||
16 | 36.9 | 37.3 | 37.7 | 27.3 | 28.5 | 27.3 | 26.6 | 26.9 | ||
17 | 34.5 | 34.3 | 34.4 | 32.2 | 34.5 | 32.2 | 32.8 | 32.6 | ||
18 | 147.8 | 142.8 | 142.8 | 45.6 | 44.9 | 45.6 | 48.0 | 47.2 | ||
19 | 124.4 | 129.9 | 129.8 | 46.9 | 47.1 | 46.9 | 46.1 | 46.8 | ||
20 | 27.1 | 32.3 | 32.3 | 31.1 | 36.3 | 31.1 | 31.1 | 31.1 | ||
21 | 28.0 | 33.3 | 33.4 | 34.7 | 73.9 | 34.7 | 34.6 | 34.7 | ||
22 | 37.5 | 40.8 | 37.4 | 37.2 | 45.3 | 37.2 | 36.9 | 37.1 | ||
23 | 27.9 | 27.6 | 28.0 | 28.0 | 28.3 | 28.8 | 27.9 | 28.1 | ||
24 | 15.4 | 16.8 | 15.4 | 16.6 | 22.4 | 15.1 | 19.4 | 16.8 | ||
25 | 16.7 | 18.1 | 16.1 | 15.5 | 25.1 | 20.1 | 19.1 | 15.5 | ||
26 | 16.1 | 17.5 | 16.7 | 16.5 | 20.9 | 21.0 | 99.1 | 16.8 | ||
27 | 14.7 | 14.8 | 14.6 | 25.7 | 20.1 | 25.3 | 23.6 | 25.9 | ||
28 | 25.5 | 25.2 | 25.3 | 28.7 | 28.6 | 28.3 | 28.7 | 28.4 | ||
29 | 70.6 | 31.3 | 31.3 | 33.2 | 28.9 | 23.7 | 33.3 | 33.3 | ||
30 | 25.7 | 29.1 | 29.2 | 23.7 | 16.9 | 33.2 | 23.7 | 23.7 | ||
1′ | 127.3 | |||||||||
2′ | 109.3 | |||||||||
3′ | 147.0 | |||||||||
4′ | 146.6 | |||||||||
5′ | 114.8 | |||||||||
6′ | 120.8 | |||||||||
7′ | 76.4 | |||||||||
8′ | 76.0 | |||||||||
9′ | 62.9 | |||||||||
OCH3 | 56.0 | |||||||||
1′ | 128.5 | |||||||||
2′ | 116.6 | |||||||||
3′ | 143.8 | |||||||||
4′ | 144.8 | |||||||||
5′ | 117.5 | |||||||||
6′ | 122.2 | |||||||||
7′ | 143.7 | |||||||||
8′ | 117.3 | |||||||||
9′ | 167.0 | |||||||||
CH3 | 20.7 | |||||||||
C=O | 170.4 | |||||||||
Ref | [191] | [191] | [220] | [198] | [187] | [68] | [221] | [126] |
C | U1 | U2 | U3 a | U4 | U5 | U6 | U7 | U8 | U9 | U10 |
---|---|---|---|---|---|---|---|---|---|---|
1 | 41.4 | 41.1 | 42.5 | 40.8 | 40.8 | 41.4 | 39.2 | 39.0 | 39.0 | 47.2 |
2 | 34.2 | 34.5 | 35.1 | 27.4 | 27.7 | 34.3 | 34.5 | 28.3 | 28.3 | 69.1 |
3 | 217.6 | 220.9 | 217.2 | 78.4 | 78.6 | 217.6 | 220.2 | 76.9 | 77.0 | 85.0 |
4 | 47.6 | 51.1 | 48.3 | 39.0 | 39.1 | 47.7 | 51.3 | 52.9 | 52.9 | 43.4 |
5 | 55.0 | 55.5 | 56.1 | 54.8 | 54.9 | 55.6 | 55.9 | 56.3 | 56.4 | 56.1 |
6 | 19.9 | 19.3 | 20.5 | 18.4 | 18.4 | 19.7 | 19.4 | 18.5 | 18.5 | 18.3 |
7 | 36.4 | 36.6 | 34.4 | 37.2 | 37.8 | 33.3 | 36.8 | 37.5 | 37.6 | 34.4 |
8 | 43.7 | 43.6 | 43.5 | 43.7 | 43.8 | 37.6 | 43.8 | 43.9 | 43.9 | 42.9 |
9 | 52.8 | 52.4 | 53.8 | 51.6 | 50.5 | 54.4 | 44.9 | 45.3 | 45.1 | 46.4 |
10 | 37.7 | 37.3 | 38.5 | 38.4 | 38.3 | 43.1 | 37.6 | 38.5 | 38.5 | 39.2 |
11 | 69.5 | 70.0 | 70.2 | 68.0 | 75.1 | 68.7 | 76.5 | 76.5 | 76.6 | 76.7 |
12 | 146.3 | 145.5 | 148.4 | 146.2 | 145.0 | 129.0 | 142.9 | 143.7 | 143.9 | 141.9 |
13 | 115.1 | 116.3 | 113.2 | 116.5 | 123.1 | 142.8 | 119.1 | 118.0 | 119.1 | 118.3 |
14 | 46.8 | 46.9 | 44.2 | 46.6 | 47.2 | 42.5 | 46.6 | 46.5 | 46.5 | 40.6 |
15 | 68.0 | 68.1 | 37.8 | 68.2 | 68.1 | 28.0 | 68.0 | 67.9 | 68.0 | 27.1 |
16 | 38.1 | 38.9 | 65.9 | 38.7 | 38.8 | 26.6 | 39.0 | 38.2 | 38.9 | 27.5 |
17 | 33.7 | 34.2 | 39.5 | 34.1 | 34.1 | 33.8 | 34.2 | 33.7 | 34.2 | 33.3 |
18 | 42.0 | 47.5 | 49.9 | 46.1 | 46.7 | 58.5 | 47.5 | 42.2 | 47.5 | 47.7 |
19 | 41.2 | 40.5 | 41.9 | 40.3 | 38.9 | 39.4 | 40.5 | 41.3 | 40.5 | 40.8 |
20 | 71.6 | 39.3 | 40.7 | 39.6 | 39.5 | 39.5 | 39.3 | 71.4 | 39.3 | 39.5 |
21 | 35.6 | 31.0 | 31.8 | 31.0 | 31.0 | 31.1 | 31.1 | 35.5 | 31.0 | 31.2 |
22 | 35.7 | 41.0 | 36.8 | 41.1 | 41.1 | 41.3 | 41.1 | 35.9 | 41.2 | 41.6 |
23 | 26.8 | 22.4 | 27.5 | 28.3 | 28.4 | 26.9 | 22.5 | 19.4 | 19.4 | 23.2 |
24 | 21.4 | 65.9 | 22.1 | 15.8 | 15.8 | 21.2 | 65.9 | 207.8 | 207.7 | 65.6 |
25 | 16.3 | 17.3 | 16.9 | 16.7 | 16.4 | 16.2 | 16.6 | 15.5 | 15.4 | 18.1 |
26 | 18.5 | 18.3 | 18.9 | 18.7 | 19.2 | 17.5 | 18.3 | 18.7 | 18.7 | 18.1 |
27 | 17.6 | 17.6 | 26.0 | 18.0 | 17.6 | 23.0 | 17.3 | 17.5 | 17.5 | 23.9 |
28 | 29.0 | 29.3 | 23.6 | 29.3 | 29.2 | 28.7 | 29.1 | 28.8 | 29.0 | 28.5 |
29 | 11.5 | 16.8 | 17.8 | 17.6 | 18.3 | 18.0 | 17.0 | 12.0 | 17.0 | 17.0 |
30 | 29.8 | 21.0 | 22.0 | 21.0 | 21.1 | 21.5 | 21.1 | 29.9 | 21.1 | 21.2 |
Ref | [193] | [193] | [190] | [54] | [54] | [228] | [193] | [193] | [193] | [193] |
C | U11 | U12 | U13 | U14 | U15 | U16 | U17 | U18 a | U19 | U20 |
1 | 40.8 | 39.0 | 38.7 | 39.0 | 38.7 | 39.0 | 39.9 | 40.6 | 39.9 | 40.3 |
2 | 34.4 | 27.5 | 27.8 | 27.5 | 27.9 | 27.5 | 27.5 | 28.5 | 26.9 | 34.2 |
3 | 218.3 | 78.6 | 80.4 | 78.6 | 80.5 | 78.7 | 78.7 | 77.9 | 78.9 | 217.9 |
4 | 47.6 | 39.1 | 43.1 | 39.1 | 43.1 | 39.2 | 30.9 | 38.5 | 39.1 | 47.6 |
5 | 55.3 | 55.1 | 55.7 | 55.1 | 56.1 | 55.5 | 54.9 | 55.8 | 55.3 | 55.2 |
6 | 19.7 | 18.4 | 18.5 | 18.4 | 18.3 | 18.2 | 18.6 | 18.8 | 18.4 | 19.6 |
7 | 33.2 | 37.3 | 37.6 | 37.4 | 34.4 | 34.2 | 36.5 | 33.6 | 33.5 | 33.0 |
8 | 42.7 | 44.2 | 44.1 | 44.2 | 40.6 | 40.6 | 44.2 | 43.2 | 42.9 | 43.2 |
9 | 50.9 | 46.9 | 46.3 | 46.3 | 46.5 | 46.4 | 52.7 | 53.1 | 52.6 | 47.2 |
10 | 37.6 | 38.4 | 38.1 | 38.5 | 38.1 | 38.4 | 38.1 | 39.7 | 38.2 | 37.3 |
11 | 77.0 | 76.4 | 76.6 | 76.4 | 76.8 | 76.7 | 76.5 | 76.7 | 76.8 | 81.7 |
12 | 124.2 | 144.0 | 143.0 | 143.1 | 142.1 | 142.1 | 125.2 | 124.9 | 124.1 | 125.4 |
13 | 143.3 | 117.9 | 119.1 | 119.2 | 118.2 | 118.2 | 144.1 | 143.1 | 143.6 | 144.2 |
14 | 42.4 | 46.4 | 46.4 | 46.4 | 42.9 | 42.9 | 47.7 | 42.2 | 41.5 | 44.2 |
15 | 26.6 | 68.0 | 68.1 | 68.1 | 27.1 | 27.2 | 68.2 | 26.7 | 27.6 | 35.8 |
16 | 27.9 | 38.0 | 38.8 | 38.7 | 27.6 | 27.6 | 38.8 | 23.7 | 28.1 | 66.7 |
17 | 33.8 | 33.6 | 34.1 | 34.1 | 33.3 | 33.3 | 33.9 | 38.6 | 33.7 | 38.5 |
18 | 58.8 | 42.2 | 47.5 | 47.5 | 47.7 | 47.7 | 58.7 | 53.8 | 58.6 | 60.3 |
19 | 39.3 | 41.3 | 40.5 | 40.5 | 40.8 | 40.8 | 39.3 | 39.8 | 39.4 | 39.4 |
20 | 39.5 | 71.5 | 39.3 | 39.3 | 39.5 | 39.5 | 39.1 | 39.4 | 39.6 | 39.2 |
21 | 31.1 | 35.5 | 31.0 | 31.0 | 31.2 | 31.3 | 30.9 | 31.1 | 31.2 | 30.4 |
22 | 41.3 | 35.9 | 41.2 | 41.2 | 41.6 | 41.6 | 41.0 | 36.1 | 42.1 | 35.0 |
23 | 26.9 | 28.3 | 22.7 | 28.4 | 22.7 | 28.4 | 28.2 | 28.8 | 28.3 | 26.0 |
24 | 21.4 | 15.8 | 64.4 | 15.8 | 64.5 | 15.8 | 15.6 | 16.6 | 15.7 | 21.4 |
25 | 16.6 | 16.3 | 16.8 | 16.2 | 16.8 | 16.2 | 17.1 | 17.4 | 17.1 | 18.0 |
26 | 18.2 | 18.7 | 18.6 | 18.7 | 18.0 | 18.1 | 18.9 | 18.3 | 18.3 | 16.2 |
27 | 22.5 | 17.7 | 17.8 | 17.8 | 23.8 | 23.9 | 16.6 | 22.7 | 22.6 | 23.2 |
28 | 28.7 | 28.7 | 29.0 | 29.0 | 28.5 | 28.5 | 29.3 | 69.1 | 28.8 | 21.9 |
29 | 17.5 | 11.9 | 17.0 | 17.0 | 17.0 | 17.0 | 17.3 | 17.6 | 17.5 | 17.7 |
30 | 21.3 | 29.9 | 21.2 | 21.2 | 21.2 | 21.2 | 21.3 | 21.6 | 21.5 | 21.2 |
OCH3 | 54.4 | 52.0 | 51.6 | 51.5 | 51.6 | 51.4 | 54.7 | 53.9 | ||
Ref | [104] | [193] | [193] | [54] | [193] | [54] | [54] | [189] | [74] | [229] |
C | U21 | U22 | U23 | U24 | U25 | U26 b | U27 | U28 | U29 a | U31 |
1 | 40.1 | 39.3 | 39.9 | 39.4 | 39.4 | 40.2 | 38.3 | 39.5 | 38.6 | 39.2 |
2 | 34.2 | 34.3 | 34.1 | 34.3 | 34.4 | 26.6 | 27.1 | 27.7 | 27.6 | 33.9 |
3 | 218.0 | 219.3 | 216.7 | 219.1 | 219.4 | 83.1 | 78.9 | 79.6 | 73.1 | 217.1 |
4 | 47.6 | 51.44 | 47.7 | 51.5 | 51.5 | 44.3 | 38.8 | 40.0 | 43.1 | 47.5 |
5 | 55.3 | 55.6 | 55.1 | 55.7 | 55.7 | 48.4 | 54.5 | 56.2 | 48.2 | 54.4 |
6 | 19.7 | 18.7 | 19.0 | 18.8 | 18.7 | 18.8 | 17.9 | 18.8 | 18.0 | 19.1 |
7 | 32.4 | 35.6 | 35.5 | 35.7 | 35.6 | 34.6 | 35.1 | 32.7 | 31.6 | 34.4 |
8 | 43.0 | 46.2 | 46.6 | 46.3 | 46.3 | 44.2 | 43.0 | 43.1 | 42.1 | 42.9 |
9 | 47.8 | 58.7 | 59.1 | 58.7 | 58.7 | 49.6 | 52.7 | 53.7 | 53.5 | 52.1 |
10 | 37.4 | 36.5 | 36.9 | 36.6 | 36.5 | 39.1 | 36.5 | 37.5 | 36.6 | 36.2 |
11 | 81.8 | 194.2 | 194.4 | 194.2 | 194.2 | 78.4 | 129.4 | 132.9 | 133.8 | 129.0 |
12 | 124.8 | 145.1 | 145.1 | 145.1 | 145.0 | 145.8 | 132.5 | 131.5 | 129.3 | 132.8 |
13 | 146.1 | 132.9 | 133.9 | 133.9 | 134.7 | 116.9 | 85.8 | 85.8 | 84.9 | 85.6 |
14 | 42.0 | 47.3 | 47.4 | 47.4 | 47.4 | 44.3 | 48.9 | 46.9 | 44.6 | 49.1 |
15 | 27.9 | 68.1 | 68.3 | 68.3 | 68.3 | 36.4 | 68.4 | 36.0 | 25.8 | 68.3 |
16 | 26.3 | 38.4 | 38.0 | 38.6 | 38.6 | 78.3 | 37.8 | 66.4 | 27.3 | 37.2 |
17 | 33.8 | 33.9 | 33.7 | 34.1 | 34.2 | 39.7 | 42.7 | 48.4 | 42.5 | 42.3 |
18 | 58.7 | 47.5 | 43.6 | 48.6 | 48.7 | 50.9 | 61.0 | 63.3 | 61.6 | 55.3 |
19 | 39.4 | 35.5 | 41.4 | 34.8 | 40.6 | 42.1 | 37.6 | 39.3 | 37.9 | 38.8 |
20 | 39.3 | 51.4 | 70.9 | 46.4 | 39.1 | 41.0 | 40.6 | 42.1 | 41.0 | 71.7 |
21 | 31.1 | 25.3 | 35.4 | 24.9 | 30.9 | 32.5 | 31.2 | 30.5 | 31.7 | 35.9 |
22 | 41.3 | 39.7 | 35.6 | 40.4 | 40.7 | 36.7 | 34.0 | 31.8 | 35.2 | 29.0 |
23 | 26.5 | 22.1 | 26.4 | 22.1 | 22.0 | 67.4 | 27.7 | 28.4 | 67.4 | 26.0 |
24 | 21.4 | 65.6 | 21.4 | 65.6 | 65.6 | 13.6 | 14.9 | 15.7 | 12.5 | 20.8 |
25 | 18.1 | 16.7 | 15.8 | 16.6 | 16.7 | 17.6 | 17.7 | 18.4 | 18.5 | 17.1 |
26 | 16.2 | 18.5 | 18.9 | 18.6 | 18.6 | 18.9 | 19.9 | 20.1 | 19.8 | 19.6 |
27 | 22.0 | 15.4 | 15.1 | 15.1 | 15.1 | 25.2 | 12.8 | 19.0 | 17.4 | 12.5 |
28 | 28.5 | 29.1 | 29.2 | 29.3 | 29.5 | 23.7 | 76.8 | 73.1 | 76.8 | 76.5 |
29 | 17.5 | 17.4 | 11.6 | 16.2 | 16.6 | 17.6 | 18.1 | 18.9 | 18.4 | 12.9 |
30 | 21.3 | 176.4 | 29.7 | 65.7 | 20.9 | 21.7 | 19.4 | 19.8 | 19.5 | 28.7 |
OCH3 | 53.5 | |||||||||
1′ | 105.8 | |||||||||
2′ | 75.7 | |||||||||
3′ | 78.4 | |||||||||
4′ | 71.8 | |||||||||
5′ | 77.6 | |||||||||
6′ | 62.8 | |||||||||
1″ | 106.1 | |||||||||
2″ | 75.7 | |||||||||
3″ | 78.3 | |||||||||
4″ | 71.6 | |||||||||
5″ | 77.8 | |||||||||
6″ | 62.9 | |||||||||
Ref | [229] | [193] | [54] | [193] | [54] | [230] | [54] | [189] | [189] | [193] |
C | U32 | U33 | U34 a | U35 | U36 a | U37 a | U38 | U39 | U40 | U41 |
1 | 40.9 | 40.9 | 39.5 | 47.1 | 48.0 | 47.9 | 38.6 | 39.8 | 39.8 | 33.5 |
2 | 28.2 | 27.4 | 34.2 | 68.6 | 68.7 | 68.8 | 23.8 | 25.9 | 34.2 | 25.3 |
3 | 76.9 | 78.7 | 217.8 | 84.9 | 85.7 | 85.8 | 81.1 | NR | 217.1 | 75.8 |
4 | 52.8 | 39.0 | 47.4 | 43.4 | 43.9 | 43.9 | 38.1 | 38.7 | 47.8 | 37.5 |
5 | 55.8 | 54.7 | 55.2 | 55.5 | 56.5 | 56.6 | 55.4 | 56.7 | 55.4 | 48.3 |
6 | 18.6 | 18.5 | 19.6 | 17.6 | 19.1 | 19.3 | 18.3 | 18.8 | 18.8 | 17.4 |
7 | 35.6 | 35.0 | 32.3 | 33.1 | 33.8 | 33.9 | 32.9 | 34.3 | 32.2 | 32.7 |
8 | 43.8 | 44.7 | 40.0 | 45.5 | 40.2 | 40.7 | 40.2 | 41.3 | 43.7 | 45.3 |
9 | 52.7 | 55.7 | 46.8 | 59.5 | 48.2 | 48.0 | 47.7 | 49.4 | 60.8 | 61.4 |
10 | 38.3 | 38.2 | 36.6 | 37.4 | 38.2 | 38.3 | 36.9 | 38.0 | 36.6 | 37.0 |
11 | 70.0 | 67.8 | 23.3 | 194.8 | 24.0 | 24.4 | 23.5 | 24.2 | 199.0 | 200.0 |
12 | 146.1 | 130.2 | 125.3 | 144.4 | 125.7 | 128.1 | 125.1 | 125.1 | 130.6 | 130.7 |
13 | 116.1 | 142.7 | 138.4 | 134.8 | 138.7 | 139.5 | 138.9 | 140.8 | 164.8 | 164.3 |
14 | 45.9 | 47.0 | 42.2 | 41.7 | 42.4 | 42.1 | 42.2 | 43.3 | 45.5 | 43.7 |
15 | 72.2 | 72.1 | 25.9 | 27.5 | 29.3 | 29.9 | 26.1 | 26.7 | 27.2 | 27.1 |
16 | 34.2 | 34.5 | 23.3 | 27.3 | 24.4 | 25.9 | 23.7 | 24.1 | 27.4 | 27.5 |
17 | 34.0 | 33.9 | 37.9 | 33.4 | 48.3 | 48.6 | 38.1 | 37.7 | 33.8 | 33.8 |
18 | 47.4 | 58.3 | 54.0 | 48.9 | 53.3 | 54.5 | 54.2 | 55.3 | 58.8 | 58.8 |
19 | 40.6 | 39.1 | 33.7 | 40.8 | 39.4 | 72.7 | 39.5 | 41.4 | 33.5 | 33.5 |
20 | 39.3 | 39.2 | 46.7 | 39.3 | 39.2 | 42.2 | 39.5 | 40.7 | 46.5 | 46.5 |
21 | 30.9 | 30.8 | 24.5 | 31.1 | 30.8 | 26.8 | 30.7 | 32.2 | 24.8 | 24.6 |
22 | 40.7 | 40.7 | 34.7 | 41.1 | 36.4 | 37.5 | 35.3 | 36.5 | 40.5 | 40.5 |
23 | 18.7 | 28.2 | 26.4 | 23.0 | 24.2 | 24.2 | 28.2 | 28.3 | 28.8 | 28.4 |
24 | 207.6 | 15.6 | 21.5 | 65.3 | 65.7 | 65.7 | 17.0 | 17.5 | 22.1 | 22.3 |
25 | 15.7 | 16.8 | 15.5 | 18.3 | 17.5 | 17.4 | 15.8 | 16.3 | 16.0 | 16.4 |
26 | 19.2 | 18.6 | 16.7 | 18.5 | 17.4 | 17.2 | 16.8 | 17.3 | 18.4 | 18.5 |
27 | 19.5 | 18.7 | 23.3 | 20.9 | 23.9 | 24.6 | 23.4 | 23.9 | 20.5 | 20.7 |
28 | 28.9 | 28.9 | 69.6 | 28.8 | 176.3 | 177.1 | 69.9 | 70.5 | 28.7 | 28.7 |
29 | 16.8 | 17.5 | 16.9 | 16.6 | 17.5 | 27.1 | 17.5 | 17.8 | 17.0 | 17.0 |
30 | 21.0 | 21.2 | 66.3 | 21.0 | 21.4 | 16.7 | 21.4 | 21.6 | 65.9 | 65.9 |
OCOPh | 165.5 | 165.6 | ||||||||
iso | 131.0 | 131.0 | ||||||||
orto | 129.5 | 129.5 | ||||||||
meta | 128.8 | 128.4 | ||||||||
para | 132.9 | 132.8 | ||||||||
1′ | 93.7 | 93.8 | 127.2 | 127.3 | ||||||
2′ | 79.2 | 79.1 | 114.0 | 129.5 | ||||||
3′ | 78.9 | 79.1 | 144.8 | 115.8 | ||||||
4′ | 70.7 | 70.8 | 147.2 | 157.4 | ||||||
5′ | 79.2 | 79.2 | 115.3 | 115.8 | ||||||
6′ | 62.1 | 62.2 | 122.1 | 129.5 | ||||||
7′ | 150.0 | 143.8 | ||||||||
8′ | 115.7 | 116.4 | ||||||||
9′ | 167.9 | 167.2 | ||||||||
1″ | 104.8 | 104.7 | ||||||||
2″ | 76.0 | 75.9 | ||||||||
3″ | 78.4 | 78.4 | ||||||||
4″ | 72.7 | 72.9 | ||||||||
5″ | 78.3 | 78.3 | ||||||||
6″ | 63.7 | 63.9 | ||||||||
Ref | [54] | [54] | [185] | [193] | [194] | [194] | [231] | [204] | [185] | [185] |
C | U42 | U43 | U44 | U45 | U46 | U47 | U48 | U49 | U50 | U51 a |
1 | 40.5 | 40.7 | 41.7 | 38.7 | 38.5 | 38.7 | 39.0 | 39.3 | 38.9 | 39.8 |
2 | 28.2 | 28.2 | 28.3 | 27.0 | 27.8 | 27.0 | 27.6 | 27.2 | 27.6 | 28.1 |
3 | 76.9 | 76.9 | 77.9 | 78.6 | 76.9 | 78.6 | 80.5 | 78.7 | 80.6 | 77.9 |
4 | 52.8 | 52.8 | 49.3 | 38.8 | 52.7 | 38.8 | 43.0 | 39.0 | 43.1 | 39.8 |
5 | 56.2 | 56.2 | 56.3 | 55.1 | 56.2 | 55.1 | 55.2 | 54.6 | 55.5 | 55.3 |
6 | 18.6 | 18.5 | 20.2 | 18.6 | 18.7 | 18.6 | 17.8 | 17.7 | 17.6 | 18.0 |
7 | 37.1 | 37.2 | 37.3 | 39.1 | 39.0 | 39.2 | 36.4 | 36.2 | 33.2 | 33.2 |
8 | 43.6 | 43.7 | 43.8 | 38.2 | 38.3 | 38.2 | 46.7 | 46.7 | 45.5 | 45.7 |
9 | 52.6 | 52.9 | 53.3 | 58.0 | 56.7 | 57.9 | 59.7 | 59.8 | 59.7 | 61.3 |
10 | 38.2 | 38.3 | 38.4 | 38.1 | 38.3 | 38.1 | 37.0 | 37.3 | 36.9 | 37.4 |
11 | 69.7 | 70.1 | 70.2 | 72.8 | 73.1 | 73.0 | 194.9 | 195.1 | 195.1 | 199.3 |
12 | 146.5 | 145.7 | 145.7 | 207.1 | 206.7 | 207.1 | 144.9 | 144.9 | 144.5 | 130.7 |
13 | 115.1 | 116.7 | 116.6 | 42.7 | 42.9 | 43.0 | 134.2 | 134.0 | 134.4 | 163.6 |
14 | 46.6 | 46.6 | 46.7 | 49.9 | 49.3 | 49.5 | 47.2 | 47.2 | 41.7 | 45.8 |
15 | 68.0 | 68.1 | 68.1 | 66.0 | 66.1 | 66.2 | 68.3 | 68.4 | 27.5 | 37.1 |
16 | 38.1 | 38.9 | 38.8 | 37.2 | 38.0 | 37.8 | 38.6 | 38.5 | 27.3 | 64.7 |
17 | 33.6 | 34.2 | 34.1 | 32.6 | 33.2 | 33.1 | 34.2 | 34.2 | 33.4 | 39.2 |
18 | 42.0 | 47.4 | 47.3 | 35.3 | 39.6 | 39.5 | 48.7 | 48.7 | 48.9 | 60.7 |
19 | 41.3 | 40.5 | 40.5 | 41.4 | 40.5 | 40.5 | 40.4 | 40.4 | 40.8 | 39.1 |
20 | 71.6 | 39.3 | 39.3 | 71.3 | 37.9 | 38.0 | 39.1 | 39.1 | 39.3 | 39.4 |
21 | 35.6 | 31.0 | 31.0 | 35.2 | 30.8 | 30.8 | 30.9 | 30.9 | 31.2 | 30.8 |
22 | 35.7 | 41.0 | 41.0 | 36.0 | 41.5 | 41.5 | 40.7 | 40.7 | 41.1 | 35.4 |
23 | 19.3 | 19.3 | 23.8 | 27.8 | 19.2 | 27.9 | 22.4 | 28.0 | 22.4 | 28.7 |
24 | 207.8 | 207.9 | 178.4 | 15.3 | 207.1 | 15.2 | 64.3 | 15.6 | 64.3 | 16.6 |
25 | 15.8 | 15.8 | 14.4 | 17.3 | 16.2 | 17.3 | 17.1 | 16.6 | 17.1 | 17.0 |
26 | 18.7 | 18.6 | 18.5 | 21.2 | 20.9 | 21.1 | 19.0 | 19.1 | 18.4 | 18.7 |
27 | 17.7 | 18.0 | 17.8 | 18.1 | 17.7 | 17.9 | 15.2 | 15.3 | 20.9 | 21.9 |
28 | 29.0 | 29.3 | 29.3 | 27.9 | 28.2 | 28.2 | 29.4 | 29.4 | 28.8 | 23.0 |
29 | 11.4 | 16.8 | 16.7 | 11.7 | 16.6 | 16.6 | 16.6 | 16.5 | 16.5 | 17.6 |
30 | 29.9 | 21.1 | 21.0 | 29.1 | 20.5 | 20.5 | 20.9 | 20.9 | 21.0 | 21.2 |
OCH3 | 51.3 | |||||||||
Ref | [193] | [54] | [54] | [193] | [193] | [193] | [193] | [54] | [54] | [190] |
C | U52 a | U54 | U55 | U56 | U57 c | U58 | U59 | U60 | U62 | U63 a |
1 | 38.5 | 39.2 | 38.4 | 38.1 | 37.9 | 38.6 | 38.5 | 38.1 | 38.5 | 40.5 |
2 | 27.6 | 27.3 | 27.5 | 23.4 | 28.7 | 23.8 | 23.7 | 26.8 | 23.6 | 36.1 |
3 | 72.8 | 78.8 | 78.0 | 80.7 | 80.0 | 81.2 | 80.6 | 78.5 | 80.6 | 216.0 |
4 | 43.1 | 39.1 | 42.3 | 37.9 | 42.8 | 37.9 | 37.8 | 38.7 | 37.7 | 54.7 |
5 | 48.1 | 54.8 | 54.6 | 55.0 | 52.5 | 55.5 | 55.3 | 54.6 | 55.3 | 49.2 |
6 | 17.9 | 17.5 | 19.3 | 17.7 | 18.5 | 18.4 | 18.3 | 17.5 | 18.2 | 67.8 |
7 | 33.0 | 32.8 | 33.3 | 31.4 | 33.3 | 33.1 | 32.9 | 31.0 | 32.9 | 41.6 |
8 | 42.1 | 45.1 | 40.9 | 41.8 | 39.9 | 40.2 | 40.1 | 41.5 | 40.0 | 42.6 |
9 | 48.9 | 61.6 | 51.1 | 53.0 | 48.7 | 47.8 | 47.7 | 52.8 | 47.6 | 46.6 |
10 | 37.0 | 36.9 | 31.0 | 36.4 | 37.1 | 37.0 | 36.8 | 36.1 | 36.8 | 37.8 |
11 | 37.4 | 199.8 | 73.3 | 133.4 | 24.4 | 23.6 | 23.4 | 128.6 | 23.4 | 77.3 |
12 | 209.8 | 130.7 | 126.0 | 129.0 | 128.0 | 124.5 | 124.4 | 133.2 | 124.3 | 145.0 |
13 | 89.4 | 164.3 | 140.4 | 89.7 | 140.2 | 139.8 | 139.7 | 89.5 | 139.6 | 116.5 |
14 | 45.9 | 43.6 | 42.5 | 42.0 | 41.7 | 42.4 | 42.1 | 41.7 | 42.1 | 41.4 |
15 | 26.3 | 27.1 | 28.4 | 25.6 | 30.6 | 28.3 | 26.6 | 25.3 | 26.6 | 27.6 |
16 | 26.4 | 27.5 | 26.0 | 30.9 | 27.6 | 26.8 | 28.1 | 22.6 | 28.1 | 28.0 |
17 | 42.7 | 33.8 | 47.8 | 45.2 | 47.0 | 33.9 | 33.8 | 44.9 | 33.7 | 33.7 |
18 | 55.0 | 58.8 | 53.5 | 40.4 | 54.6 | 59.3 | 59.1 | 60.4 | 59.1 | 47.5 |
19 | 38.0 | 33.5 | 72.1 | 38.2 | 72.4 | 39.8 | 39.6 | 37.9 | 39.6 | 41.3 |
20 | 40.7 | 46.5 | 42.5 | 60.7 | 39.7 | 39.8 | 39.7 | 40.1 | 39.7 | 40.0 |
21 | 31.6 | 24.9 | 27.4 | 22.9 | 26.8 | 31.5 | 31.3 | 30.6 | 31.2 | 31.6 |
22 | 34.9 | 40.5 | 38.3 | 31.3 | 38.5 | 41.7 | 41.6 | 31.1 | 41.5 | 42.2 |
23 | 67.2 | 28.0 | 180.6 | 27.8 | 68.4 | 28.3 | 28.1 | 27.6 | 28.1 | 66.8 |
24 | 12.9 | 22.1 | 13.7 | 16.1 | 12.8 | 16.9 | 16.8 | 14.7 | 16.8 | 20.5 |
25 | 16.1 | 16.5 | 16.7 | 19.2 | 17.0 | 16.0 | 15.7 | 17.7 | 15.7 | 17.6 |
26 | 18.7 | 18.5 | 16.9 | 19.0 | 16.8 | 17.7 | 16.9 | 18.7 | 16.9 | 20.3 |
27 | 17.7 | 20.6 | 23.9 | 16.2 | 25.0 | 23.4 | 23.3 | 15.9 | 23.2 | 24.0 |
28 | 77.2 | 28.7 | 68.7 | 18.1 | 64.5 | 29.1 | 28.8 | 179.6 | 28.7 | 28.9 |
29 | 19.1 | 17.0 | 17.4 | 17.9 | 27.1 | 17.0 | 17.5 | 17.6 | 17.5 | 17.4 |
30 | 19.8 | 65.9 | 28.6 | 179.9 | 16.2 | 21.6 | 21.4 | 18.9 | 21.4 | 21.5 |
OCH3 | 55.4 | 51.4 | ||||||||
OCH3 | 21.7 | 21.4 | 21.2 | 21.5 | ||||||
C=O | 170.4 | 171.1 | 169.9 | 171.5 | 173.5 | 173.7 | ||||
2′ | 34.9 | 34.9 | ||||||||
3′ | 25.2 | 25.2 | ||||||||
4′–13′ | 29.2–29.7 | 29.2–29.5 | ||||||||
14′ | 29.7 | 31.9 | ||||||||
15′ | 29.5 | 22.7 | ||||||||
16′ | 31.9 | 14.1 | ||||||||
17′ | 22.7 | |||||||||
18′ | 14.1 | |||||||||
Ref | [189] | [185] | [232] | [233] | [232] | [234] | [235] | [236] | [6] | [190] |
C | U64 c | U65 | U66 a | U67 | U68 | U69 a | U71 | U72 | U73c | U74 |
1 | 38.9 | 43.0 | 39.4 | 39.5 | 39.5 | 48.0 | 39.7 | 33.6 | 34.1 | 38.4 |
2 | 29.3 | 175.5 | 34.8 | 34.2 | 34.2 | 68.6 | 34.1 | 25.8 | 25.7 | 26.8 |
3 | 208.1 | 207.7 | 216.2 | 217.9 | 217.8 | 83.7 | 217.3 | 74.2 | 76.3 | 77.4 |
4 | 47.2 | 50.7 | 47.4 | 47.5 | 47.5 | 39.9 | 47.7 | 37.4 | 42.6 | 38.4 |
5 | 55.6 | 47.7 | 55.2 | 55.3 | 55.3 | 55.9 | 55.2 | 48.1 | 54.1 | 54.8 |
6 | 19.8 | 20.4 | 19.8 | 19.7 | 19.7 | 18.9 | 18.6 | 17.1 | 19.0 | 18.2 |
7 | 34.0 | 32.1 | 32.5 | 32.3 | 32.4 | 33.5 | 32.4 | 32.9 | 33.2 | 32.3 |
8 | 40.2 | 40.0 | 40.3 | 40.2 | 40.1 | 40.1 | 44.5 | 44.6 | 41.3 | 39.6 |
9 | 46.6 | 40.4 | 47.1 | 46.9 | 46.9 | 47.0 | 60.7 | 61.2 | 48.1 | 47.2 |
10 | 37.5 | 42.3 | 36.7 | 36.7 | 36.7 | 38.5 | 36.1 | 37.2 | 37.4 | 38.4 |
11 | 24.5 | 23.8 | 23.8 | 23.7 | 23.7 | 23.8 | 199.5 | 199.3 | 73.1 | 23.0 |
12 | 127.9 | 125.1 | 125.2 | 125.5 | 125.8 | 125.5 | 130.7 | 130.3 | 127.3 | 124.8 |
13 | 138.8 | 139.1 | 139.3 | 138.0 | 137.9 | 139.3 | 163.5 | 163.3 | 139.4 | 138.0 |
14 | 42.0 | 42.7 | 43.1 | 42.6 | 42.2 | 42.6 | 43.8 | 43.6 | 43.1 | 42.2 |
15 | 28.7 | 26.5 | 26.5 | 26.3 | 25.9 | 28.7 | 28.5 | 28.3 | 27.7 | 25.5 |
16 | 26.6 | 29.2 | 21.4 | 27.5 | 23.3 | 24.9 | 23.7 | 23.9 | 25.9 | 20.3 |
17 | 48.4 | 35.2 | 39.7 | 38.0 | 37.9 | 48.1 | 47.7 | 47.0 | 48.9 | 36.4 |
18 | 54.3 | 58.6 | 58.3 | 52.8 | 53.0 | 53.6 | 52.8 | 52.8 | 54.5 | 57.2 |
19 | 73.2 | 38.4 | 34.8 | 34.0 | 34.1 | 39.4 | 38.6 | 38.1 | 71.9 | 33.6 |
20 | 41.8 | 47.1 | 51.2 | 45.1 | 51.8 | 39.5 | 38.6 | 38.4 | 44.0 | 49.7 |
21 | 27.0 | 71.8 | 34.4 | 32.4 | 25.1 | 31.0 | 30.3 | 30.1 | 27.2 | 33.1 |
22 | 39.1 | 50.3 | 77.6 | 74.8 | 34.3 | 37.5 | 36.7 | 36.0 | 38.6 | 76.7 |
23 | 23.5 | 23.9 | 26.7 | 26.7 | 26.7 | 29.4 | 26.6 | 28.8 | 177.4 | 28.0 |
24 | 181.1 | 19.5 * | 21.6 | 21.6 | 21.6 | 17.7 | 21.3 | 22.1 | 13.1 | 15.3 |
25 | 15.0 | 19.4 * | 15.4 | 15.5 | 15.5 | 17.0 | 15.5 | 16.0 | 16.4 | 15.7 |
26 | 17.0 | 16.9 | 16.9 | 16.8 | 16.8 | 17.5 | 19.0 | 18.7 | 17.7 | 16.4 |
27 | 25.3 | 22.9 | 23.8 | 23.8 | 23.5 | 23.9 | 20.9 | 20.4 | 25.2 | 23.1 |
28 | 65.4 | 28.4 | 25.2 | 21.7 | 69.3 | 179.9 | 180.0 | 180.0 | 179.7 | 24.3 |
29 | 26.9 | 17.4 | 19.0 | 18.5 | 18.0 | 17.5 | 17.0 | 16.5 | 27.7 | 17.9 |
30 | 16.8 | 15.8 | 178.2 | 182.1 | 181.6 | 21.4 | 21.0 | 20.4 | 17.9 | 177.0 |
Ref | [232] | [54] | [129] | [61] | [61] | [157] | [185] | [185] | [232] | [237] |
C | U75 | U76 | U77 d | U78 a | U79 | U80 | U81 | U82 | U83 a | U84 |
1 | 42.7 | 38.1 | 39.0 | 48.0 | 40.0 | 40.9 | 40.4 | 40.8 | 33.9 | 38.8 |
2 | 34.5 | 23.8 | 28.3 | 68.6 | 34.4 | 27.3 | 27.8 | 27.4 | 28.4 | 27.3 |
3 | 74.6 | 80.8 | 79.1 | 83.9 | NR | 78.5 | 80.6 | 78.7 | 78.8 | 79.0 |
4 | 45.4 | 37.5 | 39.2 | 39.8 | 47.9 | 39.0 | 43.0 | 39.0 | 38.9 | 38.8 |
5 | 49.9 | 55.1 | 55.5 | 56.1 | 55.6 | 54.8 | 55.8 | 54.9 | 55.4 | 55.4 |
6 | 19.3 | 18.0 | 18.6 | 19.0 | 19.0 | 18.5 | 18.4 | 18.5 | 18.1 | 18.4 |
7 | 66.9 | 32.7 | 33.3 | 33.6 | 32.4 | 37.0 | 33.9 | 36.7 | 33.2 | 32.9 |
8 | 40.9 | 39.3 | 38.9 | 40.7 | 43.9 | 44.1 | 42.7 | 44.6 | 40.3 | 39.4 |
9 | 48.9 | 47.3 | 47.8 | 47.9 | 60.9 | 54.4 | 54.4 | 55.7 | 48.6 | 47.8 |
10 | 39.1 | 36.9 | 37.1 | 38.5 | 36.8 | 38.2 | 37.8 | 38.2 | 41.4 | 37.2 |
11 | 24.6 | 23.4 | 23.6 | 24.2 | 199.2 | 69.9 | 70.1 | 68.1 | 25.2 | 23.4 |
12 | 126.7 | 125.5 | 125.8 | 128.2 | 130.5 | 145.7 | 144.7 | 129.8 | 125.7 | 125.0 |
13 | 139.7 | 137.8 | 138.5 | 139.5 | 165.5 | 117.0 | 115.8 | 143.5 | 138.9 | 138.0 |
14 | 43.3 | 41.6 | 42.3 | 42.1 | 45.1 | 46.5 | 40.9 | 47.7 | 42.3 | 42.8 |
15 | 29.2 | 27.9 | 27.0 | 29.8 | 29.8 | 68.2 | 26.9 | 68.0 | 26.7 | 29.2 |
16 | 25.3 | 23.9 | 24.5 | 26.8 | 27.4 | 38.7 | 27.6 | 38.8 | 28.2 | 22.6 |
17 | 48.6 | 47.8 | 48.1 | 48.6 | 34.3 | 34.1 | 33.2 | 34.0 | 33.7 | 36.8 |
18 | 54.4 | 52.3 | 53.1 | 54.5 | 59.2 | 47.3 | 47.7 | 58.3 | 59.0 | 54.1 |
19 | 40.4 | 38.8 | 39.4 | 72.7 | 39.4 | 40.5 | 40.8 | 39.1 | 34.1 | 38.9 |
20 | 40.4 | 38.7 | 39.7 | 42.2 | 39.4 | 39.3 | 39.5 | 39.2 | 47.3 | 39.4 |
21 | 31.8 | 30.4 | 30.9 | 25.9 | 31.0 | 31.0 | 31.2 | 30.9 | 25.3 | 30.7 |
22 | 38.1 | 36.5 | 37.2 | 37.5 | 41.0 | 41.1 | 41.5 | 40.9 | 41.2 | 30.6 |
23 | 23.1 | 27.9 | 28.3 | 29.4 | 26.5 | 28.2 | 22.6 | 28.2 | 29.0 | 28.1 |
24 | 65.9 | 16.9 | 17.1 | 17.6 | 21.6 | 15.6 | 64.4 | 15.6 | 16.1 | 15.4 |
25 | 17.4 | 15.5 | 15.7 | 17.4 | 15.9 | 16.7 | 17.3 | 16.8 | 61.0 | 15.6 |
26 | 21.6 | 16.5 | 15.9 | 16.7 | 18.5 | 18.6 | 17.9 | 18.6 | 17.4 | 16.9 |
27 | 24.1 | 23.9 | 23.8 | 24.7 | 20.6 | 18.2 | 24.1 | 17.2 | 23.7 | 23.4 |
28 | 181.6 | 184.0 | 181.1 | 177.0 | 29.0 | 29.3 | 28.7 | 29.3 | 28.7 | 69.7 |
29 | 17.6 | 16.8 | 17.3 | 27.0 | 17.6 | 16.8 | 16.7 | 17.5 | 17.1 | 16.2 |
30 | 17.7 | 21.0 | 21.5 | 17.0 | 21.3 | 21.1 | 21.1 | 21.3 | 65.9 | 21.3 |
1′ | 93.7 | |||||||||
2′ | 79.3 | |||||||||
3′ | 79.0 | |||||||||
4′ | 70.9 | |||||||||
5′ | 79.1 | |||||||||
6′ | 62.4 | |||||||||
1″ | 104.8 | |||||||||
2″ | 75.9 | |||||||||
3″ | 78.3 | |||||||||
4″ | 72.9 | |||||||||
5″ | 78.1 | |||||||||
6″ | 63.9 | |||||||||
Ref | [238] | [239] | [240] | [241] | [242] | [54] | [193] | [54] | [243] | [244] |
C | U85 | U86 | U88 | |||||||
1 | 38.8 | 37.7 | 36.8 | |||||||
2 | 27.4 | 27.1 | 25.2 | |||||||
3 | 79.0 | 79.1 | 78.2 | |||||||
4 | 38.8 | 38.7 | 38.4 | |||||||
5 | 55.3 | 55.4 | 50.7 | |||||||
6 | 18.4 | 18.8 | 17.9 | |||||||
7 | 34.6 | 41.8 | 31.6 | |||||||
8 | 41.0 | 38.9 | 40.2 | |||||||
9 | 50.5 | 49.2 | 154.0 | |||||||
10 | 37.2 | 37.9 | 38.2 | |||||||
11 | 22.2 | 17.4 | 114.9 | |||||||
12 | 24.7 | 32.2 | 122.5 | |||||||
13 | 135.4 | 40.0 | 140.7 | |||||||
14 | 45.0 | 159.2 | 42.6 | |||||||
15 | 26.8 | 116.3 | 27.8 | |||||||
16 | 38.9 | 40.6 | 25.7 | |||||||
17 | 34.0 | 33.9 | 33.2 | |||||||
18 | 136.4 | 60.4 | 56.8 | |||||||
19 | 36.7 | 35.4 | 38.5 | |||||||
20 | 35.0 | 36.5 | 38.9 | |||||||
21 | 23.7 | 28.5 | 30.7 | |||||||
22 | 36.3 | 38.5 | 40.9 | |||||||
23 | 28.1 | 28.0 | 28.2 | |||||||
24 | 15.5 | 15.5 | 16.9 | |||||||
25 | 16.3 | 15.2 | 17.1 | |||||||
26 | 17.8 | 26.3 | 21.6 | |||||||
27 | 21.9 | 19.4 | 24.9 | |||||||
28 | 28.3 | 37.0 | 29.2 | |||||||
29 | 23.1 | 27.5 | 17.1 | |||||||
30 | 20.5 | 22.5 | 21.0 | |||||||
Ref | [245] | [245] | [246] |
C | OT3 | OT4 | OT5 | OT6 | OT7 | OT8 | OT9 a | OT10 a | OT11 a | OT12 |
---|---|---|---|---|---|---|---|---|---|---|
1 | 39.6 | 38.9 | 104.6 | 18.2 | 37.8 | 37.2 | 104.5 | 106.2 | 121.3 | 36.6 |
2 | 34.2 | 27.5 | 144.7 | 27.8 | 27.1 | 194.7 | 147.5 | 146.9 | 182.0 | 34.8 |
3 | 218.2 | 78.4 | 144.2 | 76.3 | 79.0 | 200.1 | 144.2 | 144.4 | 182.2 | 217.1 |
4 | 47.4 | 39.0 | 118.0 | 40.8 | 38.7 | 123.8 | 118.1 | 128.7 | 131.4 | 47.6 |
5 | 54.9 | 55.3 | 129.8 | 141.6 | 55.5 | 154.8 | 129.8 | 117.6 | 142.1 | 53.2 |
6 | 19.7 | 18.5 | 122.5 | 122.0 | 18.8 | 75.0 | 122.6 | 121.6 | 121.3 | 26.3 |
7 | 33.7 | 33.4 | 127.9 | 23.5 | 41.3 | 122.9 | 127.9 | 130.0 | 153.2 | 22.6 |
8 | 41.6 | 41.7 | 131.3 | 47.8 | 38.9 | 154.0 | 131.3 | 141.7 | 47.6 | 41.0 |
9 | 49.6 | 50.4 | 135.6 | 34.8 | 49.2 | 51.6 | 135.3 | 132.2 | 144.8 | 147.4 |
10 | 36.8 | 37.2 | 129.5 | 49.6 | 38.0 | 71.6 | 129.5 | 131.8 | 158.2 | 39.3 |
11 | 21.6 | 21.1 | 25.5 | 34.6 | 17.5 | 28.2 | 29.3 | 129.0 | 128.3 | 115.6 |
12 | 23.9 | 24.0 | 32.8 | 30.5 | 37.7 | 29.5 | 35.9 | 138.1 | 38.9 | 36.1 |
13 | 49.6 | 49.5 | 102.5 | 37.7 | 36.0 | 38.2 | 54.5 | 44.1 | 41.6 | 36.7 |
14 | 42.1 | 42.1 | 43.6 | 39.5 | 158.0 | 40.3 | 156.8 | 49.0 | 43.2 | 38.2 |
15 | 32.6 | 33.7 | 38.8 | 32.5 | 116.9 | 28.5 | 34.1 | 31.3 | 24.8 | 29.6 |
16 | 21.6 | 21.7 | 40.2 | 35.7 | 33.6 | 35.6 | 41.4 | 38.8 | 38.6 | 35.8 |
17 | 54.9 | 54.9 | 42.6 | 30.5 | 37.6 | 30.7 | 41.6 | 32.4 | 33.2 | 42.8 |
18 | 44.7 | 44.8 | 46.0 | 41.9 | 48.0 | 43.4 | 50.4 | 43.2 | 48.2 | 52.0 |
19 | 41.9 | 41.9 | 32.8 | 39.3 | 31.1 | 30.6 | 36.8 | 32.7 | 32.6 | 20.1 |
20 | 27.3 | 27.4 | 40.2 | 33.1 | 33.8 | 41.7 | 41.9 | 41.9 | 41.7 | 28.2 |
21 | 46.4 | 46.5 | 36.8 | 29.5 | 28.1 | 29.9 | 30.8 | 31.0 | 31.1 | 59.6 |
22 | 148.6 | 148.6 | 36.9 | 27.9 | 35.3 | 35.9 | 35.5 | 36.2 | 34.5 | 30.7 |
23 | 26.6 | 28.2 | 11.6 | 28.9 | 28.0 | 9.5 | 11.6 | 11.6 | 11.2 | 22.0 |
24 | 21.1 | 15.7 | 25.4 | 15.5 | 25.5 | |||||
25 | 15.7 | 16.7 | 20.5 | 16.1 | 15.4 | 27.0 | 20.7 | 19.5 | 27.7 | 21.6 |
26 | 16.4 | 15.9 | 23.2 | 18.1 | 25.9 | 21.5 | 28.0 | 20.1 | 20.5 | 16.9 |
27 | 16.6 | 16.7 | 23.2 | 20.4 | 21.1 | 28.7 | 108.3 | 23.4 | 20.5 | 15.3 |
28 | 16.1 | 16.1 | 25.1 | 32.0 | 29.9 | 31.7 | 31.3 | 31.7 | 31.8 | 13.9 |
29 | 110.1 | 110.2 | 180.5 | 74.4 | 73.9 | 178.8 | 184.7 | 183.6 | 183.2 | 22.1 |
30 | 25.0 | 25.0 | 26.3 | 26.0 | 24.6 | 32.5 | 25.9 | 32.5 | 34.0 | 23.0 |
Ref | [94] | [94] | [139] | [213] | [213] | [250] | [139] | [139] | [139] | [251] |
C | OT13 | OT14 | OT15 | OT17 | OT18 | OT19 | OT20 | OT21 | ||
1 | 110.7 | 110.6 | 98.9 | 38.5 | 18.2 | 23.6 | 36.1 | 38.1 | ||
2 | 163.7 | 163.7 | 143.2 | 27.4 | 27.8 | 18.1 | 27.8 | 27.3 | ||
3 | 178.1 | 79.0 | 76.3 | 76.2 | 79.0 | 79.2 | ||||
4 | 24.7 | 28.2 | 40.1 | 39.0 | 40.8 | 39.2 | 39.6 | 39.1 | ||
5 | 103.7 | 105.6 | 43.3 | 55.7 | 141.7 | 141.6 | 52.3 | 55.7 | ||
6 | 126.4 | 125.8 | 28.2 | 18.3 | 122.0 | 121.9 | 21.4 | 19.0 | ||
7 | 115.9 | 115.9 | 17.3 | 34.7 | 23.8 | 27.7 | 26.7 | 35.3 | ||
8 | 161.1 | 160.4 | 47.7 | 40.8 | 45.7 | 43.0 | 41.0 | 38.9 | ||
9 | 39.6 | 39.5 | 38.8 | 51.3 | 34.8 | 34.8 | 148.9 | 48.9 | ||
10 | 165.2 | 166.1 | 47.8 | 37.3 | 49.7 | 46.6 | 39.1 | 37.9 | ||
11 | 33.4 | 33.3 | 33.9 | 21.2 | 29.9 | 34.6 | 114.3 | 17.7 | ||
12 | 29.7 | 29.7 | 28.7 | 26.2 | 29.7 | 30.3 | 36.0 | 35.9 | ||
13 | 40.5 | 40.3 | 38.9 | 39.0 | 38.4 | 37.7 | 36.8 | 37.9 | ||
14 | 44.1 | 44.1 | 37.6 | 43.4 | 38.6 | 40.7 | 38.2 | 158.1 | ||
15 | 28.4 | 28.4 | 28.8 | 27.6 | 34.3 | 32.0 | 29.7 | 117.0 | ||
16 | 35.5 | 35.5 | 35.9 | 37.7 | 36.3 | 35.9 | 35.9 | 36.9 | ||
17 | 38.2 | 38.2 | 30.1 | 34.4 | 32.9 | 30.0 | 43.0 | 38.1 | ||
18 | 43.4 | 43.4 | 44.2 | 142.8 | 44.7 | 47.4 | 52.1 | 49.4 | ||
19 | 32.0 | 32.1 | 30.2 | 129.8 | 35.8 | 35.1 | 20.2 | 41.4 | ||
20 | 41.9 | 41.9 | 40.3 | 32.3 | 34.5 | 28.2 | 28.2 | 29.0 | ||
21 | 213.8 | 213.7 | 29.9 | 33.4 | 74.7 | 33.0 | 59.6 | 33.9 | ||
22 | 52.5 | 52.5 | 36.2 | 37.4 | 46.3 | 38.9 | 30.8 | 33.2 | ||
23 | 7.9 | 28.0 | 25.4 | 28.9 | 28.2 | 28.1 | ||||
24 | 99.4 | 15.4 | 28.9 | 25.4 | 15.6 | 15.6 | ||||
25 | 36.8 | 36.5 | 17.5 | 16.1 | 16.6 | 16.2 | 22.1 | 15.6 | ||
26 | 22.5 | 22.5 | 15.9 | 16.7 | 17.0 | 18.4 | 17.0 | 30.1 | ||
27 | 19.7 | 19.8 | 17.2 | 14.6 | 19.1 | 19.6 | 15.3 | 26.0 | ||
28 | 32.5 | 32.6 | 31.6 | 25.3 | 33.1 | 32.4 | 14.0 | 30.1 | ||
29 | 179.0 | 31.3 | 32.3 | 34.6 | 23.0 | 33.5 | ||||
30 | 15.1 | 15.1 | 31.8 | 29.2 | 24.6 | 32.0 | 22.2 | 21.5 | ||
OCH3 | 50.5 | 51.0 | 51.3 | |||||||
Ref | [252] | [252] | [196] | [220] | [196] | [157] | [253] | [254] |
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Camargo, K.C.; de Aguilar, M.G.; Moraes, A.R.A.; de Castro, R.G.; Szczerbowski, D.; Miguel, E.L.M.; Oliveira, L.R.; Sousa, G.F.; Vidal, D.M.; Duarte, L.P. Pentacyclic Triterpenoids Isolated from Celastraceae: A Focus in the 13C-NMR Data. Molecules 2022, 27, 959. https://doi.org/10.3390/molecules27030959
Camargo KC, de Aguilar MG, Moraes ARA, de Castro RG, Szczerbowski D, Miguel ELM, Oliveira LR, Sousa GF, Vidal DM, Duarte LP. Pentacyclic Triterpenoids Isolated from Celastraceae: A Focus in the 13C-NMR Data. Molecules. 2022; 27(3):959. https://doi.org/10.3390/molecules27030959
Chicago/Turabian StyleCamargo, Karen Caroline, Mariana Guerra de Aguilar, Acácio Raphael Aguiar Moraes, Raquel Goes de Castro, Daiane Szczerbowski, Elizabeth Luciana Marinho Miguel, Leila Renan Oliveira, Grasiely Faria Sousa, Diogo Montes Vidal, and Lucienir Pains Duarte. 2022. "Pentacyclic Triterpenoids Isolated from Celastraceae: A Focus in the 13C-NMR Data" Molecules 27, no. 3: 959. https://doi.org/10.3390/molecules27030959
APA StyleCamargo, K. C., de Aguilar, M. G., Moraes, A. R. A., de Castro, R. G., Szczerbowski, D., Miguel, E. L. M., Oliveira, L. R., Sousa, G. F., Vidal, D. M., & Duarte, L. P. (2022). Pentacyclic Triterpenoids Isolated from Celastraceae: A Focus in the 13C-NMR Data. Molecules, 27(3), 959. https://doi.org/10.3390/molecules27030959