Parathyrsoidins A–D, Four New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoides
by
Yen-Ju Tseng
1, 
Yu-Sheng Lee
1,
Shang-Kwei Wang
2,3,*,
Jyh-Horng Sheu
1,3 and
Chang-Yih Duh
1,3,* 1
Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan
2
Department of Microbiology, Kaohsiung Medical University, Kaohsiung 807, Taiwan
3
Asia-Pacific Ocean Research Center, National Sun Yat-sen University, Kaohsiung 804, Taiwan
*
Authors to whom correspondence should be addressed.
Mar. Drugs 2013, 11(7), 2501-2509; https://doi.org/10.3390/md11072501
Submission received: 22 April 2013
/
Revised: 6 June 2013
/
Accepted: 28 June 2013
/
Published: 15 July 2013
Abstract
:Four new nardosinane-type sesquiterpenoids, parathyrsoidins A–D (1–4) were isolated from the soft coral Paralemnalia thyrsoides. The structures of parathyrsoidins A–D (1–4) were determined by extensive spectral analysis and their cytotoxicity against selected cancer cell lines as well as antiviral activity against human cytomegalovirus (HCMV) were evaluated in vitro.
1. Introduction
Soft corals belonging to the genus Paralemnalia have been proved to be a rich source of sesquiterpenoids [1,2,3,4,5,6,7,8,9,10,11,12,13]. Our recent study of the chemical constituents of the soft coral P. thyrsoides has yielded a cytotoxic bisnorsesquiterpenoid, paralemnolide A [13]. Continuing chemical investigation of the same collection led to the isolation of four new nardosinanes, parathyrsoidins A–D (1–4) (Figure 1). The relative structures of these metabolites were established by extensive spectroscopic analysis. The cytotoxicity of 1–4 against P-388 (mouse lymphocytic leukemia), HT-29 (human colon adenocarcinoma), and A-549 (human lung carcinoma) cancer cell lines as well as antiviral activity against human cytomegalovirus (HCMV) were evaluated in vitro.
Figure 1.
Structures of Metabolites 1–4.
2. Results and Discussion
Parathyrsoidin A (1) was isolated as an amorphous solid. Its molecular formula, C16H26O2, was established by HRESIMS (m/z 273.1831, [M + Na]+), implying four degrees of unsaturation. The 13C NMR and DEPT (Table 1) spectroscopic data showed signals of four methyls (including one oxymethyl), five sp3 methylenes (including one oxymethylene), three sp3 methines, one sp2 methine, two sp3 (including one quaternary sp3 dioxycarbon) and one sp2 quaternary carbons. The NMR signals (Table 1) observed at δC 120.7 (CH) and 141.9 (C), δH 5.28 brd, J = 5.2 Hz showed the presence of one trisubstituted double bond. The above data accounted for one of the four degrees of unsaturation, thus, the tricyclic structure of 1 was revealed. In the 1H–1H COSY spectrum, it was possible to identify three different structural units, which were assembled with the assistance of an HMBC experiment. Key HMBC correlations of H-4 to C-14 and C-15; H-6 to C-5, C-7, C-8, C-10, C-11, C-13 and C-14; H2-8 to C-7 and C-10; H2-9 to C-1, C-5 and C-7; H-11 to C-6 and C-13; H2-12 to C-7; H3-13 to C-6, C-11 and C-12; H3-14 to C-4, C-5, C-6 and C-10; H3-15 to C-3, C-4, C-5 permitted the establishment of the nardosinane-type skeleton of 1 (Figure 2). Detailed analysis of 2D NMR correlations (Figure 2) and comparison of the 1H NMR data (in CDCl3) 1 (Supplementary Materials) with those of 2-deoxy-7-O-methyllemnacarnol [14] suggested that 1 is a closely related isomer of 2-deoxy-7-O-methyllemnacarnol. The relative configuration of 1 was proposed on the basis of key NOE correlations (Figure 3). The NOE correlations between H3-14/H-6, H3-14/H3-15, H3-14/OMe-7, and H-6/H-11 showed that H-6, H-11, H3-14, H3-15, and OMe-7 are located on the β face, whereas H-4 and H3-13 are oriented toward the opposite face. According to the aforementioned observations, the structure of parathyrsoidin A (1) was revealed to be the C-11 epimer of 2-deoxy-7-O-methyllemnacarnol. In order to rule out the possibility of 1 being an isolation artifact, a sample of 2-deoxylemnacarnol [5] obtained from Prof. Sheu laboratory was kept at room temperature for three day in the presence of RP-18 gel in MeOH. However, the formation of 2-deoxy-7-O-methyllemnacarnol was not observed.
| Position | 1 | 4 | ||
|---|---|---|---|---|
| δH a | δC b | δH a | δC b | |
| 1 | 5.28 brd (5.2) c | 120.7, CH d | 5.29 brs | 120.9, CH |
| 2 | 1.89 m, 1.94 m | 26.0, CH2 | 1.82 m, 1.88 m | 25.7, CH2 |
| 3α 3β | 1.28 m
1.42 qd (12.0, 6.0) | 27.2, CH2 | 1.28 m
1.37 qd (13.2, 6.4) | 28.9, CH2 |
| 4 | 1.78 dqd (12.0, 6.8, 3.2) | 35.0, CH | 1.71 dqd (13.2, 6.4, 3.6) | 37.8, CH |
| 5 | 38.6, qC | 39.2, qC | ||
| 6 | 2.32 d (6.0) | 52.7, CH | 118.8, qC | |
| 7 | 107.5, qC | 150.1, qC | ||
| 8α 8β | 1.81 td (13.6, 5.2)
2.31 dt (13.6, 5.2,) | 35.3, CH2 | 2.19 m | 26.4, CH2 |
| 9α 9β | 1.98 ddd (13.6, 5.2, 1.2)
2.52 tdq (13.6, 5.2, 2.4) | 29.2, CH2 | 1.95 ddd (12.8, 6.0, 1.2)
2.45 m | 29.9, CH2 |
| 10 | 141.9, qC | 142.7, qC | ||
| 11 | 1.98 qdd (7.2, 6.0, 4.0) | 36.7, CH | 2.99 qd (7.2, 1.2) | 46.4, CH |
| 12α 12β | 3.40 d (8.0)
3.78 dd (8.0, 4.0) | 74.1, CH2 | 4.82 d (1.2) | 112.5, CH |
| 13 | 1.03 d (7.2) | 15.9, CH3 | 1.12 d (7.2) | 19.6, CH3 |
| 14 | 1.19 s | 21.8, CH3 | 1.10 s | 21.5, CH3 |
| 15 | 0.80 d (6.8) | 16.4, CH3 | 0.95 d (6.4) | 18.9, CH3 |
| OMe-7 OMe-12 | 3.26 s | 48.5, CH3 | ||
| 3.28 s | 54.8, CH3 | |||
a Spectra recorded at 400 MHz in C6D6. b Spectra recorded at 100 MHz in C6D6. c J values (in Hz) are in parentheses. d Multiplicities are deduced by HSQC and DEPT experiments.
Figure 2.
Selected 1H−1H COSY ( ![Marinedrugs 11 02501 i001]()
) and HMBC ( ![Marinedrugs 11 02501 i002]()
) correlations of 1–4.
) and HMBC ( 
) correlations of 1–4.
Parathyrsoidin B (2) had the molecular formula C17H28O3, 30 mass units higher than that of 1. Comparison of the 1H and 13C NMR data (Table 2) of compounds 1 and 2 showed that both compounds should have similar structures. C-12 of 2 showed signal at downfield δC 109.0, CH relative to the corresponding signal of 1 (δC 74.1, CH2), implying the presence of an oxymethyl at C-12 of 2. In the 2D NMR spectra, including 1H–1H COSY and HMBC (Figure 2), three segregate consecutive proton spin systems, H-1 to H-4, H-4 to H3-15, H2-8 to H2-9, and H-11 to H-6, H-12 and H3-13, were found in the 1H–1H COSY spectrum. Detailed analysis of HMBC correlations (Figure 2) and comparison of 1H NMR data (in CDCl3) of 2 (Supplementary Materials) with those of 2-deoxy-12α-methoxy-7-O-methyllemnacarnol [14] revealed that they were closely related isomers. The relative configuration of 2 was determined by the analysis of NOE correlations, as shown in Figure 3. NOE correlations between H3-14/H-6, H3-14/H3-15, H3-14/OMe-7, and H-6/H-11 positioned the β-orientation of the aforementioned protons. Furthermore H3-13 (δ 1.00, d, J = 6.8 Hz) was found to show NOE interactions with H-4 (δ 1.74, dqd, J = 12.0, 6.8, 3.2 Hz) and H-12 (δ 4.37, s), suggesting the α-orientation of H-4, H-12 and H3-13. On the basis of the above findings (Figure 3), the relative structure of parathyrsoidin B (2) was determined as the C-11 epimer of 2-deoxy-12β-methoxy-7-O-methyllemnacarnol.
Figure 3.
Key NOESY Correlations for 1–3.
Parathyrsoidin C (3) possessed the same molecular formula (C17H28O3) as that of 2, as established by HRESIMS and 13C NMR spectroscopic data. Further comparison of the 1H NMR (in CDCl3) and other spectral data among 3, 2 (Table 2, Figure 2, and Supplementary Materials) and 2-deoxy-12α-methoxy-7-O-methyllemnacarnol [14] disclosed that three metabolites were closely related isomers. The significant coupling constant (JH-11,12 and JH-11,6) differences between 3 and 2 demonstrated that the configuration at C-11 for 3 differed from that of 2. NOESY correlations between H3-15/H-6, H3-15/H3-13, H3-15/H3-14 suggested the β-orientations of H3-13, H3-14, H3-15, and H-6. Furthermore, H-11 was found to show NOESY correlations with both H-12 and H-4, suggesting the α-orientations of H-12, H-11, and H-4. Therefore, 3 was elucidated as the C-11 epimer of 2.
Parathyrsoidin D (4) was also isolated as an amorphous solid and had the molecular formula C16H24O2, as determined by HRESIMS (C16H24O2 + Na, m/z found 271.1673, calculated 271.1674) indicating five degrees of unsaturation. Comparison of the NMR data (Table 1, Table 2) of compounds 2 and 4 showed both compounds should have similar structures. C-6 and C-7 of 4 showed signals at downfield δC 118.8, qC and 150.1, qC relative to the corresponding signals of 2 (δC 53.6, CH and 111.9, qC), implying the presence of a tetrasubstituted double bond at C-6 and C-7 of 4. The planar structure of 4 was also confirmed by the 1H–1H COSY and HMBC correlations (Figure 2). The relative configuration of 4 was determined by NOE correlations. NOE correlations between H3-14/H-11 and H3-14/H3-15 positioned the β-orientation of the aforementioned protons, whereas H3-13, H-4, and H-12 are oriented toward the opposite surface (Figure 4).
| Position | 2 | 3 | ||
|---|---|---|---|---|
| δH a | δC b | δH a | δC b | |
| 1 | 5.56 t (2.8) c | 120.8, CH | 5.42 brs | 122.7, CH d |
| 2 | 1.84 m, 1.90 m | 26.1, CH2 | 1.90 m, 1.96 m | 25.7, CH2 |
| 3α 3β | 1.23 m
1.35 qd (12.0, 6.0) | 27.1, CH2 | 1.29 m 1.47 qd (13.2, 7.2) | 27.1, CH2 |
| 4 | 1.74 dqd (12.0, 6.8, 3.2) | 35.2, CH | 1.71 dqd (13.2, 6.8, 3.2) | 35.3, CH |
| 5 | 38.4, qC | 40.3, qC | ||
| 6 | 2.86 dd (6.8, 2.4) | 45.8, CH | 2.40 d (10.8) | 53.6, CH |
| 7 | 109.6, qC | 111.9, qC | ||
| 8α 8β | 1.81 td (14.4, 5.2)
2.38 ddt (14.4, 5.6, 2.4) | 38.0, CH2 | 1.95 m | 32.4, CH2 |
| 9α 9β | 1.92 ddd (14.4,5.2, 2.4)
2.62 tdq (14.4, 5.6, 2.4) | 29.7, CH2 | 2.33 m 2.21 tdq (14.0, 5.6, 1.6) | 27.4, CH2 |
| 10 | 142.0, qC | 140.2, qC | ||
| 11 | 2.31 quin (6.8) | 42.0, CH | 1.83 dqd (10.8, 7.2, 5.6) | 42.1, CH |
| 12 | 4.37 s | 109.0, CH | 4.54 d (5.6) | 105.9, CH |
| 13 | 1.00 d (6.8) | 14.2, CH3 | 1.15 d (7.2) | 15.6, CH3 |
| 14 | 1.17 s | 21.0, CH3 | 1.16 s | 21.9, CH3 |
| 15 | 0.83 d (6.8) | 16.2, CH3 | 0.75 d (6.8) | 16.3, CH3 |
| OMe-7 OMe-12 | 3.33 s
3.23 s | 48.7, CH3 54.3, CH3 | 3.32 s 3.27 s | 48.9, CH3 54.5, CH3 |
a Spectra recorded at 400 MHz in C6D6. b Spectra recorded at 100 MHz in C6D6. c J values (in Hz) are in parentheses. d Multiplicities are deduced by HSQC and DEPT experiments.
Figure 4.
Key NOESY correlations for 4.
Cytotoxicity of compounds 1–4 against the proliferation of a limited panel of cancer cell lines, including P-388, A549, and HT-29, were evaluated (Table 3). Metabolites 1–4 displayed moderate cytotoxicity against P-388, with ED50 of 7.95, 13.2, 3.63 and 2.32 μM, respectively. Compounds 1–4 were also examined for antiviral activity against HCMV using a human embryonic lung (HEL) cell line. Parathyrsoidins A–D (1–4) did not show anti-HCMV activity.
| Compound | A-549 | HT-29 | P-388 |
|---|---|---|---|
| 1 | >20 | >20 | 7.95 |
| 2 | >20 | >20 | 13.2 |
| 3 | >20 | >20 | 3.63 |
| 4 Mithramycin | >20 0.17 | >20 0.19 | 2.32 0.14 |
3. Experimental Section
3.1. General Experimental Procedures
Optical rotations were measured on a JASCO P1020 digital polarimeter. IR spectra were recorded on a JASCO FT/IR4100 infrared spectrophotometer. The NMR spectra were recorded on a Varian MR 400 FT-NMR at 400 MHz for 1H (δH 7.16) and 100 MHz for 13C (δC 128.4), in C6D6 using solvent peak as internal standard. LRMS and HRMS were obtained by ESI on a Bruker APEX ÉÉ mass spectrometer. Silica gel 60 (Merck, 230–400 mesh) and LiChroprep RP-18 (Merck, 40–63 μm) were used for column chromatography. Precoated silica gel plates (Merck, Kieselgel 60 F254, 0.25 mm) and precoated RP-18 F254s plates (Merck) were used for TLC analysis. High-performance liquid chromatography was carried out using a Hitachi L-7100 pump equipped with a Hitachi L-7400 UV detector at 220 nm together with a semi-preparative reversed-phase column (Merck, Hibar LiChrospher RP-18e, 5 μm, 250 × 25 mm).
3.2. Animal Material
The octocoral P. thyrsoides was collected by hand using scuba at the Sansiantai, Taitong County, Taiwan, in July 2008, at a depth of 6 m. This soft coral was identified by Prof. Chang-Fong Dai, Institute of Oceanography, National Taiwan University. A voucher specimen (SST-07) was deposited in the Department of Marine Biotechnology and Resources, National Sun Yat-sen University.
3.3. Extraction and Separation
The frozen soft coral was chopped into small pieces and extracted with acetone in a percolator at room temperature. The acetone extract of P. thyrsoides was concentrated to a brown gum, which was partitioned with EtOAc and H2O. The EtOAc-soluble residue (20 g) was subjected to Si 60 CC using n-hexane–EtOAc mixtures of increasing polarity for elution. Fraction 14, eluted with n-hexane–EtOAc (2:1), was purified by reverse-phase HPLC (MeOH–H2O, 85:15) to afford 1 (3.0 mg) and 2 (8.0 mg). Fraction 15, eluted with n-hexane–EtOAc (1:1), was purified by reverse-phase HPLC (MeOH–H2O, 85:15) to afford 3 (6.0 mg) and 4 (1.0 mg).
Parathyrsoidin A (1): amorphous solid; [α]25D = −21 (c 0.8, CHCl3); IR (neat) νmax 2962, 2857, 1460, 1338, 1250, 1098, 854 cm−2; 1H and 13C NMR data, see Table 1; ESIMS m/z 273 [M + Na]+; HRESIMS m/z 273.1831 (calcd for C16H26O2Na, 273.1830).
Parathyrsoidin B (2): amorphous solid; [α]25D = −62 (c 2.0, CHCl3); IR (neat) νmax 2991, 2960, 1385, 1274, 1100, 855 cm−1; 1H and 13C NMR data, see Table 1; ESIMS m/z 303 [M + Na]+; HRESIMS m/z 303.1937 (calcd for C17H28O3Na, 303.1936).
Parathyrsoidin C (3): colorless oil; [α]25D = −42 (c 1.0, CHCl3); IR (neat) νmax 2929, 2831, 1385, 1108, 864 cm−1; 1H and 13C NMR data, see Table 2; ESIMS m/z 303 [M + Na]+; HRESIMS m/z 303.1934 (calcd for C17H28O3Na, 303.1936).
Parathyrsoidin D (4): colorless oil; [α]25D = −10 (c 0.1, CHCl3); IR (neat) νmax 2957, 1684, 1653, 1377, 1100, 823 cm−1; 1H and 13C NMR data, see Table 2; ESIMS m/z 271 [M + Na]+; HRESIMS m/z 271.1673 (calcd for C16H24O2Na, 271.1674).
3.4. Cytotoxicity Testing
Cytotoxicity was determined on P-388 (mouse lymphocytic leukemia), HT-29 (human colon adenocarcinoma), and A-549 (human lung epithelial carcinoma) tumor cells using a modification of the MTT colorimetric method according to a previously described procedure [15,16]. The provision of the P-388 cell line was supported by J.M. Pezzuto, formerly of the Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago. HT-29 and A-549 cell lines were purchased from the American Type Culture Collection. To measure the cytotoxic activities of tested compounds, five concentrations with three replications were performed on each cell line. Mithramycin was used as a positive control.
3.5. Anti-HCMV Assay
To determine the effects of natural products upon HCMV cytopathic effect (CPE), confluent human embryonic lung (HEL) cells grown in 24-well plates were incubated for 1 h in the presence or absence of various concentrations of tested natural products with three replications. Ganciclovir was used as a positive control. Then, cells were infected with HCMV at an input of 1000 pfu (plaque forming units) per well of a 24-well dish. Antiviral activity was expressed as IC50 (50% inhibitory concentration), or compound concentration required to reduce virus induced CPE by 50% after 7 days as compared with the untreated control. To monitor the cell growth upon treating with natural products, an MTT-colorimetric assay was employed [17].
4. Conclusions
In our continuing investigation of soft coral P. thyrsoides collected at San-Hsian-Tai (Taitong County, Taiwan) has led to the isolation of four new nardosinane-type sesquiterpenoids, parathyrsoidins A–D (1–4) exhibiting cytotoxicity against P-388 cell line with ED50 of 7.95, 13.2, 3.63 and 2.32 μg/mL, respectively. 13α-Methylated nardosinane-type metabolites have been found in soft corals Lemnalia africana and Nephthea elongata [2,4].
Acknowledgements
This research was financially supported by grants from the National Science Council (NSC99-2628-B-110-002-MY3) and NSYSUKMU Joint Project (NSYSUKMU 2013-P018) awarded to C.-Y. Duh.
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Tseng, Y.-J.; Lee, Y.-S.; Wang, S.-K.; Sheu, J.-H.; Duh, C.-Y. Parathyrsoidins A–D, Four New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoides. Mar. Drugs 2013, 11, 2501-2509. https://doi.org/10.3390/md11072501
AMA Style
Tseng Y-J, Lee Y-S, Wang S-K, Sheu J-H, Duh C-Y. Parathyrsoidins A–D, Four New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoides. Marine Drugs. 2013; 11(7):2501-2509. https://doi.org/10.3390/md11072501
Chicago/Turabian StyleTseng, Yen-Ju, Yu-Sheng Lee, Shang-Kwei Wang, Jyh-Horng Sheu, and Chang-Yih Duh. 2013. "Parathyrsoidins A–D, Four New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoides" Marine Drugs 11, no. 7: 2501-2509. https://doi.org/10.3390/md11072501
APA StyleTseng, Y. -J., Lee, Y. -S., Wang, S. -K., Sheu, J. -H., & Duh, C. -Y. (2013). Parathyrsoidins A–D, Four New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoides. Marine Drugs, 11(7), 2501-2509. https://doi.org/10.3390/md11072501
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