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Article

Antimicrobial Evaluation of Sulfonamides after Coupling with Thienopyrimidine Coplanar Structure

by
Elshaymaa I. Elmongy
1,
Wejdan S. Alanazi
2,
Alhanouf I. Aldawsari
2,
Asma A. Alfaouri
2 and
Reem Binsuwaidan
3,*
1
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Helwan University, Ain Helwan, Cairo P.O. Box 11795, Egypt
2
College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia
3
Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia
*
Author to whom correspondence should be addressed.
Pharmaceuticals 2024, 17(2), 188; https://doi.org/10.3390/ph17020188
Submission received: 22 December 2023 / Revised: 26 January 2024 / Accepted: 28 January 2024 / Published: 31 January 2024
(This article belongs to the Special Issue Computer-Aided Drug Design and Drug Discovery)
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Versions Notes

Abstract

:
This work describes the design and synthesis of three series of hybrids of thienopyrimidines and sulfonamides. Dihydrofolate reductase enzyme was selected as a target for the in-silico screening of the synthesized thienopyrimidine–sulfonamide hybrid as an antibacterial, while squalene epoxidase was selected as an antifungal target protein. All screened compounds showed promising binding affinity ranges, with perfect fitting not exceeding 1.9 Å. The synthesized compounds were tested for their antimicrobial activity using agar well diffusion and minimum inhibitory concentration tests against six bacterial strains in addition to two Candida strains. Compounds 8iii and 12ii showed varying degrees of inhibition against Staphylococcus aureus and Escherichia coli bacterial strains, whereas the best antifungal activity against Candida was displayed by compound 8iii. Compound 12ii, the cyclohexathienopyrimidine coupled with sulfadiazine at position 3, has the best antibacterial activity, which is consistent with molecular docking results at the active site of the oxidoreductase protein. Interestingly, compound 12ii also has the highest docking binding energy at the antifungal squalene epoxidase active site. Investigating the physicochemical properties of the synthesized hybrids revealed their high tolerability with cell membranes, and moderate to poor oral bioavailability, and that all are drug-like candidates, among which 4i, the cyclohexathieno[2,3-d] pyrimidine core with sulphaguanidine incorporated at position 4, recorded the best score (1.58).

1. Introduction

Scientific research is participating in significant advancements in diagnosis, prevention, and therapy. Recent studies have shifted their focus to heterocyclic compounds, especially those containing a thienopyrimidine core. These compounds have garnered attention due to their unique structural similarity to purines and their versatile pharmacological properties. They have been shown to possess antimicrobial [1], antiviral [2], and anti-inflammatory [3,4] properties, serve as β3-adrenoceptor agonists [5], exhibit anti-tuberculosis properties [6], antiprotozoal activity [7], and kinase inhibition [8,9,10,11,12], act as antioxidants [13,14,15,16], and possess anticancer activity [17,18,19,20].
A concerning global issue is the growing prevalence of pathogenic microorganism infections caused by bacteria such as Staphylococcus aureus and Escherichia coli, and the fungal strain Candida albicans. These strains have demonstrated resistance to commonly used antibiotics [21,22]. Therefore, there is an urgent need to develop novel molecules as antimicrobial agents. Recent studies on derivatives of thieno[2,3-d]pyrimidine have revealed their effectiveness against both gram-negative and gram-positive bacteria [22,23,24,25], making them promising candidates for the development of a new class of antibacterials. The molecular structure of thienopyrimidine compounds contains features necessary to interact with microbial targets, resulting in antimicrobial activity [26]. The arrangement of rings, functional groups, and bio-isosteric replacements can be adjusted to enhance potency, selectivity, and safety, making thienopyrimidines promising building blocks for the development of new antimicrobial agents [27].
Sulfonamides have diverse biological activities including bacterial [28,29] and protozoal [30,31] activities, as well as acting as dihydropteroate synthase inhibitors, thus inhibiting the biosynthesis of dihydrofolic acid [32], inhibiting carbonic anhydrase (CA) [33] and epidermal growth factor receptor (EGFR) [34,35], and inducing insulin release [36], as well as having antiviral [37], antifungal [38], anticancer [39,40], and anti-inflammatory activities [41].

Design Strategy

Scientific groups have reported on the successful implementation of the hybrid pharmacophore concept, which is performed through combining heterocycles with recognized active groups like sulfonamides [42,43]. Hybridized heterocycles with sulfonamides were successfully applied in the reported literature as seen in the interconnection between phthalazinone derivatives and sulfonamides as sulfadiazine and sulfathiazole, which was a successful strategy to synthesize broad-spectrum antibacterial compounds [28]. Also, hydrophilic ends as guanidine in sulfaguanidine are present in the residue arginine (Arg), which has been noticed in many protein binding sites. In addition, it forms an important therapeutic agent when it is incorporated in the structure due to its reported biological effects, especially in antibiotics such as trimethoprim [44]. Additionally, the thienopyrimidine heterocyclic structure has shown promising antimicrobial activity when combined with sulfa compounds. Their combination has been explored due to their potential to combat various microbial infections [44,45].
Accordingly, the design strategy of this study was based on the introduction of the cyclohexylthieno[2,3-d]pyrimidine heterocyclic as a core structure, as thieno[2,3-d]pyrimidine has been previously reported as a promising scaffold for antimicrobial compounds, followed by the incorporation of different sulfonamide derivatives, given that they are an important class of antibiotic drugs with a wide range of activity, led by compounds I–III [46,47]. Thus, our research focused on combining thienopyrimidine’s coplanar cyclic structure with various substituted sulfonamide groups, which were initially incorporated at position 4 of the thienopyrimidine core. A series of thienopyrimidine–sulfonamide hybrids, which we have designated as “4i–iii”, were synthesized, one of which—compound 4ii—exhibited mild antibacterial activity. The sulfonamides sulfadiazine and sulfamethoxazole were selected as references for comparison. Aiming to further explore the activity, the substitution was then shifted from position 4 to position 3 to synthesize the novel series “12i–iii”. The thienopyrimidine–sulfadiazine hybrid 12ii demonstrated enhanced antibacterial activity.
In an attempt to further explore the hybrids’ activities, we investigated the effect of replacing the cyclic cycloalkyl ring with a carboxylate open chain, resulting in series “8i–iii”, which revealed enhanced antifungal activity. The design strategy is illustrated below (Figure 1).

2. Results and Discussion

2.1. Molecular Modeling Studies

Molecular docking studies were performed on the prepared compounds 4i–iii, 8i–iii, and 12i–iii. The study of the prepared structures was undertaken on an antibacterial target protein (PDB ID: 2W9S) and an antifungal target protein (PDB ID: 2AIB), whose crystal structures bound to their co-crystallized ligands were downloaded from the Protein Data Bank.
Chemotherapeutic chemicals such as antibiotics are used to either suppress or kill germs. Sulfonamides are structural analogues and competitive antagonists of p-aminobenzoic acid in the manufacture of folic acid, which is necessary for bacteria to continue producing DNA. Tetrahydrofolate synthesis is inhibited by sulfonamide medications in conjunction with trimethoprim, further impeding DNA replication. The drug’s effects cause obstacles to cell division [48]. Accordingly, the dihydrofolate reductase (DHFR) enzyme was selected as a target for in-silico screening using molecular docking to compare the interactions of the newly synthesized thienopyrimidine–sulfonamide hybrids with those of the co-crystallized ligand (trimethoprim). The protein with PDB code 2W9S was downloaded and complexed with trimethoprim. All the screened compounds showed promising binding affinities ranging from −8.7115 to −7.1696, with perfect fitting not exceeding 1.9 Å (Table 1). The best binding affinity (−8.7115) was recorded by carboxylate thieno[2,3-d]pyrimidin-3(4H)-yl)-2-((4-(N-(pyrimidin-2-yl)sulfamoyl)phenyl)amino) acetamide derivative 12ii, with a root mean square deviation (RMSD) value of 1.3166 Å. The interactions with the active site occurred at three positions with the amino acid residues THR 46, LYS 45, and GLN 95. These interactions involved a hydrogen bond interaction between the NH group of compound 12ii and the acceptor oxygen of THR46, and two hydrogen bonds between the donor nitrogen atoms of both LYS 45 and GLN 95 and the acceptor sulfoxide group of thienopyrimidine–sulfadiazine-synthesized hybrid 12ii, (Figure 2). Interestingly, the compound 12ii had the best docking results as well as the best antibacterial results among the screened compounds, demonstrating enhanced antibacterial activity better than sulfadiazine alone against gram-positive S. aureus.
Moreover, squalene epoxidase (SE), cytochrome P450 sterol 14a demethylase (CYP51), and β-1,3-glucansynthase are the primary targets of antifungal screening [49]. In this work, antifungal activity was investigated using molecular docking on SE. Ergosterol production involves squalene epoxidase, and, therefore, inhibitors target this domain [50]. Ergosterol has a coplanar four-cyclic structure that resembles the core structure under investigation. The structure of the target protein with its co-crystalized ligand (PDB ID: 2AIB) was downloaded and showed that the main key interaction involves the TYR 47 amino acid residue (Figure 3). The docking results of the thienopyrimidine–sulfonamide hybrid series 4, 8, and 12 upon docking at the active site, taking the co-crystallized ligand as a placement guide, were very promising, with binding energies ranging from −6.807 kcal/mol to −9.6592 kcal/mol.
The thienopyrimidine–sulfadiazine hybrid 12ii had the best docking score, with a binding energy of −9.3391 kcal/mol and a perfect fit at the site of interaction with an RMSD value of 1.7258 Å, (Figure 4). Compound 8iii had the best antifungal results, forming two hydrogen bond interactions at −8.2032 kcal/mol with an RMSD of 1.8383 Å with the active site at TYR47, which is a promising biological result. TYR 47, THR 74, MET 50, and VAL 75 were the main receptor residues involved in most interactions between the synthesized ligands and the active site, (Figure 5). However, it is worth noting that compound 12ii—the cyclohexathienopyrimidine coupled with sulfadiazine at position 3—exhibited the best antibacterial activity, which is consistent with its molecular docking results at the active site of the DHFR oxidoreductase protein. Interestingly, 12ii also had the highest docking binding energy at the antifungal squalene epoxidase active site.
Table 1 and Table 2 present the docking results of the synthesized hybrids, which include binding affinity scores and RMSD values as well as the ligand interactions (hydrogen bonding or hydrophobic interactions) with the active site residues.

2.2. Antimicrobial Investigation

Thienopyrimidine compounds have demonstrated significant antimicrobial activity, making them a promising avenue in the search for novel antimicrobial agents [25]. One of the key factors that contributes to the antimicrobial activity of thienopyrimidine compounds is their ability to disrupt essential cellular processes in microorganisms. Thienopyrimidine compounds can be tailored to act selectively against specific microbial targets. For example, some thienopyrimidines have been shown to selectively inhibit key enzymes involved in bacterial DNA replication, transcription, translation, and cell wall synthesis [44]. Through targeting essential microbial processes, these compounds disrupt vital cellular functions, leading to the inhibition or killing of different microorganisms [25]. Furthermore, thienopyrimidines have also demonstrated effective antifungal activity [1,27,51]. The unique structures of these compounds allow them to target specific fungal enzymes, which leads to compromised cell membrane integrity and, consequently, fungal cell death.
In this study, three series of thieno[2,3-d]pyrimidine derivatives (4i–iii, 8i–iii, and 12i–iii) were investigated for their antimicrobial activity against different bacterial and fungal strains. The synthesized compounds were tested for their antimicrobial activity using agar well diffusion and MIC tests using serial dilution against the following bacterial and fungal strains: Staphylococcus aureus (ATCC 25923), Staphylococcus aureus (ATCC 29213), Staphylococcus epidermidis (ATCC 12228), Enterococcus faecalis (ATCC 29212), Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), Klebsiella pneumoniae (ATCC 700603), Candida albicans (ATCC 10231), and Candida parapsilosis (ATCC 22019). The results were expressed as the average diameter of the growth inhibition zone (GIZ) and the minimum inhibitory concentration (MIC).
Five of the investigated compounds showed activity against the gram-positive strain Staphylococcus aureus but not against Staphylococcus epidermidis and Enterococcus faecalis. Among the three tested gram-negative strains, five of the investigated thienopyrimidine–sulfonamide hybrids showed mild activity against Escherichia coli but with smaller zones of inhibition and higher MIC values than sulfonamides alone. No activity was detected against Pseudomonas aeruginosa nor Klebsiella pneumoniae, Table 3.
Regarding antifungal activity, six of the tested hybrids displayed good activity against the tested Candida strains, as tabulated in Table 4. Five of the investigated compounds—4ii, 8ii, 8iii, 12i, and 12iii—showed comparable or better activity than the investigated sulfonamides in both zones of inhibition and MICs.

2.3. Correlating Structure to Biological Activity

Linking the coplanar cyclic structure of thienopyrimidine with different substituted sulfonamide groups was initially performed at position 4 of the thienopyrimidine core. This afforded a series of thienopyrimidine–sulfonamide hybrids designated as “4i–iii”, among which the cyclohexathienopyrimidine–sulfadiazine hybrid 4ii exhibited mild antibacterial activity with zones of inhibition of 15 mm for S. aureus gram-positive bacteria and 18 mm for E. coli gram-negative bacteria in comparison to both references, sulfadiazine and sulfamethoxazole, which recorded zones of inhibition of 29.67 mm and 27.67 mm, respectively. In addition, its antifungal activity was the best among series 4, reflected by the MIC values 62.5 µg/mL and 125 µg/mL against C. albicans and C. parapsilosis, respectively.
The effect of replacing the cycloalkyl ring with a carboxylate open chain was investigated in series “8i–iii”, which revealed an enhanced antifungal activity rather than antibacterial one. The best results were recorded upon incorporating the sulfamethoxazole sulfonamide structure, as in the thienopyrimidine–sulfamethoxazole hybrid 8iii, which demonstrated mild antibacterial activity only against gram-positive S. aureus and gram-negative E. coli, recording MICs of 250 µg/mL and 125 µg/mL, respectively. On the other hand, the antifungal activity of the sulfamethoxazole hybrid structure 8iii was the best among all the tested compounds and considered promising as it demonstrated MICs of 31.25 µg/mL and 62.5 µg/mL against C. albicans and C. parapsilosis, respectively. These results were better than those of sulfamethoxazole alone (62.5 µg/mL) against both antifungal strains.
Correlating structure to the biological activity upon shifting the substitution from position 4 to position 3, which led to the synthesis of the novel series “12i–iii”, it was noticed that incorporating sulfadiazine sulfonamide in the thienopyrimidine–sulfadiazine hybrid 12ii resulted in enhanced antibacterial activity against the bacterial strains S. aureus and E. coli, which is reflected by its minimum inhibitory concentration (MIC) of 125 µg/mL for both strains. These results were better than those of sulfadiazine alone against gram-positive S. aureus (250 µg/mL) but worse than those recorded against gram-negative E. coli (31.25 µg/mL).
Notably, incorporating sulfadiazine into position 4, either in the cyclohexathienopyrimidine core or in its carboxylate analogue in compounds 4ii and 8ii, respectively, resulted in an enhanced antifungal activity than with sulfadiazine alone against Candida albicans strains and comparable activities against Candida parapsilosis, as reflected by their MIC values and inhibition zone values. However, the incorporation of sulfadiazine into position 3 of the cyclohexathieno[2,3-d]pyrimidine nucleus in series 12, as represented in 12ii, did not improve its antifungal activity. Incorporating sulfamethoxazole into position 4 among all the tested compounds in the three series revealed that compound 8iii has the highest antifungal activity against Candida albicans and Candida parapsilosis, with MIC values of 31.25 µg/mL and 62.5 µg/mL, respectively, which are better recorded values than those of both sulfadiazine and sulfamethoxazole when tested alone. It noteworthy to mention that unlike the molecular docking results that reveal the inhibitory activity of theinopyrimidine–sulfaguanidine hybrids to DHFR and SE proteins, they were inactive in all three investigated series even upon changing positions of substitution.
Overall, the results revealed that compounds 8iii—the thienopyrimidine–sulfamethoxazole hybrid–and 12ii—the cyclohexathienopyrimidine coupled with sulfadiazine at position 3—showed varying degrees of inhibition against S. aureus and E. coli bacterial strains, whereas the best antifungal activity against Candida strains was displayed by the thienopyrimidine–sulfamethoxazole hybrid 8iii. Some of the tested compounds showed relatively similar activities close to the references in both growth inhibition zone diameters and MIC values. Although the growth inhibition zone of all active compounds was less than the reference antibiotics, incorporating sulfadiazine into the thienopyrimidine scaffold in compound 12ii improved its MIC value to higher than that of sulfadiazine itself (Table 3).
All of the target compounds’ in vitro antifungal efficacies against the examined fungal strains were generally more encouraging than their antibacterial activities. Results of the antibacterial and antifungal activities are shown in Table 3 and Table 4.

2.4. In-Silico Investigation of Physicochemical Properties and Drug Likeness

An in-silico assessment of the synthesized series 4i–iii, 8i–iii, and 12i–iii was performed using both Molsoft and Swiss ADME online web tools [52,53]. Both 4i–iii and 8i–iii were investigated in silico in our previous work [54]. In reference to Lipinski’s rule of five, the number of hydrogen bond acceptors (HBAs) is less than 10, while the number of hydrogen bond donors (HBDs) ranges from two to five in all of the investigated compounds. All the tested compounds recorded iLog P < 5, which indicated their high tolerability with cell membranes. In terms of oral bioavailability, although all the screened compounds demonstrated optimum solubility (log S) (i.e., not higher than six), lipophilicity did not exceed five, and the number of rotatable bonds was less than or equal to nine, as required. Nonetheless, the compounds are expected to have moderate to poor oral bioavailability. Polarity, in terms of topological polar surface area (TPSA), ranged from 146.38 to 208.68 Å2, which suggests moderate to poor oral bioavailability of the compounds, as the optimum TPSA should not exceed 130  Å2, as reported [55] (Table 5).
When compounds have positive values, they are deemed promising candidates for drugs, as previously described [45]. The drug likeness scores for the synthesized thienopyrimidine–sulfonamide hybrids ranged from 0.73 to 1.58 (Table 5). Among the hybrids, 4i, a derivative of the cyclohexathieno[2,3-d] pyrimidine core with sulphaguanidine incorporated into position 4, resulted in the best score (1.58), Figure 6. Overall, all the screened compounds are considered promising “drug-like” molecules; none of them violated Lipinski’s rule except for those in series 12, which demonstrated violations related to the number of electronegative atoms (exceeded 10) and to molecular weight (M.Wt) (slightly exceeded 500) in both 12ii and 12iii.

3. Materials and Methods

3.1. Moelcular Modeling

Molecular Modeling studies were performed using Maestro academic version 2023-4, Molecular Operating Environment (MOE.2022.02) with the aid of Discovery Studio v21.1.0.20298. The crystal structure of the dihydrofolate reductase protein was downloaded from Protein Data Bank (PDB: 2W9S) for the in-silico investigation of antibacterial activity [56], whereas in-silico antifungal screening was performed on the downloaded structure 2AIB targeting squalene peroxidase [57]. Every structure was constructed using MOE Builder, then adjusted, its energy reduced, and saved in mol2 format. The applied protocol for molecular docking was induced fit. The force field for organic molecules was chosen as “MMFF94X”, and the gradient for energy minimization was set to 0.05. Electrostatics, bonding, and Van der Waals forces were all enabled. Calculations were made for partial charges [58].

3.2. Chemistry

Using a Stuart SMP10 device, melting points were calculated; the results were not adjusted. The Direct Inlet component of the mass analyzer in the GCMS model with the ISQ single quadrupole thermoscientific Electron Impact mode (UK) was used to perform mass spectra. For the 1H NMR spectrum investigation, a Bruker Advance 400 MHz NMR spectrometer was utilized. Tetramethylsilane (TMS) was employed as an internal standard after the chemical shift values were recorded in parts per million. A Bruker Advance 100 MHz spectrometer was used to acquire 13C NMR spectra.
A Gewald reaction was performed to prepare compounds 1 and 5 upon reaction between either cyclohexanone or ethylacetoacetate with sulfur powder, ethylcyanoacetate, and morpholine, to yield 1 and 5, respectively [59]. Reacting the aminocarboxylate esters 1 and 5 with formamide produced compounds 2 and 6, respectively, which were then chlorinated via phosphorus oxychloride to yield the chloride derivatives 3 and 7, respectively [54]. Moreover, compounds 9–11 were synthesized according to reported procedures, where a mixture of ethyl 2-(2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl) acetate (1) with acetic anhydride was heated under reflux to yield the thiophene acetamide derivative (9). The latter was refluxed with hydrazine hydrate to obtain the thienopyrimidin-4-one derivative (10), which resulted in the acetamide derivative (11) upon heating with an excess amount of chloroacetyl chloride and drops of triethylamine in dichloromethane [54].

3.2.1. General Procedure for the Synthesis of 4i–iii and 8i–iii

Equimolar amounts of the chloride derivatives 3 and 7 were refluxed with the appropriate sulfonamides, namely sulphaguanidine, sulfadiazine, and sulfamethoxazole. Reflux was performed in 15 mL of glacial acetic acid for 15 h. The reaction mixture was then left to cool to room temperature before being poured onto ice water. The formed solid was filtered and crystalized from absolute ethanol to yield the 4i–iii and 8–i-iii series, (Scheme 1 and Scheme 2), as reported in our previous investigation [54].

3.2.2. General Procedures for the Synthesis of Series 12i–iii

Equimolar amounts of 2-chloro-N-(2-methyl-4-oxo-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-3(4H)-yl)acetamide 11 (0.3 g, 0.001 mol) and appropriate sulfonamide derivatives, namely sulphaguanidine, sulfadiazine, and sulfamethoxazole (0.001 mol), were refluxed with stirring in absolute alcohol 15 mL with 3–5 drops of triethylamine (TEA) for 8 h. Then, it was left to cool and poured onto ice/water, crystallized and filtered from glacial acetic acid, and left to dry to obtain compounds 12i–iii, respectively, (Scheme 3). Moreover, all spectroscopic charts for the obtained compounds, 12i–iii, were also shown in the Supplementary Material.
2-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)-N-(2-methyl-4-oxo-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d] pyrimidin-3(4H)-yl) acetamide (12i).
m.p. 123–125 °C, yield 67% EI–MS m/z for: C22H23N7O4S2 (489.13). 1H NMR: δ 1.74, (s, 3H, CH3)—1.80–2.81 (m, 8H, cyclohexyl), 3.26 (s, 2H, CH2), 4.74 (s, 2H, NH2), 5.56 (s, 2H, NH2), 6.41 (s, 1H, NH), 7.14–7.57 (m, 4H aromatic), 10.56 (s, 1H, NH), 12.00(s, 1H, NH). 13C NMR: δ 21.17, 22.45, 22.58, 25.51, 25.89, 46.47, 112.59, 116.97, 125.21,125.55, 129.88, 131.16,133.91, 139.38, 148.23, 155.85, 157.97, 160.89, 162.66, 168.62.
N-(2-methyl-4-oxo-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-3(4H)-yl)-2-(4-(N(pyrimidin-2-yl)sulfamoyl)phenyl)amino)acetamide (12ii).
m.p. 150–152 °C, yield 71%. EI–MS m/z for: C23H23N7O4 S2 (525.6). 1H NMR: δ 1.79 (s, 3H, CH3), 1.81–2.84 (m, 8H, cyclohexyl), 3.20 (s, 2H, CH2), 4.75 (s, 1H, NH), 5.20 (s, 1H, NH), 7.45–8.29 (m, 4H aromatic ring and 3H- diazine), 11.65 (s, 1H, NH). 13C NMR: δ 21.16, 22.45, 22.58, 25.51, 25.89, 46.94, 112.58, 113.52, 116.97,127.38, 129.33, 130.88, 131.30, 133.52, 134.37, 144.78, 148.61, 156.75, 157.86, 157.97, 162.66, 168.62.
N-(2-methyl-4-oxo-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-3(4H)-yl)-2-((4-(N-(5-methylisoxazol-3-yl)sulfamoyl)phenyl)amino)acetamide (12iii).
m.p. 136–138 °C, yield 62%. EI–MS m/z for: C23H24N6O5S2 (528.6). 1H NMR: δ 1.07 (s, 3H, CH3 of oxazole), 1.79 (s, 3H, CH3 of pyrimidine ring), 1.80–2.87 (m, 8H, cyclohexyl), 3.29 (s, 2H, CH2), 4.13 (s, 1H-CH oxazole), 4.87 (s, 1H, NH), 5.23 (s, 1H, NH), 7.39–7.94 (m, 4H aromatic), 10.83 (s, 1H, NH). 13C NMR: δ 14.09, 22.17, 22.45, 22.58, 25.51, 25.89, 46.47, 95.78, 112.77, 115.90,126.83, 128.90, 129.77, 131.29, 133.56, 138.32, 148.59, 149.44, 157.50, 162.19, 167.50, 169.55.

3.3. Antimicrobial Agents

The antimicrobial agents used were sulfamethoxazole purchased from FUJIFILM Wako Pure Chemical Corporation and sulfadiazine purchased from Titan Biotech. All agents were used as standard antimicrobial agents. Stock solutions (1000 µg/mL) were prepared using 100% dimethyl sulfoxide (DMSO), which was used to dissolve all the reference antimicrobial agents and the tested compounds.

3.4. Organisms

The microbial strains used were provided by King Saud Medical City Central Laboratories. Bacterial strains include gram-positive bacterial strains Staphylococcus aureus (ATCC 25923) used for agar-well diffusion, Staphylococcus aureus (ATCC 29213) for determining the minimum inhibitory concentration, Staphylococcus epidermidis (ATCC 12228), and Enterococcus faecalis (ATCC 29212). Gram-negative strains included Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), and Klebsiella pneumoniae (ATCC 700603). Fungal strains were additionally tested and included Candida albicans (ATCC 10231) and Candida parapsilosis (ATCC 22019). All strains were cultured on Mueller Hinton agar and broth and then adjusted to 0.5 McFarland turbidity in 10 mL Mueller Hinton broth for antimicrobial assays.

3.5. Agar Well Diffusion Assay

The antimicrobial activity of the references and new compounds was determined using the agar well diffusion technique [59]. A circle of agar with a diameter of 6 mm was removed from the center of the agar plates to make a well for the addition of the compound solution. The prepared bacterial suspension was inoculated on the surface of the agar plates using a sterile cotton swab. After bacterial inoculation, 100 µL of each antimicrobial and compound (1000 µg/mL) was transferred into the agar well. The plates were incubated aerobically at 37 °C for 18–24 h. The diameters of the inhibition zones were measured around each well and recorded in mm as an average of triplicate experiments. Sulfamethoxazole and sulfadiazine were used as positive controls, and DMSO was used as a negative control. Any compound that showed antimicrobial activity was further tested using the serial dilution susceptibility test for MIC determination.

3.6. Serial Dilution Susceptibilty Test

Overnight, bacterial cultures were adjusted to 0.5 McFarland turbidity in 10 mL Mueller Hinton broth, and 150 μL of bacterial suspension was transferred to a 96-well microtiter plate. Two-fold serial dilutions of the applicable antimicrobials and compounds (150 μL) were prepared across the microtiter plate. Negative and positive controls (uninoculated media and a microbial suspension without antimicrobial agents, respectively) were added to the plates and incubated aerobically at 37 °C for 18–24 h. The MIC was described as the lowest concentration of the antimicrobial that prevented the growth of the microorganism. The turbid wells indicated microbial growth, which was compared to the clear negative control. The experiments were carried out in triplicate [60].

3.7. In-Silico Investigations

Calculating the drug likeness score of the target compounds was performed using Molsoft, while the investigation of the pharmacokinetics was performed using Swiss ADME online web tools [52,53].

4. Conclusions

This work describes the effect of incorporating different sulfonamides into different positions of the thieno[2,3-d]pyrimidine scaffold on their antimicrobial activity. To determine the synthesized hybrids’ binding affinity scores to DHFR oxidoreductase and squalene epoxidase proteins, molecular docking studies were carried out, and the outcomes were promising.
Incorporating different substituted sulfonamide groups into the coplanar structure of thienopyrimidine at position 4 of the cyclohexathienopyrimidine core resulted in mild antibacterial activity. Shifting from position 4 to position 3 demonstrated enhanced antibacterial activity by the thienopyrimidine–sulfadiazine hybrid 12ii against S. aureus bacteria, which was a better result than that of sulfadiazine alone, as reflected by the MIC values. In an attempt to further explore the hybrids’ activity, we investigated the effect of replacing the cycloalkyl ring with a carboxylate open chain, as presented in series 8i–iii, which revealed enhanced antifungal activity compared to the other two series. The best results were recorded by the thienopyrimidine–sulfamethoxazole hybrid 8iii against both Candida strains, and the results were better than those of sulfamethoxazole alone. It is worth mentioning that compared to their antibacterial action, the target compounds’ in vitro antifungal activity against the studied fungal strains was generally more encouraging. Physicochemical properties and drug likeness were assessed in silico, and all the screened compounds were found to be promising drug-like molecules. They all had no Lipinski’s rule violations except those of series 12, which demonstrated violations related to the number of electronegative atoms (exceeded 10) and to molecular weight (slightly exceeded 500) in both 12ii and 12iii.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ph17020188/s1, spectroscopic charts for 12i–iii.

Author Contributions

Conceptualization, E.I.E.; methodology, E.I.E., W.S.A., A.I.A., A.A.A. and R.B.; software, E.I.E.; validation, E.I.E. and R.B.; formal analysis, E.I.E., W.S.A., A.I.A. and A.A.A.; investigation, W.S.A., A.I.A. and A.A.A.; resources, E.I.E. and R.B.; data curation, E.I.E.; writing—original draft preparation, W.S.A., A.I.A. and A.A.A.; writing—review and editing, E.I.E. and R.B.; visualization, E.I.E. and R.B.; supervision, E.I.E.; project administration, E.I.E. and R.B.; funding acquisition, R.B. All authors have read and agreed to the published version of the manuscript.

Funding

This study was funded by Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia through the project number RI-44-0925.

Institutional Review Board Statement

The study was reviewed and approved by the Institutional Review Board of Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia on 12 October 2021 (IRB-exempt-log number 21-0373).

Informed Consent Statement

Not applicable.

Data Availability Statement

The authors confirm that all the data supporting this study are available within the article.

Acknowledgments

The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia for funding this research work through the project number RI-44-0925.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Design strategy for the synthesized theinopyrimidine–sulfonamide hybrids series 4i–iii, 8i–iii, and 12i–iii.
Figure 1. Design strategy for the synthesized theinopyrimidine–sulfonamide hybrids series 4i–iii, 8i–iii, and 12i–iii.
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Figure 2. Types of bonding between the compound with the best docking score as well as antibacterial biological results (compound 12ii; cyan balls and sticks) and the amino acid residues at the binding pocket of the protein with PBD ID 2W9S; H-bonds are represented by green dotted lines. *1 is the position of the co-crystalized ligand “trimethoprim”. (a) 2D structure; (b) 3D illustration.
Figure 2. Types of bonding between the compound with the best docking score as well as antibacterial biological results (compound 12ii; cyan balls and sticks) and the amino acid residues at the binding pocket of the protein with PBD ID 2W9S; H-bonds are represented by green dotted lines. *1 is the position of the co-crystalized ligand “trimethoprim”. (a) 2D structure; (b) 3D illustration.
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Figure 3. Ergosterol, the co-crystallized ligand of protein PDB ID 2AIB, interacting at TYR 47 of the receptor pocket; (a) 2D structure; (b) 3D illustration.
Figure 3. Ergosterol, the co-crystallized ligand of protein PDB ID 2AIB, interacting at TYR 47 of the receptor pocket; (a) 2D structure; (b) 3D illustration.
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Figure 4. The best docking results for antifungal screening (compound 12ii presents as green sticks); (a) 3D structure with the residues involved in the interaction where hydrogen bonds are green dotted lines and hydrophobic interactions are yellow dotted lines; (b) 3D illustration of 12ii totally included in the binding site of action (represented by grey net).
Figure 4. The best docking results for antifungal screening (compound 12ii presents as green sticks); (a) 3D structure with the residues involved in the interaction where hydrogen bonds are green dotted lines and hydrophobic interactions are yellow dotted lines; (b) 3D illustration of 12ii totally included in the binding site of action (represented by grey net).
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Figure 5. The best compound in antifungal biological results (compound 8iii presents as pink sticks); (a) 3D structure with the residues involved in the interaction where hydrogen bonds are green dotted lines; (b) 3D overlay complex between compound 8iii and ergosterol (the co-crystallized ligand represented in yellow sticks) at the pocket of 2AIB protein.
Figure 5. The best compound in antifungal biological results (compound 8iii presents as pink sticks); (a) 3D structure with the residues involved in the interaction where hydrogen bonds are green dotted lines; (b) 3D overlay complex between compound 8iii and ergosterol (the co-crystallized ligand represented in yellow sticks) at the pocket of 2AIB protein.
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Figure 6. Illustration of the best drug likeness scores of the 4i compound.
Figure 6. Illustration of the best drug likeness scores of the 4i compound.
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Scheme 1. Pathway for synthesis of substituted thienopyrimdine series 4i–iii.
Scheme 1. Pathway for synthesis of substituted thienopyrimdine series 4i–iii.
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Scheme 2. Pathway for synthesis of substituted thienopyrimdine series 8i–iii.
Scheme 2. Pathway for synthesis of substituted thienopyrimdine series 8i–iii.
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Scheme 3. Pathway for synthesis of substituted thienopyrimdine series 12i–iii.
Scheme 3. Pathway for synthesis of substituted thienopyrimdine series 12i–iii.
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Table 1. Molecular docking results for the thienopyrimidine–sulfonamide hybrids on DHFR reductase (PDB ID: 2W9S).
Table 1. Molecular docking results for the thienopyrimidine–sulfonamide hybrids on DHFR reductase (PDB ID: 2W9S).
CompoundBinding Energy (kcal/mol)RMSD (Å)Residues Involved in Binding and Types of Interaction
4i−7.16961.4085ASN 18 (H-donor)
ASN 18 (H-donor)
4ii−7.87301.3052ASN 18 (H-donor)
THR 46 (H-acceptor)
4iii−8.27341.7984GLN 95 (H-acceptor)
PHE 92 (H-pi)
8i−8.33541.2613ALA 7 (H-acceptor)
THR 46 (pi H)
8ii−8.35571.6653ASN 18 (H-donor)
GLN 95 (H-acceptor)
THR 46 (H-acceptor)
8iii−8.13941.9062ASP 27 (A) H-donor
12i−7.29661.2439THR 46 (H-donor)
GLN 95(H-acceptor)
ASN 18 (pi H)
12ii−8.71151.3166THR 46 (H-donor),
LYS 45 (H-acceptor),
GLN 95 (H-acceptor)
12iii−7.87471.6470THR 46 (H-donor)
LYS 45 (pi-cation)
GLN 95 (pi H)
THR 96 (pi H)
Table 2. Molecular docking results for the thienopyrimidin–sulfonamide hybrids on SE protein (PDB ID: 2AIB).
Table 2. Molecular docking results for the thienopyrimidin–sulfonamide hybrids on SE protein (PDB ID: 2AIB).
CompoundBinding Energy (kcal/mol)RMSD (Å)Residues Involved in Binding and Types of Interaction
4i−7.28351.4140MET 50 (H-donor)
4ii−7.93931.2122THR 74 (H-donor)
TYR 47 H-acceptor
VAL 75 (pi-H)
TYR 87 (pi-H)
4iii−6.86071.3582THR 74 (H-donor)
VAL75 (pi-H)
8i−7.63901.3130THR 74 (H-donor)
8ii−7.96351.4180MET 35 (pi H)
8iii−8.20321.8383TYR 47 (H-donor)
TYR 47 (H-donor)
12i−8.37121.8964TYR 12 (H-donor)
LEU 19 (pi H)
12ii−9.33911.7258MET 50 (H-donor)
TYR 47 (H-acceptor)
12iii−9.14661.4663MET 50 (H-donor)
TYR 12 (H-donor)
Table 3. Antibacterial activity of the synthesized theinopyrimidine–sulfonamides hybrids.
Table 3. Antibacterial activity of the synthesized theinopyrimidine–sulfonamides hybrids.
CompoundsGram-Positive BacteriaGram-Negative Bacteria
S. aureusS. epidermidisE. faecalisE. coliP. aeruginosaK. pneumoniae
*GIZMIC*GIZMIC*GIZMIC*GIZMIC*GIZMIC*GIZMIC
4i0-0-0-0 0-0-
4ii15.33 ± 1.155000-0-18 ± 01250-0-
4iii0-0-0-0-0-0-
8i0-0-0-0-0-0-
8ii16 ± 15000-0-17 ± 01250-0-
8iii22.33 ± 0.582500-0-17.33 ± 0.581250-0-
12i0-0-0-0 0-0-
12ii24.67 ± 0.581250-0-23.67 ± 1.531250-0-
12iii19 ± 12500-0-19.67 ± 0.581250-0-
Sulfadiazine29.67 ± 0.582500-0-27.67 ± 1.1531.250-0-
Sulfamethoxazole37.67 ± 1.1512515 ± 0-0-30.67 ± 1.1515.6250-0-
*GIZ: average diameter (mm) of growth inhibition zone in mean ± SD; MIC: minimum inhibitory concentration (µg/mL); number of replicates n = 3.
Table 4. Antifungal activity of the synthesized compounds against Candida strains.
Table 4. Antifungal activity of the synthesized compounds against Candida strains.
CompoundsC. albicansC. parapsilosis
*GIZMIC*GIZMIC
4i0-0-
4ii9 ± 062.58.33 ± 0.58125
4iii0-0-
8i0-0-
8ii9.33 ± 0.5862.59 ± 0125
8iii17.67 ± 0.5831.2515.67 ± 0.5862.5
12i11.67 ± 1.1512510.33 ± 0.58125
12ii7.67 ± 0.582508.67 ± 0.58500
12iii10.33 ± 0.581259.33 ± 0.58125
Sulfadiazine8.67 ± 1.151259 ± 0125
Sulfamethoxazole10.67 ± 0.5862.510.67 ± 0.5862.5
*GIZ: average diameter (mm) of growth inhibition zone in mean ± SD; MIC: minimum inhibitory concentration (µg/mL); number of replicates n = 3.
Table 5. Predicted physicochemical properties and drug-like candidates.
Table 5. Predicted physicochemical properties and drug-like candidates.
CompoundsM.WtHBAHBDTPSARotatable BondsLipophilicityLog SiLog PLipinski ViolationsDrug Likeness
4i402.4954170.4752.92−4.261.5101.58
4ii438.5362146.3853.8−5.142.6601.03
4iii441.5362146.6354.36−5.492.5901.08
8i434.4974196.7782.61−4.031.7501.19
8ii470.5282172.6883.48−4.912.7800.88
8iii473.5382172.9384.05−5.263.100.73
12i489.1365208.6881.6−3.69211.23
12ii525.6073184.5982.47−4.562.2321.35
12iii528.6073184.8483.04−4.922.1121.06
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Elmongy, E.I.; Alanazi, W.S.; Aldawsari, A.I.; Alfaouri, A.A.; Binsuwaidan, R. Antimicrobial Evaluation of Sulfonamides after Coupling with Thienopyrimidine Coplanar Structure. Pharmaceuticals 2024, 17, 188. https://doi.org/10.3390/ph17020188

AMA Style

Elmongy EI, Alanazi WS, Aldawsari AI, Alfaouri AA, Binsuwaidan R. Antimicrobial Evaluation of Sulfonamides after Coupling with Thienopyrimidine Coplanar Structure. Pharmaceuticals. 2024; 17(2):188. https://doi.org/10.3390/ph17020188

Chicago/Turabian Style

Elmongy, Elshaymaa I., Wejdan S. Alanazi, Alhanouf I. Aldawsari, Asma A. Alfaouri, and Reem Binsuwaidan. 2024. "Antimicrobial Evaluation of Sulfonamides after Coupling with Thienopyrimidine Coplanar Structure" Pharmaceuticals 17, no. 2: 188. https://doi.org/10.3390/ph17020188

APA Style

Elmongy, E. I., Alanazi, W. S., Aldawsari, A. I., Alfaouri, A. A., & Binsuwaidan, R. (2024). Antimicrobial Evaluation of Sulfonamides after Coupling with Thienopyrimidine Coplanar Structure. Pharmaceuticals, 17(2), 188. https://doi.org/10.3390/ph17020188

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