4-Thiazolidinone coumarin derivatives as two-component NS2B/NS3 DENV flavivirus serine protease inhibitors: synthesis, molecular docking, biological evaluation and structure-activity relationship studies.

Q1 Chemistry
Samina Khan Yusufzai, Hasnah Osman, Mohammad Shaheen Khan, Basma M Abd Razik, Mohammed Oday Ezzat, Suriyati Mohamad, Othman Sulaiman, Jualang Azlan Gansau, Thaigarajan Parumasivam
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引用次数: 0

Abstract

A series of novel 4-thiazolidinone inhibitors SKYa-SKYg, containing coumarin as a core structure were synthesized via facile and efficient method. The structures of the synthesized compounds were established by extensive spectroscopic studies (FT IR, 1D NMR, 2D NMR, LC-MS) and elemental analysis. All the synthesized hybrids were further evaluated for their potential as anti-tubercular agents against Mycobacterium tuberculosis H37Rv ATCC 25618, and anti-bacterial agents against Escherichia coli, Enterobacter aerogenes, Salmonella typhi, Streptococcus pneumoniae and Staphylococcus aureus. Interestingly, the hybrids displayed potent bioactivity. However, compounds SKYc, SKYd, and SKYe appeared to be more effective against the tested bacterial strains, among which compound SKYb showed the highest inhibition against all the bacterial strains ranging from 41 to 165 μg/mL, as compared to the standards, streptomycin, kanamycin and vancomycin. Moreover, derivative SKYa was found to be the strongest against M. tuberculosis (83 μg/mL). Additionally, the anti-dengue potential of the coumarin hybrids as two-component NS2B/NS3 DENV flavivirus serine protease inhibitors was calculated using computational molecular docking approach, with reference to the standards 4-hydroxypanduratin, panduratin and ethyl 3-(4-(hydroxymethyl)-2-methoxy-5-nitrophenoxy)propanoate with DS of - 3.379, - 3.189 and - 3.381, respectively. The docking results revealed that the synthesized hybrids exhibited potent anti-dengue activity among which compounds SKYf, SKYd, SKYc and SKYe were found to be the best ones with docking scores of - 4.014, - 3.964, - 3.905 and - 3.889. In summary, we discovered 4-thiazolidinone coumarin derivatives as a new scaffold that may eventually yield useful compounds in the treatment of bacterial and viral infections.

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作为双组分 NS2B/NS3 DENV 黄病毒丝氨酸蛋白酶抑制剂的 4-噻唑烷酮香豆素衍生物:合成、分子对接、生物学评价和结构-活性关系研究。
通过简便高效的方法合成了一系列以香豆素为核心结构的新型 4-噻唑烷酮抑制剂 SKYa-SKYg。通过广泛的光谱研究(傅立叶变换红外光谱、一维核磁共振、二维核磁共振、液相色谱-质谱联用仪)和元素分析,确定了合成化合物的结构。对所有合成的杂交化合物进行了进一步评估,以确定其作为抗结核分枝杆菌 H37Rv ATCC 25618 的抗结核剂,以及作为抗大肠杆菌、产气肠杆菌、伤寒沙门氏菌、肺炎链球菌和金黄色葡萄球菌的抗菌剂的潜力。有趣的是,杂交化合物显示出了强大的生物活性。然而,化合物 SKYc、SKYd 和 SKYe 似乎对测试的细菌菌株更有效,其中化合物 SKYb 与标准品链霉素、卡那霉素和万古霉素相比,对所有细菌菌株的抑制率最高,从 41 μg/mL 到 165 μg/mL。此外,还发现衍生物 SKYa 对结核杆菌的抗性最强(83 μg/mL)。此外,利用计算分子对接方法计算了香豆素混合物作为双组分 NS2B/NS3 DENV 黄病毒丝氨酸蛋白酶抑制剂的抗登革热潜力,参照标准物 4-羟基潘杜拉汀、潘杜拉汀和 3-(4-(羟甲基)-2-甲氧基-5-硝基苯氧基)丙酸乙酯,DS 分别为 -3.379、-3.189 和 -3.381。对接结果表明,合成的杂交化合物具有很强的抗登革热活性,其中化合物 SKYf、SKYd、SKYc 和 SKYe 的对接得分分别为 -4.014、-3.964、-3.905 和 -3.889,为最佳化合物。总之,我们发现 4-噻唑烷酮香豆素衍生物是一种新的支架,最终可能会产生治疗细菌和病毒感染的有用化合物。
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来源期刊
Chemistry Central Journal
Chemistry Central Journal 化学-化学综合
CiteScore
4.40
自引率
0.00%
发文量
0
审稿时长
3.5 months
期刊介绍: BMC Chemistry is an open access, peer reviewed journal that considers all articles in the broad field of chemistry, including research on fundamental concepts, new developments and the application of chemical sciences to broad range of research fields, industry, and other disciplines. It provides an inclusive platform for the dissemination and discussion of chemistry to aid the advancement of all areas of research. Sections: -Analytical Chemistry -Organic Chemistry -Environmental and Energy Chemistry -Agricultural and Food Chemistry -Inorganic Chemistry -Medicinal Chemistry -Physical Chemistry -Materials and Macromolecular Chemistry -Green and Sustainable Chemistry
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