一些含有 5-氯噻吩基结构的新型查耳酮衍生物:合成、表征、硅学研究和生物学评估

Q4 Chemistry Asian Journal of Chemistry Pub Date : 2024-01-31 DOI:10.14233/ajchem.2024.31013
Viralkumar A. Doshi, Yogesh S. Patel
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引用次数: 0

摘要

通过将 N-(4-乙酰苯基)-5-氯噻吩-2-甲酰胺与不同取代的芳香醛偶联,合成了一系列新型查耳酮衍生物(4a-o)。通过红外光谱、核磁共振和质谱对合成的查耳酮进行了表征。采用肉汤稀释法对这些化合物对四种细菌培养物进行了体外抗菌活性筛选,对三种真菌培养物进行了抗真菌活性筛选。化合物 4b 和 4n 对大肠杆菌(MTCC 443),化合物 4b、4e、4i、4n 和 4o 对绿脓杆菌(MTCC 1688),化合物 4c 和 4n 对金黄色葡萄球菌(MTCC 96)具有明显的抗菌活性(≤ 50 μg/mL)。此外,还对合成的查尔酮衍生物的药代动力学特性(ADME)进行了硅学研究。
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Some Novel Chalcone Derivatives containing 5-Chloro Thiophene in a Base Structure: Synthesis, Characterization, in silico Study and Biological Evaluation
A novel series of chalcone derivatives (4a-o) of N-(4-acetylphenyl)-5-chlorothiophene-2-carboxamide was synthesized by coupling it with different substituted aromatic aldehydes. Synthesized chalcones were characterized by IR, NMR and mass spectra. They were screened in vitro antibacterial activity against four bacterial cultures and antifungal activity against three fungal cultures by using broth-dilution method. The significant antibacterial activity with ≤ 50 μg/mL has been displayed by compounds 4b and 4n against E. coli (MTCC 443), compounds 4b, 4e, 4i, 4n and 4o against P. aeruginosa (MTCC 1688), compounds 4c and 4n against S. aureus (MTCC 96). In silico investigation was also carried out to predict pharmacokinetic properties (ADME) of synthesized chalcone derivatives.
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来源期刊
Asian Journal of Chemistry
Asian Journal of Chemistry 化学-化学综合
CiteScore
0.80
自引率
0.00%
发文量
229
审稿时长
4 months
期刊介绍: Information not localized
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