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Synthesis and biological evaluation of new 2-aryl-4-((4-aryl-1H-1,2,3-triazol-1-yl)methyl)thiazole derivatives

机译:新型2-芳基-4 - ((4-芳基-1H-1,2,3-三唑-1-基)甲基)噻唑衍生物的合成及生物学评价

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摘要

A series of 2-aryl-4-((4-aryl-1H-1,2,3-triazol-1-yl)methyl)thiazole derivatives (8a-p) have been synthesized. The structure of the newly synthesized compounds was determined by spectral analysis. The title compounds were screened for their preliminary antitubercular activity against Mycobacterium tuberculosis H37Ra (MTB, ATCC 25177) and Mycobacterium bovis BCG (BCG, ATCC 35743). Further, the synthesized compounds were screened for antimicrobial activity against standard Gram-negative bacteria Escherichia coli (NCIM 2576) and Pseudomonas flurescence (NCIM 2059) and Gram-positive bacteria Staphylococcus aureus (NCIM 2602) and Bacillus subtilis (NCIM 2162). Among all the synthesized compounds, 8a-c, f-h, m exhibited good activity against dormant M. bovis BCG strain. Compounds 8h, j exhibited good activity against all tested bacterial strains. All active compounds were screened for cytotoxicity and found inactive. Their high potency and promising antimycobacterial activity suggest that these compounds could serve as good leads for further optimization and development.
机译:合成了一系列2-芳基-4-((4-芳基-1H-1,2,3-三唑-1-基)甲基)噻唑衍生物(8A-P)。通过光谱分析测定新合成化合物的结构。筛选标题化合物,用于针对结核分枝杆菌H37RA(MTB,ATCC 25177)和肉杆菌BCG(BCG,ATCC 35743)的初步抗细胞活性。此外,将合成的化合物筛选用于标准革兰阴性细菌大肠杆菌(NCIM 2576)和假单胞菌(NCIM 2059)和革氏阳性细菌金黄色葡萄球菌(NCIM 2602)和枯草芽孢杆菌(NCIM 2162)的抗微生物活性。在所有合成化合物中,8A-C,F-H,M对休眠M.BOVIS BCG菌株的良好活性表现出良好的活性。化合物8h,j对所有测试的细菌菌株表现出良好的活性。将所有活性化合物筛选细胞毒性并发现无活性。它们的高效力和有前途的抗致细菌活性表明这些化合物可以作为进一步优化和发育的良好引线。

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