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设计、合成一些新的(2-氨基噻唑-4-基)甲酯衍生物作为可能的抗菌和抗结核药物。

Design, synthesis of some new (2-aminothiazol-4-yl)methylester derivatives as possible antimicrobial and antitubercular agents.

机构信息

School of Chemical Sciences, Kannur University, Payyanur Campus, Kannur, Kerala, India.

出版信息

Eur J Med Chem. 2012 Mar;49:172-82. doi: 10.1016/j.ejmech.2012.01.008. Epub 2012 Jan 12.

Abstract

A series of (2-aminothiazol-4-yl)methylester (5a-t) derivatives were synthesized in good yields and characterized by (1)H NMR, (13)C NMR, mass spectral and elemental analyses. The crystal structure of 5a was evidenced by X-ray diffraction study. The compounds were evaluated for their preliminary in vitro antibacterial, antifungal activity and were screened for antitubercular activity against Mycobacterium tuberculosis H37Rv strain. The synthesized compounds displayed interesting antimicrobial activity.

摘要

一系列(2-氨基噻唑-4-基)甲酯(5a-t)衍生物以较好的产率合成,并通过(1)H NMR、(13)C NMR、质谱和元素分析进行了表征。通过 X 射线衍射研究证实了 5a 的晶体结构。这些化合物的初步体外抗菌、抗真菌活性进行了评估,并对结核分枝杆菌 H37Rv 菌株进行了抗结核活性筛选。合成的化合物表现出有趣的抗菌活性。

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