含咔唑基团的1,4 -苯并噻唑和吡唑啉衍生物的合成及其抗微生物和抗疟疾活性

Q4 Chemistry
V. Kadnor, S. Shelke
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引用次数: 0

摘要

合成了一系列咔唑类1,4-苯并噻唑类和吡唑啉类化合物,并通过FT-IR、1H NMR、13C NMR和质谱对其结构进行了确证。对所有新衍生物4(a-f)和5(a-e)的体外抗菌活性和抗疟活性进行了筛选。与阳性对照相比,化合物4a、4b、4d、5a、5b和5c具有良好的抗菌和抗疟活性。值得注意的是,化合物4a、4b和4d对青霉菌的抗真菌活性与标准药物相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, antimicrobial and antimalarial activityof1, 4-benzothiazepine and pyrazolinederivatives incorporating carbazolemoiety
A series of carbazole-based 1,4-benzothiazepine and pyrazoline derivatives were synthesized and the structures of the newly synthesized compounds were confirmed by FT-IR, 1H NMR, 13C NMR and mass spectral studies. All new derivatives 4(a-f) and 5(a-e) were screened for their in vitro antimicrobial activity, and also for their antimalarial activity. Compounds 4a, 4b, 4d, 5a, 5b and 5c exhibited promising antimicrobial and antimalarial activities as compared to positive control. Notably, compounds 4a, 4b and 4d showed excellent antifungal activity against Penicillium sp. comparable to that of a standard drug.
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来源期刊
Bulgarian Chemical Communications
Bulgarian Chemical Communications 化学-化学综合
CiteScore
0.90
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Information not localized
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