抗真菌
抗菌活性
化学
分子
组合化学
质子核磁共振
立体化学
核化学
有机化学
微生物学
细菌
生物
遗传学
作者
Ravindra Kulkarni,Vijaykumar,H. Ramesh Babu,Krishna Kumar,Naveen Gaddam,Aneesa Fatima,Sudhakar Muvvala,Bhikshapathi D V R N,D. Sriram,Achaiah Garlapati,Jagrut Vishnav,Prashant Gurav
出处
期刊:Medicinal Chemistry
日期:2014-01-31
卷期号:10 (2): 220-227
被引量:3
标识
DOI:10.2174/15734064113099990039
摘要
A series of new N-pyrazolylbenzamides (5a–x) were synthesized by aroylation of 5-amino-1-phenyl-3-tbutylpyrazole. The structures of synthesized compounds were established based on spectral (FTIR, 1H NMR, ESI Mass) analysis and purity was ascertained by HPLC. The antibacterial screening revealed that seven molecules exhibited an excellent antibacterial activity and eight compounds demonstrated considerable antifungal activity. Three molecules of the series 5e, 5s and 5w were found to be highly effective against Klebsilla pneumoneia with MIC of 3.12 µg/ml. Compounds 5b, 5f, 5g and 5o exhibited significant antitubercular activity with MIC of 12.5 µg/ml. Keywords: Benzamides, antibacterial, antifungal, antitubercular.
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