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合成 1-(4-甲氧基苄基)-3-环丙基-1H-吡唑-5-胺衍生物作为抗菌剂。

Synthesis of 1-(4-methoxybenzyl)-3-cyclopropyl-1H-pyrazol-5-amine derivatives as antimicrobial agents.

机构信息

Department of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore, India.

出版信息

J Enzyme Inhib Med Chem. 2010 Aug;25(4):537-43. doi: 10.3109/14756360903357601.

Abstract

A series of novel substituted 1-(4-methoxybenzyl)-3-cyclopropyl-1H-pyrazol-5-amine benzamides 9(a-h) were synthesized to determine their antibacterial and antifungal activities as well as possible structure-activity relationships (SARs) to improve therapeutic efficacy. The pyrazol-5-amine benzamides were screened for their antibacterial activity against standard strains of Gram-positive (Streptococcus pyogenes NCIM 2608, Staphylococcus aureus ATCC 29737, Bacillus subtilis NCIM 2010) and Gram-negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 20852, Klebsiella pneumoniae MTCC 618) bacteria by using streptomycin as positive control. They were also tested for their antifungal activities against mycotoxic strains of Fusarium verticillioides, Aspergillus ochraceous, Aspergillus flavus, Alternaria alternata, and Penicillium chrysogenum using nystatin as positive control. Among the synthesized compounds, 9d, 9g, and 9h showed potent antimicrobial activities.

摘要

为了确定其抗菌和抗真菌活性以及可能的构效关系(SAR)以提高治疗效果,我们合成了一系列新型取代的 1-(4-甲氧基苄基)-3-环丙基-1H-吡唑-5-胺苯甲酰胺 9(a-h)。对吡唑-5-胺苯甲酰胺进行了筛选,以评估其对革兰氏阳性(化脓性链球菌 NCIM 2608、金黄色葡萄球菌 ATCC 29737、枯草芽孢杆菌 NCIM 2010)和革兰氏阴性(大肠杆菌 ATCC 25922、铜绿假单胞菌 ATCC 20852、肺炎克雷伯菌 MTCC 618)标准菌株的抗菌活性,以链霉素作为阳性对照。还使用制霉菌素作为阳性对照,测试了它们对真菌毒素菌株(串珠镰刀菌、赭曲霉、黄曲霉、交链孢霉和产黄青霉)的抗真菌活性。在所合成的化合物中,9d、9g 和 9h 表现出很强的抗菌活性。

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