喹啉衍生物作为潜在抗菌剂的设计、合成、研究及生物学评价

Vinod Kumar Gurjar, Dodiya Raj Mukeshbhai, Kushwaha Raju, Subhash Devanshi Parekh
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引用次数: 0

摘要

本文合成了几种新型喹啉-3-羧酸衍生物,对其进行了分析,并评价了其抗菌潜力。利用元素分析、红外光谱、核磁共振和质谱数据对合成的衍生物进行了鉴定。采用杯盘扩散法测定衍生物的抑菌活性。在50 μg/ml和100 μg/ml的剂量下,该物质对实验菌株表现出较强的抑菌能力。为了预测这些衍生物的药代动力学性质(ADME),还进行了计算机研究。对于目前的研究,在硅瑞士adme辅助的结果被证明是适合于衍生和合成有效的抗菌药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design synthesis in-silico study and biological evaluation of quinoline derivatives as potential antibacterial agents
The purpose of this article is to synthesize some novel quinoline-3-Carboxylic acid derivatives, analyze them, and assess their antibacterial potential. With the help of elemental analysis, IR, NMR, and mass spectral data, the synthesized derivatives were identified. Derivatives' antibacterial activity was determined using the cup and plate diffusion method. At doses of 50 μg/ml and 100 μg/ml, the substance demonstrated substantial antibacterial potential against the tested strains. To predict the pharmacokinetic properties (ADME) of these derivatives, in-silico investigations were also carried out. For the current study, the in silico Swiss ADME-assisted results were shown to be suitable for the derivation and synthesis of efficient antibacterial drugs.
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