苯并咪唑
脚手架
部分
计算生物学
化学
组合化学
广谱
模块化(生物学)
药物发现
纳米技术
生物
计算机科学
立体化学
生物化学
材料科学
遗传学
数据库
有机化学
作者
Ramalakshmi Natarajan,Padma Kumar,S. Arun-Kumar,Amuthalakshmi Siraperuman,A. Prabakaran,Richie R. Bhandare,Afzal B. Shaik
出处
期刊:Medicinal Chemistry
[Bentham Science Publishers]
日期:2023-11-10
卷期号:20 (3): 311-351
被引量:9
标识
DOI:10.2174/0115734064253813231025093707
摘要
Abstract: Benzimidazole nucleus is a predominant heterocycle displaying a wide spectrum of pharmacological activities. The privileged nature of the benzimidazole scaffold has been revealed by its presence in most small molecule drugs and in its ability to bind multiple receptors with high affinity. A literature review of the scaffold reveals several instances where structural modifications of the benzimidazole core have resulted in high-affinity lead compounds against a variety of biological targets. Hence, this structural moiety offers opportunities to discover novel, better, safe and highly potent biological agents. The goal of the present review is to compile the medicinal properties of benzimidazole derivatives with a focus on SAR (Structure-Activity Relationships)
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