An Outline on benzimidazole Containing Marketed Drugs with Proton Pump Inhibitor and H1 Receptor Antagonist Activities.

IF 3.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Sumit Tahlan, Sucheta Singh, Kailash C Pandey, Kuldeep Singh
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引用次数: 0

Abstract

Heterocyclic compounds are increasingly used in medicinal chemistry because they are the main components of many biological processes and materials. Benzimidazole remains the core center of the heterocyclic chemical group, with essential traits such as six-five-member connected rings and two nitrogen atoms at the 1,3 position in a six-membered benzene and five-membered imidazole- fused ring system. Molecules with benzimidazole derivatives serve important functions as therapeutic agents and have shown excellent results in clinical and biological research. In this comprehensive review, we summarize marketed medications that include the benzimidazole moiety. Here, we discuss two topics: PPIs and H1 receptor antagonists. Benzimidazole derivatives are important in all fields because they have the same isostructural pharmacophore as that of naturally occurring active biomolecules. While PPIs and H1 receptor antagonists are generally safe in the short term, accumulating data suggest that their long-term use may pose concerns. This systematic review aimed to assess global PPI use in the general population. This will help researchers, medicinal chemists, and pharmaceutical scientists to create breakthrough benzimidazole-based drugs. This review can help identify novel lead compounds and optimize existing benzimidazole derivatives to improve medicinal efficacy. Benzimidazole has attracted significant interest because of its high bioavailability, stability, and biological efficiency. This page reveals and discusses typical synthesis processes for marketed pharmaceuticals in the benzimidazole class of scaffolds, MOA, and therapeutic uses.

苯并咪唑类具有质子泵抑制剂和H1受体拮抗剂活性的市售药物概述。
杂环化合物是许多生物过程和材料的主要成分,因此在药物化学中的应用越来越广泛。苯并咪唑仍然是杂环化学基团的核心中心,具有六个五元连接环和在六元苯和五元咪唑融合环体系中1,3位上有两个氮原子等基本特征。具有苯并咪唑衍生物的分子具有重要的治疗功能,在临床和生物学研究中表现出优异的效果。在这篇全面的综述中,我们总结了包括苯并咪唑部分的上市药物。在这里,我们讨论两个主题:PPIs和H1受体拮抗剂。苯并咪唑衍生物在所有领域都很重要,因为它们具有与天然活性生物分子相同的同位结构药效团。虽然PPIs和H1受体拮抗剂在短期内通常是安全的,但积累的数据表明,它们的长期使用可能会引起担忧。本系统综述旨在评估全球人群中PPI的使用情况。这将有助于研究人员、药物化学家和制药科学家创造突破性的以苯并咪唑为基础的药物。本综述有助于鉴定新的先导化合物,并对现有苯并咪唑衍生物进行优化,以提高药物疗效。苯并咪唑因其高生物利用度、稳定性和生物效率而受到广泛关注。本页揭示并讨论了苯并咪唑类支架、MOA和治疗用途的上市药物的典型合成过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
0.00%
发文量
231
审稿时长
6 months
期刊介绍: The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines. Mini-Reviews in Medicinal Chemistry covers all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies. Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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