• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

新型取代苯并咪唑衍生物:专利研究综述(2010-2012)。

New substituted benzimidazole derivatives: a patent review (2010 - 2012).

机构信息

Beijing Institute of Technology, School of Chemical Engineering & the Environment, R&D Center for Pharmaceuticals, 5 South Zhongguancun Street, Beijing 100081, China.

出版信息

Expert Opin Ther Pat. 2013 Sep;23(9):1157-79. doi: 10.1517/13543776.2013.800857. Epub 2013 May 16.

DOI:10.1517/13543776.2013.800857
PMID:23675911
Abstract

INTRODUCTION

Benzimidazole is a heterocyclic aromatic system, which is part of some natural and many synthetic compounds. A large number of benzimidazoles and its derivatives are found to be biologically active against many diseases. Researchers around the world are paying greater attention to and showing increasing interests in this field.

AREAS COVERED

Areas covered in this paper include a review of the synthesis, biological effects and mechanisms of benzimidazole derivatives in the past 2 years, based on literature and patents. The patent databases SciFinder and esp@cenet were used to locate patent applications that were published between 2010 to present. Information from articles published is also included. The current state and problems are also discussed.

EXPERT OPINION

Benzimidazole derivatives possess a broad spectrum of biological activities, whose scopes of treatment ranging from ordinary antimicrobial activities to world's most deadly diseases. However, challenges such as drug resistance, relatively little knowledge of structure of receptors and rare convenient methods for synthesis of benzimidazoles still exist.

摘要

简介

苯并咪唑是一种杂环芳族体系,它是一些天然和许多合成化合物的一部分。大量的苯并咪唑及其衍生物被发现对许多疾病具有生物活性。世界各地的研究人员越来越关注这一领域,并表现出越来越大的兴趣。

涵盖领域

本文综述了过去 2 年中苯并咪唑衍生物的合成、生物效应和作用机制,参考文献和专利。专利数据库 SciFinder 和 esp@cenet 用于定位 2010 年至今公布的专利申请。还包括从已发表文章中获取的信息。目前的状况和问题也进行了讨论。

专家意见

苯并咪唑衍生物具有广泛的生物活性,其治疗范围从普通的抗菌活性到世界上最致命的疾病。然而,仍然存在一些挑战,如耐药性、对受体结构的了解相对较少以及苯并咪唑合成的便捷方法罕见等。

相似文献

1
New substituted benzimidazole derivatives: a patent review (2010 - 2012).新型取代苯并咪唑衍生物:专利研究综述(2010-2012)。
Expert Opin Ther Pat. 2013 Sep;23(9):1157-79. doi: 10.1517/13543776.2013.800857. Epub 2013 May 16.
2
New substituted benzimidazole derivatives: a patent review (2013 - 2014).新型取代苯并咪唑衍生物:专利综述(2013 - 2014年)
Expert Opin Ther Pat. 2015 May;25(5):595-612. doi: 10.1517/13543776.2015.1015987.
3
Pyrazine derivatives: a patent review (2008 - present).吡嗪衍生物:专利研究综述(2008 年至今)。
Expert Opin Ther Pat. 2012 Sep;22(9):1033-51. doi: 10.1517/13543776.2012.714370. Epub 2012 Aug 6.
4
Synthesis, in-vitro microbial and cytotoxic studies of new benzimidazole derivatives.新型苯并咪唑衍生物的合成、体外微生物及细胞毒性研究
Arch Pharm (Weinheim). 2009 Jul;342(7):412-9. doi: 10.1002/ardp.200900022.
5
Synthesis, characterization and antimicrobial studies of some new quinoline incorporated benzimidazole derivatives.合成、表征及一些新型喹啉并苯并咪唑衍生物的抗菌研究。
Eur J Med Chem. 2012 Aug;54:900-6. doi: 10.1016/j.ejmech.2012.05.027. Epub 2012 Jun 1.
6
Synthesis and QSAR evaluation of 2-(substituted phenyl)-1H-benzimidazoles and [2-(substituted phenyl)-benzimidazol-1-yl]-pyridin-3-yl-methanones.2-(取代苯基)-1H-苯并咪唑和[2-(取代苯基)-苯并咪唑-1-基]-吡啶-3-基-甲酮的合成与定量构效关系评估
Eur J Med Chem. 2009 Mar;44(3):1119-27. doi: 10.1016/j.ejmech.2008.06.009. Epub 2008 Jun 24.
7
Novel 1H-1,2,3-, 2H-1,2,3-, 1H-1,2,4- and 4H-1,2,4-triazole derivatives: a patent review (2008 - 2011).新型 1H-1,2,3-, 2H-1,2,3-, 1H-1,2,4- 和 4H-1,2,4- 三唑衍生物:专利审查(2008-2011)。
Expert Opin Ther Pat. 2013 Mar;23(3):319-31. doi: 10.1517/13543776.2013.749862. Epub 2013 Jan 6.
8
New heterocyclic derivatives of benzimidazole with germicidal activity--XII--Synthesis of N1-glycosyl-2-furyl benzimidazoles.具有杀菌活性的苯并咪唑新杂环衍生物——十二——N1-糖基-2-呋喃基苯并咪唑的合成
Farmaco. 1994 Dec;49(12):823-7.
9
Benzimidazoles in Drug Discovery: A Patent Review.药物研发中的苯并咪唑类:专利综述
ChemMedChem. 2021 Jun 17;16(12):1861-1877. doi: 10.1002/cmdc.202100004. Epub 2021 Apr 14.
10
Synthesis and potent antimicrobial activity of some novel methyl or ethyl 1H-benzimidazole-5-carboxylates derivatives carrying amide or amidine groups.一些带有酰胺或脒基的新型1H-苯并咪唑-5-羧酸甲酯或乙酯衍生物的合成及其强大的抗菌活性
Bioorg Med Chem. 2005 Mar 1;13(5):1587-97. doi: 10.1016/j.bmc.2004.12.025.

引用本文的文献

1
New Benzimidazole 3'-Deoxynucleosides: Synthesis and Antiherpes Virus Properties.新型苯并咪唑3'-脱氧核苷:合成及其抗疱疹病毒特性
Biomolecules. 2025 Jun 23;15(7):922. doi: 10.3390/biom15070922.
2
Benzimidazole(s): synthons, bioactive lead structures, total synthesis, and the profiling of major bioactive categories.苯并咪唑类:合成子、生物活性先导结构、全合成以及主要生物活性类别的剖析。
RSC Adv. 2025 Mar 28;15(10):7571-7608. doi: 10.1039/d4ra08864f. eCollection 2025 Mar 6.
3
An Outline on Benzimidazole Containing Marketed Drugs with Proton Pump Inhibitor and H Receptor Antagonist Activities.
含苯并咪唑的已上市药物的概述,这些药物具有质子泵抑制剂和H受体拮抗剂活性。
Mini Rev Med Chem. 2025;25(6):440-462. doi: 10.2174/0113895575329633240928163509.
4
Hybrids of Benzimidazole-oxadiazole: A New Avenue for Synthesis, Pharmacological Activity and Recent Patents for the Development of More Effective Ligands.苯并咪唑-噁二唑杂合体:合成、药理学活性和开发更有效配体的最新专利的新途径。
Curr Org Synth. 2024;21(8):976-1013. doi: 10.2174/0115701794260740231010111408.
5
A Review of Approaches to the Metallic and Non-Metallic Synthesis of Benzimidazole (BnZ) and Their Derivatives for Biological Efficacy.苯并咪唑(BnZ)及其衍生物的金属和非金属合成方法及其生物功效研究综述。
Molecules. 2023 Jul 18;28(14):5490. doi: 10.3390/molecules28145490.
6
Synthesis, DNA binding and biological evaluation of benzimidazole Schiff base ligands and their metal(ii) complexes.苯并咪唑席夫碱配体及其金属(II)配合物的合成、DNA结合和生物学评价
RSC Adv. 2023 Apr 17;13(18):11982-11999. doi: 10.1039/d3ra00982c.
7
Anticancer effects of imidazole nucleus in hepatocellular carcinoma cell lines via the inhibition of AKT and ERK1/2 signaling pathways.咪唑核通过抑制 AKT 和 ERK1/2 信号通路对肝癌细胞系的抗癌作用。
Mol Biol Rep. 2022 Jun;49(6):4377-4388. doi: 10.1007/s11033-022-07273-9. Epub 2022 Feb 28.
8
A Comprehensive Account on Recent Progress in Pharmacological Activities of Benzimidazole Derivatives.苯并咪唑衍生物药理活性研究进展综述
Front Pharmacol. 2021 Nov 3;12:762807. doi: 10.3389/fphar.2021.762807. eCollection 2021.
9
Imidazoles and benzimidazoles as putative inhibitors of SARS-CoV-2 B.1.1.7 (Alpha) and P.1 (Gamma) variant spike glycoproteins: A computational approach.咪唑和苯并咪唑作为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)B.1.1.7(阿尔法)和P.1(伽马)变异株刺突糖蛋白的潜在抑制剂:一种计算方法
Chem Zvesti. 2022;76(2):1107-1117. doi: 10.1007/s11696-021-01900-8. Epub 2021 Oct 18.
10
Synthesis, Crystal Study, and Anti-Proliferative Activity of Some 2-Benzimidazolylthioacetophenones towards Triple-Negative Breast Cancer MDA-MB-468 Cells as Apoptosis-Inducing Agents.某些2-苯并咪唑基硫代苯乙酮作为凋亡诱导剂对三阴性乳腺癌MDA-MB-468细胞的合成、晶体研究及抗增殖活性
Int J Mol Sci. 2016 Jul 29;17(8):1221. doi: 10.3390/ijms17081221.