Hybrids of Benzimidazole-oxadiazole: A New Avenue for Synthesis, Pharmacological Activity and Recent Patents for the Development of More Effective Ligands.

IF 1.7 4区 化学 Q3 CHEMISTRY, ORGANIC Current organic synthesis Pub Date : 2024-01-01 DOI:10.2174/0115701794260740231010111408
Gunjan Bhasker, Salahuddin, Avijit Mazumder, Rajnish Kumar, Greesh Kumar, Mohamed Jawed Ahsan, Mohammad Shahar Yar, Fahad Khan, Bhupinder Kapoor
{"title":"Hybrids of Benzimidazole-oxadiazole: A New Avenue for Synthesis, Pharmacological Activity and Recent Patents for the Development of More Effective Ligands.","authors":"Gunjan Bhasker, Salahuddin, Avijit Mazumder, Rajnish Kumar, Greesh Kumar, Mohamed Jawed Ahsan, Mohammad Shahar Yar, Fahad Khan, Bhupinder Kapoor","doi":"10.2174/0115701794260740231010111408","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Two significant families of compounds i.e. 1,3,4-oxadiazole and benzimidazole, have undergone extensive investigation into their pharmacological characteristics and possible therapeutic applications. Both classes have shown their potential in a variety of applications, and because of their synergistic interactions, they may have an even better therapeutic impact when combined.</p><p><strong>Objectives: </strong>To produce a specific molecule with potent therapeutic properties, it is now common methods to combine at least two pharmacophores. This facilitates interaction with several targets, enhances biological functions, or eliminates adverse effects associated with them.</p><p><strong>Conclusion: </strong>The synthesis of benzimidazole-1,3,4-oxadiazole hybrid compounds has recently involved the use of several synthetic techniques, all of which are detailed in the literature along with the advantages and disadvantages. It has been noted that the structure-activity relationship relates their pharmacological actions to their molecular structure. In order to set the stage for future research, the study aims to provide researchers with an effective toolbox and an understanding of benzimidazole and 1,3,4-oxadiazole hybrid compounds.</p>","PeriodicalId":11101,"journal":{"name":"Current organic synthesis","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current organic synthesis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.2174/0115701794260740231010111408","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Two significant families of compounds i.e. 1,3,4-oxadiazole and benzimidazole, have undergone extensive investigation into their pharmacological characteristics and possible therapeutic applications. Both classes have shown their potential in a variety of applications, and because of their synergistic interactions, they may have an even better therapeutic impact when combined.

Objectives: To produce a specific molecule with potent therapeutic properties, it is now common methods to combine at least two pharmacophores. This facilitates interaction with several targets, enhances biological functions, or eliminates adverse effects associated with them.

Conclusion: The synthesis of benzimidazole-1,3,4-oxadiazole hybrid compounds has recently involved the use of several synthetic techniques, all of which are detailed in the literature along with the advantages and disadvantages. It has been noted that the structure-activity relationship relates their pharmacological actions to their molecular structure. In order to set the stage for future research, the study aims to provide researchers with an effective toolbox and an understanding of benzimidazole and 1,3,4-oxadiazole hybrid compounds.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
苯并咪唑-恶二唑的杂交:合成、药理活性和开发更有效配体的最新专利的新途径。
背景:两个重要的化合物家族,即1,3,4-恶二唑和苯并咪唑,已经对其药理特性和可能的治疗应用进行了广泛的研究。这两类药物在各种应用中都显示出了它们的潜力,由于它们的协同作用,当它们结合在一起时,可能会产生更好的治疗效果。目的:为了产生具有有效治疗特性的特定分子,现在常用的方法是结合至少两个药效团。这促进了与几个靶标的相互作用,增强了生物功能,或消除了与之相关的不良影响。结论:苯并咪唑-1,3,4-恶二唑杂化化合物的合成最近涉及到几种合成技术的使用,所有这些技术都在文献中详细介绍了其优缺点。已经注意到,结构-活性关系将它们的药理作用与其分子结构联系起来。为了为未来的研究奠定基础,该研究旨在为研究人员提供苯并咪唑和1,3,4-恶二唑杂化化合物的有效工具箱和基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Current organic synthesis
Current organic synthesis 化学-有机化学
CiteScore
3.40
自引率
5.60%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Current Organic Synthesis publishes in-depth reviews, original research articles and letter/short communications on all areas of synthetic organic chemistry i.e. asymmetric synthesis, organometallic chemistry, novel synthetic approaches to complex organic molecules, carbohydrates, polymers, protein chemistry, DNA chemistry, supramolecular chemistry, molecular recognition and new synthetic methods in organic chemistry. The frontier reviews provide the current state of knowledge in these fields and are written by experts who are internationally known for their eminent research contributions. The journal is essential reading to all synthetic organic chemists. Current Organic Synthesis should prove to be of great interest to synthetic chemists in academia and industry who wish to keep abreast with recent developments in key fields of organic synthesis.
期刊最新文献
A Pharmacological Overview and Recent Patent of Triazine Scaffold in Drug Development: A Review Development of a Suitable Method for the Synthesis of New Thiadiazoles Using Hydrazonoyl Halides Synthesis of Heterocyclic Sulfonium Triflates by Cu-Catalyzed Selective Sarylation with Aryl(mesityl)iodonium Salts Co2(CO)8 as a CO-source for Pd-catalyzed Carbonylations: An Update Synthesis and Characterization of Novel Polythiadiazoles from Bis-hydrazonoyl Dichlorides and Bis-(methyl-2-arylidene hydrazone carbodithioates)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1