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取代的噁二唑类化合物:专利审查(2010-2012 年)。

Substituted oxadiazoles: a patent review (2010 - 2012).

机构信息

Shahid Beheshti University of Medical Sciences, School of Pharmacy, Department of Medicinal Chemistry, P.O. Box: 14155-6153, Tehran, Iran.

出版信息

Expert Opin Ther Pat. 2013 Sep;23(9):1209-32. doi: 10.1517/13543776.2013.797409. Epub 2013 May 10.

Abstract

INTRODUCTION

The oxadiazoles represent a class of five-membered heterocyclic compounds which are of considerable interest in different areas of medicinal chemistry and drug discovery. Oxadiazoles can exist in different regioisomeric forms and employ in various agents with a broad range of biological activities. This review covers the work reported on various biological activities of oxadiazole derivatives from 2010 to 2012.

AREAS COVERED

Oxadiazole derivatives attract great attention due to their different kinds of pharmaceutical activities including antiviral, antimicrobial, anticancer, anticonvulsant, antidiabetic and anti-inflammatory activity. This paper provides a general review of oxadiazole derivatives published in international journals and patented between 2010 and 2012.

EXPERT OPINION

Oxadiazoles have been used frequently in drug-like molecules as bioisosteres for ester and amide functionalities and displayed numerous prominent pharmacological effects. The broad pharmacological profile of oxadiazole derivatives has attracted the attention of many researchers to explore this scaffold to its multiple potential against several activities. Therefore, oxadiazole motif is likely to be present in other therapeutic molecules in the future.

摘要

简介

恶二唑是一类五元杂环化合物,在药物化学和药物发现的多个领域都具有相当大的研究兴趣。恶二唑可以存在于不同的区域异构体形式,并用于具有广泛生物活性的各种试剂中。本综述涵盖了 2010 年至 2012 年报道的关于恶二唑衍生物的各种生物活性的研究工作。

涵盖领域

恶二唑衍生物由于具有多种药物活性,如抗病毒、抗菌、抗癌、抗惊厥、抗糖尿病和抗炎活性,引起了极大的关注。本文综述了 2010 年至 2012 年期间在国际期刊上发表的专利中关于恶二唑衍生物的研究。

专家意见

恶二唑经常被用作酯和酰胺官能团的药物类似物,在药物设计中被广泛应用,具有多种显著的药理学作用。恶二唑衍生物广泛的药理学特性引起了许多研究人员的关注,他们试图探索这种结构,以挖掘其对多种活性的潜在作用。因此,恶二唑结构很可能会出现在未来的其他治疗性分子中。

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