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新型组蛋白去乙酰化酶抑制剂。

New patented histone deacetylase inhibitors.

机构信息

Chemistry Discovery, S*BIO Pte Ltd, The Capricorn, Singapore Science Park II, Singapore, Singapore.

出版信息

Expert Opin Ther Pat. 2009 Dec;19(12):1727-57. doi: 10.1517/13543770903393789.

Abstract

IMPORTANCE OF THE FIELD

Following FDA approval of vorinostat in 2006, several novel HDAC inhibitors (HDACis) have entered clinical trials, and there are numerous published patent applications claiming novel HDACis which were optimized as potential drug candidates, designed for regional or systemic release, and created as dual or multifunctional inhibitors. Given the breadth and depth of recent reporting of novel HDACis, there has emerged a need to review the field from a chemist's perspective in one compact article.

AREAS COVERED IN THIS REVIEW

This review provides a summary of published patent applications claiming novel HDACis from 2007 until mid-2009, covering mainly classes I, II and IV anticancer HDACis including those that have recently advanced to the clinic.

WHAT THE READER WILL GAIN

Readers will rapidly gain an overview of the majority of HDACi scaffolds with representative structure-activity relationships; they will learn how these new compounds were created, how their drug like properties were improved and which companies are the main players in the field.

TAKE HOME MESSAGE

Although competition in this field is intense, the future application of HDACis to treat human disease either as single agents or in combination with existing drugs holds real promise.

摘要

重要性的领域

继 FDA 批准伏立诺他在 2006 年,几种新型 HDAC 抑制剂(HDACis)已进入临床试验,并有大量公布的专利申请声称新型 HDACis 进行了优化,作为潜在的药物候选物,设计为区域或全身释放,并创建为双或多功能抑制剂。鉴于最近报道的新型 HDACis 的广度和深度,已经出现了从化学家的角度审查该领域的需要在一个紧凑的文章。

涵盖的领域在这篇综述中

这篇综述提供了一个总结发表的专利申请声称新型 HDACis 从 2007 年到 2009 年年中,主要涵盖 I 类、II 类和 IV 类抗癌 HDACis,包括那些最近已进入临床。

读者将获得

读者将迅速获得概述的大多数 HDACi 支架与代表性的构效关系;他们将了解如何创建这些新化合物,他们的药物样性质得到改善,哪些公司是该领域的主要参与者。

带回家的消息

虽然在这一领域的竞争是激烈的,未来的应用程序的 HDACis 治疗人类疾病无论是作为单一制剂或与现有的药物真正有希望。

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