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组胺H3受体配体在众多显著的治疗领域取得了突破。

Histamine H3 receptor ligands break ground in a remarkable plethora of therapeutic areas.

作者信息

Wijtmans Maikel, Leurs Rob, de Esch Iwan

机构信息

Vrije Universiteit Amsterdam, Leiden/Amsterdam Center of Drug Research, Division of Medicinal Chemistry, Faculty of Sciences, De Boelelaan 1083, Amsterdam, The Netherlands.

出版信息

Expert Opin Investig Drugs. 2007 Jul;16(7):967-85. doi: 10.1517/13543784.16.7.967.

Abstract

The neurotransmitter histamine exerts its action through four distinct histamine receptors. The histamine H(1) and H(2) receptor are well established drug targets, whereas the histamine H(4) receptor is undergoing rigorous characterisation at present. The histamine H(3) receptor (H(3)R) is a G(i/o)-protein coupled receptor and is mostly expressed in the CNS. A remarkably large and different array of therapeutic areas, in which ligands for the H(3)R may prove useful, has been identified and a massive research undertaking is underway to substantiate the high expectations for H(3)R ligands. At present, several ligands for the H(3)R are being evaluated in clinical studies. In this review, the many potential therapeutic areas for H(3)R antagonists, inverse agonists and agonists is discussed. Promising medicinal chemistry and toxicological developments, as well as the advancement of several H(3)R ligands into the clinic, will be highlighted. This review also describes the problems that have been overcome and the questions that remain in developing H(3)R-related drugs. Considering the tremendous efforts by industry, it can be expected that the first H(3)R drugs will reach the market soon.

摘要

神经递质组胺通过四种不同的组胺受体发挥作用。组胺H(1)和H(2)受体是已确立的药物靶点,而组胺H(4)受体目前正在进行严格的特性描述。组胺H(3)受体(H(3)R)是一种与G(i/o)蛋白偶联的受体,主要在中枢神经系统中表达。已经确定了一系列非常广泛且不同的治疗领域,其中H(3)R配体可能会被证明是有用的,并且正在进行大量的研究工作以证实对H(3)R配体的高度期望。目前,几种H(3)R配体正在临床研究中进行评估。在这篇综述中,将讨论H(3)R拮抗剂、反向激动剂和激动剂的许多潜在治疗领域。将重点介绍有前景的药物化学和毒理学进展,以及几种H(3)R配体进入临床的情况。这篇综述还描述了在开发与H(3)R相关药物过程中已经克服的问题和仍然存在的问题。考虑到制药行业付出的巨大努力,可以预期首批H(3)R药物将很快上市。

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