Suppr超能文献

茚并[化]物——性质、制备及在 G 蛋白偶联受体配体中的存在。

Indanes--Properties, Preparation, and Presence in Ligands for G Protein Coupled Receptors.

机构信息

Division of Medicinal Chemistry, Leiden Academic Centre for Drug Research, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands.

出版信息

Med Res Rev. 2015 Nov;35(6):1097-126. doi: 10.1002/med.21352. Epub 2015 May 27.

Abstract

The indane (2,3-dihydro-1H-indene) ring system is an attractive scaffold for biologically active compounds due to the combination of aromatic and aliphatic properties fused together in one rigid system. This bicyclic structure provides a wide range of possibilities to incorporate specific substituents in different directionalities, thus being an attractive scaffold for medicinal chemists. Notably, many indane-based compounds are being used in the clinic to treat various diseases, such as indinavir, an HIV-1 protease inhibitor; indantadol, a potent Monoamine Oxidase (MAO)-inhibitor; the amine uptake inhibitor indatraline; and the ultra-long-acting β-adrenoceptor agonist indacaterol. Given the diversity of targets these drugs act on, one could argue that the indane ring system is a privileged substructure. In the present review, the synthetic and medicinal chemistry of the indane ring system is described. In more detail, it contains a comprehensive overview of compounds bearing the indane substructure with G protein coupled receptor (GPCR) activity, with particular emphasis on their structure-activity relationships (SAR).

摘要

茚满(2,3-二氢-1H-茚)环系是一种有吸引力的生物活性化合物骨架,因为其结合了在一个刚性系统中融合在一起的芳香族和脂肪族性质。这种双环结构提供了广泛的可能性,可以将特定取代基引入不同的方向,因此成为药物化学家的有吸引力的支架。值得注意的是,许多基于茚满的化合物正在临床上用于治疗各种疾病,例如 HIV-1 蛋白酶抑制剂茚地那韦;强效单胺氧化酶(MAO)抑制剂吲哚达托;胺摄取抑制剂吲哚拉明;和超长效β-肾上腺素受体激动剂茚达特罗。鉴于这些药物作用的靶点多样性,可以说茚满环系是一种特权亚结构。在本综述中,描述了茚满环系的合成和药物化学。更详细地说,它包含了具有 G 蛋白偶联受体(GPCR)活性的含茚满亚结构的化合物的全面概述,特别强调了它们的结构-活性关系(SAR)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验