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痕量胺相关受体 1(TAAR1)调节剂:专利审查(2010 年至今)。

Trace amine associated receptor 1 (TAAR1) modulators: a patent review (2010-present).

机构信息

Dipartimento di Farmacia, Università di Genova, Viale Benedetto XV 3, Genova, Italy.

出版信息

Expert Opin Ther Pat. 2020 Feb;30(2):137-145. doi: 10.1080/13543776.2020.1708900. Epub 2019 Dec 25.

Abstract

: The greater interest in TAAR1-mediated potential for the treatment of different pathologies, especially those related to CNS disorders, has given a considerable boost to the search for developing TAAR1-selective small molecules.: During the last decade, the medicinal chemistry efforts have allowed the yield of various chemotypes to be properly dressed toward TAAR1 receptor. The more relevant chemical features and structure-activity relationship studies on the TAAR1 ligands will be discussed in order to guide future drug discovery investigations.: The discovery of TAAR receptors has allowed better investigation of the role played by TAs, not only as secondary neuromodulators, but also as neurotransmitters, even if it should still be completely clarified. This has drawn new ways for further insights around the TAAR1 involvement in numerous diseases. Despite this, the limited number of promising ligands targeting TAAR1 orthologue makes the discovery of novel compounds still a challenging task. Relevant efforts have to be focused on safe ligands, devoid of any side-efficacy toward other highly related GPCR (monoaminergic systems). Moreover, species-specificity preferences experienced by numerous compounds so far investigated, based on rodent models and translated to the human environment, turn in a critical bottleneck in drug discovery.

摘要

:人们对 TAAR1 介导的治疗各种疾病的潜力(尤其是与中枢神经系统疾病相关的疾病)越来越感兴趣,这极大地推动了寻找开发 TAAR1 选择性小分子的研究。:在过去的十年中,药物化学的努力已经产生了各种不同的化学类型,这些类型都经过适当修饰以适应 TAAR1 受体。将讨论 TAAR1 配体的更相关的化学特征和构效关系研究,以指导未来的药物发现研究。:TAAR 受体的发现使人们能够更好地研究 TAs 所扮演的角色,不仅作为次级神经调节剂,而且作为神经递质,尽管这仍需完全阐明。这为进一步了解 TAAR1 在许多疾病中的作用提供了新的途径。尽管如此,针对 TAAR1 同源物的有前途的配体数量有限,使得发现新化合物仍然是一项具有挑战性的任务。相关的努力必须集中在安全的配体上,这些配体对其他高度相关的 GPCR(单胺能系统)没有任何副作用。此外,迄今为止基于啮齿动物模型并转化为人类环境的许多化合物所经历的物种特异性偏好,成为药物发现的一个关键瓶颈。

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