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2型大麻素(CB)受体激动剂及其治疗潜力的最新进展

Recent Advances on Type-2 Cannabinoid (CB) Receptor Agonists and their Therapeutic Potential.

作者信息

Gasperi Valeria, Guzzo Tatiana, Topai Alessandra, Gambacorta Nicola, Ciriaco Fulvio, Nicolotti Orazio, Maccarrone Mauro

机构信息

Department of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy.

C4T S.r.l Colosseum Combinatorial Chemistry Centre for Technology, Rome, Italy.

出版信息

Curr Med Chem. 2023;30(12):1420-1457. doi: 10.2174/0929867329666220825161603.

Abstract

In the last decade, selective modulators of type-2 cannabinoid receptor (CB) have become a major focus to target endocannabinoid signaling in humans. Indeed, heterogeneously expressed within our body, CB actively regulates several physio-pathological processes, thus representing a promising target for developing specific and safe therapeutic drugs. If CB modulation has been extensively studied since the very beginning for the treatment of pain and inflammation, the more recent involvement of this receptor in other pathological conditions has further strengthened the pursuit of novel CB agonists in the last five years. Against this background, here we discuss the most recent evidence of the protective effects of CB against pathological conditions, emphasizing central nervous system disorders, bone and synovial diseases, and cancer. We also summarize the most recent advances in the development of CB agonists, focusing on the correlation between different chemical classes and diverse therapeutic applications. Data mining includes a review of the CB ligands disclosed in patents also released in the last five years. Finally, we discuss how the recent elucidation of CB tertiary structure has provided new details for the rational design of novel and more selective CB agonists, thus supporting innovative strategies to develop effective therapeutics. Our overview of the current knowledge on CB agonists provides pivotal information on the structure and function of different classes of molecules and opens possible avenues for future research.

摘要

在过去十年中,2型大麻素受体(CB)的选择性调节剂已成为人类内源性大麻素信号传导靶向研究的主要焦点。事实上,CB在我们体内异质表达,积极调节多种生理病理过程,因此是开发特异性和安全治疗药物的一个有前景的靶点。自最初以来,CB调节在疼痛和炎症治疗方面已得到广泛研究,而该受体在其他病理状况中的最新参与,在过去五年中进一步强化了对新型CB激动剂的探索。在此背景下,我们讨论CB对病理状况保护作用的最新证据,重点关注中枢神经系统疾病、骨骼和滑膜疾病以及癌症。我们还总结了CB激动剂开发的最新进展,着重于不同化学类别与多样治疗应用之间的相关性。数据挖掘包括对过去五年发布的专利中披露的CB配体的综述。最后,我们讨论最近对CB三级结构的阐明如何为新型和更具选择性的CB激动剂的合理设计提供了新细节,从而支持开发有效治疗方法的创新策略。我们对CB激动剂当前知识的概述提供了关于不同类别分子结构和功能的关键信息,并为未来研究开辟了可能的途径。

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