临床前和临床开发中的选择性雄激素受体调节剂。

Nuclear receptor signaling Pub Date : 2008-01-01 Epub Date: 2008-11-26 DOI:10.1621/nrs.06010
Ramesh Narayanan, Michael L Mohler, Casey E Bohl, Duane D Miller, James T Dalton
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引用次数: 133

摘要

雄激素受体(雄激素受体)在主要和辅助性器官、骨骼肌和骨骼等器官的功能中起着至关重要的作用,使其成为理想的治疗靶点。选择性雄激素受体调节剂(SARMs)与AR结合并表现出骨和肌合成代谢活性;然而,与睾酮和其他合成代谢类固醇不同,这些非甾体类药物对前列腺和其他第二性器官的生长作用较小。SARMs为多种疾病提供了治疗机会,包括与烧伤、癌症或终末期肾病、骨质疏松、虚弱和性腺功能减退相关的肌肉萎缩。本文综述了sarm的研究和开发现状、sarm的晶体学、可能的作用机制以及这类新兴药物的潜在治疗适应症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Selective androgen receptor modulators in preclinical and clinical development.

Selective androgen receptor modulators in preclinical and clinical development.

Selective androgen receptor modulators in preclinical and clinical development.

Selective androgen receptor modulators in preclinical and clinical development.

Androgen receptor (AR) plays a critical role in the function of several organs including primary and accessory sexual organs, skeletal muscle, and bone, making it a desirable therapeutic target. Selective androgen receptor modulators (SARMs) bind to the AR and demonstrate osteo- and myo-anabolic activity; however, unlike testosterone and other anabolic steroids, these nonsteroidal agents produce less of a growth effect on prostate and other secondary sexual organs. SARMs provide therapeutic opportunities in a variety of diseases, including muscle wasting associated with burns, cancer, or end-stage renal disease, osteoporosis, frailty, and hypogonadism. This review summarizes the current standing of research and development of SARMs, crystallography of AR with SARMs, plausible mechanisms for their action and the potential therapeutic indications for this emerging class of drugs.

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