Department of Physiology & Pharmacology, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd, Portland, OR 97239-3098, USA.
Heart Fail Rev. 2010 Mar;15(2):177-82. doi: 10.1007/s10741-008-9122-x. Epub 2008 Nov 11.
Sobetirome, also known as GC-1 and QRX-431, is a member of a class of compounds known as selective thyromimetics (Scanlan et al., Curr Opin Drug Discov Dev 4:614-622). These compounds are synthetic structural analogs of thyroid hormone that have tissue-specific thyroid hormone actions. Many of the compounds in this class, including sobetirome, also are subtype-selective thyroid hormone receptor (TR) agonists. Sobetirome selectively binds to and activates TRbeta over TRalpha and this receptor selectivity led to the hypothesis that sobetirome would lower cholesterol through activation of liver TRbeta without stimulating cardiac function through TRalpha activation in the heart. The tissue selective thyromimetic properties of sobetirome have been demonstrated in numerous animal models, which led to its clinical development as a novel cholesterol-lowering agent. This review will describe the discovery and development journey of sobetirome as a case history.
索贝替尔,又称 GC-1 和 QRX-431,是一类称为选择性甲状腺模拟物(Scanlan 等人,Curr Opin Drug Discov Dev 4:614-622)的化合物中的一员。这些化合物是甲状腺激素的合成结构类似物,具有组织特异性的甲状腺激素作用。该类中的许多化合物,包括索贝替尔,也是亚型选择性甲状腺激素受体(TR)激动剂。索贝替尔选择性地与 TRβ结合并激活 TRβ,而不是与 TRα结合并激活,这种受体选择性导致了这样的假设,即索贝替尔通过激活肝脏 TRβ来降低胆固醇,而不会通过激活心脏中的 TRα来刺激心脏功能。索贝替尔在许多动物模型中表现出组织选择性甲状腺模拟物的特性,这导致了其作为新型降胆固醇药物的临床开发。本综述将描述索贝替尔作为一个案例研究的发现和开发历程。