化学
敌手
体内
甲状腺
内分泌学
效力
内科学
小分子
激素
受体
口服
药理学
体外
生物化学
医学
生物
生物技术
作者
Willem F. J. Karstens,Wiro M.B.P. Menge,Gijs Martens,Sanne J.N. op het Veld,Jacobus Th.H. van Eupen,Marco Demon,Tanja A.E. van Achterberg,Monica J. Arisse-Thijssen,Ellen W.H. Santegoeds-Lenssen,Miranda M.C. van der Lee,Ruud Ubink,Roel J. Arends,Aloys L.A. Sesink,Marion Blomenröhr,C. Marco Timmers
标识
DOI:10.1016/j.bmc.2023.117258
摘要
The thyrotropin receptor (TSH-R) regulates the thyroid gland and is normally activated by thyrotropin. In patients with Graves’ disease, TSH-R is also stimulated by stimulatory TSH-R autoantibodies leading to hyperthyroidism. In this paper, we describe the discovery of SYD5115 (67), a novel small molecule TSH-R antagonist with nanomolar potency. SYD5115 also blocks stimulating antibody induced synthesis of the thyroid hormone thyroxine (T4) in vivo, after a single oral dose. During optimization, several issues had to be addressed such as the low metabolic stability and the potential mutagenicity of our first series of compounds.
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