SB756050是选择性的TGR5激动剂，目前正处于临床一期实验用于治疗二型糖尿病。
CAS：447410-57-3
分子式：C21H28N2O8S2
分子量：500.59
纯度：98%
存储：Store at -20°C

Background:

SB756050 is a selective TGR5 agonist currently in phase 1clinical trials for the treatment of type 2 diabetes.

TGR5 is a bile acid receptor and a potential target for the treatment of type 2 diabetes (T2D)[1].

SB756050 is well‐ olerated; it is readily absorbed, exhibited nonlinear pharmacokinetics with a less than dose‐proportional increase in plasma exposure above 100 mg, and demonstrates no significant changes in exposure when co‐administered with sitagliptin. SB756050 demonstrates highly variable pharmacodynamic effects both within dose groups and between doses, with increases in glucose seen at the two lowest doses and no reduction in glucose seen at the two highest doses. The glucose effects of SB756050 ? sitagliptin are comparable to those of sitagliptin alone, even though gut hormone plasma profiles are different[1].

[1]. Hodge RJ, et al. Safety, Pharmacokinetics, and Pharmacodynamic Effects of a Selective TGR5 Agonist, SB-756050, in Type 2 Diabetes. Clin Pharmacol Drug Dev. 2013 Jul;2(3):213-22.