生物利用度
口服活性
药代动力学
兴奋剂
药理学
口服
化学
受体
2型糖尿病
配体(生物化学)
医学
糖尿病
生物化学
内分泌学
作者
Stefan Peukert,Richard L. Hughes,Jill Nunez,Guo‐Wei He,Zhao Yan,Rishi K. Jain,Luis Llamas,Sarah J. Luchansky,Adam Carlson,Guiqing Liang,Vidya Kunjathoor,Mike Pietropaolo,Jeffrey Shapiro,Anja Castellana,Xiaoping Wu,Avirup Bose
摘要
The identification of highly potent and orally bioavailable GPR39 agonists is reported. Compound 1, found in a phenotypic screening campaign, was transformed into compound 2 with good activity on both the rat and human GPR39 receptor. This compound was further optimized to improve ligand efficiency and pharmacokinetic properties to yield GPR39 agonists for the potential oral treatment of type 2 diabetes. Thus, compound 3 is the first potent GPR39 agonist (EC50s ≤ 1 nM for human and rat receptor) that is orally bioavailable in mice and robustly induced acute GLP-1 levels.
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