化学
苯乙胺类
二肽基肽酶-4
葡萄糖稳态
立体化学
二肽基肽酶
哌啶
生物化学
组合化学
药理学
糖尿病
酶
2型糖尿病
内分泌学
胰岛素抵抗
医学
作者
Zhonghua Pei,Xiaofeng Li,Thomas W von Geldern,K.L. Longenecker,Daisy Pireh,Kent D. Stewart,Bradley J. Backes,Chunqiu Lai,Thomas Lübben,Stephen J. Ballaron,David W. A. Beno,Anita J. Kempf-Grote,Hing L. Sham,James M. Trevillyan
摘要
Dipeptidyl peptidase IV (DPP4) inhibitors are emerging as a new class of therapeutic agents for the treatment of type 2 diabetes. They exert their beneficial effects by increasing the levels of active glucagon-like peptide-1 and glucose-dependent insulinotropic peptide, which are two important incretins for glucose homeostasis. Starting from a high-throughput screening hit, we were able to identify a series of piperidinone- and piperidine-constrained phenethylamines as novel DPP4 inhibitors. Optimized compounds are potent, selective, and have good pharmacokinetic profiles.
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