4-Aminophenylalanine and 4-aminocyclohexylalanine derivatives as potent, selective, and orally bioavailable inhibitors of dipeptidyl peptidase IV

被引:18
作者
Duffy, Joseph L. [1 ]
Kirk, Brian A.
Wang, Liping
Eiermann, George J.
He, Huaibing
Leiting, Barbara
Lyons, Kathryn A.
Patel, Reshma A.
Patel, Sangita B.
Petrov, Alexsandr
Scapin, Giovanna
Wu, Joseph K.
Thornberry, Nancy A.
Weber, Ann E.
机构
[1] Merck Res Labs, Dept Med Chem, Rahway, NJ 07065 USA
[2] Merck Res Labs, Dept Pharmacol, Rahway, NJ 07065 USA
[3] Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA
关键词
dipeptidyl peptidase IV; DPP-4; Kazmaier Claisen; Buchwald amidation; X-ray;
D O I
10.1016/j.bmcl.2007.02.066
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel series of 4-aminophenylalanine and 4-aminocyclohexylalanine derivatives were designed and evaluated as inhibitors of dipeptidyl peptidase IV (DPP-4). The phenylalanine series afforded compounds such as 10 that were potent and selective (DPP-4, IC50 = 28 nM), but exhibited limited oral bioavailability. The corresponding cyclohexylalanine derivatives such as 25 afforded improved PK exposure and efficacy in a murine OGTT experiment. The X-ray crystal structure of 25 bound to the DPP-4 active site is presented. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2879 / 2885
页数:7
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