Spiroimidazolidinone NPC1L1 inhibitors. Part 2: Structure-activity studies and in vivo efficacy

被引:16
|
作者
Howell, Kobporn L. [1 ]
DeVita, Robert J. [1 ]
Garcia-Calvo, Margarita [2 ]
Meurer, Roger D. [3 ]
Lisnock, JeanMarie [2 ]
Bull, Herbert G. [2 ]
McMasters, Daniel R. [4 ]
McCann, Margaret E. [3 ]
Mills, Sander G. [1 ]
机构
[1] Merck & Co Inc, Dept Med Chem, Rahway, NJ 07065 USA
[2] Merck & Co Inc, Dept Metab Disorders Diabet, Rahway, NJ 07065 USA
[3] Merck & Co Inc, Dept Pharmacol, Rahway, NJ 07065 USA
[4] Merck & Co Inc, Dept Mol Syst, Rahway, NJ 07065 USA
关键词
Ezetimibe; Cholesterol-absorption inhibitor; Hypercholesterolemia; Niemann-Pick C1-Like 1 protein; Spiroimidazolidinone; CHOLESTEROL ABSORPTION INHIBITOR; EZETIMIBE; DISPOSITION; DISCOVERY; SCH58235; POTENT;
D O I
10.1016/j.bmcl.2010.09.138
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ezetimibe (Zetia (R)), a cholesterol-absorption inhibitor (CAI) approved by the FDA for the treatment of hypercholesterolemia, is believed to target the intestine protein Niemann-Pick C1-Like 1 (NPC1L1) or its pathway. A spiroimidazolidinone NPC1L1 inhibitor identified by virtual screening showed moderate binding activity but was not efficacious in an in vivo rodent model of cholesterol absorption. Synthesis of analogs established the structure-activity relationships for binding activity, and resulted in compounds with in vivo efficacy, including 24, which inhibited plasma cholesterol absorption by 67% in the mouse, thereby providing proof-of-concept that non-beta-lactams can be effective CAIs. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6929 / 6932
页数:4
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