Transporters as Drug Targets: Discovery and Development of NPC1L1 Inhibitors

被引:17
作者
Betters, J. L. [1 ]
Yu, L. [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Pathol, Winston Salem, NC 27103 USA
关键词
INTESTINAL CHOLESTEROL ABSORPTION; NIEMANN-PICK C1-LIKE-1; EZETIMIBE; MICE; RECEPTOR; BINDING; CELLS; HYPERCHOLESTEROLEMIA; PROTEIN; ACIDS;
D O I
10.1038/clpt.2009.209
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The potent cholesterol absorption inhibitor ezetimibe was developed as a first-in-class drug for treating hypercholesterolemia even before its molecular target, Niemann-Pick C1-like 1 (NPC1L1), had been identified. The NPC1L1 protein mediates sterol transport across the enterocyte brush border membrane and is essential for intestinal cholesterol absorption, a major pathway controlling whole-body cholesterol homeostasis. An elucidation of the mechanism underlying NPC1L1-dependent cholesterol absorption would greatly facilitate the discovery and development of new cholesterol-lowering agents for treating hypercholesterolemia and other cholesterol-related metabolic disorders.
引用
收藏
页码:117 / 121
页数:5
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