共 32 条
Transporters as Drug Targets: Discovery and Development of NPC1L1 Inhibitors
被引:17
作者:

Betters, J. L.
论文数: 0 引用数: 0
h-index: 0
机构:
Wake Forest Univ, Bowman Gray Sch Med, Dept Pathol, Winston Salem, NC 27103 USA Wake Forest Univ, Bowman Gray Sch Med, Dept Pathol, Winston Salem, NC 27103 USA

Yu, L.
论文数: 0 引用数: 0
h-index: 0
机构:
Wake Forest Univ, Bowman Gray Sch Med, Dept Pathol, Winston Salem, NC 27103 USA Wake Forest Univ, Bowman Gray Sch Med, Dept Pathol, Winston Salem, NC 27103 USA
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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