Phosphaisocoumarins as a new class of potent inhibitors for pancreatic cholesterol esterase

被引:69
|
作者
Li, Baojian [1 ]
Zhou, Binhua [1 ]
Lu, Hailiang [1 ]
Ma, Lin [1 ]
Peng, Ai-Yun [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cholesterol esterase; Inhibitor; Isocoumarin; Phosphaisocoumarin; INTESTINAL-CELLS; HYDROLYSIS; LIPASE; SERINE; 2-(1-ALKYNYL)PHENYLPHOSPHONATES; 4-HALOPHOSPHAISOCOUMARINS; HALOCYCLIZATION; TRANSPORT; PROTEASES; ENZYMES;
D O I
10.1016/j.ejmech.2010.01.038
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Due to the importance of pancreatic cholesterol esterase (CEase) as a potential target in atherosclerosis and for the development of hypocholesterolemic agents, there are increasing interests in designing and synthesizing CEase inhibitors. In the present study, we prepared forty-five isocoumarin phosphorus analogues (i.e., phosphaisocoumarins) and investigated the inhibition of these compounds on the CEase. The results showed that some phosphaisocoumarins could act as potent inhibitors of CEase. The most potent inhibitors, compounds 9d, 10a and 12e give IC(50) values of 4.8 mu M, 2.3 mu M and 1.9 mu M, respectively. The inhibition mechanism and kinetic characterization studies indicate that they are reversible competitive inhibitors. (C) 2010 Published by Elsevier Masson SAS.
引用
收藏
页码:1955 / 1963
页数:9
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