Memapsin 2 (beta-secretase) inhibitors: Drug development

被引:51
|
作者
Ghosh, Arun K. [1 ,2 ]
Kumaragurubaran, Nagaswamy [1 ,2 ]
Hong, Ling [3 ]
Koelsh, Gerald [3 ]
Tang, Jordan [4 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Med Chem, W Lafayette, IN 47907 USA
[3] CoMentis Inc, San Francisco, CA 94080 USA
[4] Univ Oklahoma, Hlth Sci Ctr, Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA
关键词
D O I
10.2174/156720508783954730
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Memapsin 2 (secretase, BACE 1) processing of beta-amyloid precursor protein is the first step in the pathway leading to the production of amyloid-beta, thus, it is a major target for the development of inhibitor drug for the treatment of Alzheimers's Disease. Although there are distinctive advantages of this protease as a drug target, the development of drug-like memapsin 2 inhibitors has been somewhat slow since the cloning of the protease seven years ago. Here we review the progress of memapsin 2 inhibitor development using crystal structure-based design cycles. Recent progress has evolved the inhibitors into sizes sufficiently small to penetrate cell membranes and the blood-brain barrier yet retain potency for the inhibition of A beta production in cultured cells and experimental animals. Such progress lends optimism that clinically useful memapsin 2 inhibitors will eventually be developed.
引用
收藏
页码:121 / 131
页数:11
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