Memapsin 2 (Beta-Secretase) Inhibitors: Drug Development

2008 ◽  
Vol 5 (2) ◽  
pp. 121-131 ◽  
Author(s):  
Arun Ghosh ◽  
Nagaswamy Kumaragurubaran ◽  
Ling Hong ◽  
Gerald Koelsh ◽  
Jordan Tang
2007 ◽  
Vol 21 (12) ◽  
pp. 3184-3196 ◽  
Author(s):  
Wan‐Pin Chang ◽  
Deborah Downs ◽  
Xiang‐Ping Huang ◽  
Huining Da ◽  
Kar‐Ming Fung ◽  
...  

2006 ◽  
Vol 2 ◽  
pp. S20-S21
Author(s):  
Wan-Pin Chang ◽  
Gerald Koelsch ◽  
Deborah Downs ◽  
Kar-Ming Fung ◽  
Huining Da ◽  
...  

2007 ◽  
Vol 4 (4) ◽  
pp. 418-422 ◽  
Author(s):  
Arun Ghosh ◽  
Geoffrey Bilcer ◽  
Lin Hong ◽  
Gerald Koelsch ◽  
Jordan Tang

2008 ◽  
Vol 4 ◽  
pp. T467-T467
Author(s):  
Wan-Pin Chang ◽  
Huining Da ◽  
Xiangping Huang ◽  
Deborah Downs ◽  
Kar-Ming Fung ◽  
...  

2003 ◽  
Vol 70 ◽  
pp. 213-220 ◽  
Author(s):  
Gerald Koelsch ◽  
Robert T. Turner ◽  
Lin Hong ◽  
Arun K. Ghosh ◽  
Jordan Tang

Mempasin 2, a ϐ-secretase, is the membrane-anchored aspartic protease that initiates the cleavage of amyloid precursor protein leading to the production of ϐ-amyloid and the onset of Alzheimer's disease. Thus memapsin 2 is a major therapeutic target for the development of inhibitor drugs for the disease. Many biochemical tools, such as the specificity and crystal structure, have been established and have led to the design of potent and relatively small transition-state inhibitors. Although developing a clinically viable mempasin 2 inhibitor remains challenging, progress to date renders hope that memapsin 2 inhibitors may ultimately be useful for therapeutic reduction of ϐ-amyloid.


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