Structure-Based Design: Potent Inhibitors of Human Brain Memapsin 2 (β-Secretase)
Journal of Medicinal Chemistry2001Vol. 44(18), pp. 2865–2868
Citations Over TimeTop 10% of 2001 papers
Arun K. Ghosh, Geoffrey Bilcer, Cynthia Harwood, Reiko Kawahama, Dong-Woo Shin, Khaja Azhar Hussain, Hong Lin, Jeffrey A. Loy, Chan Nguyen, Gerald Koelsch, Jacques Ermolieff, Jordan Tang
Abstract
Memapsin 2 (beta-secretase) is one of two proteases that cleave the beta-amyloid precursor protein (APP) to produce the 40-42 residue amyloid-beta peptide (Abeta) in the human brain, a key event in the progression of Alzheimer's disease. On the basis of the X-ray crystal structure of our lead inhibitor (2, OM99-2 with eight residues) bound to memapsin, we have reduced the molecular weight and designed potent memapsin inhibitors. Structure-based design and preliminary structure-activity studies have been presented.
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