Structure-based design:: Potent inhibitors of human brain memapsin 2 (β-secretase)

被引:208
作者
Ghosh, AK
Bilcer, G
Harwood, C
Kawahama, R
Shin, D
Hussain, KA
Hong, L
Loy, JA
Nguyen, C
Koelsch, G
Ermolieff, J
Tang, J
机构
[1] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[2] Zapaq Inc, Oklahoma City, OK 73104 USA
[3] Oklahoma Med Res Fdn, Prot Studies Program, Oklahoma City, OK 73104 USA
[4] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73104 USA
关键词
D O I
10.1021/jm0101803
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 (A beta) 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.
引用
收藏
页码:2865 / 2868
页数:4
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