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Beta-secretase (BACE-1) inhibitors: accounting for 10s loop flexibility using rigid active sites.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2007 Feb 15; Vol. 17 (4), pp. 1117-21. Date of Electronic Publication: 2006 Nov 06. - Publication Year :
- 2007
-
Abstract
- BACE-1 is a flexible enzyme with experimentally determined motion in the flap region, the catalytic aspartates, and the 10s loop. Four in-house crystallographically determined complexes of tertiary carbinamine inhibitors revealed 10s loop motion in the S(3) pocket. These X-ray structures were used to correlate K(i) values, which span over five orders of magnitude, with the calculated interaction energy, using the Merck Molecular Force Field for a series of 19 tertiary carbinamine inhibitors.
- Subjects :
- Aspartic Acid analogs & derivatives
Aspartic Acid chemistry
Aspartic Acid pharmacology
Binding Sites
Catalysis
Chemical Phenomena
Chemistry, Physical
Crystallography, X-Ray
Enzyme Inhibitors chemistry
Ligands
Molecular Conformation
Structure-Activity Relationship
Thermodynamics
Amyloid Precursor Protein Secretases antagonists & inhibitors
Enzyme Inhibitors pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 17
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 17112725
- Full Text :
- https://doi.org/10.1016/j.bmcl.2006.11.003