2b8l: Difference between revisions
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'''Crystal structure of human beta secretase complexed with inhibitor''' | '''Crystal structure of human beta secretase complexed with inhibitor''' | ||
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[[Category: Kuo, L.]] | [[Category: Kuo, L.]] | ||
[[Category: Munshi, S K.]] | [[Category: Munshi, S K.]] | ||
[[Category: | [[Category: Aspartyl protease]] | ||
[[Category: | [[Category: Bace]] | ||
[[Category: | [[Category: Hydrolase]] | ||
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Revision as of 16:59, 3 May 2008
Crystal structure of human beta secretase complexed with inhibitor
Overview
We have synthesized and evaluated a series of conformationally biased P3 amide replacements based on an isophthalamide lead structure. The studies resulted in the identification of the beta-secretase inhibitor 7m which has an in vitro IC(50)=35 nM. The synthesis and biological activities of these compounds are described.
About this Structure
2B8L is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Conformationally biased P3 amide replacements of beta-secretase inhibitors., Stachel SJ, Coburn CA, Steele TG, Crouthamel MC, Pietrak BL, Lai MT, Holloway MK, Munshi SK, Graham SL, Vacca JP, Bioorg Med Chem Lett. 2006 Feb;16(3):641-4. Epub 2005 Nov 2. PMID:16263281 Page seeded by OCA on Sat May 3 19:59:01 2008