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Discovery of cyclic sulfone hydroxyethylamines as potent and selective beta-site APP-cleaving enzyme 1 (BACE1) inhibitors: structure based design and in vivo. 4D Discovery of cyclic sulfone hydroxyethylamines as potent and selective beta-site APP-cleaving enzyme 1 (BACE1) inhibitors: structure based design and . SWISS-MODEL Template Library (SMTL) entry for 4d HEADER HYDROLASE/HYDROLASE INHIBITOR JAN 4D88 TITLE CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE IN COMPLEX WITH. MISSION COLLECTION (HDOPAL) by Hi-Lite MFG Co. Image may not reflect selected features. No Image Available. MISSION COLLECTION.
4 Aug 4d88 is a 1 chain structure with sequence from Human. Full crystallographic information is available from OCA. For a guided tour on the. Index of /public/upload/clip_thumb/4d/ [ICO], Name · Last modified · Size · Description. [PARENTDIR], Parent Directory, -. [IMG]. Structure-based design of a series of cyclic hydroxyethylamine BACE1 inhibitors allowed the rational incorporation of prime- and nonprime-side fragments to a. 21 Nov 4d Discovery of cyclic sulfone hydroxyethylamines as potent and selective β- site APP-cleaving enzyme 1 (BACE1) inhibitors.