A NOVEL INHIBITOR OF HUMAN ALPHA-L-FUCOSIDASE - ENANTIOSELECTIVE SYNTHESIS OF L-FUCOAMIDRAZONE
[摘要] A short, chiral synthesis of the title inhibitor 1 is reported from D-galactosamine by chain end interchange. The L-fucoamidrazone is a good competitive inhibitor of human alpha-L-fucosidase (K-i = 820 nM).
[发布日期] 1994-06-06 [发布机构]
[效力级别] [学科分类]
[关键词] [时效性]