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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] 
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