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Deoxynojirimycin enzyme inhibition

Support for the proposal that the non-covalent event required by the kinetic data results in the placing of the pyranose ring in the 2 5B conformation comes from the failure of the alkaloid castanospermine [53] to inhibit this enzyme (Saul et al., 1983), even though deoxynojirimycin [54] does. Castanospermine cannot adopt the equivalent of the 2,5B conformation, whereas deoxynojirimycin can. [Pg.144]

An improved, three-step synthesis of iV-butyl-l-deoxynojiromycin from D-glucose has been described, involving an enzymic oxidation ofN-butylglucamine. A synthesis ofA/ -[ C]methyl-1-deoxynojirimycin and its manno epimer has been reported in a study of glycosidase inhibition. l,3,4-Trideoxy-3-fluoronojirimycin and its manno epimer have been characterized and stereochemically distinguished by mass-analyzed ion kinetic energy spectroscopy. ... [Pg.259]

See other pages where Deoxynojirimycin enzyme inhibition is mentioned: [Pg.196]    [Pg.399]    [Pg.340]    [Pg.343]    [Pg.236]    [Pg.356]    [Pg.357]    [Pg.59]    [Pg.221]    [Pg.224]    [Pg.247]    [Pg.248]    [Pg.198]    [Pg.159]    [Pg.198]    [Pg.1916]    [Pg.2341]    [Pg.113]    [Pg.321]    [Pg.11]    [Pg.194]    [Pg.197]    [Pg.243]    [Pg.249]    [Pg.251]    [Pg.398]    [Pg.179]    [Pg.113]    [Pg.1191]    [Pg.90]    [Pg.52]   
See also in sourсe #XX -- [ Pg.157 ]



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