EC Number |
Reaction |
Reference |
---|
2.4.1.81 | UDP-glucose + 5,7,3',4'-tetrahydroxyflavone = UDP + 7-O-beta-D-glucosyl-5,7,3',4'-tetrahydroxyflavone |
- |
- |
2.4.1.81 | UDP-glucose + 5,7,3',4'-tetrahydroxyflavone = UDP + 7-O-beta-D-glucosyl-5,7,3',4'-tetrahydroxyflavone |
GTs are generally regarded as unidirectional catalysts that drive the formation of glycosidic bonds from NDP-sugar donors and aglycon acceptors according to a nucleophilic substitution mechanism (SN2). An SN2 attack by the aromatic hydroxyl or carboxylate oxygen to the anomeric carbon of UDP-glucose is performed in the aromatic O-glucoside or acyl-glucose ester forming reactions |
759388 |
2.4.1.81 | UDP-glucose + 5,7,3',4'-tetrahydroxyflavone = UDP + 7-O-beta-D-glucosyl-5,7,3',4'-tetrahydroxyflavone |
GTs are generally regarded as unidirectional catalysts that drive the formation of glycosidic bonds from NDP-sugar donors and aglycon acceptors according to a nucleophilic substitution mechanism (SN2). An SN2 attack by the aromatic hydroxyl or carboxylate oxygen to the anomeric carbon of UDP-glucose is performed in the aromatic O-glucoside or acyl-glucoseester forming reactions |
759388 |