kaempferol 4′-O-methyltransferase EC#: 2.1.1.155; ChemWhat Code: 1376355

Product Name kaempferol 4′-O-methyltransferase
Example Structure Example Structure of kaempferol 4'-O-methyltransferase EC#: 2.1.1.155
Synonyms 4’OMT, CrOMT6, F 4¡¯-OMT, flavonoid methyltransferase, flavonoid O-methyltransferase, methyltransferase, flavonoid, S-adenosyl-L-methionine:flavonoid 4¡¯-O-methyltransferase
EC Number 2.1.1.155
CAS Registry Number
Comments The enzyme acts on the hydroxy group in the 4′-position of some flavones, flavanones and isoflavones. Kaempferol, apigenin and kaempferol triglucoside are substrates, as is genistein, which reacts more slowly. Compounds with an hydroxy group in the 3′ and 4′ positions, such as quercetin and eriodictyol, do not act as substrates. Similar to EC 2.1.1.75, apigenin 4′-O-methyltransferase and EC 2.1.1.83, 3,7-dimethylquercetin 4′-O-methyltransferase.
Cofactor
History
Reactions S-adenosyl-L-methionine + kaempferol = S-adenosyl-L-homocysteine + kaempferide.

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