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Results 1 - 6 of 6

EC Number	Natural Substrates	Commentary (Nat. Sub.)
2.1.1.337	more	RNMT shows a strong preference for substrates with a tertiary amine, although alkaloids containing a secondary amine (e.g. (R,S)-tetrahydropapaverine, (S)-coclaurine) are also accepted as substrates. In the case of substrates with secondary amines, RNMT catalyzes two sequential N-methylations
2.1.1.337	S-adenosyl-L-methionine + (+)-bulbocapnine	75% substrate conversion
2.1.1.337	S-adenosyl-L-methionine + (+)-glaucine	47% substrate conversion
2.1.1.337	S-adenosyl-L-methionine + (R)-reticuline	98% substrate conversion
2.1.1.337	S-adenosyl-L-methionine + (S)-corytuberine	82% substrate conversion
2.1.1.337	S-adenosyl-L-methionine + (S)-reticuline	47% substrate conversion

Results 1 - 6 of 6

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Release 2023.1 (January 2023)