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HRID1359898

反应详情

EQUATION

反应方程式

HRID 1359898 的结构方程式

REACTANTS

反应物

2
结构：C[S+](CC[C@H](N)C(=O)O)C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
HCID34756

5'-[[(3S)-3-Amino-3-carboxypropyl]methylsulfonio]-5'-deoxy-adenosine

C15H23N6O5S+

结构：O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(O)c(O)c(O)c1)c1cc(O)c(O)c(O)c1
HCID65064

(-)-Epigallocatechin gallate

C22H18O11

PRODUCTS

生成物

1
结构：Oc1cc(O)c2c(c1)OC(c1ccc(O)c(O)c1)C(O)C2
HCID1203

2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

C15H14O6

PROCEDURE

实验过程

The purified enzyme is suspended in a buffer having a pH of 4.5 to 8.5, preferably 6.5 to 8. To this suspension, EGCG or ECG is added along with S-adenosyl-L-methionine (SAM) and the reaction is allowed to proceed at 5 to 60° C., preferably at 20 to 40° C., to form a methylated catechin.

WORKUP

后处理

  1. customto proceed at 5 to 60° C., preferably at 20 to 40° C.