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Results 1 - 5 of 5
EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.12environmental protection as a potential biocatalyst, the enzyme is promising in controlling cyclohexylamine pollution and deracemization of chiral amines 764760
Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.12synthesis chemoenzymatic deracemization is applied to prepare D-valine from racemic valine ethyl ester or L-valine ethyl ester in high yield (up to 95%) with excellent optical purity (more than 99% enantiomeric excess) by employing cyclohexylamine oxidase (CHAO) variant Y321I/M226T exhibiting catalytic efficiency that is 30times higher than that of the wild type enzyme -, 764488
Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.12synthesis deracemization of racemic beta-amino alcohols is conducted by cyclohexylamine oxidase-catalyzed enantioselective deamination and transaminase-catalyzed enantioselective amination to afford (S)-beta-amino alcohols in excellent conversion (78-94%) and enantiomeric excess (above 99%) 764479
Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.12synthesis stereoselective synthesis of various enantioenriched 1-benzyl-octahydroisoquinoline derivatives of potential pharmaceutical importance at a semipreparative scale -, 765258
Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.12synthesis the enzyme is a useful biocatalyst for the kinetic resolution and dereacemization of amines -, 724688
Results 1 - 5 of 5