1.4.3.12: cyclohexylamine oxidase
This is an abbreviated version!
For detailed information about cyclohexylamine oxidase, go to the full flat file.
Word Map on EC 1.4.3.12
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1.4.3.12
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brevibacterium
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deracemization
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oxydans
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monoamine
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alicyclic
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cyclohexanone
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biocatalytic
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deamination
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flavin
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monooxygenase
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stereoselective
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cage
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flavoprotein
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enantiomeric
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dextromethorphan
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fad
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prosthetic
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racemic
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oxidases
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chaas
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synthesis
- 1.4.3.12
- brevibacterium
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deracemization
- oxydans
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monoamine
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alicyclic
- cyclohexanone
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biocatalytic
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deamination
- flavin
- monooxygenase
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stereoselective
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cage
- flavoprotein
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enantiomeric
- dextromethorphan
- fad
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prosthetic
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racemic
- oxidases
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chaas
- synthesis
Reaction
Synonyms
ArCHAO, CF596_10820, chaA, CHAO, CHAOCCH12-C2
ECTree
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Application
Application on EC 1.4.3.12 - cyclohexylamine oxidase
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environmental protection
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as a potential biocatalyst, the enzyme is promising in controlling cyclohexylamine pollution and deracemization of chiral amines
synthesis
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the enzyme is a useful biocatalyst for the kinetic resolution and dereacemization of amines
synthesis
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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
synthesis
Arthrobacter sp. TYUT010-15
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%)
synthesis
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stereoselective synthesis of various enantioenriched 1-benzyl-octahydroisoquinoline derivatives of potential pharmaceutical importance at a semipreparative scale
synthesis
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stereoselective synthesis of various enantioenriched 1-benzyl-octahydroisoquinoline derivatives of potential pharmaceutical importance at a semipreparative scale
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synthesis
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the enzyme is a useful biocatalyst for the kinetic resolution and dereacemization of amines
-
synthesis
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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
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