Ligand Cyclohex-1-enecarbaldehyde
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Basic Ligand Information
Molecular Structure
C7H10O
Cyclohex-1-enecarbaldehyde
OANSOJSBHVENEI-UHFFFAOYSA-N
1-cyclohexene-1-carboxaldehyde, cyclohex-1-ene-1-carbaldehyde, cyclohexene-2-al
Roles as Enzyme Ligand
Substrate in Enzyme-catalyzed Reactions (4 results)
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1-cyclohexene-1-carboxaldehyde + NADPH + H+ = cyclohexanecarbaldehyde + NADP+
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cyclohex-1-ene-1-carbaldehyde + 2-oxoglutarate = (5R)-5-cyclohex-1-en-1-yl-5-hydroxy-4-oxopentanoic acid + CO2
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cyclohex-1-ene-1-carbaldehyde + acetaldehyde = (S)-1-Cyclohex-1-enyl-2-hydroxy-propan-1-one
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Cyclohex-1-enecarbaldehyde + acetaldehyde = 1-Cyclohex-1-enyl-2-hydroxy-propan-1-one
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Enzyme Kinetic Parameters
References & Links
Literature References (4)
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Benzoylformate decarboxylase from Pseudomonas putida as stable catalyst for the synthesis of chiral 2-hydroxy ketones
2000
Iding, H.; Dünnwald, T.; Greiner, L.; Liese, A.; Müller, M.; et al.
Chem. Eur. J.
6
1483-1495
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Enantioselective synthesis of (S)-2-hydroxypropanone derivatives by benzoylformate decarboxylase catalyzed C-C bond formation
2000
Dünnwald, T.; Demir, A.S.; Siegert, P.; Pohl, M.; Muller, M.
Eur. J. Org. Chem.
2000
2161-2170
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MenD as a versatile catalyst for asymmetric synthesis
2009
Kurutsch, A.; Richter, M.; Brecht, V.; Sprenger, G.; Müller, M.
J. Mol. Catal. B
61
56-66
Biocatalytic asymmetric alkene reduction: crystal structure and characterization of a double bond reductase from Nicotiana tabacum
2013
Mansell, D.J.; Toogood, H.S.; Waller, J.; Hughes, J.M.X.; Levy, C.W.; Gardiner, J.M.; Scrutton, N.S.
ACS Catal.
3
370-379
Links to other databases for Cyclohex-1-enecarbaldehyde
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