Ligand 4-(1-hydroxyethyl)phenol
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Basic Ligand Information
Molecular Structure
C8H10O2
4-(1-hydroxyethyl)phenol
PMRFBLQVGJNGLU-UHFFFAOYSA-N
(RS)-1-(4-hydroxyphenyl)ethanol, 1-(4'-hydroxyphenyl)ethanol
Show all BRENDA pathways known for 4-(1-hydroxyethyl)phenol
Roles as Enzyme Ligand
Substrate in Enzyme-catalyzed Reactions (1 result)
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(RS)-1-(4-hydroxyphenyl)ethanol + acceptor + H2O = ?
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Product in Enzyme-catalyzed Reactions (6 results)
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4-ethylphenol + O2 + H2O = 1-(4'-hydroxyphenyl)ethanol + H2O2
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4-ethylphenol + O2 = 1-(4'-hydroxyphenyl)ethanol + 4-vinylphenol + 4-hydroxyacetophenone
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4-ethylphenol + acceptor + H2O = 1-(4'-hydroxyphenyl)ethanol + reduced acceptor
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4-ethylphenol + H2O + acceptor = 4-(1-hydroxyethyl)phenol + acceptor
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4-ethylphenol + H2O + ferricenium = 4-(1-hydroxyethyl)phenol + ferrocene
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4-ethylphenol + H2O + ferricenium = 4-(1-hydroxyethyl)phenol + ferrocenium
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Enzyme Kinetic Parameters
References & Links
Literature References (4)
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Regio- and stereospecific conversion of 4-alkylphenols by the covalent flavoprotein vanillyl-alcohol oxidase
1998
Van der Heuvel, R.H.H.; Fraaije, M.W.; Laane, C.; van Berkel, W.J.H.
J. Bacteriol.
180
5646-5651
Enantioselective hydroxylation of 4-alkylphenols by vanillyl alcohol oxidase
1998
Drijfhout, F.P.; Fraaije, M.W.; Jongejan, H.; van Berkel, W.J.H.; Franssen, M.C.R.
Biotechnol. Bioeng.
59
171-177
Stereochemistry of 1-(4-hydroxyphenyl)ethanol produced by hydroxylation of 4-ethylphenol by p-cresol methylhydroxylase
1984
McIntire, W.; Hopper, D.J.; Craig, J.C.; Everhart, E.T.; Webster, R.V.; Causer, M.J.; Singer, T.P.
Biochem. J.
224
617-621
p-Cresol methylhydroxylase. assay and general properties
1985
McIntire, W.; Hopper, D.J.; Singer, T.P.
Biochem. J.
228
325-335
Links to other databases for 4-(1-hydroxyethyl)phenol
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