Ligand 2,4,6-trichlorophenol

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Basic Ligand Information

Molecular Structure
Picture of 2,4,6-trichlorophenol (click for magnification)
Molecular Formula
BRENDA Name
InChIKey
C6H3ClO
2,4,6-trichlorophenol
LINPIYWFGCPVIE-UHFFFAOYSA-N
Synonyms:
2,4,6-trichlorphenol, trichlorophenol, trichloro phenol

Roles as Enzyme Ligand

In Vivo Substrate in Enzyme-catalyzed Reactions (2 results)

EC NUMBER
PROVEN IN VIVO REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE

Substrate in Enzyme-catalyzed Reactions (18 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
2,4,6-trichlorophenol + O2 = ?
show the reaction diagram
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2,4,6-trichlorophenol + H2O2 = ?
show the reaction diagram
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2,4,6-trichlorophenol + H2O2 = ? + H2O
show the reaction diagram
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2,4,6-trichlorophenol + H2O2 + H+ = ?
show the reaction diagram
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2,4,6-trichlorophenol + NADH + H+ + O2 = 2,6-dichlorohydroquinone + 6-chloro-2-hydroxyquinol + ? + NAD+ + H2O
show the reaction diagram
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2,4,6-trichlorophenol + NADPH + O2 = ?
show the reaction diagram
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2,4,6-trichlorphenol + O2 = 2,6-dichlorohydroquinone + H2O + Cl-
show the reaction diagram
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2,4,6-trichlorophenol + reduced acceptor = 4-chlorophenol + chloride + oxidized acceptor
show the reaction diagram
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UDP-glucose + 2,4,6-trichlorophenol = UDP + 2,4,6-trichlorophenylglucoside
show the reaction diagram
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Product in Enzyme-catalyzed Reactions (2 results)

EC NUMBER
REACTION
REACTION DIAGRAM
LITERATURE
ENZYME 3D STRUCTURE
1,3,5-trichlorobenzene + putidaredoxin + O2 = 2,4,6-trichlorophenol + oxidized putidaredoxin + H2O
show the reaction diagram
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2',4',6'-trichlorophenyl alpha-L-arabinofuranoside + H2O = 2,4,6-trichlorophenol + alpha-L-arabinofuranose
show the reaction diagram
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-

Activator in Enzyme-catalyzed Reactions (1 result)

EC NUMBER
COMMENTARY
LITERATURE
ENZYME 3D STRUCTURE
induction of MAR activity in wild type strain
-

Inhibitor in Enzyme-catalyzed Reactions (4 results)

EC NUMBER
COMMENTARY
LITERATURE
ENZYME 3D STRUCTURE
substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP; substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP
-

Enzyme Kinetic Parameters

kcat Value (Turnover Number) (4 results)

EC NUMBER
TURNOVER NUMBER [1/S]
TURNOVER NUMBER MAXIMUM [1/S]
COMMENTARY
LITERATURE
11.28
-
in 0.1 M acetate buffer pH 5.0, at 25°C

KM Value (4 results)

EC NUMBER
KM VALUE [MM]
KM VALUE MAXIMUM [MM]
COMMENTARY
LITERATURE
0.1359
-
-

IC50 Value (1 result)

EC NUMBER
IC50 VALUE
IC50 VALUE MAXIMUM
COMMENTARY
LITERATURE
0.00037
-
in 0.1 M sodium phosphate, pH 7.2, and 2 mM EDTA for 30 min at 16°C

References & Links

Links to other databases for 2,4,6-trichlorophenol

ChEBI
PubChem
ChEBI
PubChem