Compile Data Set for Download or QSAR
Report error Found 8 Enz. Inhib. hit(s) with all data for entry = 5706
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 92749BDBM92749(Pentachlorophenol (PCP))
Affinity DataKd: <50nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 92751BDBM92751(Tetrachlorohydroquinone (TCHQ))
Affinity DataKd:  4.20E+3nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 92752BDBM92752(2,4,6-Trichlorophenol (2,4,6-TriCP))
Affinity DataKd:  7.00E+3nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 92750BDBM92750(2,3,4,6-Tetrachlorophenol (TCP))
Affinity DataKd:  1.10E+4nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 92753BDBM92753(2,6-Dichlorophenol | 2,6-Dichlorophenol (2,6-DCP))
Affinity DataKd:  4.55E+4nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 92754BDBM92754(3,5-Dichlorphenol (3,5-DCP))
Affinity DataKd: >5.00E+5nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 91350BDBM91350(SMR001307309 | cid_11859 | 3,4,5-tris(chloranyl)ph...)
Affinity DataKd: >5.00E+5nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed
TargetPentachlorophenol 4-monooxygenase(Sphingobium chlorophenolicum)
University of Colorado Boulder

LigandChemical structure of BindingDB Monomer ID 36301BDBM36301(2-Chlorophenol (2-CP) | 2-chlorophenol)
Affinity DataKd: >1.00E+6nMAssay Description:Formation of the hydroxylated product and depletion of NADPH were measured following ethyl acetate extraction of the reaction mixture.More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/5/2013
Entry Details Article
PubMed