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PubMed code 20060304

Compile data set for download or QSAR
Found 9 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310362
PNG
(3-(2'-Methoxyphenyl)-1H-naphtho[2,1-b]pyran-1-one ...)
Show SMILES COc1ccccc1-c1cc(=O)c2c(ccc3ccccc23)o1
Show InChI InChI=1S/C20H14O3/c1-22-17-9-5-4-8-15(17)19-12-16(21)20-14-7-3-2-6-13(14)10-11-18(20)23-19/h2-12H,1H3
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Article
PubMed
n/an/an/an/a 270n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310363
PNG
(3-(2'-Pyridinyl)-1H-naphtho[2,1-b]pyran-1-one | CH...)
Show SMILES O=c1cc(oc2ccc3ccccc3c12)-c1ccccn1
Show InChI InChI=1S/C18H11NO2/c20-15-11-17(14-7-3-4-10-19-14)21-16-9-8-12-5-1-2-6-13(12)18(15)16/h1-11H
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n/an/an/an/a 450n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50137506
PNG
((B(a)P) | 3,4-BP | 3,4-Benzopyrene | 3,4-Benzpyren...)
Show SMILES c1ccc2c(c1)cc1ccc3cccc4ccc2c1c34
Show InChI InChI=1S/C20H12/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14/h1-12H
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Article
PubMed
n/an/an/an/a 2.70E+3n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310359
PNG
(3-(2',6'-Dimethylphenyl)-1H-naphtho[2,1-b]pyran-1-...)
Show SMILES Cc1cccc(C)c1-c1cc(=O)c2c(ccc3ccccc23)o1
Show InChI InChI=1S/C21H16O2/c1-13-6-5-7-14(2)20(13)19-12-17(22)21-16-9-4-3-8-15(16)10-11-18(21)23-19/h3-12H,1-2H3
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PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310361
PNG
(3-(2',6'-Difluorophenyl)-1H-naphtho[2,1-b]pyran-1-...)
Show SMILES Fc1cccc(F)c1-c1cc(=O)c2c(ccc3ccccc23)o1
Show InChI InChI=1S/C19H10F2O2/c20-13-6-3-7-14(21)19(13)17-10-15(22)18-12-5-2-1-4-11(12)8-9-16(18)23-17/h1-10H
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PubMed
n/an/an/an/a 200n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50028963
PNG
(3-Phenyl-1H-naphtho[2,1-b]pyran-1-one | 3-Phenyl-b...)
Show SMILES O=c1cc(oc2ccc3ccccc3c12)-c1ccccc1
Show InChI InChI=1S/C19H12O2/c20-16-12-18(14-7-2-1-3-8-14)21-17-11-10-13-6-4-5-9-15(13)19(16)17/h1-12H
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PubMed
n/an/an/an/a 1.40E+3n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310358
PNG
(3-(2'-Methylphenyl)-1H-naphtho[2,1-b]pyran-1-one |...)
Show SMILES Cc1ccccc1-c1cc(=O)c2c(ccc3ccccc23)o1
Show InChI InChI=1S/C20H14O2/c1-13-6-2-4-8-15(13)19-12-17(21)20-16-9-5-3-7-14(16)10-11-18(20)22-19/h2-12H,1H3
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PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310360
PNG
(3-(2'-Fluorophenyl)-1H-naphtho[2,1-b]pyran-1-one |...)
Show SMILES Fc1ccccc1-c1cc(=O)c2c(ccc3ccccc23)o1
Show InChI InChI=1S/C19H11FO2/c20-15-8-4-3-7-14(15)18-11-16(21)19-13-6-2-1-5-12(13)9-10-17(19)22-18/h1-11H
PDB

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Article
PubMed
n/an/an/an/a 330n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
Aryl hydrocarbon receptor


(Homo sapiens (Human))
BDBM50310357
PNG
(CHEMBL599552 | indigo)
Show SMILES O=C1C(Nc2ccccc12)=C1Nc2ccccc2C1=O |w:2.2|
Show InChI InChI=1S/C16H10N2O2/c19-15-9-5-1-3-7-11(9)17-13(15)14-16(20)10-6-2-4-8-12(10)18-14/h1-8,17-18H
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Article
PubMed
n/an/an/an/a 1.70E+3n/an/an/an/a



The University of Tokyo

Curated by ChEMBL


Assay Description
Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assay


Bioorg Med Chem 18: 1194-203 (2010)


Article DOI: 10.1016/j.bmc.2009.12.036
BindingDB Entry DOI: 10.7270/Q2GX4BNF
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%