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BDBM50234039 CHEMBL4082553

SMILES: COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1

InChI Key: InChIKey=QPDYRCCMWUATHL-UHFFFAOYSA-N

Data: 9 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50234039   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cytochrome P450 2C9


(Homo sapiens (human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 (unknown origin)


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 1A


(Homo sapiens)
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 (unknown origin)


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 (unknown origin)


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 (unknown origin)


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 2B6


(Homo sapiens (Human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP2B6 (unknown origin)


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 (unknown origin) using BZR as substrate


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 2C8


(Homo sapiens (Human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP2C8 (unknown origin)


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1


(Homo sapiens (human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a 49n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of IDO1 in IFN-gamma stimulated human HeLa cells assessed as inhibition of kynurenine production preincubated with cells followed by IFN-g...


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (human))
BDBM50234039
PNG
(CHEMBL4082553)
Show SMILES COc1ccc(cc1C(O)=O)-c1ccc(Oc2cccc3CCCCc23)c(NC(=O)Nc2ccccc2C)c1
Show InChI InChI=1S/C32H30N2O5/c1-20-8-3-6-12-26(20)33-32(37)34-27-19-23(22-14-16-28(38-2)25(18-22)31(35)36)15-17-30(27)39-29-13-7-10-21-9-4-5-11-24(21)29/h3,6-8,10,12-19H,4-5,9,11H2,1-2H3,(H,35,36)(H2,33,34,37)
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n/an/a>3.00E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 (unknown origin) using BFC as substrate


Bioorg Med Chem Lett 27: 582-585 (2017)

More data for this
Ligand-Target Pair