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SMILES: CC1(CC(=O)NCc2ccccc2Sc2ccccc2CO)CC2(CCCCC2)OO1

InChI Key: InChIKey=XHQRQWJOOLSDNW-UHFFFAOYSA-N

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 5 hits for monomerid = 50301847   
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 1A2


(Homo sapiens (Human))
BDBM50301847
PNG
(CHEMBL565360 | N-(2-(2-(hydroxymethyl)phenylthio)b...)
Show SMILES CC1(CC(=O)NCc2ccccc2Sc2ccccc2CO)CC2(CCCCC2)OO1
Show InChI InChI=1S/C25H31NO4S/c1-24(18-25(30-29-24)13-7-2-8-14-25)15-23(28)26-16-19-9-3-5-11-21(19)31-22-12-6-4-10-20(22)17-27/h3-6,9-12,27H,2,7-8,13-18H2,1H3,(H,26,28)
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n/an/a>5.00E+3n/an/an/an/an/an/a



Institute Infectious Diseases Initiative

Curated by ChEMBL


Assay Description
Inhibition of human CYP1A2


Bioorg Med Chem Lett 19: 5657-60 (2009)


Article DOI: 10.1016/j.bmcl.2009.08.024
BindingDB Entry DOI: 10.7270/Q22R3RRX
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50301847
PNG
(CHEMBL565360 | N-(2-(2-(hydroxymethyl)phenylthio)b...)
Show SMILES CC1(CC(=O)NCc2ccccc2Sc2ccccc2CO)CC2(CCCCC2)OO1
Show InChI InChI=1S/C25H31NO4S/c1-24(18-25(30-29-24)13-7-2-8-14-25)15-23(28)26-16-19-9-3-5-11-21(19)31-22-12-6-4-10-20(22)17-27/h3-6,9-12,27H,2,7-8,13-18H2,1H3,(H,26,28)
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n/an/a 2.20E+3n/an/an/an/an/an/a



Institute Infectious Diseases Initiative

Curated by ChEMBL


Assay Description
Inhibition of human CYP2C9


Bioorg Med Chem Lett 19: 5657-60 (2009)


Article DOI: 10.1016/j.bmcl.2009.08.024
BindingDB Entry DOI: 10.7270/Q22R3RRX
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50301847
PNG
(CHEMBL565360 | N-(2-(2-(hydroxymethyl)phenylthio)b...)
Show SMILES CC1(CC(=O)NCc2ccccc2Sc2ccccc2CO)CC2(CCCCC2)OO1
Show InChI InChI=1S/C25H31NO4S/c1-24(18-25(30-29-24)13-7-2-8-14-25)15-23(28)26-16-19-9-3-5-11-21(19)31-22-12-6-4-10-20(22)17-27/h3-6,9-12,27H,2,7-8,13-18H2,1H3,(H,26,28)
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n/an/a 1.20E+3n/an/an/an/an/an/a



Institute Infectious Diseases Initiative

Curated by ChEMBL


Assay Description
Inhibition of human CYP3A4


Bioorg Med Chem Lett 19: 5657-60 (2009)


Article DOI: 10.1016/j.bmcl.2009.08.024
BindingDB Entry DOI: 10.7270/Q22R3RRX
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50301847
PNG
(CHEMBL565360 | N-(2-(2-(hydroxymethyl)phenylthio)b...)
Show SMILES CC1(CC(=O)NCc2ccccc2Sc2ccccc2CO)CC2(CCCCC2)OO1
Show InChI InChI=1S/C25H31NO4S/c1-24(18-25(30-29-24)13-7-2-8-14-25)15-23(28)26-16-19-9-3-5-11-21(19)31-22-12-6-4-10-20(22)17-27/h3-6,9-12,27H,2,7-8,13-18H2,1H3,(H,26,28)
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PC sid
UniChem
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n/an/a>5.00E+3n/an/an/an/an/an/a



Institute Infectious Diseases Initiative

Curated by ChEMBL


Assay Description
Inhibition of human CYP2D6


Bioorg Med Chem Lett 19: 5657-60 (2009)


Article DOI: 10.1016/j.bmcl.2009.08.024
BindingDB Entry DOI: 10.7270/Q22R3RRX
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50301847
PNG
(CHEMBL565360 | N-(2-(2-(hydroxymethyl)phenylthio)b...)
Show SMILES CC1(CC(=O)NCc2ccccc2Sc2ccccc2CO)CC2(CCCCC2)OO1
Show InChI InChI=1S/C25H31NO4S/c1-24(18-25(30-29-24)13-7-2-8-14-25)15-23(28)26-16-19-9-3-5-11-21(19)31-22-12-6-4-10-20(22)17-27/h3-6,9-12,27H,2,7-8,13-18H2,1H3,(H,26,28)
PDB
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n/an/a 2.90E+3n/an/an/an/an/an/a



Institute Infectious Diseases Initiative

Curated by ChEMBL


Assay Description
Inhibition of human CYP2C19


Bioorg Med Chem Lett 19: 5657-60 (2009)


Article DOI: 10.1016/j.bmcl.2009.08.024
BindingDB Entry DOI: 10.7270/Q22R3RRX
More data for this
Ligand-Target Pair