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BDBM50366426 CHEMBL4161819

SMILES: Cl.Cl.CCc1ccncc1-c1ccc(CN)s1

InChI Key: InChIKey=PMFPLVYHUVJODG-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 = 50366426   
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 2B6


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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n/an/a 93n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2B6 in human liver microsomes using bupropion as substrate preincubated for 5 mins followed by addition of NADPH-regenerating system...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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PubMed
n/an/a 4.00E+3n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate preincubated for 5 mins followed by addition of NADPH-regenerating syste...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 2C8


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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n/an/a 1.50E+3n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2C8 in human liver microsomes using amodiaquine as substrate preincubated for 5 mins followed by addition of NADPH-regenerating syst...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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n/an/a 1.60E+4n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 in human liver microsomes using diclofenac as substrate preincubated for 5 mins followed by addition of NADPH-regenerating syste...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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n/an/a 1.30E+4n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 in human liver microsomes using midazolam as substrate preincubated for 5 mins followed by addition of NADPH-regenerating system...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 2E1


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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n/an/a 230n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2E1 in human liver microsomes using chlorzoxazone as substrate preincubated for 5 mins followed by addition of NADPH-regenerating sy...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
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PubMed
n/an/a 840n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using omeprazole as substrate preincubated for 5 mins followed by addition of NADPH-regenerating syst...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 2A6


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
PDB
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PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 17n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2A6 in human liver microsomes using coumarin as substrate preincubated for 5 mins followed by addition of NADPH-regenerating system ...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50366426
PNG
(CHEMBL4161819)
Show SMILES Cl.Cl.CCc1ccncc1-c1ccc(CN)s1
Show InChI InChI=1S/C12H14N2S/c1-2-9-5-6-14-8-11(9)12-4-3-10(7-13)15-12/h3-6,8H,2,7,13H2,1H3
PDB

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PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 4.50E+3n/an/an/an/an/an/a



Washington State University

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 in human liver microsomes using dextromethorphan as substrate preincubated for 5 mins followed by addition of NADPH-regenerating...


J Med Chem 61: 7065-7086 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00084
BindingDB Entry DOI: 10.7270/Q2QN69B5
More data for this
Ligand-Target Pair