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BDBM50366410 CHEMBL4163694

SMILES: Cl.Cl.NCC#Cc1cnccc1-c1ccco1

InChI Key: InChIKey=ZDBFFUPFHFIASN-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 = 50366410   
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 1A


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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n/an/a 1.40E+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 2C9


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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n/an/a 2.80E+3n/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 2C8


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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n/an/a 7.50E+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 2C19


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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n/an/a 3.70E+3n/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 2B6


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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UniChem
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n/an/a 5.00E+3n/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 2D6


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 3.90E+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
Cytochrome P450 2E1


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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UniChem
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n/an/a 1.90E+3n/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 3A4


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
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UniChem
Article
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n/an/a 1.10E+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 2A6


(Homo sapiens (Human))
BDBM50366410
PNG
(CHEMBL4163694)
Show SMILES Cl.Cl.NCC#Cc1cnccc1-c1ccco1
Show InChI InChI=1S/C12H10N2O/c13-6-1-3-10-9-14-7-5-11(10)12-4-2-8-15-12/h2,4-5,7-9H,6,13H2
PDB
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Reactome pathway
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UniChem
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n/an/a 560n/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