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BDBM50078824 2-Phenyl-1H-imidazole::CHEMBL14189::US9138393, 2-Phenylimidazole::US9144538, 2-Phenylimidazole

SMILES: c1c[nH]c(n1)-c1ccccc1

InChI Key: InChIKey=ZCUJYXPAKHMBAZ-UHFFFAOYSA-N

Data: 1 KI  5 IC50  2 Kd

PDB links: 3 PDB IDs match this monomer.

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 8 hits for monomerid = 50078824   
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
Nischarin


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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Article
PubMed
1.26E+3n/an/an/an/an/an/an/an/a



Universit£ d'Orl£ans

Curated by ChEMBL


Assay Description
Binding affinity for imidazoline receptor I-2 in rabbit kidney homogenate (relative to [3H]-Idazoxan radioligand)


J Med Chem 43: 1109-22 (2000)


Article DOI: 10.1021/jm991124t
BindingDB Entry DOI: 10.7270/Q2SB48G9
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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US Patent
n/an/a>1.00E+4n/an/an/an/an/an/a



The Procter & Gamble Company

US Patent


Assay Description
A commercially available P450-GLO Assay kit (Promega Corporation, Madison Wis.) is used to screen various compounds for CYP3A4A inhibition activity. ...


US Patent US9138393 (2015)


BindingDB Entry DOI: 10.7270/Q2GF0S8J
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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US Patent
n/an/a>5.00E+5n/an/an/an/a7.4n/a



The Procter & Gamble Company

US Patent


Assay Description
All procedures were carried out under minimal light in order to prevent degradation of the retinoid samples.Microsomal preparation: one lobe of fresh...


US Patent US9144538 (2015)


BindingDB Entry DOI: 10.7270/Q22806DV
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase mTOR


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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n/an/an/a 1.00E+5n/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Dissociation constant when binding to FK506 binding protein (FKBP).


J Med Chem 42: 2498-503 (1999)


Article DOI: 10.1021/jm990073x
BindingDB Entry DOI: 10.7270/Q2639NZB
More data for this
Ligand-Target Pair
Nitric Oxide Synthase, inducible


(Mus musculus (mouse))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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n/an/a>1.00E+6n/an/an/an/an/an/a



Wake Forest University Winston-Salem

Curated by ChEMBL


Assay Description
Inhibition of purified mouse inducible nitric oxide synthase catalyzed [14C]-L-citrulline production at a compound concentration of 1 mM in presence ...


Bioorg Med Chem Lett 9: 2953-8 (1999)


BindingDB Entry DOI: 10.7270/Q27943W9
More data for this
Ligand-Target Pair
Adenosine kinase


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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n/an/an/a 3.00E+6n/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human adenosine kinase


J Med Chem 43: 4781-6 (2000)


BindingDB Entry DOI: 10.7270/Q289154F
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
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US Patent
n/an/a>5.00E+5n/an/an/an/a7.44



The Procter & Gamble Company

US Patent


Assay Description
Microsomal preparation: One lobe of fresh pig liver is obtained (e.g., at about the time of slaughter from a food-processing company) and immediately...


US Patent US9138393 (2015)


BindingDB Entry DOI: 10.7270/Q2GF0S8J
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50078824
PNG
(2-Phenyl-1H-imidazole | CHEMBL14189 | US9138393, 2...)
Show SMILES c1c[nH]c(n1)-c1ccccc1
Show InChI InChI=1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
PDB
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US Patent
n/an/a>1.00E+4n/an/an/an/an/an/a



The Procter & Gamble Company

US Patent


Assay Description
Cytochrome P450 is a large and diverse group of enzymes that catalyze the oxidation of organic substances. Some members of the CYP family contribute ...


US Patent US9144538 (2015)


BindingDB Entry DOI: 10.7270/Q22806DV
More data for this
Ligand-Target Pair