null

SMILES O=C1C(CCc2ccccc12)=Cc1cnc[nH]1

InChI Key InChIKey=SEHNFQNDEFTGRO-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50049763   

TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Rattus norvegicus)
American University of Ras Al Khaimah

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of rat ovarian aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC84Q6PubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed