BDBM50517833 CHEMBL4472621

SMILES O=C(Nc1ccccc1)c1cn2cc(ccc2n1)-c1ccccn1

InChI Key InChIKey=VMCCGRKQGHMWMG-UHFFFAOYSA-N

Data  3 IC50  3 EC50

  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 6 hits for monomerid = 50517833   

TargetCytochrome P450 2C9(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50517833(CHEMBL4472621)
Affinity DataIC50:  8.60E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50517833(CHEMBL4472621)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNuclear receptor subfamily 4 group A member 2(Mus musculus)
Sanofi

Curated by ChEMBL
LigandPNGBDBM50517833(CHEMBL4472621)
Affinity DataEC50:  1nMAssay Description:Agonist activity at Nurr1 in mouse N2A cells harboring NBRE by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50517833(CHEMBL4472621)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNuclear receptor subfamily 4 group A member 2(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50517833(CHEMBL4472621)
Affinity DataEC50:  140nMAssay Description:Agonist activity at full-length Gal4-fused NOT (unknown origin) expressed in CHO cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50517833(CHEMBL4472621)
Affinity DataEC50: >1.00E+4nMAssay Description:Activation of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed