BDBM50313698 CHEMBL1082237::N-(6-(4-hydroxyphenyl)-1H-indazol-3-yl)butyramide::N-[6-(4-hydroxyphenyl)-1H-indazol-3-yl]butanamide

SMILES CCCC(=O)Nc1n[nH]c2cc(ccc12)-c1ccc(O)cc1

InChI Key InChIKey=VCIZMGNKKFEEHA-UHFFFAOYSA-N

Data  4 IC50

  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 4 hits for monomerid = 50313698   

TargetAurora kinase B(Human)
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313698(N-[6-(4-hydroxyphenyl)-1H-indazol-3-yl]butanamide ...)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Aurora kinase 2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetCytochrome P450 1A2(Human)
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313698(N-[6-(4-hydroxyphenyl)-1H-indazol-3-yl]butanamide ...)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human recombinant CYP1A2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetGlycogen synthase kinase-3 beta(Human)
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313698(N-[6-(4-hydroxyphenyl)-1H-indazol-3-yl]butanamide ...)
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of human recombinant GSK3-beta by kinetic assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetGlycogen synthase kinase-3 beta(Human)
Sanofi-Aventis

Curated by ChEMBL
LigandPNGBDBM50313698(N-[6-(4-hydroxyphenyl)-1H-indazol-3-yl]butanamide ...)
Affinity DataIC50: 44nMAssay Description:Inhibition of human recombinant GSK3-beta using gamma[33P]-ATP after 30 mins by scintillation proximity assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed