BDBM50310357 CHEMBL599552::indigo

SMILES O=C1C(Nc2ccccc12)=C1Nc2ccccc2C1=O

InChI Key InChIKey=COHYTHOBJLSHDF-UHFFFAOYSA-N

Data  7 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50310357   

TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of GST-tagged recombinant human CDK2/cyclin E expressed in insect SF-9 cells after 10 mins by scintillation counting analysis in presence ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAryl hydrocarbon receptor(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataEC50:  1.70E+3nMAssay Description:Agonist activity at aryl hydrocarbon receptor in human MCF7 cells after 24 hrs CYP1A1-dependent EROD assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50:  7.00E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 2 (CDK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Vanderbilt University School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50:  2.80E+4nMAssay Description:Inhibition of Src tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMalate dehydrogenase(Thermus thermophilus)
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50:  6.00E+4nMAssay Description:Inhibitory activity against malate dehydrogenase (MDH) from Thermus flavusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 1-cyclin B of M-phase Marthasterias glacialis oocytesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen B(Homo sapiens (Human))
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50310357(CHEMBL599552 | indigo)
Affinity DataIC50:  9.00E+4nMAssay Description:Inhibitory activity against Chymotrypsinogen from Thermus flavusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed