BDBM7722 (3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-sulfamoylphenyl)hydrazin-1-ylidene]-2,3-dihydro-1H-indole-5-carboxamide::3-{[4-(Aminosulfonyl)phenyl]hydrazono}-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-2,3-dihydro-1H-indole-5-carboxamide::CS261::Oxindole-Based Inhibitor 58

SMILES NS(=O)(=O)c1ccc(NN=C2C(=O)Nc3ccc(cc23)C(=O)NCCc2cnc[nH]2)cc1

InChI Key InChIKey=CQSUILWVYSOEJC-UHFFFAOYSA-N

Data  4 IC50  4 Kd

  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 8 hits for monomerid = 7722   

TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Glaxosmithkline

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataIC50:  69nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence 1.4 uM ATP/[gamma-32P] ATP. A...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Glaxosmithkline

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataIC50:  12nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence 1.4 uM ATP/[gamma-32P] ATP. A...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Csar

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataKd:  251nMpH: 7.5 T: 2°CAssay Description:OctetRedMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Csar

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataIC50:  12nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Csar

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataKd:  1.28E+3nMpH: 7.5 T: 2°CAssay Description:ITCMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Glaxosmithkline

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataKd:  82nMpH: 7.5 T: 2°CAssay Description:OctetRedMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
University Of Zurich

Curated by ChEMBL
LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataIC50:  60nMAssay Description:Inhibition of CDK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Csar

LigandPNGBDBM7722((3Z)-N-[2-(1H-imidazol-4-yl)ethyl]-2-oxo-3-[2-(4-s...)
Affinity DataKd:  3.12E+3nMpH: 7.5 T: 2°CAssay Description:ThermofluorMore data for this Ligand-Target Pair
In DepthDetails PubMed