null

SMILES CC(C)c1nn(-c2c(Cl)cccc2Cl)c2nc(Cc3ccc(OCCO)cc3)[nH]c(=O)c12

InChI Key InChIKey=RSQPNXBTPUXMQN-UHFFFAOYSA-N

PDB links: 1 PDB ID matches this monomer.

  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 13 hits for monomerid = 59227   

TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 839nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetCyclin-dependent kinase 6/G1/S-specific cyclin-D3(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 282nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 51nMAssay Description:Inhibition of HCT116 cell proliferation after 72hr of incubation with compounds was determined by SRB Assay.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetCyclin-dependent kinase 3/G1/S-specific cyclin-E1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 754nMAssay Description:Inhibition of GSK3-betaChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB82RHPubMed
TargetCDK-activating kinase assembly factor MAT1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 71nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 754nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed
TargetCyclin-H/Cyclin-dependent kinase 7(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 71nMAssay Description:Inhibition of Cdk7/H/MAT1Checked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB82RHPubMed
TargetCyclin-dependent kinase 6/G1/S-specific cyclin-D3(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 282nMAssay Description:Inhibition of Cdk6/cyclin D3Checked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB82RHPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of Cdk9Checked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB82RHPubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59227(Pyrazolopyrimidone analog, RGB-286147)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of in vitro kinase activity of purified CDKs.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3BR6PubMed