Compile Data Set for Download or QSAR
Found 20 Enz. Inhib. hit(s) with all data for assayid = 1 entry = 4262
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59229(Pyrazolopyrimidone analog, RGB-286331)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay 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.

LigandPNGBDBM59228(Pyrazolopyrimidone analog, RGB-285940)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay 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 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
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59230(Pyrazolopyrimidone analog, RGB-285960)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
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
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/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59229(Pyrazolopyrimidone analog, RGB-286331)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay 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: 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
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
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM50079331(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(3-hydroxy-1-m...)copy SMILEScopy InChI
Affinity DataIC50: 155nMAssay 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.

LigandPNGBDBM59228(Pyrazolopyrimidone analog, RGB-285940)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay 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.

LigandPNGBDBM59230(Pyrazolopyrimidone analog, RGB-285960)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay 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.

LigandPNGBDBM50079331(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(3-hydroxy-1-m...)copy SMILEScopy InChI
Affinity DataIC50: 485nMAssay 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.

LigandPNGBDBM50079331(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(3-hydroxy-1-m...)copy SMILEScopy InChI
Affinity DataIC50: 663nMAssay 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))
GPC Biotech, Inc.

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-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 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
GPC Biotech, Inc.

LigandPNGBDBM59228(Pyrazolopyrimidone analog, RGB-285940)copy SMILEScopy InChI
Affinity DataIC50: 858nMAssay 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.

LigandPNGBDBM50079331(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(3-hydroxy-1-m...)copy SMILEScopy InChI
Affinity DataIC50: 1.34E+3nMAssay 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.

LigandPNGBDBM59230(Pyrazolopyrimidone analog, RGB-285960)copy SMILEScopy InChI
Affinity DataIC50: 1.75E+3nMAssay 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