BDBM8037 2-Anilino-4-(thiazol-5-yl)pyrimidine deriv. 8::4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamine::4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine::4-(dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine, 1::CS12

SMILES Cc1nc(C)c(s1)-c1ccnc(N)n1

InChI Key InChIKey=CTFDMGIBHFQWKB-UHFFFAOYSA-N

Data  4 KI  3 IC50  2 Kd  1 Koff  1 Kon

  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 11 hits for monomerid = 8037   

TargetCyclin-dependent kinase 2(Human)
Cyclacel

LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataIC50: 6.50E+3nMAssay Description:In vitro inhibition assay using human recombinant CDK2 and human recombinant cyclin A2.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataIC50: 6.50E+3nMAssay Description:In vitro inhibition assay using human recombinant CDK2 and human recombinant cyclin A2.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKd:  3.03E+4nMpH: 7.5 T: 2°CAssay Description:OctetRedMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCyclin-dependent kinase 2(Human)
Cyclacel

LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKd:  3.03E+4nMAssay Description:OctetRed_Method2More data for this Ligand-Target Pair
In DepthDetails
D3R

TargetCyclin-dependent kinase 2(Human)
Cyclacel

LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKoff:  8.22E+4s-1Assay Description:OctetRed_Method3More data for this Ligand-Target Pair
In DepthDetails
D3R

TargetCyclin-dependent kinase 2(Human)
Cyclacel

LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKon:  1.42M-1s-1Assay Description:OctetRed_Method3More data for this Ligand-Target Pair
In DepthDetails
D3R

TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataIC50: 6.46E+3nMAssay Description:Inhibition of CDK2/Cyclin E (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Cyclacel

LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKi:  396nMAssay Description:Inhibition of CDK2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKi:  6.50E+3nM ΔG°:  -7.19kcal/molepH: 7.4 T: 2°CAssay Description:In vitro kinase assay using purified enzyme, was incubated at 30 °C with substrate, and test compounds in the presence of 100 uM ATP/ [gamma-32P...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Human)
University of Tours

Curated by ChEMBL
LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKi:  6.50E+3nMAssay Description:Inhibition of recombinant human His6-tagged CDK2/cyclin E expressed in baculovirus infected sf9 cells using histone H1 susbtrate in presence of [gamm...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM8037(4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-amine...)
Affinity DataKi:  1.60E+4nM ΔG°:  -6.65kcal/moleT: 2°CAssay Description:In vitro kinase assay using purified enzyme, was incubated at 30 °C with substrate, and test compounds in the presence of 100 uM ATP/ [gamma-32P...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed