BDBM8065 2-Anilino-4-(thiazol-5-yl)pyrimidine deriv. 36::3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino]-benzonitrile::3-{[4-(2,4-dimethyl-1,3-thiazol-5-yl)pyrimidin-2-yl]amino}benzonitrile::CS15

SMILES Cc1nc(C)c(s1)-c1ccnc(Nc2cccc(c2)C#N)n1

InChI Key InChIKey=JFMGVNVAZVRZMU-UHFFFAOYSA-N

Data  2 KI  5 Kd  2 Koff  2 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 = 8065   

TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKd:  2.59E+3nMpH: 7.5 T: 2°CAssay Description:ThermofluorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2012
Entry Details PubMed
TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKd:  557nMpH: 7.5 T: 2°CAssay Description:OctetRedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2012
Entry Details PubMed
LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKd:  161nMpH: 7.5 T: 2°CAssay Description:OctetRedMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2012
Entry Details PubMed
TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKd:  161nMAssay Description:OctetRed_Method2More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/10/2017
Entry Details
D3R

TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKoff:  1.58E+5s-1Assay Description:OctetRed_Method3More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/10/2017
Entry Details
D3R

TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKon:  0.0200M-1s-1Assay Description:OctetRed_Method3More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/10/2017
Entry Details
D3R

TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKd:  557nMAssay Description:OctetRed_Method1More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/10/2017
Entry Details
D3R

TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKoff:  1.13E+5s-1Assay Description:OctetRed_Method3More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/10/2017
Entry Details
D3R

TargetCyclin-dependent kinase 2(Human)
Csar

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKon:  0.0367M-1s-1Assay Description:OctetRed_Method3More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/10/2017
Entry Details
D3R

LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKi:  300nM ΔG°:  -9.04kcal/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 Depth
Date in BDB:
3/13/2006
Entry Details Article
PubMed
LigandPNGBDBM8065(3-[4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-ylamino...)
Affinity DataKi:  480nM ΔG°:  -8.76kcal/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 Depth
Date in BDB:
3/13/2006
Entry Details Article
PubMed