null

SMILES CCCCn1c2nc(Nc3ccccc3)ncc2ccc1=O

InChI Key InChIKey=ZEHXSPZMRLUPSR-UHFFFAOYSA-N

  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 5 hits for monomerid = 6250   

TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1 [L188C](Homo sapiens (Human))
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6250(8-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:The enzyme was assayed with substrate GST- retinoblastoma in the presence of 25 uM ATP/[gamma-32P] ATP. IC50 is the inhibitor concentration, which in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00N4PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6250(8-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:The enzyme was assayed with substrate GST- retinoblastoma in the presence of 12 uM ATP/[gamma-32P] ATP. IC50 is the inhibitor concentration, which in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00N4PubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6250(8-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 5.29E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00N4PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6250(8-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:The enzyme was assayed with substrate GST- retinoblastoma in the presence of 12 uM ATP/[gamma-32P] ATP. IC50 is the inhibitor concentration, which in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00N4PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6250(8-Butyl-2-phenylamino-8H-pyrido[2,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:The enzyme was assayed with substrate GST- retinoblastoma in the presence of 12 uM ATP/[gamma-32P] ATP. IC50 is the inhibitor concentration, which in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00N4PubMed