BDBM6248 2-(phenylamino)-8-propyl-7H,8H-pyrido[2,3-d]pyrimidin-7-one::N8 Pyrido[2,3-d]pyrimidin-7-one deriv. 40

SMILES CCCn1c2nc(Nc3ccccc3)ncc2ccc1=O

InChI Key InChIKey=ZEJXJYCOUVOWGJ-UHFFFAOYSA-N

Data  5 IC50

  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 = 6248   

TargetCyclin-A2/Cyclin-dependent kinase 2(Human)
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6248(2-(phenylamino)-8-propyl-7H,8H-pyrido[2,3-d]pyrimi...)
Affinity DataIC50: 50nMAssay 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 Depth
Date in BDB:
10/20/2005
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Human)
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6248(2-(phenylamino)-8-propyl-7H,8H-pyrido[2,3-d]pyrimi...)
Affinity DataIC50: 112nMAssay 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 Depth
Date in BDB:
10/20/2005
Entry Details Article
PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Human)
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6248(2-(phenylamino)-8-propyl-7H,8H-pyrido[2,3-d]pyrimi...)
Affinity DataIC50: 299nMAssay 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 Depth
Date in BDB:
10/20/2005
Entry Details Article
PubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1 [L188C](Human)
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6248(2-(phenylamino)-8-propyl-7H,8H-pyrido[2,3-d]pyrimi...)
Affinity DataIC50: 553nMAssay 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 Depth
Date in BDB:
10/20/2005
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
Parke-Davis Pharmaceutical Research

LigandPNGBDBM6248(2-(phenylamino)-8-propyl-7H,8H-pyrido[2,3-d]pyrimi...)
Affinity DataIC50: 6.60E+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 Depth
Date in BDB:
10/20/2005
Entry Details Article
PubMed