BDBM5590 2-arylamino-pyrimidine deriv. 8b::4-{[4-amino-6-(cyclohexylmethoxy)pyrimidin-2-yl]amino}benzene-1-sulfonamide

SMILES Nc1cc(OCC2CCCCC2)nc(Nc2ccc(cc2)S(N)(=O)=O)n1

InChI Key InChIKey=ALNJIRVGTQKZMG-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 5590   

TargetCyclin-A2 [171-432]/Cyclin-dependent kinase 2(Human)
University of Newcastle

LigandPNGBDBM5590(4-{[4-amino-6-(cyclohexylmethoxy)pyrimidin-2-yl]am...)
Affinity DataIC50: 2.90E+3nMpH: 7.5 T: 2°CAssay Description:The enzyme was assayed with substrate histone H1 in the presence of 12.5 uM ATP/[gamma-32P] ATP. IC50 is the inhibitor concentration, which inhibits ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2005
Entry Details Article
PubMed
LigandPNGBDBM5590(4-{[4-amino-6-(cyclohexylmethoxy)pyrimidin-2-yl]am...)
Affinity DataIC50: 2.93E+3nMAssay Description:Inhibition of CDK2/cyclinA (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article

TargetCyclin-dependent kinase 1/G2/mitotic-specific cyclin-B(Spiny starfish)
University of Newcastle

LigandPNGBDBM5590(4-{[4-amino-6-(cyclohexylmethoxy)pyrimidin-2-yl]am...)
Affinity DataIC50: 5.30E+3nMpH: 7.5 T: 2°CAssay Description:The enzyme was assayed with substrate histone H1 in the presence of 12.5 uM ATP/[gamma-32P] ATP. IC50 is the inhibitor concentration, which inhibits ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2005
Entry Details Article
PubMed