BDBM5476 6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine::CHEMBL407876::O6-Substituted Guanine Deriv. 16

SMILES CC(=C)COc1nc(N)nc2nc[nH]c12

InChI Key InChIKey=SKVCEFNZQMPWEN-UHFFFAOYSA-N

Data  6 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 6 hits for monomerid = 5476   

TargetMethylated-DNA--protein-cysteine methyltransferase(Human)
Newcastle University

Curated by ChEMBL
LigandPNGBDBM5476(6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine |...)
Affinity DataIC50: 1.35E+4nMAssay Description:concentration required to reduce AGT activity to 50% of control rate in intact HT-29 human colorectal carcinoma cells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMethylated-DNA--protein-cysteine methyltransferase(Human)
Newcastle University

Curated by ChEMBL
LigandPNGBDBM5476(6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine |...)
Affinity DataIC50: 1.35E+4nMAssay Description:concentration required to reduce AGT activity to 50% of control rate in intact HT-29 human colorectal carcinoma cells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetMethylated-DNA--protein-cysteine methyltransferase(Human)
Newcastle University

Curated by ChEMBL
LigandPNGBDBM5476(6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine |...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of AGT activity to 50% of control rate in HT-29 cell extractMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCyclin-dependent kinase 1/G2/mitotic-specific cyclin-B(Spiny starfish)
University of Newcastle

LigandPNGBDBM5476(6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine |...)
Affinity DataIC50: 3.20E+4nMAssay 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:
8/17/2005
Entry Details Article
PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Human)
University of Zurich

Curated by ChEMBL
LigandPNGBDBM5476(6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine |...)
Affinity DataIC50: 3.20E+4nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetCyclin-A2 [171-432]/Cyclin-dependent kinase 2(Human)
University of Newcastle

LigandPNGBDBM5476(6-[(2-methylprop-2-en-1-yl)oxy]-9H-purin-2-amine |...)
Affinity DataIC50: 3.50E+4nMAssay 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:
8/17/2005
Entry Details Article
PubMed