BDBM50323734 3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)ethynyl)phenol::3-{[4-amino-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]ethynyl}phenol::CHEMBL1213120

SMILES CC(C)n1nc(C#Cc2cccc(O)c2)c2c(N)ncnc12

InChI Key InChIKey=HFGDXJQGICLTIE-UHFFFAOYSA-N

Data  6 IC50

PDB links: 1 PDB ID matches this monomer.

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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50323734   

TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
Medical Research Council-Laboratory Of Molecular Biology

Curated by ChEMBL
LigandPNGBDBM50323734(3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidi...)
Affinity DataIC50:  34nMAssay Description:Inhibition of p110alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
Medical Research Council-Laboratory Of Molecular Biology

Curated by ChEMBL
LigandPNGBDBM50323734(3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidi...)
Affinity DataIC50:  316nMAssay Description:Inhibition of p110betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
University Of Southern California

Curated by ChEMBL
LigandPNGBDBM50323734(3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidi...)
Affinity DataIC50:  8nMAssay Description:Inhibition of human wild-type Abl after 30 mins by phosphocellulose paper disk assay using 0.1 mM EAIYAAPFAKKK peptide substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
Medical Research Council-Laboratory Of Molecular Biology

Curated by ChEMBL
LigandPNGBDBM50323734(3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidi...)
Affinity DataIC50:  21nMAssay Description:Inhibition of p110deltaMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
University Of Southern California

Curated by ChEMBL
LigandPNGBDBM50323734(3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidi...)
Affinity DataIC50:  8nMAssay Description:Inhibition of Abl T315I mutant (unknown origin) after 30 mins by phosphocellulose paper disk assay using 0.1 mM EAIYAAPFAKKK peptide substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
Medical Research Council-Laboratory Of Molecular Biology

Curated by ChEMBL
LigandPNGBDBM50323734(3-((4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidi...)
Affinity DataIC50:  69nMAssay Description:Inhibition of p110gammaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed