null

SMILES COc1ccc(Cl)c(Nc2nc3ccccc3nc2NS(=O)(=O)c2cccc(NC(=O)C(C)(C)N)c2)c1

InChI Key InChIKey=QINPEPAQOBZPOF-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50197062   

TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
Curtin University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human recombinant PI3Kgamma by luciferase-luciferin-coupled chemiluminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PG1TPXPubMed
TargetPhosphatidylinositol 3-kinase catalytic subunit type 3(Homo sapiens (Human))
Curtin University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of N-terminal tagged full-length human VPS34 by luciferase-luciferin-coupled chemiluminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PG1TPXPubMed
TargetDNA-dependent protein kinase catalytic subunit(Homo sapiens (Human))
Curtin University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human DNA-PK by by luciferase-luciferin-coupled chemiluminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PG1TPXPubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
Ain Shams University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Reversible competitive inhibition of PI3K p110beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HCBPubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
Curtin University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 383nMAssay Description:Reversible competitive inhibition of PI3K p110gamma (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HCBPubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
Ain Shams University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Reversible competitive inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HCBPubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
Ain Shams University

Curated by ChEMBL
LigandPNGBDBM50197062(Pilaralisib | SAR-245408 | XL-147)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Reversible competitive inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HCBPubMed