BDBM50177662 CHEMBL3813842
SMILES CC1(C)OCCn2c1nc1c(nc(nc21)-c1cnc(N)nc1)N1CCOCC1
InChI Key InChIKey=LGWACEZVCMBSKW-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 8 hits for monomerid = 50177662
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
University of Calabria
Curated by ChEMBL
University of Calabria
Curated by ChEMBL
Affinity DataIC50: 2nMAssay Description:Inhibition of P13Kalpha (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Human)
University of Calabria
Curated by ChEMBL
University of Calabria
Curated by ChEMBL
Affinity DataIC50: 46nMAssay Description:Inhibition of P13Kbeta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Human)
University of Calabria
Curated by ChEMBL
University of Calabria
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of P13Kgamma (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
University of Calabria
Curated by ChEMBL
University of Calabria
Curated by ChEMBL
Affinity DataIC50: 3nMAssay Description:Inhibition of P13Kdelta (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 70nMAssay Description:Inhibition of mTOR (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
University of Calabria
Curated by ChEMBL
University of Calabria
Curated by ChEMBL
Affinity DataKi: 2nMAssay Description:Inhibition of recombinant PI3Kalpha (unknown origin) using dioctanoylglycerol-PIP2 as substrate incubated for 30 mins in presence of TAMRA-PIP3 by fl...More data for this Ligand-Target Pair
Affinity DataKi: 70nMAssay Description:Inhibition of human recombinant mTOR (1360 to 2549 residues) expressed in insect cells assessed as inhibition of GFP-labeled 4-EBP1 phosphorylation a...More data for this Ligand-Target Pair
