Report error Found 16693 Enz. Inhib. hit(s) with Target = 'Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform'
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.00100nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.00300nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.00300nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.00500nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.00500nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.00700nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.0200nMAssay Description:Inhibition of P13Kdelta (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.0240nMAssay Description:Binding affinity to p110 delta (unknown origin) assessed as inhibition constant in presence of ATP by TR-FRET assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0350nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0350nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0360nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0400nMAssay Description:Inhibition of PI3Kdelta (unknown origin) preincubated for 30 mins followed by insulin stimulation for 5 mins by Western blot analysisMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0430nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0430nMAssay Description:Enzymatic activity of the class I PI3K isoforms in the presence of the compounds of Table 1 above was measured using a time-resolved fluorescence res...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0430nMAssay Description:The TR-FRET assay can monitor formation of the product 3,4,5-inositol triphosphate molecule (PIP3) as it competed with fluorescently labeled PIP3 for...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0480nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0600nMAssay Description:Inhibition of PI3Kdelta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.0790nMAssay Description:PI3K Binding assays are intended for determining the biochemical potency of small molecule PI3K inhibitors. The PI3K lipid kinase reaction is perform...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.0794nMAssay Description:Inhibition of PI3Kdelta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.0794nMAssay Description:Inhibition of PI3Kdelta (unknown origin) using PIP2 as substrate preincubated for 15 mins followed by substrate addition measured after 60 mins by HT...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0800nMAssay Description:Inhibition of recombinant human full length P13Kdelta expressed in Sf9 cells assessed as reduction in ATP-dependent phosphorylation by chromatography...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0860nMAssay Description:Enzymatic activity of the class I PI3K isoforms in the presence of the compounds of Table 1 above was measured using a time-resolved fluorescence res...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.0860nMAssay Description:The TR-FRET assay can monitor formation of the product 3,4,5-inositol triphosphate molecule (PIP3) as it competed with fluorescently labeled PIP3 for...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:Inhibition of PI3Kdelta (unknown origin) after 60 mins using fluorescein-labeled kinase tracer by HTRF assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:Inhibition of PI3Kdelta (unknown origin) assessed as inhibition of AKT phosphorylation by cell-based HTRF assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:Inhibition of PI3Kdelta in human SUDHL6 cellsMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:Inhibition of PI-3K delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:Inhibition of PI3Kdelta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.100nMAssay Description:TR-FRET monitored the formation of 3,4,5-inositol triphosphate molecule that competed with fluorescently labeled PIP3 for binding to the GRP-1 plecks...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.102nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.106nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.107nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.116nMAssay Description:Inhibition of p110 delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.120nMAssay Description:Inhibition of PI3Kdelta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.122nMAssay Description:Inhibition of human PI3KdeltaMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKi: 0.126nMAssay Description:Inhibition of PI3Kdelta (unknown origin) using PIP2 as substrate preincubated for 15 mins followed by substrate addition measured after 60 mins by HT...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.140nMAssay Description:Enzymatic activity of the class I PI3K isoforms in the presence of the compounds of Table 1 above was measured using a time-resolved fluorescence res...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.140nMAssay Description:The TR-FRET assay can monitor formation of the product 3,4,5-inositol triphosphate molecule (PIP3) as it competed with fluorescently labeled PIP3 for...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.160nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.178nMpH: 7.5Assay Description:PI3K enzymatic activity was assayed by measuring the amount of product phosphatidylinositol 3,4,5-phosphate (PIP3) formed from substrate 4,5 phosphat...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.180nMAssay Description:Inhibition of PI3Kdelta (unknown origin) using PIP2 as substrate by ADP-Glo assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.180nMAssay Description:1) Preparation of buffer salt solution: A 10× buffer salt solution with a pH of 7.5 containing 500 mM HEPES, 500 mM NaCl, and 30 mM MgCl2 was prepare...More data for this Ligand-Target Pair
Ligand InfoSimilars
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.180nMAssay Description:Inhibition of PI3Kdelta (unknown origin) using PIP2 as substrate incubated for 1 hr in presence of ATP by ADP-Glo assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataKd: 0.200nMAssay Description:Binding affinity to PI3Kdelta in human HL60 cell extract measured after 2 hrs by kinobeads based pull down assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:The ADP-Glo format PI3K assays were performed in Proxiplate 384-well plates (Perkin Elmer #6008280). The final assay volume was 2 μl prepared fr...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:The ADP-Glo format PI3K assays were performed in Proxiplate 384-well plates (Perkin Elmer #6008280). The final assay volume was 2 μl prepared fr...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:The ADP-Glo format PI3K assays were performed in Proxiplate 384-well plates (Perkin Elmer #6008280). The final assay volume was 2 μl prepared fr...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:The ADP-Glo format PI3K assays were performed in Proxiplate 384-well plates (Perkin Elmer #6008280). The final assay volume was 2 μl prepared fr...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:Inhibition of PI3Kdelta (unknown origin) by biochemical Alphascreen assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Cancer Chemotherapy Center
Curated by ChEMBL
Cancer Chemotherapy Center
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:PI-3 Kinase HTRF kit (ref. #33-037) and the different PI3K recombinant isoforms (ref. #14-602, ref. #14-603, ref. #14-604, ref. #15-558 for Alpha, Be...More data for this Ligand-Target Pair




























3D Structure (crystal)












