TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 3.50E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 3.80E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 3.80E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 4.40E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 4.50E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 4.90E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 5.40E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 5.50E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 5.70E+4nMAssay Description:Inhibition of EGFR in human MDA231 cells assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 6.10E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan
Curated by ChEMBL
The University Of Jordan
Curated by ChEMBL
Affinity DataIC50: 6.40E+4nMAssay Description:Inhibition of PI3Kalpha in human HCT116 cells coexpressing PI3Kalpha H1047R mutant assessed as growth inhibition after 24 hrs by MTT assayMore data for this Ligand-Target Pair