Found 21 with Last Name = 'mubarak' and Initial = 'ms' 
Affinity DataIC50: 900nMAssay Description:Inhibition of beta-glucuronidase (unknown origin) using p-nitrophenyl-beta-D-glucuronide substrate incubated for 30 mins by spectrophotometryMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 1/12/13/14/2/3/4/5A, mitochondrial/5B, mitochondrial/6/7/9(Homo sapiens (Human))
King Saud University
Curated by ChEMBL
King Saud University
Curated by ChEMBL
Affinity DataIC50: 1.86E+3nMAssay Description:Inhibition of carbonic anhydrase (unknown origin)More 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: 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
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
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: 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
Affinity DataIC50: 4.58E+4nMAssay Description:Inhibition of beta-glucuronidase (unknown origin) using p-nitrophenyl-beta-D-glucuronide substrate incubated for 30 mins by spectrophotometryMore 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
TargetCarbonic anhydrase 1/12/13/14/2/3/4/5A, mitochondrial/5B, mitochondrial/6/7/9(Homo sapiens (Human))
King Saud University
Curated by ChEMBL
King Saud University
Curated by ChEMBL
Affinity DataIC50: 2.70E+5nMAssay Description:Inhibition of carbonic anhydrase (unknown origin)More data for this Ligand-Target Pair
TargetCarbonic anhydrase 1/12/13/14/2/3/4/5A, mitochondrial/5B, mitochondrial/6/7/9(Homo sapiens (Human))
King Saud University
Curated by ChEMBL
King Saud University
Curated by ChEMBL
Affinity DataIC50: 4.42E+5nMAssay Description:Inhibition of carbonic anhydrase (unknown origin)More data for this Ligand-Target Pair
