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Found 21 with Last Name = 'mubarak' and Initial = 'ms'
TargetBeta-glucuronidase(Homo sapiens (Human))
King Saud University

Curated by ChEMBL
LigandPNGBDBM50028013(CHEMBL3360798)
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
In DepthDetails ArticlePubMed
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
LigandPNGBDBM50028010(AD-810 | CHEBI:10127 | CI-912 | PD-110843 | Zonegr...)
Affinity DataIC50:  1.86E+3nMAssay Description:Inhibition of carbonic anhydrase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165853(CHEMBL3798658)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165853(CHEMBL3798658)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165851(CHEMBL3800448)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165852(CHEMBL3798556)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165852(CHEMBL3798556)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165851(CHEMBL3800448)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165854(CHEMBL3799332)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165854(CHEMBL3799332)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165849(CHEMBL3799956)
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
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Homo sapiens (Human))
King Saud University

Curated by ChEMBL
LigandPNGBDBM50008907(D-Saccharic Acid 1,4-Lactone)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165850(CHEMBL3799345)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165848(CHEMBL3797839)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165850(CHEMBL3799345)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165849(CHEMBL3799956)
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
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165847(CHEMBL3800262)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165848(CHEMBL3797839)
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
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University Of Jordan

Curated by ChEMBL
LigandPNGBDBM50165847(CHEMBL3800262)
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
In DepthDetails ArticlePubMed