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Found 31 with Last Name = 'landau' and Initial = 'm'
TargetNa(+)/H(+) antiporter NhaA(Escherichia coli (strain K12))
Tel-Aviv University

Curated by ChEMBL
LigandPNGBDBM50010751(1H,3H-Perimidin-2-ylideneamine | 2-aminoperimidine...)
Affinity DataIC50:  1.70E+3nMAssay Description:Antiporter activity in Escherichia coli K12 wild type EcNhaA assessed as effect on sodium chloride-induced pH changes by acridine orange fluorescence...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNa(+)/H(+) antiporter NhaA(Escherichia coli (strain K12))
Tel-Aviv University

Curated by ChEMBL
LigandPNGBDBM50010751(1H,3H-Perimidin-2-ylideneamine | 2-aminoperimidine...)
Affinity DataIC50:  2.20E+3nMAssay Description:Antiporter activity in Escherichia coli K12 wild type EcNhaA assessed as effect on lithium chloride-induced pH changes by acridine orange fluorescenc...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Yale University

Curated by ChEMBL
LigandPNGBDBM50495830(CHEMBL1530518)
Affinity DataIC50:  5.10E+4nMAssay Description:Inhibition of Toxoplasma gondii TS-DHFR using methylenetetrahydrofolate/dUMP as sustrate preincubated for 10 mins followed by substrate additionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Yale University

Curated by ChEMBL
LigandPNGBDBM50495829(CHEMBL3112972)
Affinity DataIC50:  7.40E+4nMAssay Description:Inhibition of Toxoplasma gondii TS-DHFR using methylenetetrahydrofolate/dUMP as sustrate preincubated for 10 mins followed by substrate additionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Yale University

Curated by ChEMBL
LigandPNGBDBM50495830(CHEMBL1530518)
Affinity DataIC50:  1.39E+5nMAssay Description:Inhibition of Toxoplasma gondii TS-DHFR by Michaelis-Menten plot analysis in presence of bovine serum albuminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Yale University

Curated by ChEMBL
LigandPNGBDBM50495830(CHEMBL1530518)
Affinity DataIC50:  1.42E+5nMAssay Description:Inhibition of Toxoplasma gondii TS-DHFR using methylenetetrahydrofolate/dUMP as sustrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional dihydrofolate reductase-thymidylate synthase(Toxoplasma gondii)
Yale University

Curated by ChEMBL
LigandPNGBDBM50495829(CHEMBL3112972)
Affinity DataIC50:  1.90E+5nMAssay Description:Inhibition of Toxoplasma gondii TS-DHFR using methylenetetrahydrofolate/dUMP as sustrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067123(5-Methyl-2-phenyl-4-[1-phenyl-1-(4-o-tolyl-piperaz...)
Affinity DataEC50:  680nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067126(1-(3-tert-Butylamino-2-hydroxy-propyl)-5-methyl-2-...)
Affinity DataEC50:  7.76E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067125(1-(2-Hydroxy-3-propylamino-propyl)-5-methyl-2-phen...)
Affinity DataEC50:  6.31E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50034682((R)-2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-py...)
Affinity DataEC50:  60nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067121(1-(3-tert-Butylamino-2-hydroxy-propyl)-5-methyl-2-...)
Affinity DataEC50:  7.24E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067128(4-Benzoyl-1-(3-diisopropylamino-2-hydroxy-propyl)-...)
Affinity DataEC50:  2.41E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067129(1-(3-Butylamino-2-hydroxy-propyl)-5-methyl-2-pheny...)
Affinity DataEC50:  2.69E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067132(2,5-Dimethyl-4-[1-phenyl-1-propylamino-meth-(Z)-yl...)
Affinity DataEC50:  2.73E+5nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067133(1-(2-(2-hydroxy-3-(propylamino)propoxy)phenyl)-3-p...)
Affinity DataEC50:  320nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067131(1-(3-Methyl-1-phenyl-5-propylamino-1H-pyrazol-4-yl...)
Affinity DataEC50:  8.38E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067135(1-(2-Hydroxy-3-isopropylamino-propyl)-5-methyl-2-p...)
Affinity DataEC50:  1.23E+5nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067130(1-(2-Hydroxy-3-isopropylamino-propyl)-5-methyl-2-p...)
Affinity DataEC50:  1.18E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067137((3-Methyl-1-phenyl-5-propylamino-1H-pyrazol-4-yl)-...)
Affinity DataEC50:  1.10E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067136(CHEMBL339825 | [5-(3-Diisopropylamino-2-hydroxy-pr...)
Affinity DataEC50:  1.06E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067138(CHEMBL131459 | [5-(3-Diisopropylamino-2-hydroxy-pr...)
Affinity DataEC50:  1.21E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067140(4-Benzoyl-1-(2-hydroxy-3-isopropylamino-propyl)-5-...)
Affinity DataEC50:  8.32E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067134(4-Benzoyl-1-(3-tert-butylamino-2-hydroxy-propyl)-5...)
Affinity DataEC50:  8.13E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067139(4-Benzoyl-1-[2-hydroxy-3-(4-o-tolyl-piperazin-1-yl...)
Affinity DataEC50:  890nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067124(4-Benzoyl-1-(3-diisopropylamino-2-hydroxy-propyl)-...)
Affinity DataEC50:  1.26E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067118(1-(2-Hydroxy-3-propylamino-propyl)-5-methyl-2-phen...)
Affinity DataEC50:  7.24E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM81939(CAS_52-53-9 | NSC_62969 | VERAPAMIL)
Affinity DataEC50:  120nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067119(1-[2-Hydroxy-3-(4-o-tolyl-piperazin-1-yl)-propyl]-...)
Affinity DataEC50:  210nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067120(4-Benzoyl-1-(2-hydroxy-3-propylamino-propyl)-5-met...)
Affinity DataEC50:  2.82E+4nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50067122(5-Methyl-2-phenyl-4-[3-phenyl-1-propylamino-prop-(...)
Affinity DataEC50:  3.79E+3nMAssay Description:Compound was tested for inhibition of daunomycin efflux in the resistant human T-lymphoblast cell line CEM vcr1000.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed