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Found 105 with Last Name = 'greenbaum' and Initial = 'd'
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339789((S)-2-((2S,3R)-3-amino-2-hydroxy-4-(4-methoxypheny...)
Affinity DataKi:  43nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM23971((2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanami...)
Affinity DataKi:  190nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339790((S)-2-((2S,3R)-3-amino-4-(4-(benzyloxy)phenyl)-2-h...)
Affinity DataKi:  490nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339784((S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamid...)
Affinity DataKi:  900nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339785((S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamid...)
Affinity DataKi:  1.45E+3nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339791((S)-2-((2S,3R)-3-amino-2-hydroxy-4-(naphthalen-2-y...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339792((S)-2-((2S,3R)-3-amino-2-hydroxyheptanamido)-4-met...)
Affinity DataKi:  5.30E+3nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339788((S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamid...)
Affinity DataKi: >1.50E+4nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339786((S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamid...)
Affinity DataKi: >1.50E+4nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50339787((S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamid...)
Affinity DataKi: >1.50E+4nMAssay Description:Inhibition of Plasmodium falciparum recombinant M1-aminopeptidase expressed in Escherichia coli after 40 mins uisng fluorigenic substrate L-Leucyl-7-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University of California San Francisco

LigandPNGBDBM36812(CA-074)
Affinity DataIC50:  40nMpH: 5.5 T: 2°CAssay Description:Inhibition assay using pre-treatment of recombinant cathepsin-L-like cysteine protease cruzain lacking the carboxy-terminal domain or cathepsin B fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50114651((1E)-1-(3-bromophenyl)ethan-1-one thiosemicarbazon...)
Affinity DataIC50:  50nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University of California San Francisco

LigandPNGBDBM36813(CA-074b)
Affinity DataIC50:  60nMpH: 5.5 T: 2°CAssay Description:Inhibition assay using pre-treatment of recombinant cathepsin-L-like cysteine protease cruzain lacking the carboxy-terminal domain or cathepsin B fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCruzipain(Trypanosoma cruzi)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50114651((1E)-1-(3-bromophenyl)ethan-1-one thiosemicarbazon...)
Affinity DataIC50:  60nMAssay Description:Inhibition of cruzain from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148049((1E)-1-(1,1'-biphenyl-4-yl)ethan-1-one thiosemicar...)
Affinity DataIC50:  90nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22097(6-{[(3,4-dichlorophenyl)methyl]amino}-9-(3-hydroxy...)
Affinity DataIC50:  270nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148061((1Z)-1-{3-[(1E)-N-(aminocarbonothioyl)ethanehydraz...)
Affinity DataIC50:  330nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
University of California San Francisco

LigandPNGBDBM36814(MB-074)
Affinity DataIC50:  400nMpH: 5.5 T: 2°CAssay Description:Inhibition assay using pre-treatment of recombinant cathepsin-L-like cysteine protease cruzain lacking the carboxy-terminal domain or cathepsin B fr...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148055((1E)-1-(3-phenoxyphenyl)ethan-1-one thiosemicarbaz...)
Affinity DataIC50:  550nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22087(6-{[(4-chlorophenyl)methyl]amino}-9-(3-hydroxyprop...)
Affinity DataIC50:  570nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22100(6-{[(3,4-dichlorophenyl)methyl]amino}-9-[3-(methox...)
Affinity DataIC50:  800nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148057((1E)-1-(3-anilinophenyl)ethan-1-one thiosemicarbaz...)
Affinity DataIC50:  800nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22099(6-{[(3,4-dichlorophenyl)methyl]amino}-9-(5-hydroxy...)
Affinity DataIC50:  930nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148053((1E)-1-(1,1'-biphenyl-3-yl)ethan-1-one thiosemicar...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22098(6-{[(3,4-dichlorophenyl)methyl]amino}-9-(2,3-dihyd...)
Affinity DataIC50:  1.20E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22094(6-{[(3,4-dichlorophenyl)methyl]amino}-9-(2-hydroxy...)
Affinity DataIC50:  1.40E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148060((1E)-1-(3-bromophenyl)ethan-1-one N,N-diethylthios...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22051(9-benzyl-6-(cyclohexylamino)-9H-purine-2-carbonitr...)
Affinity DataIC50:  2.30E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22101(6-{[(3,4-dichlorophenyl)methyl]amino}-9-(3-methoxy...)
Affinity DataIC50:  2.50E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22082(6-(benzylamino)-9-{[3-(trifluoromethyl)phenyl]meth...)
Affinity DataIC50:  2.80E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22063(9-benzyl-6-{[(3-methylphenyl)methyl]amino}-9H-puri...)
Affinity DataIC50:  3.30E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22085(9-benzyl-6-{[(4-fluorophenyl)methyl]amino}-9H-puri...)
Affinity DataIC50:  3.30E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22102(6-{[(3,4-dichlorophenyl)methyl]amino}-9-(3,3-dimet...)
Affinity DataIC50:  3.40E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148058(CHEMBL326220 | N'-[(1E)-1-(3-bromophenyl)ethyliden...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148052(CHEMBL108700 | N'-[(1E)-1-(3-bromophenyl)ethyliden...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22095(9-butyl-6-{[(3,4-dichlorophenyl)methyl]amino}-9H-p...)
Affinity DataIC50:  4.10E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22076(9-(3-hydroxypropyl)-6-{[(4-methylphenyl)methyl]ami...)
Affinity DataIC50:  4.20E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22075(9-benzyl-6-{[(4-methoxyphenyl)methyl]amino}-9H-pur...)
Affinity DataIC50:  4.50E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22088(6-{[(4-chlorophenyl)methyl]amino}-9-(4-hydroxybuty...)
Affinity DataIC50:  4.80E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCruzipain(Trypanosoma cruzi)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148058(CHEMBL326220 | N'-[(1E)-1-(3-bromophenyl)ethyliden...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of cruzain from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCruzipain(Trypanosoma cruzi)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148061((1Z)-1-{3-[(1E)-N-(aminocarbonothioyl)ethanehydraz...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of cruzain from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22048(9-benzyl-6-{[(2S)-2-methylbutyl]amino}-9H-purine-2...)
Affinity DataIC50:  5.00E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCruzipain(Trypanosoma cruzi)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148060((1E)-1-(3-bromophenyl)ethan-1-one N,N-diethylthios...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of cruzain from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCruzipain(Trypanosoma cruzi)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148049((1E)-1-(1,1'-biphenyl-4-yl)ethan-1-one thiosemicar...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of cruzain from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCruzipain(Trypanosoma cruzi)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148052(CHEMBL108700 | N'-[(1E)-1-(3-bromophenyl)ethyliden...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of cruzain from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22066(9-benzyl-6-(benzylamino)-9H-purine-2-carbonitrile ...)
Affinity DataIC50:  6.00E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22074(9-butyl-6-{[(4-methoxyphenyl)methyl]amino}-9H-puri...)
Affinity DataIC50:  6.00E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22059(9-cyclopentyl-6-{[(4-methoxyphenyl)methyl]amino}-9...)
Affinity DataIC50:  7.00E+3nMpH: 5.5 T: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22084(9-butyl-6-{[(4-fluorophenyl)methyl]amino}-9H-purin...)
Affinity DataIC50:  7.10E+3nMT: 2°CAssay Description:Enzyme activity was assayed in a 96-well plate format. TbcatB was incubated with inhibitor compound at room temperature for 20 min before the additio...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50148050((1E)-1-(4-phenoxyphenyl)ethan-1-one thiosemicarbaz...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of rhodesain from Trypanosoma brucei rhodesienseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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