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Found 66 with Last Name = 'harbut' and Initial = 'm'
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
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
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
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
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
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
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
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
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
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
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

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

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
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22049(6-(cyclohexylamino)-9-propyl-9H-purine-2-carbonitr...)
Affinity DataIC50:  8.30E+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

LigandPNGBDBM22050(9-cyclohexyl-6-(cyclohexylamino)-9H-purine-2-carbo...)
Affinity DataIC50:  8.30E+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

LigandPNGBDBM22091(6-{[(4-bromophenyl)methyl]amino}-9-butyl-9H-purine...)
Affinity DataIC50:  8.40E+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
TargetCathepsin B-like cysteine protease(Trypanosoma brucei)
University of California San Francisco

LigandPNGBDBM22071(6-[(2-phenylethyl)amino]-9-(pyridin-3-ylmethyl)-9H...)
Affinity DataIC50:  1.00E+4nMpH: 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

LigandPNGBDBM22067(9-butyl-6-{[(4-chlorophenyl)methyl]amino}-9H-purin...)
Affinity DataIC50:  1.00E+4nMpH: 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

LigandPNGBDBM22080(6-(benzylamino)-9-(oxan-2-ylmethyl)-9H-purine-2-ca...)
Affinity DataIC50:  1.10E+4nMT: 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

LigandPNGBDBM22081(6-(benzylamino)-9-[(4-methoxyphenyl)methyl]-9H-pur...)
Affinity DataIC50:  1.10E+4nMT: 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

LigandPNGBDBM22060(9-butyl-6-{[(3-methylphenyl)methyl]amino}-9H-purin...)
Affinity DataIC50:  1.10E+4nMpH: 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

LigandPNGBDBM22079(6-(benzylamino)-9-(3-hydroxypropyl)-9H-purine-2-ca...)
Affinity DataIC50:  1.20E+4nMT: 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

LigandPNGBDBM22064(6-(benzylamino)-9-butyl-9H-purine-2-carbonitrile |...)
Affinity DataIC50:  1.40E+4nMpH: 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

LigandPNGBDBM22046(9-cyclopentyl-6-{[(2S)-2-methylbutyl]amino}-9H-pur...)
Affinity DataIC50:  1.40E+4nMpH: 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

LigandPNGBDBM22096(9-benzyl-6-{[(3,4-dichlorophenyl)methyl]amino}-9H-...)
Affinity DataIC50:  1.50E+4nMT: 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

LigandPNGBDBM22072(9-butyl-6-[(2-phenylethyl)amino]-9H-purine-2-carbo...)
Affinity DataIC50:  1.60E+4nMpH: 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

LigandPNGBDBM22083(6-{[(4-fluorophenyl)methyl]amino}-9-(4-hydroxybuty...)
Affinity DataIC50:  1.80E+4nMT: 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

LigandPNGBDBM22068(6-{[(4-chlorophenyl)methyl]amino}-9-cyclopentyl-9H...)
Affinity DataIC50:  1.90E+4nMpH: 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

LigandPNGBDBM22089(6-{[(4-chlorophenyl)methyl]amino}-9-[(4-methoxyphe...)
Affinity DataIC50:  2.30E+4nMT: 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

LigandPNGBDBM22061(9-cyclopentyl-6-{[(3-methylphenyl)methyl]amino}-9H...)
Affinity DataIC50: >2.50E+4nMpH: 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

LigandPNGBDBM22077(9-butyl-6-{[(4-methylphenyl)methyl]amino}-9H-purin...)
Affinity DataIC50: >2.50E+4nMT: 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

LigandPNGBDBM22078(9-benzyl-6-{[(4-methylphenyl)methyl]amino}-9H-puri...)
Affinity DataIC50: >2.50E+4nMT: 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
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