Compile Data Set for Download or QSAR
Found 102 with Last Name = 'royo' and Initial = 's'
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463145(CHEMBL4244085)copy SMILEScopy InChI
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463145(CHEMBL4244085)copy SMILEScopy InChI
Affinity DataKi:  7.80E+5nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298372((S)-1-((S)-1-(4-(benzyloxy)-3-(trifluoromethyl)ben...)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298372((S)-1-((S)-1-(4-(benzyloxy)-3-(trifluoromethyl)ben...)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298373((S)-1-((S)-1-(4-(benzyloxy)-3-fluorobenzoyl)-4,4-d...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298373((S)-1-((S)-1-(4-(benzyloxy)-3-fluorobenzoyl)-4,4-d...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463157(CHEMBL4244656)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463142(CHEMBL4238441)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298357((S)-1-((2S,4S)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 13.1nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298357((S)-1-((2S,4S)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 13.1nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetCruzipain(Trypanosoma cruzi)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463157(CHEMBL4244656)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of Trypanosoma cruzi cruzainMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCruzipain(Trypanosoma cruzi)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463142(CHEMBL4238441)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of Trypanosoma cruzi cruzainMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463157(CHEMBL4244656)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463154(CHEMBL4251480)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463142(CHEMBL4238441)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298355((S)-1-((2S)-1-(4-(benzyloxy)-3,5-dimethoxybenzoyl)...)copy SMILEScopy InChI
Affinity DataIC50: 48.7nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298355((S)-1-((2S)-1-(4-(benzyloxy)-3,5-dimethoxybenzoyl)...)copy SMILEScopy InChI
Affinity DataIC50: 48.7nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463143(CHEMBL4245127)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463157(CHEMBL4244656)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463154(CHEMBL4251480)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463142(CHEMBL4238441)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine proteinase falcipain 2a(Plasmodium falciparum)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463154(CHEMBL4251480)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of Plasmodium falciparum falcipain-2 using Cbz-Phe-Arg-AMC as substrate measured for 15 mins by spectrofluorimetric methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298352((S)-1-((2S,4R)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 60.4nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298352((S)-1-((2S,4R)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 60.4nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298345((S)-1-((2S,4R)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 63.8nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298345((S)-1-((2S,4R)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 63.8nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463154(CHEMBL4251480)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463149(CHEMBL4248915)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463152(CHEMBL4242138)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463148(CHEMBL4247707)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCruzipain(Trypanosoma cruzi)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463143(CHEMBL4245127)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of Trypanosoma cruzi cruzainMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463146(CHEMBL4240920)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463147(CHEMBL4237990)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463147(CHEMBL4237990)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463147(CHEMBL4237990)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298363((S)-1-((2S)-1-(4-benzoyloxy-3,5-dimethoxybenzoyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 111nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298363((S)-1-((2S)-1-(4-benzoyloxy-3,5-dimethoxybenzoyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 111nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463151(CHEMBL4249696)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCathepsin B(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463146(CHEMBL4240920)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human cathepsin B using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463151(CHEMBL4249696)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463143(CHEMBL4245127)copy SMILEScopy InChI
Affinity DataIC50: 145nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463148(CHEMBL4247707)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463152(CHEMBL4242138)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain using Cbz-Phe-Arg-AMC as substrate measured for 30 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298356((S)-1-((2S,4S)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 176nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase-like(Human)
UNIVERSITAT DE BARCELONA; FUNACIÓ INSTITUT DE RECERCA BIOMÉDICA; IPROTEOS S.L.

US Patent
LigandPNGBDBM298359((S)-1-((2S,4S)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 176nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2377CQKUS Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298359((S)-1-((2S,4S)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 176nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetProlyl endopeptidase(Homo sapiens (Human))
UNIVERSITAT DE BARCELONA; FUNDACIO INSTITUT DE RECERCA BIOMEDICA (IRB BARCELONA); IPROTEOS S.L.

US Patent
LigandPNGBDBM298356((S)-1-((2S,4S)-1-(4-(benzyloxy)-3,5-dimethoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 176nMAssay Description:POP activity was determined following the method described by Toide et al (Toide K et al., J. Pharmacol. Exp. Ther. 1995; 274:1370-8), using Z-G-P-AM...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J6DX3US Patent
TargetProcathepsin L(Homo sapiens (Human))
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463152(CHEMBL4242138)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibition of human cathepsin L using Cbz-Phe-Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCysteine proteinase falcipain 2a(Plasmodium falciparum)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463146(CHEMBL4240920)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of Plasmodium falciparum falcipain-2 using Cbz-Phe-Arg-AMC as substrate measured for 15 mins by spectrofluorimetric methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
TargetCruzipain(Trypanosoma cruzi)
Universitat Jaume I

Curated by ChEMBL
LigandPNGBDBM50463147(CHEMBL4237990)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of Trypanosoma cruzi cruzainMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1TPMPubMed
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