Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Genome polyprotein (Human rhinovirus B) | BDBM50112584 (2-(2-{2-[2-(2-{2-[2-(2-Amino-3-methyl-pentanoylami...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370072 (CHEMBL1790422) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 100 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50468724 (CHEMBL4294334) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 120 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50468723 (CHEMBL4279824) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 160 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112580 (CHEMBL268148 | PWGF(CH2NH)WWFW) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 200 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Falcipain 2 (Plasmodium falciparum) | BDBM50183767 ((2R,3R)-dibenzyl 1-((S)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 400 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Plasmodium falciparum falcipain 2 using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Procathepsin L (Homo sapiens (Human)) | BDBM50183767 ((2R,3R)-dibenzyl 1-((S)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 400 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of human cathepsin-L using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Falcipain 2 (Plasmodium falciparum) | BDBM50468724 (CHEMBL4294334) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 450 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Plasmodium falciparum falcipain 2 using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50183767 ((2R,3R)-dibenzyl 1-((S)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112597 (2-{2-[2-(2-{2-[2-[2-(2-Amino-3-carboxy-propionylam...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Similars | PubMed | 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112581 (6-Amino-2-(2-{2-[2-(6-amino-2-{2-[6-amino-2-(2-ami...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 600 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50468724 (CHEMBL4294334) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 710 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50183757 ((2S,3S)-dibenzyl 1-((S)-1-((R)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 790 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50183776 ((2S,3S)-dibenzyl 1-((R)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 900 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112596 (6-Amino-2-{2-[2-(2-{2-[2-[6-amino-2-(2-amino-3-car...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112594 (CHEMBL266692 | ChaALF(CH2NH)YMYY) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50183757 ((2S,3S)-dibenzyl 1-((S)-1-((R)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50183776 ((2S,3S)-dibenzyl 1-((R)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Falcipain 2 (Plasmodium falciparum) | BDBM50468723 (CHEMBL4279824) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.26E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Plasmodium falciparum falcipain 2 using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50468729 (CHEMBL4288606) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50468725 (CHEMBL4279254) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50468729 (CHEMBL4288606) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50183762 ((2S,3S)-dibenzyl 1-((S)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50183747 ((2S,3S)-dibenzyl 1-((R)-1-((R)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Procathepsin L (Homo sapiens (Human)) | BDBM50183757 ((2S,3S)-dibenzyl 1-((S)-1-((R)-2-(tert-butoxycarbo...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of human cathepsin-L using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112583 (1-{2-[2-[2-(6-Amino-2-{2-[2-(2-amino-3-methyl-pent...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 5.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50468722 (CHEMBL4292021) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 5.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Procathepsin L (Homo sapiens (Human)) | BDBM50183776 ((2S,3S)-dibenzyl 1-((R)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 6.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of human cathepsin-L using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112579 (6-Amino-2-(2-{2-[2-(6-amino-2-{2-[2-(2-amino-3-cyc...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 6.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112591 (2-(2-{2-[2-(2-{2-[2-(2-Amino-4-methylsulfanyl-buty...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 6.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112585 (2-[3-Cyclohexyl-2-(2-{2-[2-(3-(3H-imidazol-4-yl)-2...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 6.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Procathepsin L (Homo sapiens (Human)) | BDBM50468724 (CHEMBL4294334) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 7.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of human cathepsin-L using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50468726 (CHEMBL4283566) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 7.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50468727 (CHEMBL4286203) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 7.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112582 (6-Amino-2-[2-(2-{2-[2-(2-{6-amino-2-[(pyrrolidine-...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 8.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370073 (CHEMBL1790421) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.01E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Procathepsin L (Homo sapiens (Human)) | BDBM50468729 (CHEMBL4288606) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of human cathepsin-L using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370068 (CHEMBL1790423) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cysteine protease (Trypanosoma brucei rhodesiense) | BDBM50468721 (CHEMBL4289948) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.52E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma brucei rhodesiense rhodesain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cathepsin B-like protease (Leishmania major) | BDBM50468725 (CHEMBL4279254) | UniProtKB/TrEMBL GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.82E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Leishmania major MHOM/IL/81/FE/BNI His6-tagged CPC expressed in Pichia pastoris using Cbz-Phe-Arg-AMC as substrate by fluorescence spec... | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370070 (CHEMBL1790419) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.86E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370074 (CHEMBL1790420) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Falcipain 2 (Plasmodium falciparum) | BDBM50183757 ((2S,3S)-dibenzyl 1-((S)-1-((R)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 2.83E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Plasmodium falciparum falcipain 2 using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Falcipain 2 (Plasmodium falciparum) | BDBM50468728 (CHEMBL4290479) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 2.86E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Plasmodium falciparum falcipain 2 using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370069 (CHEMBL1790418) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Similars | PubMed | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cruzipain (Trypanosoma cruzi) | BDBM50468721 (CHEMBL4289948) | PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 3.09E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Trypanosoma cruzi cruzain using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112592 (6-Amino-2-(2-{2-[2-(2-{6-amino-2-[6-amino-2-(2-ami...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 3.11E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Falcipain 2 (Plasmodium falciparum) | BDBM50183776 ((2S,3S)-dibenzyl 1-((R)-1-((S)-2-(tert-butoxycarbo...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 4.39E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johannes Gutenberg-Universit£t Mainz Curated by ChEMBL | Assay Description Inhibition of Plasmodium falciparum falcipain 2 using Z-Phe-Arg-AMC as substrate by fluorometric assay | Eur J Med Chem 156: 587-597 (2018) Article DOI: 10.1016/j.ejmech.2018.07.012 BindingDB Entry DOI: 10.7270/Q2CN76MS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50112587 (2-(2-{2-[2-[2-[2-[2-(2-Amino-propionylamino)-3-met...) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Similars | PubMed | 4.47E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Genome polyprotein (Human rhinovirus B) | BDBM50370071 (CHEMBL1790424) | PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 5.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Carlsberg Laboratory Curated by ChEMBL | Assay Description Inhibition of Leishmania mexicana Cysteine protease B (CPB2.8deltaCTE) was obtained in a solution-phase assay | J Med Chem 45: 1971-82 (2002) BindingDB Entry DOI: 10.7270/Q29887QH | |||||||||||
More data for this Ligand-Target Pair |
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