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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM223314 (YPYSCWARHVRIREN | piHA-D1) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1 | n/a | n/a | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description The release of 2-chloro-4-nitrophenol resulting from the HPA-catalyzed hydrolysis of 2-chloro-4-nitrophenyl a-maltotrioside (CNPG3) was monitored at ... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM223315 (YPYSCWVRHSDPHKF | piHA-D3) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 2.70 | n/a | n/a | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description The release of 2-chloro-4-nitrophenol resulting from the HPA-catalyzed hydrolysis of 2-chloro-4-nitrophenyl a-maltotrioside (CNPG3) was monitored at ... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM223316 (YPYSCWVRH | piHA-Dm) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 7 | n/a | n/a | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description The release of 2-chloro-4-nitrophenol resulting from the HPA-catalyzed hydrolysis of 2-chloro-4-nitrophenyl a-maltotrioside (CNPG3) was monitored at ... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163646 (Montbretin A (MbA)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 8.10 | -47.0 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163647 (MbA-G (1)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 9.10 | -46.7 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cathepsin K (Homo sapiens (Human)) | BDBM50201794 (CHEMBL3897445) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 11 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia Curated by ChEMBL | Assay Description Competitive inhibition of human recombinant cathepsin K using Z-FR-MCA fluorogenic substrate by Handerson plot analysis | J Nat Prod 79: 1962-70 (2016) Article DOI: 10.1021/acs.jnatprod.6b00215 BindingDB Entry DOI: 10.7270/Q2F76FHF | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163648 (MbA-R (2)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 21.3 | -44.5 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cathepsin K (Homo sapiens (Human)) | BDBM50201793 (CHEMBL3899320) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 41 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia Curated by ChEMBL | Assay Description Competitive inhibition of human recombinant cathepsin K using Z-FR-MCA fluorogenic substrate by Handerson plot analysis | J Nat Prod 79: 1962-70 (2016) Article DOI: 10.1021/acs.jnatprod.6b00215 BindingDB Entry DOI: 10.7270/Q2F76FHF | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163649 (MbA-RX (3)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 42.4 | -42.8 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163650 (MbA-GR (4)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 79.3 | -41.2 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163651 (MbA-GRX (5) | mini-MbA) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid PDB UniChem Similars | PDB Article PubMed | 93.3 | -40.8 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Cathepsin K (Homo sapiens (Human)) | BDBM50201793 (CHEMBL3899320) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 105 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia Curated by ChEMBL | Assay Description Competitive inhibition of human recombinant cathepsin K using Z-FR-MCA fluorogenic substrate by Dixon plot analysis | J Nat Prod 79: 1962-70 (2016) Article DOI: 10.1021/acs.jnatprod.6b00215 BindingDB Entry DOI: 10.7270/Q2F76FHF | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cathepsin K (Homo sapiens (Human)) | BDBM50201793 (CHEMBL3899320) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 105 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia Curated by ChEMBL | Assay Description Competitive inhibition of human recombinant cathepsin K using Z-FR-MCA fluorogenic substrate by Dixon plot analysis | J Nat Prod 79: 1962-70 (2016) Article DOI: 10.1021/acs.jnatprod.6b00215 BindingDB Entry DOI: 10.7270/Q2F76FHF | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cathepsin K (Homo sapiens (Human)) | BDBM50201795 (CHEMBL3972383) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 163 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia Curated by ChEMBL | Assay Description Competitive inhibition of human recombinant cathepsin K using Z-FR-MCA fluorogenic substrate by Dixon plot analysis | J Nat Prod 79: 1962-70 (2016) Article DOI: 10.1021/acs.jnatprod.6b00215 BindingDB Entry DOI: 10.7270/Q2F76FHF | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Trehalose synthase/amylase TreS (Mycobacterium tuberculosis) | BDBM18351 ((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars | Article PubMed | 250 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia | Assay Description The inhibition of TreS by a range of known alpha-glucosidase inhibitor was assayed. | J Biol Chem 286: 35601-9 (2011) Article DOI: 10.1074/jbc.M111.280362 BindingDB Entry DOI: 10.7270/Q2VM49V1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cathepsin K (Homo sapiens (Human)) | BDBM50201792 (CHEMBL3942776) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 393 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia Curated by ChEMBL | Assay Description Competitive inhibition of human recombinant cathepsin K using Z-FR-MCA fluorogenic substrate by Dixon plot analysis | J Nat Prod 79: 1962-70 (2016) Article DOI: 10.1021/acs.jnatprod.6b00215 BindingDB Entry DOI: 10.7270/Q2F76FHF | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163652 (MbA-C (6)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 730 | -35.6 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163653 (MbA-CG (7)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 2.24E+3 | -32.8 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Trehalose synthase/amylase TreS (Mycobacterium tuberculosis) | BDBM92460 (Casuarine) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | MMDB PC cid PC sid PDB UniChem Similars | Article PubMed | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia | Assay Description The inhibition of TreS by a range of known alpha-glucosidase inhibitor was assayed. | J Biol Chem 286: 35601-9 (2011) Article DOI: 10.1074/jbc.M111.280362 BindingDB Entry DOI: 10.7270/Q2VM49V1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163656 (3-O-(6-(4-(Caffeamidomethyl)-triazolyl)hexyl)querc...) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 1.39E+4 | -28.2 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163654 (MbA-CR (8)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 4.68E+4 | -25.1 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Homo sapiens (Human)) | BDBM163655 (MbA-CGR (9)) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | 1.28E+5 | -22.6 | n/a | n/a | n/a | n/a | n/a | n/a | 30 |
University of British Columbia | Assay Description Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor... | Nat Chem Biol 11: 691-6 (2015) Article DOI: 10.1038/nchembio.1865 BindingDB Entry DOI: 10.7270/Q2KD1WP4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Trehalose synthase/amylase TreS (Mycobacterium tuberculosis) | BDBM50182801 ((3R,4R,5R)-5-(Hydroxymethyl)piperidine-3,4-diol, 8...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars | Article PubMed | 1.40E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of British Columbia | Assay Description The inhibition of TreS by a range of known alpha-glucosidase inhibitor was assayed. | J Biol Chem 286: 35601-9 (2011) Article DOI: 10.1074/jbc.M111.280362 BindingDB Entry DOI: 10.7270/Q2VM49V1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Pancreatic alpha-amylase (Sus scrofa (Pig)) | BDBM223316 (YPYSCWVRH | piHA-Dm) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 8.5 | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description After kinetic analysis with HPA, piHA-Dm was tested as an inhibitor of ten additional enzymes. The conditions are listed as follows: Agrobacterium fa... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Alpha-amylase 1A (Homo sapiens (Human)) | BDBM223316 (YPYSCWVRH | piHA-Dm) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 34 | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description After kinetic analysis with HPA, piHA-Dm was tested as an inhibitor of ten additional enzymes. The conditions are listed as follows: Agrobacterium fa... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Maltase-glucoamylase (Homo sapiens (Human)) | BDBM223316 (YPYSCWVRH | piHA-Dm) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 520 | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description After kinetic analysis with HPA, piHA-Dm was tested as an inhibitor of ten additional enzymes. The conditions are listed as follows: Agrobacterium fa... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Soluble maltase-glucoamylase (Mus musculus (Mouse)) | BDBM223316 (YPYSCWVRH | piHA-Dm) | UniProtKB/TrEMBL GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 990 | n/a | n/a | n/a | n/a | 7.0 | n/a |
The University of Tokyo | Assay Description After kinetic analysis with HPA, piHA-Dm was tested as an inhibitor of ten additional enzymes. The conditions are listed as follows: Agrobacterium fa... | Cell Chem Biol 24: 381-390 (2017) Article DOI: 10.1016/j.chembiol.2017.02.001 BindingDB Entry DOI: 10.7270/Q27D2T0M | |||||||||||
More data for this Ligand-Target Pair |