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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Sucrase-isomaltase (Mus musculus) | BDBM18355 ((2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-...) | UniProtKB/TrEMBL GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars | Article PubMed | n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of wild type C57BL/6 mouse small intestinal sucrase/isomaltase using sucrose as substrate after 30 mins | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Lysosomal alpha-glucosidase (Rattus norvegicus) | BDBM18355 ((2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-...) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars | Article PubMed | n/a | n/a | 5.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of rat liver lysosomal alpha-glucosidase using p-nitrophenyl alpha-D-glucopyranoside as substrate by colorimetric method | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Lysosomal alpha-glucosidase (Homo sapiens (Human)) | BDBM18355 ((2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-...) | PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars | Article PubMed | n/a | n/a | 1.58E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of recombinant human GAA by UV-visible spectrophotometric method | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Lysosomal acid/Non-lysosomal glucosylceramidase (Homo sapiens (Human)) | BDBM18355 ((2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-...) | PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars | PDB Article PubMed | n/a | n/a | 1.80E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of [3H]cocaine binding to the dopamine transporter. | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Lysosomal acid glucosylceramidase (Homo sapiens (Human)) | BDBM18355 ((2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars | MMDB PDB Article PubMed | n/a | n/a | 3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of recombinant human GBA1 | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Sucrase-isomaltase (Mus musculus) | BDBM50243651 (CHEMBL4061367) | UniProtKB/TrEMBL GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of wild type C57BL/6 mouse small intestinal sucrase/isomaltase using sucrose as substrate after 30 mins | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Beta-galactosidase (Mus musculus) | BDBM50243651 (CHEMBL4061367) | PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 5.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Napoli Federico II Curated by ChEMBL | Assay Description Inhibition of [3H]WIN-35428 binding to the dopamine transporter | J Med Chem 60: 9462-9469 (2017) Article DOI: 10.1021/acs.jmedchem.7b00646 BindingDB Entry DOI: 10.7270/Q2SJ1P1C | |||||||||||
More data for this Ligand-Target Pair |