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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Maltase-glucoamylase (Homo sapiens (Human)) | BDBM50316180 ((1S,2R,3S,4S)-1-{(1S)-2-[(2R,3S,4S)-3,4-dihydroxy-...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Patents Similars | Article PubMed | 100 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Simon Fraser University Curated by ChEMBL | Assay Description Inhibition of recombinant human maltase glucoamylase N-terminal catalytic domain | Bioorg Med Chem 18: 2829-35 (2010) Article DOI: 10.1016/j.bmc.2010.03.027 BindingDB Entry DOI: 10.7270/Q22B8Z5J | |||||||||||
More data for this Ligand-Target Pair |