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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Aldo-keto reductase family 1 member B1 (Homo sapiens (Human)) | BDBM50016633 (4-Chloro-2-(2,5-dioxo-imidazolidin-4-yl)-N-pentyl-...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc. Curated by ChEMBL | Assay Description Inhibition of human placental aldose reductase (HPAR) activity with glyceraldehyde as substrate | J Med Chem 32: 1208-13 (1989) BindingDB Entry DOI: 10.7270/Q24B309G | |||||||||||
More data for this Ligand-Target Pair |