BDBM50037763 6-[2-Imidazol-1-yl-1,3-diphenyl-prop-(E)-ylideneaminooxy]-hexanoic acid::CHEMBL120284
SMILES: OC(=O)CCCCCO\N=C(\C(Cc1ccccc1)n1ccnc1)c1ccccc1
InChI Key: InChIKey=HYJNXVDECKJAJZ-SHHOIMCASA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Prostanoid TP receptor (Homo sapiens (Human)) | BDBM50037763 (6-[2-Imidazol-1-yl-1,3-diphenyl-prop-(E)-ylideneam...) | UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia-Farmitalia Carlo Erba Curated by ChEMBL | Assay Description In vitro thromboxane-A2 receptor binding affinity to displace by 50% [3H]-SQ 29548 binding from washed human platelets | J Med Chem 37: 3588-604 (1994) BindingDB Entry DOI: 10.7270/Q2C24VFD | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50037763 (6-[2-Imidazol-1-yl-1,3-diphenyl-prop-(E)-ylideneam...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia-Farmitalia Carlo Erba Curated by ChEMBL | Assay Description In vitro inhibition of thromboxane-A2 synthase in rat whole blood during clotting at 37 degrees centigrade | J Med Chem 37: 3588-604 (1994) BindingDB Entry DOI: 10.7270/Q2C24VFD | |||||||||||
More data for this Ligand-Target Pair |