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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Prostaglandin G/H synthase 1/2 (RAT) | BDBM50022309 (3,5-Dioxo-1,2-diphenyl-4-n-butylpyrazolidine | 4-b...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL MMDB PC cid PC sid PDB UniChem Patents Similars | PubMed | n/a | n/a | 1.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was tested for inhibition of prostaglandin synthetase when administered perorally | J Med Chem 23: 734-8 (1980) BindingDB Entry DOI: 10.7270/Q28W3GHQ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Prostaglandin G/H synthase 1/2 (RAT) | BDBM50222214 (CHEMBL162115) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 7.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was tested for inhibition of prostaglandin synthetase when administered perorally | J Med Chem 23: 734-8 (1980) BindingDB Entry DOI: 10.7270/Q28W3GHQ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Prostaglandin G/H synthase 1/2 (RAT) | BDBM50222213 (TIARAMIDE HYDROCHLORIDE | Tiaramide HCl) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase PC cid PC sid UniChem Similars | PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was tested for inhibition of prostaglandin synthetase when administered perorally | J Med Chem 23: 734-8 (1980) BindingDB Entry DOI: 10.7270/Q28W3GHQ | |||||||||||
More data for this Ligand-Target Pair |