Reaction Details Report a problem with these data
Target
Prostaglandin G/H synthase 1 [582-599]
Ligand
BDBM17638
Substrate
n/a
Meas. Tech.
Enzyme Inhibition Assay
IC50
2.6e+2± 3.2e+2 nM
Citation
 Bekhit, AA; Ashour, HM; Bekhit, Ael-D; Abdel-Rahman, HM; Bekhit, SA Synthesis of some pyrazolyl benzenesulfonamide derivatives as dual anti-inflammatory antimicrobial agents. J Enzyme Inhib Med Chem 24:296-309 (2009) [PubMed]  Article 
Target
Name:
Prostaglandin G/H synthase 1 [582-599]
Synonyms:
COX-1 | COX1 | Cyclooxygenase | Cyclooxygenase-1 | Cyclooxygenase-1 (COX-1) | PGH synthase 1 | PGH1_HUMAN | PGHS-1 | PHS 1 | PTGS1 | Prostaglandin G/H synthase 1 | Prostaglandin H2 synthase 1 | Prostaglandin-endoperoxide synthase 1
Type:
Protein
Mol. Mass.:
1879.89
Organism:
Homo sapiens (Human)
Description:
Q6LCE7
Residue:
18
Sequence:
PDASQDDGPAVERPSTEL
  
Inhibitor
Name:
BDBM17638
Synonyms:
2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl-1H-indol-3-yl}acetic acid | CHEMBL6 | Indocin | Indomethacin | US11478464, Compound Indomethacin | US11786535, Compound Indomethacin | US9271961, Indomethacin | indometacin
Type:
Small organic molecule
Emp. Form.:
C19H16ClNO4
Mol. Mass.:
357.788
SMILES:
COc1ccc2n(C(=O)c3ccc(Cl)cc3)c(C)c(CC(O)=O)c2c1
Structure:
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