Reaction Details |
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Target | Prostaglandin G/H synthase 1 [582-599] |
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Ligand | BDBM17638 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Enzyme Inhibition Assay |
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IC50 | 2.6e+2± 3.2e+2 nM |
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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 Chem24:296-309 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin G/H synthase 1 [582-599] |
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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: | |
BDBM17638 |
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n/a |
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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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