| aceclofenac, acebutolol, acarbose | |
| acenocoumarol, acetazolamide, acetic acid |
| Systematic (IUPAC) name | |
|---|---|
| 2-[2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetyl]oxyacetic acid | |
| Clinical data | |
| AHFS/Drugs.com | International Drug Names |
| Pregnancy cat. | ? |
| Legal status | POM (UK) |
| Identifiers | |
| CAS number | 53164-05-9 |
| ATC code | M01AB11 |
| PubChem | CID 1981 |
| ChemSpider | 1904 |
| UNII | 5V141XK28X |
| KEGG | D01582 |
| ChEMBL | CHEMBL189171 |
| Chemical data | |
| Formula | C21H18ClNO6 |
| Mol. mass | 415.82372 g/mol |
| SMILES | eMolecules & PubChem |
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Acemetacin is a non-steroidal anti-inflammatory drug, used for the treatment of osteoarthritis, rheumatoid arthritis, lower back pain, and relieving post-operative pain. It is manufactured by Merck under the tradename Emflex, and is available in the UK as a prescription-only drug. Other brand names for acemetacin include Rheutrop (Austria), Acemetadoc, Acephlogont, Azeat, Rantudil (Germany), Gamespir (Greece), Oldan, Reudol (Spain), Tilur (Switzerland) ost-map (egypt).
Acemetacin, a glycolic acid ester of indometacin, acts as a prodrug; in the body, it is metabolized to indometacin, which then acts as an inhibitor of cyclooxygenase, producing the anti-inflammatory effects. An advantage of acemetacin is that it reduces gastric damage when compared to indometacin.
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