Archival research
A nonsteroidal anti-inflammatory drug
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CAS Number | 54300-20-8 |
PubChem | 68770 |
DrugBank | |
ChemSpider | 62020 |
KEGG | D02899 |
Antrafenine is a nonsteroidal anti-inflammatory drug (NSAID) that was developed for the treatment of pain and inflammation. It is part of a class of drugs that work by inhibiting the production of prostaglandins, which are compounds involved in the inflammatory response.
Pharmacology[edit | edit source]
Antrafenine functions by inhibiting the cyclooxygenase (COX) enzymes, specifically COX-1 and COX-2. These enzymes are responsible for the conversion of arachidonic acid to prostaglandins, which mediate inflammation, pain, and fever. By blocking these enzymes, antrafenine reduces the synthesis of prostaglandins, thereby alleviating symptoms associated with inflammation.
Clinical Use[edit | edit source]
Antrafenine is used primarily for its analgesic and anti-inflammatory properties. It is indicated for the treatment of conditions such as arthritis, musculoskeletal pain, and other inflammatory disorders. The drug is administered orally and is absorbed through the gastrointestinal tract.
Side Effects[edit | edit source]
As with other NSAIDs, antrafenine can cause a range of side effects. Common adverse effects include gastrointestinal discomfort, such as nausea, vomiting, and gastric ulceration. Long-term use may increase the risk of cardiovascular events and renal impairment. Patients are advised to use the lowest effective dose for the shortest duration necessary to minimize these risks.
Synthesis[edit | edit source]
The synthesis of antrafenine involves the chemical modification of a phenylpropionic acid derivative. The process includes the introduction of a chloro group to the aromatic ring, followed by the formation of the propanoic acid moiety. The detailed synthetic pathway is illustrated in the accompanying diagram.
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