Fenoprofen
- CasNo:31879-05-7
Product Description
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1.What is the Fenoprofen ?
ChEBI: Propanoic acid in which one of the hydrogens at position 2 is substituted by a 3-phenoxyphenyl group. A non-steroidal anti-inflammatory drug, the dihydrate form of the calcium salt is used for the management of mild to moderate pain and for the relief of p in and inflammation associated with disorders such as arthritis. It is pharmacologically similar to aspirin, but causes less gastrointestinal bleeding.
Fenoprofen, also known as Nalfon, is a non-steroidal anti-inflammatory drug (NSAID) that belongs to the propionic acid class. It is characterized by the presence of a 3-phenoxyphenyl group substituted at position 2 of the propanoic acid. Fenoprofen is rapidly absorbed orally, reaches peak plasma levels within 2 hours, and has a short plasma half-life of 3 hours. It is highly protein-bound, similar to other NSAIDs, and caution is needed when used concurrently with other medications.
2.What is the CAS number for Fenoprofen ?
The CAS number of Fenoprofen is 31879-05-7.
3.What are another words for Fenoprofen ?
Synonyms?for?Fenoprofen 31879-05-7:benzeneacetic acid, α-methyl-3-phenoxy-;2-[3-(phenyloxy)phenyl]propanoic acid;PROGESIC;
4.What is Fenoprofen (31879-05-7) used for?
Fenoprofen is used in treating symptoms of rheumatoid arthritis and osteoarthritis; however, fenoprofen exhibits a number of undesirable side effects.
Fenoprofen (Nalfon) is chemically and pharmacologically similar to ibuprofen and is used in the treatment of rheumatoid arthritis, osteoarthritis, and mild to moderate pain. GI effects such as dyspepsia and pain are most common, although dizziness, pruritus, and palpitations may occur. GI bleeding, sometimes severe, has been reported, and interstitial nephritis has been rarely associated with this drug. Concomitant administration of aspirin decreases the biological half-life of fenoprofen by increasing the metabolic clearance of hydroxylated fenoprofen. Chronic administration of phenobarbital also decreases the drug’s half-life.
InChI:InChI=1/2C15H14O3.Ca/c2*1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13;/h2*2-11H,1H3,(H,16,17);/q;;-1/p-2
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Palladium-Catalyzed Asymmetric Markovnikov Hydroxycarbonylation and Hydroalkoxycarbonylation of Vinyl Arenes: Synthesis of 2-Arylpropanoic Acids |
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