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Usage

Uses

Used in Veterinary Medicine:
Cicloprofen is used as an anti-inflammatory and analgesic agent for the treatment of conditions such as osteoarthritis, joint pain, and musculoskeletal injuries in animals. It is effective in reducing inflammation and alleviating pain by inhibiting the production of prostaglandins, which are the chemical mediators of these symptoms.
Used in Pain Management for Animals:
Cicloprofen serves as a pain management tool in veterinary practice, providing relief to animals suffering from various painful conditions. Its use helps to improve the quality of life for animals by reducing discomfort and promoting mobility.
Used in Various Forms:
Cicloprofen is available in different forms such as tablets, chewable treats, and injectable solutions, catering to the varying needs and preferences of animals and their owners. This versatility allows for easier administration and compliance with treatment plans.
Used with Veterinary Supervision:
Due to potential side effects such as gastrointestinal upset, decreased kidney function, and liver toxicity, cicloprofen is used under the supervision and monitoring of a veterinarian. This ensures that the medication is administered safely and effectively, minimizing the risk of adverse effects.

InChI:InChI=1/C16H14O2/c1-10(16(17)18)11-6-7-15-13(8-11)9-12-4-2-3-5-14(12)15/h2-8,10H,9H2,1H3,(H,17,18)

Upstream product

• 75-69-4 trichlorofluoromethane 
• 124-38-9 carbon dioxide 
• 42914-78-3 2-(1-chloro-ethyl)-fluorene 
• 1117-96-0 Diazoethan 
• 7507-40-6 9H-fluorene-2-carboxylic acid 
• 42914-03-4 methyl α-methylfluorene-2-acetic acid 
• 37411-84-0 2-(9H-fluoren-2-yl)propanenitrile 
• 37411-79-3 α-methylene fluorene-2acetic acid 

Relevant academic research and scientific papers

Electrosynthesis of 2-arylpropionic acids from α-methylbenzyl chlorides and carbon dioxide by [Co(Salen)]

The electrochemical synthesis of the 2-arylpropionic acid group of nonsteroidal anti-inflammatory agents such as ibuprofen, naproxen, indoprofen, biprofen, cicloprofen, and fenoprofen has been carried out in dimethylformamide (DMF) containing tetra-n-butylammonium perchlorate (nBu4NClO 4) by electrochemical carboxylation of α-methylbenzyl chlorides catalyzed by a schiff-base complex [Co(salen)] in an undivided cell equipped with a platinum cathode and magnesium anode under constant current density of 10 mA/cm2 in good yields. Cyclic voltammetric studies have also been carried out to investigate the mechanism by which [Co(salen)] catalyzes the cathodic reaction of α-methylbenzyl chlorides in presence of CO 2 by taking α-phenylethylchloride as the model compound. Copyright Taylor & Francis, Inc.

Synthesis of α,α-disubstituted acetic acids using low-valent titanium

Digalogenocarbenes generated using low-valent titanium (LVT) undergo a one-pot cycloaddition to diaryl, aryl alkyl or dialkyl ketones to give α,α-disubstituted acetic acids such as (R,S)-2-arylpropanoic acids.TiI4 proved most effective in this reaction for which the product yield was optimized by use of an excess of reducing agent.

Derivatives of antiphlogistically effective carboxylic acids, their preparation and medicinal use

Compounds of Formula I STR1 wherein R1 is the residue of an antiphlogistically effective carboxylic acid of the formula R1 COOH, n is an integer 1, 2, or 3, and X is oxygen, sulfur, or optionally alkylated nitrogen have valuable antiinflammatory activity.

Method of using fluorene-2-acetic acid derivatives

Novel fluorene-2-acetic acid derivatives and methods for preparing these derivatives are provided. Inflammatory conditions may be treated by administering these novel compounds. Additionally, it has been found that the treatment of inflammatory conditions is a new use for certain known compounds; specifically, fluorene-2-acetic acid and its 7-halo, 7-amino, and 7-nitro derivatives.