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Fluproquazone: Wikis

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Fluproquazone
Systematic (IUPAC) name
4-(4-fluorophenyl)-7-methyl-1-propan-2-ylquinazolin-2-one
Identifiers
CAS number 40507-23-1
ATC code none
PubChem 38503
Chemical data
Formula C 18H17FN2O 
Mol. mass 296.339 g/mol
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.  ?
Legal status
Routes  ?

Fluproquazone (Tormosyl) is a quinazolinone derivative with potent analgesic[1][2] and antipyretic[3] effects and also anti-inflammatory action. It has been shown to be effective in a variety of animal species after both oral and parenteral administration, and has a duration of action of several hours. The compound is many times more potent than acetylsalicylic acid and clinically generally resembles ibuprofen and indoprofen in its pharmacological effects, but with significantly less ulcerogenic activity.[4] It is mainly used in the treatment of arthritis[5] and post-operative pain.[6]

References

  1. ^ Mohing W, Suckert R, Lataste X. Comparative study of fluproquazone in the management of post-operative pain. Arzneimittelforschung. 1981;31(5a):918-20.
  2. ^ Wheatley D. Analgesic properties of fluproquazone. Rheumatology and Rehabilitation. 1982 May;21(2):98-100.
  3. ^ Fankhauser S, Laube W, Marti HR, Schultheiss HR, Vogtlin J, von Graffenried B. Antipyretic activity of fluproquazone in man. Arzneimittelforschung. 1981;31(5a):934-5.
  4. ^ Gillberg R, Korsan-Bengtsen K, Magnusson B, Nyberg G. Gastrointestinal blood loss, gastroscopy and coagulation factors in normal volunteers during administration of acetylsalicylic acid and fluproquazone. Scandinavian Journal of Rheumatology. 1981;10(4):342-6.
  5. ^ Huskisson EC, Bryans R, Scott J. Fluproquazone for osteoarthritis. Rheumatology and Rehabilitation. 1981 May;20(2):122-4.
  6. ^ Haanaes HR, Benterud UJ, Skoglund LA. RF 46-790 versus paracetamol: effect on post-operative pain. International Journal of Clinical Pharmacology, Therapy, and Toxicology. 1986 Nov;24(11):598-601.
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