Propyphenazone

Summary

Propyphenazone (known as isopropylantipyrine in Japan)[1] is a derivative of phenazone[2] with similar analgesic and antipyretic effects. Originally patented in 1931,[3] propyphenazone is marketed as a combination formulation with paracetamol and caffeine for treatment of primary headache disorder.[4]

Propyphenazone
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
Identifiers
  • 1,5-Dimethyl-2-phenyl-4-propan-2-yl-pyrazol-3-one
CAS Number
  • 479-92-5 ☒N
PubChem CID
  • 3778
ChemSpider
  • 3646 checkY
UNII
  • OED8FV75PY
ChEBI
  • CHEBI:135538 checkY
ChEMBL
  • ChEMBL28318 checkY
CompTox Dashboard (EPA)
  • DTXSID6023529 Edit this at Wikidata
ECHA InfoCard100.006.855 Edit this at Wikidata
Chemical and physical data
FormulaC14H18N2O
Molar mass230.311 g·mol−1
3D model (JSmol)
  • Interactive image
  • O=C1C(C(C)C)=C(C)N(C)N1c2ccccc2
  • InChI=1S/C14H18N2O/c1-10(2)13-11(3)15(4)16(14(13)17)12-8-6-5-7-9-12/h5-10H,1-4H3 checkY
  • Key:PXWLVJLKJGVOKE-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)
Saridon (Combination drug with Propyphenazone) from Hoffman-La Roche, ca. 1950/60

Serious adverse events edit

Case reports have described acute inferior-wall myocardial infarctions characterized by low atrial rhythms[vague] (Kounis syndrome) secondary to propyphenazone use.[5]

Excerpt from WHO comments edit

Propyphenazone, a pyrazolone derivative with anti-inflammatory, analgesic and antipyretic activity, was introduced in 1951 for the treatment of rheumatic disorders. As it is structurally related to aminophenazone it has been associated with severe blood dyscrasias. However, it cannot be transformed into potentially carcinogenic nitrosamines and has therefore been widely used as a replacement drug for aminophenazone. In certain countries, products containing propyphenazone have now been restricted in their indications, whereas in others they are still available, sometimes as over-the-counter preparations.[6]

Banned edit


See also edit

References edit

  1. ^ "Isopropylantipyrine". Drugs.com. Retrieved 8 March 2018.
  2. ^ Göres E, Kossowicz J, Schneider HG (March 2004). "[Propyphenazone. Pharmacology and use]" [Propyphenazone. Pharmacology and use]. Medizinische Monatsschrift für Pharmazeuten (in German). 27 (3): 72–6. PMID 15032249.
  3. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 530. ISBN 9783527607495.
  4. ^ "SC exempts painkiller Saridon from the banned list in India". The Economic Times. February 21, 2019.
  5. ^ Akyel A, Alsancak Y, Yayla Ç, Sahinarslan A, Özdemir M (May 2011). "Acute inferior myocardial infarction with low atrial rhythm due to propyphenazone: Kounis syndrome". International Journal of Cardiology. 148 (3): 352–3. doi:10.1016/j.ijcard.2010.05.038. PMID 20541820.
  6. ^ Consolidated List of Products whose Consumption and/or Sale have been Banned, Withdrawn, Severely Restricted or not Approved by Governments, Twelfth Issue (PDF). New York: Department of Economic and Social Affairs of the United Nations Secretariat. 2005. p. 232.
  7. ^ a b c "Multi-Country Survey On Banned And Restricted Pharmaceuticals". Health Action International Asia Pacific. August 2008. p. 7.