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Pipamazine

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Chemical compound Pharmaceutical compound
Pipamazine
Chemical structure of Pipamazine
Clinical data
Pregnancy
category
Routes of
administration
Oral, intramuscular injection
ATC code
  • None
Legal status
Legal status
  • Withdrawn
Identifiers
IUPAC name
  • 1-piperidine-4-carboxamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.001.375 Edit this at Wikidata
Chemical and physical data
FormulaC21H24ClN3OS
Molar mass401.95 g·mol
3D model (JSmol)
SMILES
  • C1CN(CCC1C(=O)N)CCCN2C3=CC=CC=C3SC4=C2C=C(C=C4)Cl
InChI
  • InChI=1S/C21H24ClN3OS/c22-16-6-7-20-18(14-16)25(17-4-1-2-5-19(17)27-20)11-3-10-24-12-8-15(9-13-24)21(23)26/h1-2,4-7,14-15H,3,8-13H2,(H2,23,26)
  • Key:OSJJYEUEJRVVOD-UHFFFAOYSA-N
  (what is this?)  (verify)

Pipamazine (INN; trade names Mornidine, Mometine, Nausidol) is a drug of the phenothiazine class formerly used as an antiemetic. It is chemically related to chlorpromazine, but has negligible antipsychotic activity and produces few extrapyramidal side effects.

Pipamazine was introduced to the U.S. market in 1959 by G. D. Searle & Company. It was advertised for morning sickness and postoperative nausea and vomiting, and was claimed to reduce the need for postoperative analgesia. It was eventually withdrawn from the U.S. market in 1969, after reports of hepatotoxicity (liver injury).

There is very little published information on pipamazine; it is mostly absent from modern-day sources, apart from a few passing mentions in the pharmacological literature.

Adverse effects

Mornidine advertisements for postoperative recovery claimed "unusually low side effects". However, contemporary comparative trials found that hypotension (low blood pressure) was a substantial concern when the drug was given at normal dosages for this indication; blood pressure reductions of up to 70 mmHg were reported. Reductions in dosage mitigated hypotension while maintaining antiemetic efficacy.

In his book The Creation of Psychopharmacology, Irish psychiatrist David Healy states that the failure of pipamazine to perform as a neuroleptic and its negative side effect profile helped Searle lose interest in the antipsychotic sector, and contributed to the company's refusal to market haloperidol in the United States.

Synthesis

Thieme Patents:

The alkylation of 2-chloro-10-(3-chloropropyl)phenothiazine (1) with Isonipecotamide (2) gives pipamazine (3).

References

  1. ^ Frota LH (2003). Cinqüenta anos de medicamentos antipsicóticos em psiquiatria (PDF) (in Portuguese) (1st ed.). Rio de Janeiro: UFRJ. p. 486. ISBN 85-903827-1-0. Archived from the original (PDF) on 2011-07-06. Retrieved 2010-09-28.
  2. (July 1959). "Now she can cook breakfast again..." Canadian Medical Association Journal. 81 (1): 59. PMC 1830735. Advertisement.
  3. ^ (April 1960). "Lessened postoperative vomiting with MORNIDINE". Annals of Surgery. 151 (4). PMC 1613578. Advertisement.
  4. 34 FR 12051. July 17, 1969.
  5. Wysowski DK, Swartz L (June 2005). "Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002: the importance of reporting suspected reactions". Archives of Internal Medicine. 165 (12): 1363–9. doi:10.1001/archinte.165.12.1363. PMID 15983284.
  6. Blatchford E (March 1961). "Studies of anti-emetic drugs: A comparative study of cyclizine (Marzine), pipamazine (Mornidine), trimethobenzamide (Tigan), and hyoscine". Canadian Journal of Anesthesia. 8 (2): 159–65. doi:10.1007/BF03021345.
  7. Healy D (2002). "Explorations in a new world". The creation of psychopharmacology. Cambridge: Harvard University Press. pp. 123–4. ISBN 0-674-01599-1.
  8. John W Cusic, Dr Henry William Sause, DE 1089386  (1960 to Searle & Co).
  9. John W Cusic, Sause Henry William, U.S. patent 2,957,870 (1960 to Searle & Co).
Antiemetics (A04)
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