PF-592,379

PF-592,379
Clinical data
Routes of
administration		 Oral
Legal status
Legal status
  • Investigational (discontinued)
Identifiers
PubChem CID
IUPHAR/BPS
ChemSpider
Chemical and physical data
Formula C13H21N3O
Molar mass 235.33 g/mol
3D model (JSmol)

PF-592,379 is a drug developed by Pfizer which acts as a potent, selective and orally active agonist for the dopamine D3 receptor, which is under development as a potential medication for the treatment of female sexual dysfunction and male erectile dysfunction. Unlike some other less selective D3 agonists, PF-592,379 showed no evidence of abuse potential in animal studies, and so was selected for further development and potentially human clinical trials.[1][2] Development has since been discontinued.[3]

See also

References

  1. ↑ Attkins, N.; Betts, A.; Hepworth, D.; Heatherington, A. C. (2010). "Pharmacokinetics and elucidation of the rates and routes of N-glucuronidation of PF-592379, an oral dopamine 3 agonist in rat, dog, and human". Xenobiotica. 40 (11): 730–742. PMID 20836725. doi:10.3109/00498254.2010.514961.
  2. ↑ Collins, G. T.; Butler, P.; Wayman, C.; Ratcliffe, S.; Gupta, P.; Oberhofer, G.; Caine, S. B. (2012). "Lack of abuse potential in a highly selective dopamine D3 agonist, PF-592,379, in drug self-administration and drug discrimination in rats". Behavioural Pharmacology. 23 (3): 280–291. PMC 3365486 Freely accessible. PMID 22470105. doi:10.1097/FBP.0b013e3283536d21.
  3. ↑ "Drug Profile: PF 592379".


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