PF-592,379
From Wikipedia, the free encyclopedia
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| Routes of administration |
Oral |
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| PubChem (CID) | 10263487 |
| IUPHAR/BPS | 7683 |
| ChemSpider | 8438966 |
| Chemical and physical data | |
| Formula | C13H21N3O |
| Molar mass | 235.33 g/mol |
| 3D model (Jmol) | Interactive image |
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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]
See also[edit]
References[edit]
- ^ 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. doi:10.3109/00498254.2010.514961. PMID 20836725.
- ^ 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. doi:10.1097/FBP.0b013e3283536d21. PMC 3365486
. PMID 22470105.
