PF-592,379
Dopamine receptor agonist compound
- Investigational (discontinued)
- 5-[(2R,5S)-5-methyl-4-propylmorpholin-2-yl]pyridin-2-amine
- 710655-15-5
Y
- 10263487
- 7683
- 8438966
- 66B7UY5K7I
- DTXSID901030407
- Interactive image
- CCCN([C@@H](C)CO1)C[C@H]1C2=CN=C(N)C=C2
InChI
- InChI=1S/C13H21N3O/c1-3-6-16-8-12(17-9-10(16)2)11-4-5-13(14)15-7-11/h4-5,7,10,12H,3,6,8-9H2,1-2H3,(H2,14,15)/t10-,12-/m0/s1
- Key:DFTCYTDJDXZFSK-JQWIXIFHSA-N
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, a research study showed that PF-592,379 has little 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
- 7-OH-DPAT
- PD-128,907
- PF-219,061
References
- ^ Attkins N, Betts A, Hepworth D, Heatherington AC (November 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; the Fate of Foreign Compounds in Biological Systems. 40 (11): 730–42. doi:10.3109/00498254.2010.514961. PMID 20836725. S2CID 30288414.
- ^ Collins GT, Butler P, Wayman C, Ratcliffe S, Gupta P, Oberhofer G, Caine SB (June 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): 280–91. doi:10.1097/FBP.0b013e3283536d21. PMC 3365486. PMID 22470105.
- ^ "Drug Profile: PF 592379". Adis Insight. Springer Nature Switzerland AG.
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- See also: Receptor/signaling modulators
- Adrenergics
- Serotonergics
- Monoamine reuptake inhibitors
- Monoamine releasing agents
- Monoamine metabolism modulators
- Monoamine neurotoxins
