PF-592,379

PF-592,379

Systematic (IUPAC) name
5-[(2R,5S)-5-methyl-4-propylmorpholin-2-yl]pyridin-2-amine
Clinical data
Routes of administration	Oral
Identifiers
PubChem	CID 10263487
IUPHAR/BPS	7683
ChemSpider	8438966
Chemical data
Formula	C13H21N3O
Molar mass	235.33 g/mol
SMILES 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, 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

• 7-OH-DPAT
• PD-128,907
• PF-219,061

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. doi:10.3109/00498254.2010.514961. PMID 20836725.
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. doi:10.1097/FBP.0b013e3283536d21. PMC 3365486. PMID 22470105.