PF-592,379

PF-592,379
Clinical data
Routes of; administration	Oral
Legal status
Legal status	Investigational (discontinued);
Identifiers
	IUPAC name 5-[(2R,5S)-5-methyl-4-propylmorpholin-2-yl]pyridin-2-amine;
PubChem CID	10263487;
IUPHAR/BPS	7683;
ChemSpider	8438966;
Chemical and physical data
Formula	C13H21N3O
Molar mass	235.33 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	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, 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]

References

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.
"Drug Profile: PF 592379".

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[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.

[3] "Drug Profile: PF 592379".

PF-592,379

See also

References