Cypionic acid

Cypionic acid
Names
IUPAC name
3-Cyclopentylpropanoic acid
Other names
3-Cyclopentylpropionic acid; Cypionate; Cipionate
Identifiers
140-77-2 YesY
3D model (Jmol) Interactive image
ChemSpider 8487
ECHA InfoCard 100.004.940
PubChem 8818
Properties
C8H14O2
Molar mass 142.20 g·mol−1
Density 0.996 g/mL[1]
Melting point 130 to 132 °C (266 to 270 °F; 403 to 405 K) (12 mmHg)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Cypionic acid is a carboxylic acid with the molecular formula C8H14O2. Its salts and esters are known as cypionates or cipionates.

The primary use of cypionic acid is in pharmaceutical formulations. Cypionic acid is used to prepare ester prodrugs which have increased half-lives relative to the parent compound. The lipophilicity of the cypionate group allows the prodrug to be sequestered in fat depots after intramuscular injection.[2] The ester group is slowly hydrolyzed by metabolic enzymes, releasing steady doses of the active ingredient. Examples include testosterone cypionate, estradiol cypionate, hydrocortisone cypionate, and oxabolone cypionate.

References

  1. 3-Cyclopentylpropionic acid at Sigma-Aldrich
  2. VJ. Stella, W.N A. Charman and V.H. Naringrekar (1985). "Prodrugs: Do They Have Advantages in Clinical Practice?". Drugs. 29 (5): 455–473. doi:10.2165/00003495-198529050-00002. PMID 3891303.
This article is issued from Wikipedia - version of the 1/31/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.