3-Hydroxypentanoic acid
Names | |
---|---|
IUPAC name
3-Hydroxypentanoic acid | |
Other names
3-Hydroxyvalerate 3-Hydroxy valeric acid beta-Hydroxyvaleric acid beta-Hydroxypentanoate | |
Identifiers | |
10237-77-1 | |
3D model (Jmol) | Interactive image Interactive image |
ChemSpider | 96952 |
ECHA InfoCard | 100.123.761 |
PubChem | 107802 |
| |
| |
Properties | |
C5H10O3 | |
Molar mass | 118.13 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
3-Hydroxypentanoic acid, or beta-hydroxypentanoate is a 5-carbon ketone body. It is made from odd carbon fatty acids in the liver and rapidly enters the brain. As opposed to 4-carbon ketone bodies, 3-hydroxypentanoic acid is anaplerotic, meaning it can refill the pool of TCA cycle intermediates. The triglyceride triheptanoin is used clinically to produce beta-hydroxypentanoate.[1]
References
- ↑ Renée P. Kinman; Takhar Kasumov; Kathryn A. Jobbins; Katherine R. Thomas; Jillian Adams; Lisa N. Brunengraber; Gerd Kutz; Wolf-Ulrich Brewer; Charles R. Roe & Henri Brunengraber (2006). "Parenteral and Enteral Metabolism of Anaplerotic Triheptanoin in Normal Rats". Am J Physiol Endocrinol Metab. 291 (4): E860–E866. doi:10.1152/ajpendo.00366.2005. PMID 16705058. Reprint
This article is issued from Wikipedia - version of the 5/17/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.