For research use only. Not for therapeutic Use.
9(R)-PAHSA is a stereoisomer of 9-PAHSA (Item No. <span class=/itemid/>17037</span>), an endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). 9-PAHSA is a FAHFA in which palmitic acid (Item No. <span class=/itemid/>10006627</span>) is esterified to 9-hydroxy stearic acid. 9(R)-PAHSA is the predominant form that accumulates in adipose tissues in AG4OX mice, which overexpress Glut4 specifically in adipose tissue. Also, cell lines favor the production of 9(R)-PAHSA, and carboxyl ester lipase selectively hydrolyzes 9(S)-PAHSA (Item No. <span class=/itemid/>18023</span>).
| Catalog Number | R065686 |
| CAS Number | 2097130-84-0 |
| Synonyms | 9R-[(1-oxohexadecyl)oxy]-octadecanoic acid |
| Molecular Formula | C34H66O4 |
| Purity | ≥95% |
| Storage | -20°C |
| InChI | InChI=1S/C34H66O4/c1-3-5-7-9-11-12-13-14-15-16-18-23-27-31-34(37)38-32(28-24-20-17-10-8-6-4-2)29-25-21-19-22-26-30-33(35)36/h32H,3-31H2,1-2H3,(H,35,36)/t32-/m1/s1 |
| InChIKey | MHQWHZLXDBVXML-JGCGQSQUSA-N |
| SMILES | OC(CCCCCCC[C@H](OC(CCCCCCCCCCCCCCC)=O)CCCCCCCCC)=O |
| Reference | 1.Yore, M.M.,Syed, I.,Moraes-Vieira, P.M., et al. Discovery of a class of endogenous mammalian lipids with anti-diabetic and anti-inflammatory effects. Cell. 159(2), 318-332 (2014). |
