| Identification | Back Directory | [Name]
9-Octadecenoic acid (9Z)-, 12-carboxy-1-pentyldodecyl ester | [CAS]
1997286-67-5 | [Synonyms]
9-Octadecenoic acid (9Z)-, 12-carboxy-1-pentyldodecyl ester | [Molecular Formula]
C36H68O4 | [MOL File]
1997286-67-5.mol | [Molecular Weight]
564.92 |
| Chemical Properties | Back Directory | [Boiling point ]
639.8±38.0 °C(Predicted) | [density ]
0.918±0.06 g/cm3(Predicted) | [solubility ]
DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 20 mg/ml; Ethanol:PBS(pH 7.2) (1:1): 0.5 mg/ml | [pka]
4.78±0.10(Predicted) |
| Hazard Information | Back Directory | [Description]
Branched fatty acid esters of hydroxy fatty acids (FAHFAs) are newly identified endogenous lipids regulated by fasting and high-fat feeding and associated with insulin sensitivity.1 13-OAHSA is a form of FAHFA in which oleic acid is esterified to 13-hydroxy stearic acid. Among the FAHFA family members, OAHSAs are the most abundantly expressed in the serum of glucose tolerant AG4OX mice, which overexpress the Glut4 glucose transporter specifically in adipose tissue.1 As other FAHFAs improve glucose tolerance, stimulate insulin secretion, and have anti-inflammatory effects, 13-OAHSA may be a bioactive lipid with roles in metabolic syndrome and inflammation.1 | [Uses]
13-OAHSA is one of fatty acid esters of hydroxy fatty acids (FAHFAs). 13-OAHSA increases glucose-stimulated insulin secretion (GSIS) at a high glucose concentration[1]. | [IC 50]
Human Endogenous Metabolite | [References]
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). |
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