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| | 9-Octadecenoic acid (9Z)-, 9-carboxy-1-octylnonyl ester Basic information |
| | 9-Octadecenoic acid (9Z)-, 9-carboxy-1-octylnonyl ester Chemical Properties |
| 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) |
| | 9-Octadecenoic acid (9Z)-, 9-carboxy-1-octylnonyl ester Usage And Synthesis |
| Description | 10-OAHSA is a newly identified endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). It is a FAHFA in which oleic acid is esterified to 10-hydroxy stearic acid. Among the FAHFA family members, PAHSAs are the most abundant in the adipose tissue 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, 10-OAHSA may be a bioactive lipid with roles in metabolic syndrome and inflammation.1 | | Uses | 10-OAHSA is one of fatty acid esters of hydroxy fatty acids (FAHFAs). 10-POHSA increases glucose-stimulated insulin secretion (GSIS) at a high glucose concentration. 10-OAHSA reduces LPS (HY-D1056)-induced Tnf-α secretion in bone marrow-derived dendritic cells (BMDCs)[1]. | | 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). |
| | 9-Octadecenoic acid (9Z)-, 9-carboxy-1-octylnonyl ester Preparation Products And Raw materials |
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