ChemicalBook--->CAS DataBase List--->2748208-06-0

2748208-06-0

2748208-06-0 Structure

2748208-06-0 Structure
IdentificationBack Directory
[Name]

9-PAHSA-d31
[CAS]

2748208-06-0
[Synonyms]

9-PAHSA-d31
9-[(1-oxohexadecyl)oxy-2,2',3,3',4,4',5,5',6,6',7,7',8,8',9,9',10,10',11,11',12,12',13,13',14,14',15,15',16,16,16-d31]-octadecanoicacid
[Molecular Formula]

C34H35D31O4
[MOL File]

2748208-06-0.mol
[Molecular Weight]

570.076
Chemical PropertiesBack Directory
[solubility ]

DMF: 20 mg/ml
DMSO: 15 mg/ml
Ethanol: 20 mg/ml
Ethanol: PBS(pH 7.2) (1:1): 0.5 mg/ml
Hazard InformationBack Directory
[Description]

9-PAHSA-d31 is intended for use as an internal standard for the quantification of 9-PAHSA (Item No. 17037) by GC- or LC-mass spectrometry. 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 Structurally, these esters are comprised of a C-16 or C-18 fatty acid (e.g., palmitoleic, palmitic, oleic, or stearic acid) linked to a hydroxylated C-16 or C-18 lipid. 9-PAHSA is a FAHFA in which palmitic acid is esterified to 9-hydroxy stearic acid. PAHSAs are the most abundant forms of FAHFA in serum as well as white and brown adipose tissues of glucose tolerant AG4OX mice, which overexpress Glut4 specifically in adipose tissue.1 9-PAHSA is the predominant isomer of PAHSA in wild type and AG4OX mice.1 It is found in humans and is reduced in the serum and adipose tissues of insulin-resistant humans.1 9-PAHSA improves glucose tolerance, stimulates insulin secretion, and has anti-inflammatory effects in mice.1WARNING This product is not for human or veterinary use.
[References]

[1] MARK M YORE. Discovery of a class of endogenous mammalian lipids with anti-diabetic and anti-inflammatory effects.[J]. Cell, 2014, 159 2: 318-332. DOI: 10.1016/j.cell.2014.09.035
[2] DAN TAN. Discovery of FAHFA-Containing Triacylglycerols and Their Metabolic Regulation[J]. Journal of the American Chemical Society, 2019, 141 22: 8798-8806. DOI: 10.1021/jacs.9b00045
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