2097130-87-3
2097130-87-3
Chemical Structure
9(S)-PAHSA
- CAS No.: 2097130-87-3
- Formula:C34H66O4
- Molecular Weight:538.89
IUPAC Name: (S)-9-(palmitoyloxy)octadecanoic acid
InChIKey: MHQWHZLXDBVXML-YTTGMZPUSA-N
SMILES: CCCCCCCCC[C@H](OC(CCCCCCCCCCCCCCC)=O)CCCCCCCC(O)=O
Biological Activity: 9(S)-PAHSA is a S-enantiomer of 9-PAHSA. 9-PAHSA is an orally available anti-inflammatory lipid that lowers blood sugar and reduces inflammation[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
9(S)-PAHSA | 9(S)-PAHSA is a S-enantiomer of 9-PAHSA. 9-PAHSA is an orally available anti-inflammatory lipid that lowers blood sugar and reduces inflammation. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Wang YM, et al. 9-PAHSA promotes browning of white fat via activating G-protein-coupled receptor 120 and inhibiting lipopolysaccharide / NF-kappa B pathway. Biochem Biophys Res Commun. 2018 Nov 17;506(1):153-160. [Content Brief]
- [2]. Nelson AT, et al. Stereochemistry of Endogenous Palmitic Acid Ester of 9-Hydroxystearic Acid and Relevance of Absolute Configuration to Regulation. J Am Chem Soc. 2017 Apr 5;139(13):4943-4947. [Content Brief]
