For research use only. Not for therapeutic Use.
N-<wbr></wbr>Acyl ethanolamines (NAEs) have diverse biological actions that are strongly affected by the associated acyl group. Eicosapentaenoyl ethanolamide (EPEA) has potential signaling roles in aging, cancer, inflammation, and neurological development. At least some of EPEA’s effects are mediated through cannabinoid (CB) receptors, while some NAEs also act as vanilloid receptor agonists. R-<wbr></wbr>(+)-<wbr></wbr>Eicosapentaenyl-<wbr></wbr>1’-<wbr></wbr>hydroxy-<wbr></wbr>2’-<wbr></wbr>propylamide is a homolog of EPEA, characterized by the addition of an (R)-<wbr></wbr>α-<wbr></wbr>methyl group at the methylene carbon adjacent to the amide nitrogen. A similar modification of arachidonoyl ethanolamide (Item No. <span class=/itemid/>90050</span>) to produce R-<wbr></wbr>1 methanandamide (Item No. <span class=/itemid/>90070</span>) imparts higher affinity for the CB receptor as well as improved metabolic stability. The physiological actions of this compound have not been evaluated.
| Catalog Number | R067538 |
| Synonyms | N-((R)-1-hydroxypropan-2-yl)icosa-5Z,8Z,11Z,14Z,17Z-pentaenamide |
| Molecular Formula | C23H37NO2 |
| Purity | ≥95% |
| Storage | -20°C |
| InChI | InChI=1S/C23H37NO2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23(26)24-22(2)21-25/h4-5,7-8,10-11,13-14,16-17,22,25H,3,6,9,12,15,18-21H2,1-2H3,(H,24,26)/b5-4-,8-7-,11-10-,14-13-,17-16-/t22-/m1/s1 |
| InChIKey | XOYVLIGJHWVUFH-DZUHFYEBSA-N |
| SMILES | CC/C=CC/C=CC/C=CC/C=CC/C=CCCCC(N[C@H](C)CO)=O |
| Reference | 1.Brown, I.,Cascio, M.G.,Wahle, K.W.J., et al. Cannabinoid receptor-dependent and -independent anti-proliferative effects of omega-3 ethanolamides in androgen receptor-positive and -negative prostate cancer cell lines. Carcinogenesis 31(9), 1584-1591 (201 |
