For research use only. Not for therapeutic Use.
Arachidonoyl PAF C-<wbr></wbr>16 is the product of acylation of lyso-<wbr></wbr>PAF C-<wbr></wbr>16 by a CoA-<wbr></wbr>independent transacylase. It is the most common precursor for formation of PAF C-<wbr></wbr>16 by the remodeling pathway.
| Catalog Number | R067314 |
| CAS Number | 86288-11-1 |
| Synonyms | 1-O-hexadecyl-2-Arachidonoyl-sn-glycero-3-Phosphocholine |
| Molecular Formula | C44H82NO7P |
| Purity | ≥95% |
| Storage | -20°C |
| IUPAC Name | [(2R)-3-hexadecoxy-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyl]oxypropyl] 2-(trimethylazaniumyl)ethyl phosphate |
| InChI | InChI=1S/C44H82NO7P/c1-6-8-10-12-14-16-18-20-22-23-24-25-27-29-31-33-35-37-44(46)52-43(42-51-53(47,48)50-40-38-45(3,4)5)41-49-39-36-34-32-30-28-26-21-19-17-15-13-11-9-7-2/h14,16,20,22,24-25,29,31,43H,6-13,15,17-19,21,23,26-28,30,32-42H2,1-5H3/b16-14-,22-20-,25-24-,31-29-/t43-/m1/s1 |
| InChIKey | DUUSFCFZBREELS-WWBBCYQPSA-N |
| SMILES | CCCCCCCCCCCCCCCCOCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCC=CCC=CCC=CCC=CCCCCC |
| Reference | 1.Kramer, R.M.,Patton, G.M.,Pritzker, C.R., et al. Metabolism of platelet-activating factor in human platelets. The Journal of Biological Chemisty 259, 13316-13320 (1984). |
