For research use only. Not for therapeutic Use.
| Catalog Number | R017190 |
| CAS Number | 18194-25-7 |
| Synonyms | L-α-Dilauroylglyceryl-3-phosphorylcholine; 1,2-Didodecanoyl-sn-glycero-3-phosphocholine; 1,2-Didodecanoyl-sn-glycero-3-phosphocholine; 1,2-Dilaurin Dihydrogen Phosphate Monoester with L-Choline Hydroxide Inner Salt; 1,2-Dilauroyl-L-phosphatidylcholi |
| Molecular Formula | C32H64NO8P |
| Purity | ≥95% |
| Target | Liposome |
| Solubility | Soluble to 100 mM in ethanol |
| Storage | Store at -20C |
| IUPAC Name | [(2R)-2,3-di(dodecanoyloxy)propyl] 2-(trimethylazaniumyl)ethyl phosphate |
| InChI | InChI=1S/C32H64NO8P/c1-6-8-10-12-14-16-18-20-22-24-31(34)38-28-30(29-40-42(36,37)39-27-26-33(3,4)5)41-32(35)25-23-21-19-17-15-13-11-9-7-2/h30H,6-29H2,1-5H3/t30-/m1/s1 |
| InChIKey | IJFVSSZAOYLHEE-SSEXGKCCSA-N |
| SMILES | CCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCC |
| Reference | <br>1. H. Lin et al. “The Grapefruit Juice Effect Is Not Limited to Cytochrome P450 (P450) 3A4: Evidence for Bergamottin-Dependent Inactivation, Heme Destruction, and Covalent Binding to Protein in P450s 2B6 and 3A5” JPET, Vol. 313 pp. 154-164, 2005 <br>2. M. Billah and J. Anthes “The regulation and cellular functions of phosphatidylcholine hydrolysis” Biochemistry Journal, Vol. 269 pp. 281-291, 1990<br>3. J. Exton “Signaling through Phosphatidylcholine Breakdown” The Journal of Biological Chemistry, Vol. 265(1) pp. 1-4, 1990<br>4. Z. Li and D. Vance “Phosphatidylcholine and choline homeostasis” Journal of Lipid Research, Vol. 49 pp. 1187-1194, 2008</br></br></br></br> |
