Synthesis of 1-O-[hexadecyl-1′,2′-3H]hexadecyl 2-acetyl-sn-glyceryl 3-phosphorylcholine and 1-O-alkyl [32P]lysophosphatidycholine
✍ Scribed by Un Hoi Do; Yang Hong; Peter Tam; Puliyur Srinivasan
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- French
- Weight
- 480 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
1 -0-[hexadecyl-1',2'-3H]Hexadecyl 2-acetyl-sn-glyceryl3-phosphorylcholine (GPC) was prepared by acetylation of 1-0-alkenyl lysophosphatidylcholine, reduction of the alkenyl lipid with tritium gas over palladium oxide, and separation of molecular species of 1-0-[3H]alkyl2-acetyl GPC by reverse phase thin-layer chromatography. I-O-Alkyl[32P]lysophosphatidylcholine was prepared by mild alkaline hydrolysis of I-0-alkyl 2-acyl [32P]phos hatidylcholine, which was 1-0-hexadecyl2-acetyl-sn-glycerol in the presence of rat liver microsomes. The resulting radiolabeled ether phospholipids possessed high specific radioactivity suitable for metabolic and binding studies. enzymatically produced by treating cytidine 5'-[ 3 l P]diphosphocholine with
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## Abstract The syntheses of N‐substituted 1‐O‐alkyl‐2‐desoxy‐2‐amino‐__sn__‐glycero‐3‐[^32^P]phosphocholines were performed in four steps starting from [^32^P] POCl~3~ and the corresponding 1‐O‐alkyl‐2‐amino‐propane‐3‐ols in 5‐7% total yield.
## Abstract A mixed‐acid monounsaturated lecithin, 1‐palmitoyl‐2‐oleyl‐__sn__‐glycero‐3‐phosphorylcholine (POL), has been synthesized by phospholipase A~2~ digestion of 1,2 dipalmitoyl‐__sn__‐glycero‐3‐phosphorylcholine followed by reacylation of the lysolecithin with oleic anhydride. ^1^H (90 MHz