Sripada P K
Department of Medicine, Boston University School of Medicine, Housman Medical Research Center, MA 02118.
Chem Phys Lipids. 1988 Sep;48(1-2):147-51. doi: 10.1016/0009-3084(88)90143-0.
Cholesterol oleate with the 13C-label in oleic acid at the carbonyl and/or in the sterol ring at position 4 was synthesized by two methods: (1) cholesterol was condensed with oleic anhydride, prepared from [1-13C] oleic acid, in the presence of dimethylaminopyridine (DMAP) in anhydrous chloroform at room temperature for 4--5 h; (2) cholesterol or 13C-enriched cholesterol at position 4 were reacted with 90% [1-13C]-oleic acid in the presence of dicyclohexylcarbodiimide (DCC) and DMAP at room temperature in anhydrous chloroform for 1.25 h. The single-13C and double-13C-labeled cholesterol oleate were obtained in 90% yields after purification by silicic acid column chromatography. Their purity was assessed by thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC) and 13C-NMR spectroscopy. Tritium-labeled cholesterol oleate was also synthesized by method 1 using the fatty acid anhydride.
通过两种方法合成了在油酸的羰基处和/或在4位的甾醇环中带有13C标记的油酸胆固醇:(1)在无水氯仿中,于室温下,在4 - 5小时内,胆固醇与由[1-13C]油酸制备的油酸酐在4 - 5小时内缩合,在二甲基氨基吡啶(DMAP)存在下进行;(2)胆固醇或4位富含13C的胆固醇与90%的[1-13C]油酸在二环己基碳二亚胺(DCC)和DMAP存在下,于室温下在无水氯仿中反应1.25小时。通过硅酸柱色谱纯化后,以90%的产率获得了单13C和双13C标记的油酸胆固醇。通过薄层色谱(TLC)、高效液相色谱(HPLC)和13C核磁共振光谱对其纯度进行了评估。还通过方法1使用脂肪酸酐合成了氚标记的油酸胆固醇。