Itoh Toshimasa, Tomiyasu Ayako, Yamamoto Keiko
Laboratory of Drug Design and Medicinal Chemistry, Showa Pharmaceutical University, 3-3165 Higashi-Tamagawagakuen, Machida, Tokyo, 194-8543, Japan.
Lipids. 2011 May;46(5):455-61. doi: 10.1007/s11745-011-3541-5. Epub 2011 Feb 24.
Tetracosahexaenoic acid (C(24):6n-3, THA, 3) is an essential biosynthetic precursor in mammals of docosahexaenoic acid (C(22):6n-3, DHA, 1), the end-product of the metabolism of n-3 fatty acids. THA 3 is present in commercially valuable fishes, such as flathead flounder. Tricosahexaenoic acid (C(23):6n-3, TrHA, 2), an odd-numbered-chain fatty acid, has been identified from marine organisms such as the dinoflagellate, Amphidinium carterae. To date, few studies have examined THA 3 and TrHA 2 due to difficulties in detecting and identifying these compounds, so their chemical and biological properties remain poorly characterized. Only one methodology for the chemical synthesis of THA 3 has been presented, and no method for the synthesis of TrHA 2 has been reported. We report here the efficient synthesis of THA 3 in four steps in 56% overall yield, and the synthesis of TrHA 2 in six steps in 48% overall yield. We also present the synthesis of Δ(2)-THA 4, an intermediate of β-oxidation of THA 3 to DHA 1, in three steps in 73% overall yield.
二十四碳六烯酸(C(24):6n-3,THA,3)是哺乳动物中二十二碳六烯酸(C(22):6n-3,DHA,1)的必需生物合成前体,而DHA是n-3脂肪酸代谢的终产物。THA 3存在于具有商业价值的鱼类中,如太平洋扁头鲽。二十三碳六烯酸(C(23):6n-3,TrHA,2)是一种奇数碳链脂肪酸,已从海洋生物如双鞭毛虫卡特亚双鞭藻中鉴定出来。迄今为止,由于检测和鉴定这些化合物存在困难,很少有研究对THA 3和TrHA 2进行研究,因此它们的化学和生物学特性仍知之甚少。仅有一种THA 3的化学合成方法被报道,而尚未有TrHA 2的合成方法被报道。我们在此报告了以四步反应高效合成THA 3,总产率为56%,以及以六步反应合成TrHA 2,总产率为48%。我们还展示了以三步反应合成Δ(2)-THA 4,它是THA 3氧化为DHA 1的β-氧化过程中的中间体,总产率为73%。