Rådmark O, Malmsten C, Samuelsson B, Goto G, Marfat A, Corey E J
J Biol Chem. 1980 Dec 25;255(24):11828-31.
Leukotriene A, an unstable intermediate in the conversion of arachidonic acid to stable leukotrienes, was isolated from human polymorphonuclear leukocytes. The allylic epoxide intermediate is rapidly hydrolyzed under acidic conditions. A method was therefore developed for esterification and extraction of the intermediate as the methyl ester from an alkaline aqueous phase, into an aprotic solvent. This was achieved by addition of methanol and an excess of diazomethane in ether to the incubatio mixture, followed by addition of water, and phase separation. The identity of the isolated compound with the previously synthesized methyl ester of 5 (S)-trans-5,6-oxido-7,9-trans-11,14-cis-eicostatetraenoic acid (leukotriene A), was established by comparing chromatographic and chemical properties of the isolated compound and synthetic leukotriene A.
白三烯A是花生四烯酸转化为稳定白三烯过程中的不稳定中间体,它是从人多形核白细胞中分离出来的。烯丙基环氧化物中间体在酸性条件下会迅速水解。因此,人们开发了一种方法,用于将中间体作为甲酯从碱性水相酯化并萃取到非质子溶剂中。具体做法是,向孵育混合物中加入甲醇和过量的乙醚重氮甲烷,随后加水并进行相分离。通过比较分离出的化合物与合成的5(S)-反式-5,6-环氧-7,9-反式-11,14-顺式二十碳四烯酸甲酯(白三烯A)的色谱和化学性质,确定了分离出的化合物与之前合成的白三烯A甲酯的一致性。