Ishiyama S, Hiraga K, Tuboi S
Biochem Int. 1984 Feb;8(2):305-11.
Carboxyatractyloside was labeled with [3H]KBH4 after oxidation of the primary alcohol of the glucose disulfate moiety by dicyclohexylcarbodiimide and P2O5 under anhydrous conditions in a dimethylsulfoxide medium. The 3H-labeled product was purified by DE 52 column chromatography followed by Cellulofine GCL 25 column chromatography. The final 3H-labeled product gave a single spot on a thin-layer chromatogram, and its Rf value was the same as that of authentic carboxyatractyloside. The biological activities (such as inhibition of state 3 respiration and binding to the adenine nucleotide carrier) were also comparable with those of authentic carboxyatractyloside.
在二甲基亚砜介质中,在无水条件下,通过二环己基碳二亚胺和P2O5将葡萄糖二硫酸部分的伯醇氧化后,用[3H]KBH4标记羧基苍术苷。3H标记的产物先通过DE 52柱色谱法纯化,然后通过Cellulofine GCL 25柱色谱法纯化。最终的3H标记产物在薄层色谱上显示为单一斑点,其Rf值与 authentic羧基苍术苷相同。其生物活性(如对状态3呼吸的抑制和与腺嘌呤核苷酸载体的结合)也与 authentic羧基苍术苷相当。