Banskota Arjun H, Usia Tepy, Tezuka Yasuhiro, Kouda Kyoji, Nguyen Nhan Trung, Kadota Shigetoshi
Institute of Natural Medicine, Toyama Medical and Pharmaceutical University, 2630-Sugitani, Toyama 930-0194, Japan.
J Nat Prod. 2002 Nov;65(11):1700-2. doi: 10.1021/np020235j.
Three new C-14 oxygenated taxane-type diterpenes, hongdoushans A-C (1-3), were isolated from the wood of Taxus yunnanensis together with four known diterpenes and two lignans. The absolute stereochemistry of the 2-methylbutyryloxy group attached at C-14 of the taxane skeleton was determined to be S by GC analysis of the methyl ester of 2-methylbutyric acid obtained after alkaline hydrolysis of 1 and 4 followed by treatment with CH(2)N(2). The complete stereostructure of the known compound 2alpha,5alpha,10beta-triacetoxy-14beta-[(S)-2-methylbutyryloxy]-4(20),11-taxadiene (4) was established for the first time. The isolates obtained were evaluated for their antiproliferative activity toward murine colon 26-L5 carcinoma and human HT-1080 fibrosarcoma cell lines.
从云南红豆杉木材中分离出三种新的C-14氧化紫杉烷型二萜,红豆衫山A-C(1-3),以及四种已知的二萜和两种木脂素。通过对1和4进行碱性水解后用CH(2)N(2)处理得到的2-甲基丁酸甲酯进行气相色谱分析,确定紫杉烷骨架C-14处连接的2-甲基丁酰氧基的绝对立体化学为S型。首次确定了已知化合物2α,5α,10β-三乙酰氧基-14β-[(S)-2-甲基丁酰氧基]-4(20),11-紫杉二烯(4)的完整立体结构。对所获得的分离物进行了对小鼠结肠26-L5癌和人HT-1080纤维肉瘤细胞系的抗增殖活性评估。