Mimaki Y, Kanmoto T, Kuroda M, Sashida Y, Nishino A, Satomi Y, Nishino H
School of Pharmacy, Tokyo University of Pharmacy and Life Science, Japan.
Chem Pharm Bull (Tokyo). 1995 Jul;43(7):1190-6. doi: 10.1248/cpb.43.1190.
Phytochemical study on the underground parts of Hosta longipes gave six new steroidal saponins together with a known one. The structures of the new compounds were determined by detailed analysis of their 1H- and 13C-NMR spectra including two-dimensional NMR spectroscopy, acid-catalyzed hydrolysis followed by chemical correlation, and by comparison with spectral data of known compounds. The isolated saponins and their aglycones were examined for inhibitory activity on 12-O-tetradecanoylphorbol-13-acetate (TPA)-stimulated 32P-incorporation into phospholipids of HeLa cells to identify new antitumor-promoter compounds.
对长梗玉簪地下部分进行的植物化学研究得到了六种新的甾体皂苷以及一种已知的甾体皂苷。通过对其1H-和13C-NMR光谱进行详细分析(包括二维NMR光谱)、酸催化水解后进行化学关联,并与已知化合物的光谱数据进行比较,确定了新化合物的结构。对分离得到的皂苷及其苷元进行了检测,以考察它们对12-O-十四烷酰佛波醇-13-乙酸酯(TPA)刺激的32P掺入HeLa细胞磷脂的抑制活性,从而鉴定新的抗肿瘤促进剂化合物。