芒柄花素
异黄酮
糖苷
立体化学
二维核磁共振波谱
化学
类黄酮
生物
生物化学
抗氧化剂
染料木素
内分泌学
大豆黄酮
作者
Süheyla Kırmızıgül,Nezhun Gören,Shu‐Wei Yang,Geoffrey A. Cordell,Candan Bozok-Johansson
摘要
The roots of Ononis spinosa subsp. leiosperma (Leguminosae) afforded a new glycoside, spinonin (1), possessing a novel skeleton, in addition to the known isoflavonoid glycoside, ononin [7beta-(glucosyloxy)formononetin] (2) and the known pterocarpan, 7-demethoxy-7-D-(glucosyloxy)homopterocarpin (3). The structure of the new isolate was elucidated by spectral methods including 1H and 13C NMR, COSY, APT, HETCOR, HMBC, NOESY, CD, FABMS, HRMS, EIMS, CIMS, and some chemical reactions. Spinonin was inactive against a number of human cancer cell lines and HIV-1 reverse transcriptase. The compounds 1 and 3 showed weak activity against Pseudomonas aeruginosa, whereas 2 was active against beta-hemolytic Streptococcus.
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