Homoisoflavonoids fromOphiopogon japonicus

Autor: Li Zou, Li-She Gan, Qiaojun He, Chang-Xin Zhou, Xue-Yao Wang, Jian-Xia Mo, Bo Yang
Rok vydání: 2013
Předmět:
Zdroj: Helvetica Chimica Acta. 96:1397-1405
ISSN: 0018-019X
DOI: 10.1002/hlca.201200493
Popis: Phytochemical study on the root tubers of Ophiopogon japonicus resulted in the isolation and identification of 13 homoisoflavonoids, including three new compounds, 8-formyl-7-hydroxy-5,4′-dimethoxy-6-methylhomoisoflavone (1), 6-formylisoophiopogonone B (2), and 8-formylophiopogonanone B (4), and the ten known homoisoflavonoids 3, and 5–13. The absolute configurations of 8-formylophiopogonanone B (4) and 8-formyl-7-hydroxy-5,4′-dimethoxy-6-methylhomoisoflavanone (5) were confirmed by time-dependent density-functional-theory (TD DFT) calculations of their theoretical electronic circular dichroism (ECD) spectra. The structure of the formerly reported ‘6-aldehydoisoophiopogonone B’ was revised to 8-formylophiopogonone B (3). All compounds were evaluated for their cytotoxic activities against the human-lung-tumor A549 cell line, and compounds 3, 9, 10, and 13 exhibited promising antiproliferative activities with IC50 values of 10.01, 6.40, 0.84, and 1.66 μM, respectively.
Databáze: OpenAIRE