甘草
A549电池
传统医学
化学
IC50型
细胞培养
细胞毒性T细胞
药理学
生物化学
立体化学
体外
生物
医学
遗传学
病理
替代医学
作者
Kai Li,Shuai Ji,Wei Song,Yi Kuang,Yan Lin,Shunan Tang,Ze-Xu Cui,Xue Qiao,Siwang Yu,Min Ye
标识
DOI:10.1021/acs.jnatprod.6b00783
摘要
In an attempt to discover bioactive agents from the herbal medicine Glycyrrhiza glabra (widely known as licorice), 11 new phenolic compounds, glycybridins A–K (1–11), along with 47 known phenolics (12–58) were isolated. Their structures were elucidated on the basis of extensive NMR and MS analyses as well as experimental and computed ECD data. According to the clinical therapeutic effects of licorice, enzyme or cell-based bioactivity screenings of 1–58 were conducted. A number of compounds significantly activate Nrf2, inhibit tyrosinase or PTP1B, inhibit LPS-induced NO production and NF-κB transcription, and inhibit the proliferation of human cancer cells (HepG2, SW480, A549, MCF7). Glycybridin D (4) showed moderate cytotoxic activities against the four cancer cell lines, with IC50 values ranging from 4.6 to 6.6 μM. Further studies indicated that 4 (10 mg/kg, ip) decreased tumor mass by 39.7% on an A549 human lung carcinoma xenograft mice model, but showed little toxicity.
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