药效学
药理学
化学
芒柄花素
葡萄糖醛酸化
黄芩苷
大黄素
黄芩素
新陈代谢
药代动力学
生物化学
医学
色谱法
微粒体
体外
内科学
大豆黄酮
高效液相色谱法
染料木素
作者
Zi Hui Ni,Li Wu,Ke Cao,Xi Qiong Zhang,Dan Yu Wang,Yu Wei Zeng,Li-Bo Liang,Xian Dan Qiu,Ruiqian Guo,Haibo Cheng,Zhi Peng Chen
标识
DOI:10.1016/j.jep.2019.112332
摘要
Dahuang Zhechong pill (DHZCP) is a commonly used traditional Chinese medicine for the treatment of hepatocarcinoma. Previous studies have found that DHZCP can exert anti-hepatocarcinoma effects and reverse drug resistance by inhibiting energy metabolism. The goal of this study was to further explore the pharmacodynamic substances that inhibit energy metabolism. The components of DHZCP absorbed into plasma were identified by UHPLC-Q-TOF-MS/MS. The Swiss and STITCH databases were used for target collection. The DAVID database was used for pathway enrichment analysis. Cytoscape software was used for network construction. The CCK-8 method detected cell viability. Chemiluminescence was used to detect ATP levels. A total of 89 components absorbed into plasma were identified by UHPLC-Q-TOF-MS/MS. Based on this, 24 potential pharmacodynamic substances were selected by network pharmacology. Among them, 11 components such as rhein can significantly inhibit ATP levels. Rhein, emodin, chrysophanol, hypoxanthine, baicalein, baicalin, wogonoside, acteoside, formononetin, isoliquiritigenin, and glycyrrhizic acid were the pharmacodynamic substances responsible for inhibition of energy metabolism of DHZCP.
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