Benzophenones from <i>Anemarrhena asphodeloides</i> Bge. Exhibit Anticancer Activity in HepG2 Cells via the NF-κB Signaling Pathway
De-Ling Wu,
Zhen-Dong Liao,
Fang-Fang Chen,
Wei Zhang,
Ya-Shuo Ren,
Can-Can Wang,
Xiao-Xiao Chen,
Dai-Yin Peng,
Ling-Yi Kong
Affiliations
De-Ling Wu
Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, China
Zhen-Dong Liao
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Fang-Fang Chen
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Wei Zhang
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Ya-Shuo Ren
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Can-Can Wang
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Xiao-Xiao Chen
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Dai-Yin Peng
School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
Ling-Yi Kong
Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, China
A chemical investigation of the fibrous roots of Anemarrhena asphodeloides Bge. led to the isolation of four benzophenones, including one new compound (1) and three known ones (2−4). Comprehensive 1D, 2D NMR and HRESIMS data established the structures of the isolated compounds. The absolute configurations were determined by comparison of the calculated optical rotation (OR) with experimental data. All the isolates were evaluated for their cytotoxicities on hepatocellular carcinoma cell lines (HepG2 and Hep3B). Compound 1 showed strong cytotoxicity against HepG2 and Hep3B cells, with IC50 values at 153.1 and 180.6 nM. Through MTT assay, flow cytometry and Western blot analysis, compound 1 demonstrated the ability to stimulate apoptosis via the NF-κB signaling pathway in HepG2 cells. These benzophenones are potential lead compounds for the development of better treatments for hepatocellular carcinoma.