Yan-Zhe Jia, Yu-Pei Yang, Shao-Wu Cheng, Liang Cao, Qing-Ling Xie, Meng-Yun Wang, Bin Li, Yu-Qing Jian, Bin Liu, Cai-Yun Peng, Wei Wang
Phytochemistry 2021 AprPhytochemical investigations on the fresh fruits of Kadsura coccinea (Lem.) A. C. Sm. have led to the isolation of fourteen undescribed 2,2'-cyclolignans named heilaohuguosus A-N, four undescribed aryltetrahydronaphthalene lignans, heilaohuguosus O-R and one tetrahydrofuran lignan, heilaohuguosu S, with twenty-seven previously described lignan analogues. Their structures and absolute configurations of heilaohuguosus A-S were established by spectroscopic methods including 1D and 2D-NMR techniques and CD experiments. All isolated compounds were evaluated for their hepatoprotective activity against APAP-induced toxicity in HepG-2 cells, four 2,2'-cyclolignans, heilaohuguosus A and L, tiegusanin I and kadsuphilol I showed good hepatoprotective activities against APAP toxicity in HepG-2 cells with cell survival rates of 53.5 ± 1.7%, 55.2 ± 1.2%, 52.5 ± 2.4%, and 54.0 ± 2.2% (positive control bicyclol, 52.1 ± 1.3%) at 10 μM, respectively. Copyright © 2021 Elsevier Ltd. All rights reserved.
Yan-Zhe Jia, Yu-Pei Yang, Shao-Wu Cheng, Liang Cao, Qing-Ling Xie, Meng-Yun Wang, Bin Li, Yu-Qing Jian, Bin Liu, Cai-Yun Peng, Wei Wang. Heilaohuguosus A-S from the fruits of Kadsura coccinea and their hepatoprotective activity. Phytochemistry. 2021 Apr;184:112678
PMID: 33550198
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