| Literature DB >> 27116597 |
Linzhen Hu1,2, Yu Zhang2, Hucheng Zhu1, Junjun Liu1, Hua Li1, Xiao-Nian Li3, Weiguang Sun1, Junfen Zeng4, Yongbo Xue1, Yonghui Zhang1.
Abstract
Seven filicinic acid-based meroterpenoids (1-7), possessing 6/6/11, 6/6/7/5, or 6/6/10 ring systems, were isolated from Hypericum japonicum. All of them have novel skeletons with the incorporation of sesquiterpenoid moieties to an acylated filicinic acid. Compounds 2a and 4 exhibited significant efficacy on anti-Epstein-Barr virus, with EC50 values of 0.57 and 0.49 μM, respectively. Furthermore, compounds 2a and 4 were well accommodated to the binding pocket of 2GV9 predicted by the molecular docking.Entities:
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Year: 2016 PMID: 27116597 DOI: 10.1021/acs.orglett.6b00906
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005