Japonicones A-C: Three lindenane sesquiterpenoid dimers with a 12-membered ring core from Chloranthus japonicus

被引:24
|
作者
Yan, Huan [1 ,2 ]
Qin, Xu-Jie [1 ,2 ]
Li, Xu-Hong [1 ,2 ]
Yu, Qian [3 ]
Ni, Wei [1 ,2 ]
He, Li [4 ]
Liu, Hai-Yang [1 ,2 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
[2] Yunnan Key Lab Nat Med Chem, Kunming 650201, Yunnan, Peoples R China
[3] Sun Yat Sen Univ, Sch Pharmaceut Sci, Inst Med Chem & Chem Biol, Guangzhou 510006, Guangdong, Peoples R China
[4] Kunming Med Univ, Affiliated Hosp 1, Dept Dermatol, Kunming 650032, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
Chloranthus japonicus; Lindenane sesquiterpenoid dimer; Japonicones A-C; ECD calculation; CHEMICAL-CONSTITUENTS; PLANTS;
D O I
10.1016/j.tetlet.2019.01.040
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Japonicones A-C (1-3), three new dimeric lindenane-type sesquiterpenoids featuring a rare 12-membered ring framework, were isolated from the whole plants of Chloranthus japonicus Sieb. Their structures and absolute configurations were unequivocally established by a combination of spectroscopic data, ECD calculation, and X-ray crystallography. Compounds 1-3 were evaluated for their DNA Topoisomerase I (Top1) inhibitory, cytotoxic, and antibacterial activities. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:713 / 717
页数:5
相关论文
共 11 条
  • [11] Ascomylactams A-C, Cytotoxic 12-or 13-Membered-Ring Macrocyclic Alkaloids Isolated from the Mangrove Endophytic Fungus Didymella sp. CYSK-4, and Structure Revisions of Phomapyrrolidones A and C
    Chen, Yan
    Liu, Zhaoming
    Huang, Yun
    Liu, Lan
    He, Jianguo
    Wang, Lan
    Yuan, Jie
    She, Zhigang
    JOURNAL OF NATURAL PRODUCTS, 2019, 82 (07): : 1752 - 1758