Sesquiterpene lactone dimers from the fruit of Carpesium abrotanoides L

被引:6
作者
Wang, Yu-Fang [1 ]
Fu, Yan [1 ,2 ]
Ji, Yan-Nan [1 ]
Shi, Ning-Ning [1 ]
Sauriol, Francoise [3 ]
Lu, Xin-Hua [4 ]
Gu, Yu-Cheng [5 ]
Shi, Qing-Wen [1 ]
Huo, Chang-Hong [1 ]
机构
[1] Hebei Med Univ, Sch Pharmaceut Sci, Key Lab Innovat Drug Dev & Evaluat, Shijiazhuang 050017, Hebei, Peoples R China
[2] Hebei Med Univ, Core Facil & Ctr, Shijiazhuang 050017, Hebei, Peoples R China
[3] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
[4] North China Pharmaceut Grp Corp, New Drug Res & Dev Ctr, Shijiazhuang 050015, Hebei, Peoples R China
[5] Syngenta Jealotts Hill Int Res Ctr, Bracknell RG42 6EY, Berks, England
基金
中国国家自然科学基金;
关键词
Carpesium abrotanoides L; Asteraceae; Sesquiterpene lactone dimer; Cytotoxicity; A-D; INHIBITORS;
D O I
10.1016/j.phytochem.2022.113389
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Seven undescribed sesquiterpene lactone dimers (SLDs) (carpeabrodilactones A-G), one known SLD, and six known sesquiterpenes were isolated from the fruit of Carpesium abrotanoides L. Carpeabrodilactone A was a dimeric carabrane featuring a rare C-13-C-13 & PRIME; linkage. Carpeabrodilactones B and C are the first two SLDs to be described possessing a carabranolide unit and a guaianolide unit connected by an O-ether linkage. The structures of the SLDs were assigned based on HRESIMS, NMR analysis, C-13 NMR calculation, ECD calculation, and modified Mosher's method. Four SLDs showed potent cytotoxicity against K562 and/or A549 cells, with IC50 values below 10 mu M, but none inhibited protein tyrosine phosphatases at 40 mu M, including PTP1B, SHP1, CD45, and TCPTP.
引用
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页数:8
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