NATURAL PRODUCT RESEARCH AND DEVELOPMENT ›› 2019, Vol. 31 ›› Issue (4): 643-647.doi: 10.16333/j.1001-6880.2019.4.014

• Article • Previous Articles     Next Articles

Eremophilane-type sesquiterpenoids from Ligularia veitchiana

XU Jian-long,ZOU Kun,YANG Di,LI Wen-cong,QIAO Ting,LU Ying,CHENG Fan,WANG Hui*   

  1. Hubei Key Laboratory of Natural Products Research and Development,College of Biological and Pharmaceutical Sciences,China Three Gorges University,Yichang 443002,China
  • Online:2019-04-29 Published:2019-04-29

Abstract: To investigate eremophilane-type sesquiterpenoids from L.veitchiana,various chromatographic techniques,including silica gel column chromatography,ODS and preparative HPLC were used.The structures of the compounds were identified by means of spectroscopic and chemical data.As a result,13 eremophilane-type sesquiterpenoids were isolated from the 95% ethanol extract from Ligularia veitchiana and identified as eremophilenolide (1),eremophila-7(11),9-dien-8-one (2),eremophil-6-en-11-ol (3),8-oxo-eremophil-6-en-11-one (4),(6α,8α)-6-hydroxyeremophil-7(11)-en-12,8-olide (5),8β-hydroxyeremophil-7(11)-en-12,8α-olide (6),6β-hydroxy-8α-methoxyeremophil-7(11)-12,8β-olide (7),2α-hydroxyeremophil-11-en-9-one (8),6β-methoxy-8β-hydroxyeremophil-7(11)-en-12,8α-olide (9),6β-hydroxyeremophil-7(11)-en-12,8β-olide (10),6β-hydroxy-8β-methoxyeremophil-7(11)-12,8α-olide (11),6β,8β-dihydroxyeremophil-7(11)-en-12,8α-olide (12) and 6β,8α-dihydroxyeremophil-7(11)-en-12,8β-olide (13).Among them,compounds 5 and 10,7 and 11,12 and 13 are three pairs of diastereomers.Except for compound 3 and 5,all the above sesquiterpenoids were isolated from the plant for the first time.Cytotoxicities of all the compounds against cancer cell lines were evaluated in vitro by MTT assay,none of them showed significant growth inhibition of tumor cells HGC-27 and Caski.

Key words: L.veitchiana, eremophilane-type, sesquiterpenoid, anti-tumor

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