| Literature DB >> 26832425 |
Yong-Jin Yang1, Juan Yao1, Xiao-Jie Jin1, Zhuan-Ning Shi1, Tian-Fei Shen1, Jian-Guo Fang1, Xiao-Jun Yao1, Ying Zhu2.
Abstract
A sulfated guaiane sesquiterpene lactone, an unusual pyridinium alkaloid with a sulfated guaiane sesquiterpene lactone nucleus, an amino conjugate of a sulfated guaiane sesquiterpene lactone, a bisabolane sesquiterpene, three tirucallane triterpenes, and six known compounds, were isolated from roots of Scorzonera divaricata. Their structures and absolute configurations were established based on chemical and spectroscopic methods, X-ray single crystal crystallography, and also by comparison with experimental and calculated ECD spectra. One of the tirucallane triterpenes exhibited significant cytotoxic activities against four human cancer cell lines (HL60, HeLa, HepG2, and SMMC-7721) in vitro. Two of sulfated guaiane sesquiterpenoids also exhibited antioxidant activities by scavenging ABTS cation free radicals. Tirucallane-type and dammarane-type triterpenes were not previously known in the genus Scorzonera. The study suggests that sulfated guaiane-type sesquiterpenoids are a valuable marker for systematic chemical studies in the Lactuceae tribe of the Asteraceae.Entities:
Keywords: ABTS radical scavenging capacity; Asteraceae; Circular dichroism; Cytotoxicity; Scorzonera divaricata; Sesquiterpenoid; Structure elucidation; Triterpenoids; X-ray single crystal diffraction
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Year: 2016 PMID: 26832425 DOI: 10.1016/j.phytochem.2016.01.015
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072