| Literature DB >> 27889540 |
ZhenXing Zou1, KangPing Xu2, PingSheng Xu3, XiaoMin Li3, Fei Cheng2, Jing Li2, Xia Yu2, DongSheng Cao2, Dan Li3, Wei Zeng3, GuoGang Zhang4, GuiShan Tan5.
Abstract
Six new flavonoids, seladoeflavones A-F (1-6), were isolated from the whole herbs of Selaginella doederleinii, together with one known flavonoid (7). Their structures including absolute configuration were characterized on the basis of extensive spectroscopic methods including NMR, HRMS, and electronic circular dichroism (ECD). All compounds consist of an aryl substituent at the C-3' position of naringenin or apigenin skeletons, and compounds 1 and 6 were identified as R configurations, which are uncommonly encountered in nature. A possible biosynthetic pathway was postulated. In addition, bioassay of the isolates revealed that 5-7 exhibited moderate cytotoxicity against three human cancer cell lines NCI-H460, A549, and K562 in vitro with IC50 values ranging from 8.17 to 18.66μM.Entities:
Keywords: Cytotoxicity; Selaginella; Selaginella doederleinii; Unique flavonoids
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Year: 2016 PMID: 27889540 DOI: 10.1016/j.fitote.2016.11.014
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882