| Literature DB >> 29658323 |
Rui Liu1,2, Hui Zou2,3, Zhen-Xing Zou1, Fei Cheng1, Xia Yu2, Ping-Sheng Xu1, Xiao-Min Li1, Dai Li1, Kang-Ping Xu2, Gui-Shan Tan1,2.
Abstract
Two new anthraquinone derivatives, selaginones A (1) and B (2), and one new triarylbenzophenone analog, selagibenzophenone B (3), were isolated from Selaginella tamariscina (Beauv.) Spring. Their structures were established by 1D-, 2D-NMR and HR-ESI-MS data. Compounds 1 and 2 represent the uncommon examples of aryl substituted anthraquinone derivatives. Especially, compound 2 is a unique anthranone with exceptional structural feature, in which a p-hydroxyphenyl moiety is attached to the C-10 position. Compound 3 is the second naturally occurring triarylbenzophenone and showed moderate activity against SMCC-7721 and MHCC97-H cell lines with IC50 values of 39.8, 51.5 μM respectively.Entities:
Keywords: Selaginella tamariscina; anthranone; anthraquinone; hepatocellular carcinoma; selagibenzophenone B; selaginone A; selaginone B
Year: 2018 PMID: 29658323 DOI: 10.1080/14786419.2018.1452008
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861