Literature DB >> 24841969

Cytotoxic triterpenoid glycosides from the roots of Camellia oleifera.

Xia Li1, Jianping Zhao2, Cuiping Peng1, Zhong Chen1, Yanli Liu1, Qiongming Xu1, Ikhlas A Khan1, Shilin Yang1.   

Abstract

Eight new triterpenoid saponins, oleiferosides A-H (1-8), were isolated from the EtOH extract of the roots of Camellia oleifera. Their structures were elucidated by a combination of 1D and 2D NMR techniques, mass spectrometry, and chemical methods. All were characterized to be oleanane-type saponins with sugar moieties linked to C-3 of the aglycone. Cytotoxic activities of these saponins were evaluated against four human tumor cell lines (A549, B16, BEL-7402, and MCF-7) by using the MTT in vitro assay. Compound 3 exhibited potent cytotoxic activitiy against all the tested cell lines with IC50 values < 10 µM. Compounds 1, 2, 4, and 5 showed moderate cytotoxic activities toward the tested cell lines. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2014        PMID: 24841969     DOI: 10.1055/s-0034-1368428

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  1 in total

1.  Phytochemical constituents of Camellia osmantha fruit cores with antithrombotic activity.

Authors:  Li Yang; Gui-Liang Xie; Jin-Lin Ma; Xiao-Qiong Huang; Yao Gu; Lei Huang; Hai-Yan Chen; Xi-Lin Ouyang
Journal:  Food Sci Nutr       Date:  2022-03-21       Impact factor: 3.553

  1 in total

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