| Literature DB >> 27351981 |
Yuka Kanehira1, Susumu Kawakami2, Sachiko Sugimoto1, Katsuyoshi Matsunami1, Hideaki Otsuka3,4.
Abstract
Extensive isolation work on the 1-BuOH-soluble fraction of a MeOH extract of the aerial parts of Dianthus japonicus afforded three further triterpene glycosyl estsers, termed dianthosaponins G-I, an anthranilic acid amide glucoside and a C-glycosyl flavonoid along with one known triterpene saponin. Their structures were elucidated from spectroscopic evidence. The cytotoxicity of the isolated compounds toward A549 cells was evaluated.Entities:
Keywords: Anthranilic acid amide glucoside; Caryophyllaceae; Dianthus japonicus; Flavonoid glycoside; Oleanane; Triterpene saponin
Mesh:
Substances:
Year: 2016 PMID: 27351981 DOI: 10.1007/s11418-016-1019-8
Source DB: PubMed Journal: J Nat Med ISSN: 1340-3443 Impact factor: 2.343