| Literature DB >> 28209279 |
Takahiro Matsumoto1, Seikou Nakamura1, Souichi Nakashima1, Tomoe Ohta1, Keiko Ogawa1, Masashi Fukaya1, Junko Tsukioka1, Tomohiro Hasei1, Tetsushi Watanabe1, Hisashi Matsuda2.
Abstract
Six neolignan glucosides, named isodonosides I-VI, and a megastigmane glucoside named isodonmegastigmane I, were isolated together with 15 known compounds from the methanolic extract of aerial parts of Isodon japonicus cultivated in Tokushima, Japan. The chemical structures of the compounds were elucidated based on their MS and NMR spectroscopic analysis. The absolute configurations of the neolignan and megastigmane glucosides were determined by derivatizations, by ECD (electronic circular dicroism) Cotton effect approximation, and by the modified Mosher's method. In addition, a significant cell protective effects of neolignan glucosides on benzo[a]pyrene-induced cytotoxicity was found.Entities:
Keywords: Glucoside; Isodon japonicus; Isodonmegastigmane; Isodonoside; Lamiaceae; Megastigmane; Neolignan
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Year: 2017 PMID: 28209279 DOI: 10.1016/j.phytochem.2017.02.007
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072