Three 2′,4′,6′-Trioxygenated flavanones in roots of Echinosophora koreensis

作者: Munekazu Iinuma , Masayoshi Ohyama , Toshiyuki Tanaka , Mizuo Mizuno , Soon-Keun Hong

DOI: 10.1016/0031-9422(92)90056-V

关键词: FlavanoneKetoneEchinosophora koreensisChemistryMoietyPratenseinGenisteinFlavonoidScopoletinStereochemistry

摘要: Abstract Further investigation of the phenolic constituents roots Echinosophora koreensis , led to isolation 11 compounds. Their structures were determined as (2 S )-6-geranyl-5,7,2′,4′,6′-pentahydroxyflavanone (sophoraflavanone D), )-8-geranyl-5,7,2′,4′,6′-pentahydroxyflavanone E), )-6,8-di(γ,γ-dimethylallyl)-5,7,2′,4′,6′-pentahydroxyflavanone (kenusanone B), sophoraisoflavanone A, isosophoranone, 2,3-dehydrokievitone, sophoracarpane B, sophoronol, pratensein, genistein and scopoletin. Three them are novel flavanones possessing a 2′,4′,6′-trihydroxyl moiety on B ring.

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