4.3 Article

Medicinal foodstuffs.: XXXIV.: Structures of new prenylchalcones and prenylflavanones with TNF-α and aminopeptidase N inhibitory activities from Boesenbergia rotunda

Journal

CHEMICAL & PHARMACEUTICAL BULLETIN
Volume 56, Issue 7, Pages 956-962

Publisher

PHARMACEUTICAL SOC JAPAN
DOI: 10.1248/cpb.56.956

Keywords

Boesenbergia rotunda; Zingiberaceae; krachaizin; rotundaflavone; tumor necrosis factor-alpha inhibitory activity; aminopeptidase N inhibitor

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The methanolic extract from the rhizomes of Boesenbergia rotunda (Zingiberaceae) was found to show inhibitory effect on tumor necrosis factor-alpha (TNF-alpha)-induced cytotoxicity in L929 cells (IC50=6.1 mu g/ml). By bioassay-guided separation, four new prenylcalcones, (+)-krachaizin A (1a) (-)-krachaizin A (1b), (+)-krachaizin B (2a), and (-)-krachaizin B (2b), and four new prenylflavanones, rotundaflavones Ia (3a), Ib (3b), IIa (4a), and IIb (4b), were isolated together with 18 known constituents (5a-7b and 8-19). The structures of eight new compounds were elucidated on the basis of physicochemical evidence. Among them, (+)-krachaizin B (2a), (-)krachaizin B (2b), (+)-4-hydroxypanduratin A (6a), (-)-4-hydroxypanduratin A (6b), (+)-isopanduratin A (7a), (-)-isopanduratin A (7b), alpinetin (10), cardamonin (14), and 2,6-dihydroxy-4-methoxydihydrochalcone (15) significantly inhibited TNF-alpha-induced cytotoxicity in L929 cells at 10 mu M. In addition, 2a, 2b, (+)-panduratins A (5a), (-)-panduratin A (5b), 6a, 7b, and geranyl-2,4-dihydroxy-6-phenylbenzoate (17) were found to show strong inhibitory effects on aminopeptidase N activity.

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