Antibacterial and cytotoxic phenolic metabolites from the fruits of Amorpha fruticosa

Autor: Raha Orfali, Adriana Díaz, Nidja Rehberg, Peter Proksch, Rini Muharini, Wenhan Lin, Rainer Kalscheuer, Zhen Liu, Weaam Ebrahim, Rudolf Hartmann, Tibor Kurtán, Attila Mándi
Rok vydání: 2017
Předmět:
Zdroj: Phytotherapie 2017 „Von der Innovation zur Evidenz“.
ISSN: 1438-9584
DOI: 10.1055/s-0037-1607173
Popis: Fourteen new natural products, namely, 2-[(Z)-styryl]-5-geranylresorcin-1-carboxylic acid (1), amorfrutin D (2), 4-O-demethylamorfrutin D (3), 8-geranyl-3,5,7-trihydroxyflavanone (4), 8-geranyl-5,7,3′-trihydroxy-4′-methoxyisoflavone (5), 6-geranyl-5,7,3′-trihydroxy-4′-methoxyisoflavone (6), 8-geranyl-7,3′-dihydroxy-4′-methoxyisoflavone (7), 3-O-demethyldalbinol (8), 6a,12a-dehydro-3-O-demethylamorphigenin (9), (6aR,12aR,5′R)-amorphigenin (10), amorphispironones B and C (11 and 12), resokaempferol 3-O-β-d-glucopyranosyl-(1→2)-β-d-glucopyranoside-7-O-α-l-rhamnopyranoside (13), and daidzein 7-O-β-d-glucopyranosyl-(1→2)-β-d-glucopyranoside (14), together with 40 known compounds, were isolated from the fruits of Amorpha fruticosa. The structures of the new compounds were elucidated by 1D and 2D NMR spectroscopic analysis as well as from the mass spectrometry data. ECD calculations were performed to determine the absolute configurations of 11 and 15. Compounds 1, 4–6, and 16–23 showed potent to moderate antibac...
Databáze: OpenAIRE