
pmid: 29980108
Thirteen flavonoids were isolated from the fresh sweet fruit of Averrhoa carambola L. (Oxalidaceae), commonly known as star fruit, and their structures were determined by spectroscopic and chemical methods. 8-Carboxymethyl-(+)-epicatechin methyl ester, pinobanksin 3-O-β-d-glucoside, and carambolasides M-Q were undescribed structures. (+)-Epicatechin, aromadendrin 3-O-β-d-glucoside, helicioside A, taxifolin 3'-O-β-d-glucoside, galangin 3-O-rutinoside, and isorhamnetin 3-O-rutinoside were reported from this species for the first time. Pinobanksin 3-O-β-d-glucoside and carambolasides M-Q showed more potent 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) radical cation scavenging activity (IC50 = 5.3-2.3 μM) than l-ascorbic acid (10.5 μM). Further, (+)-epicatechin, pinobanksin 3-O-β-d-glucoside, isorhamnetin 3-O-rutinoside, and carambolasides O-Q exhibited weak porcine pancreatic lipase inhibitory activity.
Flavonoids, Averrhoa, Fruit, Molecular Conformation, Stereoisomerism, Biodiversity, Taxonomy
Flavonoids, Averrhoa, Fruit, Molecular Conformation, Stereoisomerism, Biodiversity, Taxonomy
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