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Antioxidant Principles from <i>Bauhinia </i><i>t</i><i>arapotensis</i>

Journal of Natural Products · 2001 · Vol. 64(7) · pp. 892–895
Alessandra BracaNunziatina De TommasiLorenzo Di BariCosimo PìzzaMatteo PolitiIvano Morelli

Abstract

A new cyclohexenone (1) and a new caffeoyl ester derivative (2), together with the known compounds (-)-isolariciresinol 3-alpha-O-beta-D-glucopyranoside (3), (+)-1-hydroxypinoresinol 1-O-beta-D-glucopyranoside (4), isoacteoside (5), luteolin 4'-O-beta-D-glucopyranoside (6), and indole-3-carboxylic acid (7), were isolated from the leaves of Bauhinia tarapotensis. The structures of these new compounds were determined by spectroscopic data analysis. The antioxidant activities of 1-7 were determined by measuring their free radical scavenging effects, using the 1,1-diphenyl-2-dipicrylhydrazyl free radical (DPPH) and Trolox equivalent antioxidant activity (TEAC) methods, and the coupled oxidation of beta-carotene and linoleic acid. Compounds 3-5 showed good activities in the DPPH and TEAC tests, while compounds 1 and 2 were active in the coupled oxidation of beta-carotene and linoleic acid bioassay.

Phytochemicals and Antioxidant ActivitiesPhytochemistry and Biological ActivitiesNatural Antidiabetic Agents StudiesDPPHLinoleic acidTroloxChemistryAntioxidantTrolox equivalent antioxidant capacityOrganic chemistryStereochemistryFatty acid

MeSH terms

AntioxidantsBiphenyl CompoundsCaffeic AcidsChromansChromatography, High Pressure LiquidCyclohexanonesEcuadorFlavonoidsGlucosidesIndolesFabaceaeMagnetic Resonance SpectroscopyPhenolsPicratesPlants, Medicinal
Citations
980
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0.92
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12
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67%
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References
Antioxidant properties of phenolic compounds
Trends in Plant Science · 1997 · 4,292 citations
Structure-antioxidant activity relationships of flavonoids and phenolic acids
Free Radical Biology and Medicine · 1996 · 8,862 citations
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