2014
DOI: 10.1021/jf500977d
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Characterization of Phenolic Compounds in Brazilian Pepper (Schinus terebinthifolius Raddi) Exocarp

Abstract: The objective of this study was to characterize the phenolic composition of Brazilian pepper (Schinus terebinthifolius Raddi) exocarp extract. Using UHPLC-DAD-MS/MS analysis, four anthocyanins, three biflavonoids, gallic acid, and two types of hydrolyzable tannins (galloyl glucoses, galloyl shikimic acids) were tentatively identified. The structure of the so far unknown 7-O-methylpelargonidin 3-O-β-D-galactopyranoside was elucidated by 2D NMR. Within the group of gallotannins, galloyl shikimic acids with uncom… Show more

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Cited by 60 publications
(52 citation statements)
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“…Solid samples were extracted by acidified methanol/water (Wu et al, 2004), liquid samples were diluted appropriately by the same solvent. Anthocyanins were analysed by HPLC and quantified at 500 nm using cyanidin 3-O-glucoside as reference as described elsewhere (Feuereisen et al, 2014).…”
Section: Methodsmentioning
confidence: 99%
“…Solid samples were extracted by acidified methanol/water (Wu et al, 2004), liquid samples were diluted appropriately by the same solvent. Anthocyanins were analysed by HPLC and quantified at 500 nm using cyanidin 3-O-glucoside as reference as described elsewhere (Feuereisen et al, 2014).…”
Section: Methodsmentioning
confidence: 99%
“…[ 65 ] These are specific phenolic lipids (6‐alkylsalicylic acids) that have been also found in other members of the Anacardiaceae family such as the pistachio nut ( Pistacia vera L.) [ 66 ] and Brazilian pepper ( Schinus terebinthifolius Raddi). [ 67 ] Interestingly, anacardic acids isolated from cashew nuts have been shown to have a variety of biological properties including potential antioxidant activity. [ 65,68 ]…”
Section: Chemistry and Quality Of Nut Oilsmentioning
confidence: 99%
“…Equipment and experimental conditions are described elsewhere (Feuereisen et al, 2014) with the following modifications: the gradient started with 2% B and raised linearly to 36.3% within 20 min, then to 100% B within 1 min and holding for 2 min as a washing step; back to 2% B within 2 min and equilibrating for 2 min. Eluent A was water with 0.1% formic acid, eluent B was acetonitrile with 0.1% formic acid, the flow was 0.4 mL/min on a BEH Shield RP18 column (150 mm  2.1 mm, 1.7 mm) by Waters (Milford, MA) at 40 C. The peaks were identified by MS/MS, i.e.…”
Section: Analysis Of Polyphenolsmentioning
confidence: 99%