2015
DOI: 10.1016/j.indcrop.2015.01.068
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RP-HPLC–ESI–QTOF/MS2 based strategy for the comprehensive metabolite profiling of Sclerocarya birrea (marula) bark

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Cited by 30 publications
(16 citation statements)
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References 117 publications
(72 reference statements)
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“…The six compounds identified either tentatively or with the use of standards (quinic acid, catechin, epigallocatechin-3-gallate, epicatechin-3-O-gallate-epicatechin, procyanidin B2-3′3 di-O-gallate, epicatechin gallate) in this study have been previously tentatively identified in Marula stem bark in a study by Jimenez et al [ 15 ]. Additionally, in another study by Russo et al [ 14 ] the same compounds from our study were tentatively identified in Marula stem bark with the exception of quinic acid.…”
Section: Discussionmentioning
confidence: 59%
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“…The six compounds identified either tentatively or with the use of standards (quinic acid, catechin, epigallocatechin-3-gallate, epicatechin-3-O-gallate-epicatechin, procyanidin B2-3′3 di-O-gallate, epicatechin gallate) in this study have been previously tentatively identified in Marula stem bark in a study by Jimenez et al [ 15 ]. Additionally, in another study by Russo et al [ 14 ] the same compounds from our study were tentatively identified in Marula stem bark with the exception of quinic acid.…”
Section: Discussionmentioning
confidence: 59%
“…The variation in anti-elastase activity observed in our study from that reported in literature is difficult to explain as in our case elafin, the positive control gave the inhibitory activity as expected indicating the validity of the assay. Peak 5 and peak 6 had similar fragmentation patterns to the compounds epicatechin-3-O-gallate-epicatechin and procyanidin B2-3′3 di-O-gallate respectively, which were tentatively identified in Marula stem bark [ 14 , 15 ].…”
Section: Discussionmentioning
confidence: 99%
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“…The proposed method allowed the characterisation of 24 flavonoids and its derivatives, being the most abundant chemical group detected in the sample. In this sense, two isomers (peaks 2 and 5) with molecular ions at m/z 577.1351 were unambiguously identified as (epi)catechin–(epi)catechin (proanthocyanidin B2), according to characteristic fragments at m/z 289.0727 and 407.0778 . Peaks 4 and 8 displayed the same precursor ions [M – H] − at m/z 289.0718 and MS/MS product ions at m/z 109.0295 [M – H – 180 Da] − and 123.0452 [M – H – 166 Da] − .…”
Section: Resultsmentioning
confidence: 97%
“…Moreover, water and acetone extracts of stem bark show anticancer and proapoptotic activities [ 13 ]. Previous studies [ 14 , 15 , 16 ] investigated the phytochemical profile of different parts of S. birrea and it was found that polyphenols, including phenolic acid, flavonoids and their glycosides and procyanidins, were the main compounds. Considering the antioxidant and proapoptotic activity of the methanol extract of S. birrea root [ 12 ] and in order to clarify the biological activity of different parts of this plant, the aim of this study was to investigate the in vitro antioxidant properties and the cytotoxic activity of leaf and bark methanol extracts in a carcinoma cell line (HepG2).…”
Section: Introductionmentioning
confidence: 99%