2011
DOI: 10.1016/j.foodchem.2011.04.078
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Characterisation of phenolic acid derivatives and flavonoids from different morphological parts of Helichrysum obconicum by a RP-HPLC–DAD-(−)–ESI-MSn method

Abstract: a b s t r a c tThe phenolic composition from different morphological parts of Helichrysum obconicum was investigated for the first time and 50 different phenolic compounds were detected. Phenolic acid conjugates, mainly mono-and di-caffeoylquinic acid derivatives, were the major components; some flavonoid derivatives were also detected in small amounts. Their separation and identification was performed by a high-performance liquid chromatography/electron spray ionisation tandem ion trap mass spectrometry metho… Show more

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Cited by 97 publications
(58 citation statements)
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“…The MS/MS spectrum on precursor ion at m/z 340.8 produced a fragment at m/z 178.7 (100%) (deprotonated caffeic acid) ( Table 1). The hexoside group probably was linked to caffeoyl moiety, since a base peak was observed at m/z 340.8 (Gouveia & Castilho, 2011;Negri et al, 2011). Compound 1 was characterized as a rosmarinic acid diglucoside, which was also found in bee pollen samples (Negri et al, 2011).…”
Section: Passiflora Sidifoliamentioning
confidence: 93%
“…The MS/MS spectrum on precursor ion at m/z 340.8 produced a fragment at m/z 178.7 (100%) (deprotonated caffeic acid) ( Table 1). The hexoside group probably was linked to caffeoyl moiety, since a base peak was observed at m/z 340.8 (Gouveia & Castilho, 2011;Negri et al, 2011). Compound 1 was characterized as a rosmarinic acid diglucoside, which was also found in bee pollen samples (Negri et al, 2011).…”
Section: Passiflora Sidifoliamentioning
confidence: 93%
“…The fragmentation pattern of Compound B displays an ion peak at m/z 515, indicating the loss of the first caffeoyl, loss of the second caffeoyl at m/z 353, and loss of the third caffeoyl at m/z 191 to yield quinic acid, a loss of caffeic acid at m/z 179, and another caffeoyl at m/z 135. Thus, the compound was characterized as 3,4-O-dicaffeoylquinic acid (Lin and Harnly, 2008;Gouveia and Castilho, 2011). Compound C exhibits fragment ions at m/z 179 and m/z 135, the characteristic ions of caffeic acid (Luo et al, 2003;Lin and Harnly, 2008;Plazonic et al, 2011).…”
Section: Fraction Yield and Lcms-ms Analysismentioning
confidence: 99%
“…Samples rich in flavonoids are known to possess low LD50 values against Artemia salina [29,30]. Several flavonoids were identified in H. devium [13] and H. melaleucum [17], while H. obconicum was rich in quinic acid derivatives [18]. These differences in the composition can contribute to the different toxicity of each plant.…”
Section: Artemia Salina Toxicitymentioning
confidence: 99%
“…However, this hypothesis is excluded based on our recent studies [13,17,18] where the polar extracts of H. devium, melaleucum and obconicum were analyzed by HPLC-DAD-ESI/MS n and the major compounds identified were hydroxycinnamic acids, mainly quinic acid derivatives, and flavonoids normally in their O-glycosilated form, and no high molecular weight compounds were discovered. (H. obconicum, methanol) ( Table 1).…”
Section: Radical Scavenging Activitymentioning
confidence: 99%