1987
DOI: 10.1007/bf02311411
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Comparison of the sequential simplex method and linear solvent strength theory in HPLC gradient elution optimization of multicomponent flavonoid mixtures

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Cited by 20 publications
(2 citation statements)
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“…Apigenin does not appear to accumulate in chamomile flowers in the free form (Schreiber et al, 1990), and there is evidence to suggest that the aglycone is actually a product of post-harvest degradation (Maier et al, 1991). Besides apigenin and its derivatives, chamomile flowers also contain luteolin, quercetin, patuletin (and their glycosides), herniarin and umbelliferone (Redaelli et al, 1981a) as well as several phenylpropanoid derivatives (Dondi et al, 1987;Mulinacci et al, 2000).…”
Section: Introductionmentioning
confidence: 99%
“…Apigenin does not appear to accumulate in chamomile flowers in the free form (Schreiber et al, 1990), and there is evidence to suggest that the aglycone is actually a product of post-harvest degradation (Maier et al, 1991). Besides apigenin and its derivatives, chamomile flowers also contain luteolin, quercetin, patuletin (and their glycosides), herniarin and umbelliferone (Redaelli et al, 1981a) as well as several phenylpropanoid derivatives (Dondi et al, 1987;Mulinacci et al, 2000).…”
Section: Introductionmentioning
confidence: 99%
“…Nine compounds were confirmed via a comparison with the standards (37, 42–44, 57, 59, 63, 65, and 66) and the others were tentatively identified via examination of the MS spectra. Some flavonoids specific for chamomile, such as 6-methoxyapigenin or hispidulin, 6-methoxyluteolin or nepetin [ 22 ], 6-hydroxyquercetin or quercetagetin [ 23 ], and 6-methoxyquercetin or patuletin [ 24 ], were also found in this study. Compound 50 was marked as an apigenin derivative, because its exact structure could not be suggested.…”
Section: Resultsmentioning
confidence: 56%