2012
DOI: 10.1055/s-0032-1321285
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New flavonol glycosides from the leaves of Allium victorialis var. platyphyllum

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“…Further isolation was carried out via semi-preparative HPLC for fractions M2 and M3, resulting in the isolation of nine metabolites, including glycosidic metabolites and caffeoylshikimic acids (Figure 1). The isolated compounds were identified as kaempferol 3,7-di-O-β-D-glucopyranoside (1) [31], icariside B 2 (2) [32], (Z)-3-hexenyl β-D-glucopyranoside (3) [33], luteolin 5-O-β-D-glucopyranoside (4) [34], 4-O-β-D-glucopyranosyl caffeic acid (5) [35], clemastanin B (6) [36], 4-O-caffeoylshikimic acid (7) [37], (7S,8S)-threo-7,9,9 -trihydroxy-3,3 -dimethoxy-8-O-4 -neolignan-4-O-β-D-glucopyranoside (8) [38], 3-O-caffeoylshikimic acid (9) [39]. These identifications were based on the comparison of their NMR spectra with reported data and HR-ESI-MS analysis (Figures S1-S18).…”
Section: Isolation and Identification Of The Compoundsmentioning
confidence: 99%
“…Further isolation was carried out via semi-preparative HPLC for fractions M2 and M3, resulting in the isolation of nine metabolites, including glycosidic metabolites and caffeoylshikimic acids (Figure 1). The isolated compounds were identified as kaempferol 3,7-di-O-β-D-glucopyranoside (1) [31], icariside B 2 (2) [32], (Z)-3-hexenyl β-D-glucopyranoside (3) [33], luteolin 5-O-β-D-glucopyranoside (4) [34], 4-O-β-D-glucopyranosyl caffeic acid (5) [35], clemastanin B (6) [36], 4-O-caffeoylshikimic acid (7) [37], (7S,8S)-threo-7,9,9 -trihydroxy-3,3 -dimethoxy-8-O-4 -neolignan-4-O-β-D-glucopyranoside (8) [38], 3-O-caffeoylshikimic acid (9) [39]. These identifications were based on the comparison of their NMR spectra with reported data and HR-ESI-MS analysis (Figures S1-S18).…”
Section: Isolation and Identification Of The Compoundsmentioning
confidence: 99%
“…In this study, chromatographic separation of EtOAc and BuOH fractions from Sample 6 of the Drynaria fortunei J. Smith species was performed. The isolated compounds were identified as gallic acid (1) [25], 5-hydroxymethylfurfural (2) [26], protocatechuic acid (3) [27], coumaric acid 4-O-β-D-glucopyranoside (4) [28][29][30], caffeic acid 4-O-β-D-glucopyranoside (5) [31][32][33][34][35], 4-hydroxybenzoic acid (6) [26], lavandoside (7) [29,36], trans-p-sinapoyl-β-D-glucopyranoside (8) [33,36], 5,7-dihydroxychromone-7-O-neohesperidoside (9) [9,31], kaempferol 3-O-rhamnoside 7-O-glucoside (10) [31], kaempferol 3-O-glucopyranoside-7-O-arabinofuranoside (11) [31,37], neoeriocitrin (12) [7], naringin (13) [38], and hesperidin ( 14) [38] through NMR and MS analyses and comparison with previous research results. The chemical structure of the isolated compound is presented in Figure 1, and the corresponding NMR and MS data are provided in Table S1.…”
Section: Structural Identification Of Isolated Compounds 1-14mentioning
confidence: 99%