2016
DOI: 10.20307/nps.2016.22.1.41
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Flavonoid Glycosides from the Flowers ofPulsatilla koreanaNakai

Abstract: − Extraction and fractionation of Pulsatilla koreana flowers followed by, repeated open column chromatography for EtOAc and n-BuOH fractions yielded four flavonoid glycosides, namely, astragalin (1), tiliroside (2), buddlenoide A (3), and apigenin-7-O-(3''-E-p-coumaroyl)-glucopyranoside (4). The chemical structures of these flavonoid glycosides were elucidated on the basis of various spectroscopic methods including electronic ionization mass spectrometry (EI-MS), 1D NMR ( 1 H, 13C, DEPT), 2D NMR (gCOSY, gHSQC,… Show more

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Cited by 13 publications
(8 citation statements)
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“…C-NMR data of F1 with the data published previously [10]. The 1 3 C-NMR data obtained from the current study were collected in dimethylsulfoxide-d6, and those published previously were in dimethylsulfoxide-d6 position 1 3 C-NMR data obtained from the current study collected in dimethylsulfoxide-d6/ ppm C-NMR data of F3 with the data published previously [9]. The 1 3 C-NMR data obtained from the current study were collected in dimethylsulfoxide-d6, and those published previously were in methanol-d4 position 1 3 C-NMR data obtained from the current study collected in dimethylsulfoxide-d6/ ppm A comparison of the 13 C-NMR data of F1 with the data published previously [11] was listed in Table 3.…”
Section: Resultsmentioning
confidence: 65%
See 1 more Smart Citation
“…C-NMR data of F1 with the data published previously [10]. The 1 3 C-NMR data obtained from the current study were collected in dimethylsulfoxide-d6, and those published previously were in dimethylsulfoxide-d6 position 1 3 C-NMR data obtained from the current study collected in dimethylsulfoxide-d6/ ppm C-NMR data of F3 with the data published previously [9]. The 1 3 C-NMR data obtained from the current study were collected in dimethylsulfoxide-d6, and those published previously were in methanol-d4 position 1 3 C-NMR data obtained from the current study collected in dimethylsulfoxide-d6/ ppm A comparison of the 13 C-NMR data of F1 with the data published previously [11] was listed in Table 3.…”
Section: Resultsmentioning
confidence: 65%
“…5A). A comparison of the 13 C-NMR data of F3 with the data published previously [9] was listed in Table 1.…”
Section: Resultsmentioning
confidence: 99%
“…The structures of the nine major compounds in the EA and n-BuOH fractions were predicted based on their MS/MS fragment patterns (Figure 2A [19,20], and kaempferol 7-O-α-l-rhamnopyranoside ( 9) [21] by comparing their physicochemical properties and NMR spectra with those previously reported. 2D).…”
Section: Bioactivity-guided Isolation and Dereplication Of The Active Compoundsmentioning
confidence: 99%
“…Thus, 3 was confirmed as chrysoeriol (3′-methoxy-4′,5,7-trihydroxyflavone). 2) [11]. Thus, the compound 5 was confirmed as kaempferol 3-O-β-D-glucopyranoside or astragalin.…”
Section: Extraction and Isolationmentioning
confidence: 89%