2015
DOI: 10.1080/14786419.2015.1055492
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A new monoterpene glucoside and complete assignments of dihydroflavonols ofPulicaria jaubertii: potential cytotoxic and blood pressure lowering activity

Abstract: One new monoterpene glucoside and five dihydroflavonols were isolated for the first time from the aerial parts of Pulicaria jaubertii and identified as p-menthane-2-O-β-D-glucopyranoside [1], dihydroquercetin (taxifolin) [2], 7,3'-di-O-methyltaxifolin [3], 3'-O-methyltaxifolin [4], 7-O-methyltaxifolin (padmatin) [5] and 7-O-methyl-dihydrokampferol (7-O-methylaromadenderin) [6]. The structures of these compounds were unambiguously assigned on the basis of NMR spectroscopic data ((1)H, (13)C, DEPT, HSQC, HMBC) a… Show more

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Cited by 25 publications
(25 citation statements)
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“…The EtOAc extract was the most active and was not toxic to RBL-2H3 cells (Figure 1). This extract was subjected to silica gel column chromatography, Sephadex LH-20 column chromatography, and RP HPLC to yield ten known flavonoids, such as, padmatin ( 1 ) [14], aromadendrin ( 2 ) [15], apigenin ( 3 ) [16], (2 R , 3 S , 2′’ R , 3′’ S )-wikstaiwanone C ( 4 ) [17], taxifolin ( 5 ) [14], (2 R , 3 R , 2′’ R , 3′’ S )-neochamaejasmine B ( 6 ) [18], (2 S , 3 R , 2′’ S , 3′’ R )-chamaejasmine ( 7 ) [18], naringenin ( 8 ) [16], afzelechin ( 9 ) [19], and catechin ( 10 ) [20] (Figure 2). These ten flavonoids were identified using 2D-NMR and HR-MS data.…”
Section: Resultsmentioning
confidence: 99%
“…The EtOAc extract was the most active and was not toxic to RBL-2H3 cells (Figure 1). This extract was subjected to silica gel column chromatography, Sephadex LH-20 column chromatography, and RP HPLC to yield ten known flavonoids, such as, padmatin ( 1 ) [14], aromadendrin ( 2 ) [15], apigenin ( 3 ) [16], (2 R , 3 S , 2′’ R , 3′’ S )-wikstaiwanone C ( 4 ) [17], taxifolin ( 5 ) [14], (2 R , 3 R , 2′’ R , 3′’ S )-neochamaejasmine B ( 6 ) [18], (2 S , 3 R , 2′’ S , 3′’ R )-chamaejasmine ( 7 ) [18], naringenin ( 8 ) [16], afzelechin ( 9 ) [19], and catechin ( 10 ) [20] (Figure 2). These ten flavonoids were identified using 2D-NMR and HR-MS data.…”
Section: Resultsmentioning
confidence: 99%
“…Pure compound 9 was identified from spectroscopic data as maltol 3-[6″-(2-(E)-butenoyl)-glucoside]. Ten other compounds were identified in SCAE by comparing 1 H-NMR, 13 C-NMR, and MS data with literature values; these compounds were benzoic acid (1), 20 daphnoretin (2), 21 apigenin 3, 22 genkwanin (4), 23 taxifolin 5, 24 apigenin 7-Oglucoside (6), 25 luteolin 7-Osambubioside 7, 26 genkwanin 5-Oglucoside (8), 27,28 matairesinoside (10), 29 and lariciresinol (11). 30 A β-hexosaminidase assay was used to assess the antiallergic effects of the 11 compounds isolated from S. chamaejasme (Figure 3).…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, dihydrochalcones are widely found in apple trees, other edible and medicinal plants 29 . Dihydroflavonols are mainly isolated from diets bicolour (Iridaceae), willow and pulicaria jaubertii 30‐32 …”
Section: Brief Overview Of Flavonoids: Structure Classification and Main Sourcesmentioning
confidence: 99%