1997
DOI: 10.1590/s0103-50531997000600012
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Two new norphenylpropanoid glucosides and hemipholin from the flowers of Ononis vaginalis

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Cited by 13 publications
(7 citation statements)
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“…Moreover, several flavanones (dihydroflavones) were also characterized for first time in V. faba : eriodictyol‐di‐ C ‐dihexoside ( 60 ) , naringenin 6,8‐di‐ C ‐hexoside ( 88 ) , naringenin 6‐ C ‐α‐ d ‐glucoside (hemipholin; 101 ) , naringenin 7‐ O ‐glucoside (prunin; 131 ) , and pinocembrin ( 144 ) . Compounds 60 , 84 , 88 , 91 , 101 , and 110 gave a fragmentation pattern typical of C ‐glycosides, as commented above.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, several flavanones (dihydroflavones) were also characterized for first time in V. faba : eriodictyol‐di‐ C ‐dihexoside ( 60 ) , naringenin 6,8‐di‐ C ‐hexoside ( 88 ) , naringenin 6‐ C ‐α‐ d ‐glucoside (hemipholin; 101 ) , naringenin 7‐ O ‐glucoside (prunin; 131 ) , and pinocembrin ( 144 ) . Compounds 60 , 84 , 88 , 91 , 101 , and 110 gave a fragmentation pattern typical of C ‐glycosides, as commented above.…”
Section: Resultsmentioning
confidence: 99%
“…The methanol extract (6.5 g) yielded taxifolin ( 1 ) [ 8 ], astragalin ( 2 ) [ 9 ], isorhamnetin 3- O -β- d -glucoside ( 3 ) [ 10 ], (−)-catechin ( 4 ) [ 11 ], benzoate glucoside ( 5 ) [ 12 ], benzyl-β- d -glucoside ( 6 ) [ 13 ], benzyl-β- d -rutinoside ( 7 ) [ 14 ], 2-methoxy-phenyl-β- d -glucoside ( 8 ) [ 15 ], 3,4-dimethoxyphenyl-β- d -glucoside ( 9 ) [ 16 ], raspberry ketone ( 10 ) [ 17 ], p-anisic acid ( 11 ) [ 18 ], 4-hydroxybenzoic acid 4- O -β- d -glucoside ( 12 ) [ 19 ], p-coumaric acid ( 13 , 6.0 mg) and its glucoside ( 14 ) [ 20 , 21 ], trans -vaginoside ( 15 ) [ 22 ] and abscisic alcohol glucoside ( 16 ) [ 23 ]. The methanol:water (5:1) extract afforded kaempferol-3- O -β-rutinoside ( 17 ) [ 24 ], kaempferide-3- O -β-rutinoside ( 18 ) [ 25 ], tiliroside ( 19 ) [ 26 ], and syringetin 3- O -β- d -glucoside ( 20 ) [ 27 ] ( Figure 1 ).…”
Section: Resultsmentioning
confidence: 99%
“…Compound 2 was identified as quercitrin, a 3-O-rhamnosylquercetin, by comparison of its 1 H NMR spectral data with those found in the literature (Pyo et al, 2002). Compound 3 was identified as 6-C-glycosylnaringenin through comparison of its spectral data with those reported 1 H and 13 C NMR spectral data in literature (Budzianowski and Skrzypczakowa, 1978;Abdel-Kader, 1997). Compound 4 was an impure catechin derivative and due to the weak inhibitory activity further efforts for the structure elucidation were not applied.…”
Section: Tablementioning
confidence: 99%