2010
DOI: 10.1016/j.foodchem.2009.07.004
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Flavonoid glycosides in the shoot system of Okinawa Taumu (Colocasia esculenta S.)

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Cited by 47 publications
(39 citation statements)
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“….4 (C-1 00 ), 70.8 (C-2 00 ), 78.7 (C-3 00 ), 70.6 (C-4 00 ), 81.9 (C-5 00 ), 61.3 (C-6 00 ). Comparison of these data with the literature led to the identification of this compound as vitexin (Leong et al, 2010). compound is identified as quercetin (Guvenalp & Demirezer, 2005;Markham, 1978).…”
mentioning
confidence: 97%
See 1 more Smart Citation
“….4 (C-1 00 ), 70.8 (C-2 00 ), 78.7 (C-3 00 ), 70.6 (C-4 00 ), 81.9 (C-5 00 ), 61.3 (C-6 00 ). Comparison of these data with the literature led to the identification of this compound as vitexin (Leong et al, 2010). compound is identified as quercetin (Guvenalp & Demirezer, 2005;Markham, 1978).…”
mentioning
confidence: 97%
“…It was identified as orientin (Leong et al, 2010). .4 (C-1 00 ), 70.8 (C-2 00 ), 78.7 (C-3 00 ), 70.6 (C-4 00 ), 81.9 (C-5 00 ), 61.3 (C-6 00 ).…”
mentioning
confidence: 99%
“…The structures of isolated compounds were identified by a combination of spectroscopic methods (MS, 1 D NMR and 2D NMR) and comparisons with the literature data as a mixture of quercetin 3-β-Ogalactopyranoside or hyperoside (1) and quercetin 3-β-Oglucopyranoside or isoquercitrin (1:1) (2) (Almeida et al, 1998;Costa et al, 2007;Ohguchi et al, 2010), quercetin 3-O-α-rhamnoside or quercitrin (3) (Zhong et al, 1997), luteolin 6-C-β-glucopyranoside or orientin (4) (Li et al, 2009), apigenin-6-C-glucoside or isovitexin (5) (Leong et al, 2010), kaempferol 3-O-α-rhamnoside (6) (Fossen et al, 1999) and lupenone (7) (Prachayasittikul et al, 2010), respectively. Characterization of the sugar moieties from the mixture of quercetin 3-β-galactopyranoside (1) and quercetin 3-β-glucopyranoside (2) was performed according Cota et al 2008b.…”
Section: Resultsmentioning
confidence: 82%
“…Chromatography indicated that it was pure and led to its identification as compound 6 (324 mg). Thus, on the basis of nuclear magnetic resonance (NMR) 1 H and 13 C NMR data analysis, the structures of compounds 1-6 were identified as protocatechuic acid, 19 methyl gallate, 20 isoquercitrin, 21 isovitexin, 22,23 rutin, 21 and corilagin, 24 respectively (Fig. 1).…”
Section: Isolation and Identification Of Compounds From Agfmentioning
confidence: 99%