1988
DOI: 10.1055/s-2006-962418
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Isolation of Flavonol Glycosides fromGinkgo bilobaLeaves

Abstract: 6-Hydroxykynurenic acid and nine flavonol glycosides were isolated and identified from the leaves of GINKGO BILOBA: three of them were identified in Ginkgo for the first time, and two others are unusual P-coumaroyl esters.

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Cited by 31 publications
(11 citation statements)
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“…MS/MS spectra of compound 19 showed major fragment ions at m / z 509 [(M + H)-146] + and 347 [(M + H)-146-162] + , indicating the loss of deoxyhexose and hexose groups. Furthermore, comparing the 1 H-NMR spectral data with those in the literature, they were assigned as syringetin 3- O -β- d -glucopyranoside ( 18 ) (Guo et al 2010) and syringetin 3- O -rutinoside ( 19 ) (Victoire et al 1988). …”
Section: Resultsmentioning
confidence: 99%
“…MS/MS spectra of compound 19 showed major fragment ions at m / z 509 [(M + H)-146] + and 347 [(M + H)-146-162] + , indicating the loss of deoxyhexose and hexose groups. Furthermore, comparing the 1 H-NMR spectral data with those in the literature, they were assigned as syringetin 3- O -β- d -glucopyranoside ( 18 ) (Guo et al 2010) and syringetin 3- O -rutinoside ( 19 ) (Victoire et al 1988). …”
Section: Resultsmentioning
confidence: 99%
“…In addition, 13 known compounds were elucidated as uracil, 7) isorhamnetin 3-O-a-arabinopyranoside, 8) rhamnetin 3-O-b-glucopyranoside (4), 9) rhamnocitrin 3-O-b-glucopyranoside (5), 10) adenosine, 11) quercetin 3-O-a-arabinopyranoside, 8,12) isorhamnetin 3-O-b-glucopyranoside (6), 13) genistein 4Ј-O-b-glucopyranoside (7), 14) dihydrokaempferol 4Ј-Ob-glucopyranoside (8), 15) acacetin 7-O-b-rutinoside (9), 16) isorhamnetin 3-O-b-rutinoside (10), 17,18) quercetin 3-O-bglucopyranoside (11), 19) and rutin (12), 19) by spectroscopic analysis.…”
Section: Resultsmentioning
confidence: 99%
“…To confirm the site of glucosylation by rNTGT2, the glucosylated product of kaempferol was purified by preparative HPLC. The glucosylated product of kaempferol was identified as kaempferol 7-O-β-glucopyranoside by the comparisons of its FAB-MS, 1 H-NMR and 13 C-NMR spectra with those described in the literature [25]. The site of glucosylation, 7-OH, was finally confirmed by the 1 H-Detected Heteronuclear Multiple Bond Connectivity experiment, in which, the correlation of the anomeric proton (δ H 5.05) with C-7 (δ 164.3) was observed.…”
Section: Properties Of Recombinant Ntgt2 Enzymementioning
confidence: 99%