2013
DOI: 10.1002/pca.2430
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Characterisation of Homoflavonoids from Three Ophioglossum Species Using Liquid Chromatography with Diode Array Detection and Electrospray Ionisation Tandem Mass Spectrometry

Abstract: The HPLC-DAD-ESI/MS(n) method obtained in the present study provided a powerful tool for identifying homoflavonoids from ferns in the genus Ophioglossum.

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Cited by 6 publications
(7 citation statements)
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“…Six homoflavonoids, ophioglonin, ophioglonin 7-O-β-Dglucopyranoside, ophioglonol, ophioglonol prenyl ether, ophioglonol 4′-O-β-D-glucopyranoside, and isoophioglonin 7-O-β-D-glucopyranoside, quercetin, luteolin, kaempferol, 3,5,7,3′,4′-pentahydroxy-8-prenylflavone, and quercetin 3-O-methyl ether, were isolated from O. petiolatum (Lin et al 2005a, b). Homoflavonoids were also found in O. vulgatum and O. thermale (Wan et al 2013). These compounds can be divided to two groups: type I homoflavonoids, which have an additional carbon atom attached to the C-3 position of ring C, and undergo competing losses of H 2 O and CH 2 O from their aglycone ions; and type II homoflavonoids, which bear an additional carbon atom at the C-2′ position of ring B, forming a new ring (Wan et al 2013;Lin et al 2005a, b;Wan et al 2012).…”
Section: Ophioglossaceaementioning
confidence: 90%
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“…Six homoflavonoids, ophioglonin, ophioglonin 7-O-β-Dglucopyranoside, ophioglonol, ophioglonol prenyl ether, ophioglonol 4′-O-β-D-glucopyranoside, and isoophioglonin 7-O-β-D-glucopyranoside, quercetin, luteolin, kaempferol, 3,5,7,3′,4′-pentahydroxy-8-prenylflavone, and quercetin 3-O-methyl ether, were isolated from O. petiolatum (Lin et al 2005a, b). Homoflavonoids were also found in O. vulgatum and O. thermale (Wan et al 2013). These compounds can be divided to two groups: type I homoflavonoids, which have an additional carbon atom attached to the C-3 position of ring C, and undergo competing losses of H 2 O and CH 2 O from their aglycone ions; and type II homoflavonoids, which bear an additional carbon atom at the C-2′ position of ring B, forming a new ring (Wan et al 2013;Lin et al 2005a, b;Wan et al 2012).…”
Section: Ophioglossaceaementioning
confidence: 90%
“…Homoflavonoids were also found in O. vulgatum and O. thermale (Wan et al 2013). These compounds can be divided to two groups: type I homoflavonoids, which have an additional carbon atom attached to the C-3 position of ring C, and undergo competing losses of H 2 O and CH 2 O from their aglycone ions; and type II homoflavonoids, which bear an additional carbon atom at the C-2′ position of ring B, forming a new ring (Wan et al 2013;Lin et al 2005a, b;Wan et al 2012).…”
Section: Ophioglossaceaementioning
confidence: 90%
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“…The commonest example in many forest states has been observed to be the Ophioglossum ( Figure 4 e) species on the ground and Marsilea spp ( Figure 4 f) from the aquatic ecosystem. Flavonoids were isolated from the aerial parts of the pteridophyte O. vulgatum ., including 3- O -methylquercetin and its glucosides, 5’-isoprenyl-3- O -ethylquercetin 4’,7-di-β- d -glucopyranoside, 3- O -methylquercetin 4’-β- d -glucopyranoside 7-[ O -β- d- glucopyranosyl-(1 → 2)-β- d -glucopyranoside [ 18 , 52 ]. Seven new homoflavonoid glucosides, pedunculosumosides A–G, were isolated from the ethanolic extracts of whole O .…”
Section: Methods: Field Work and Descriptionmentioning
confidence: 99%
“…Six homoflavonoids, ophioglonin, ophioglonin 7- O -β- d- glucopyranoside, ophioglonol, ophioglonol prenyl ether, ophioglonol 4’- O -β- d -glucopyranoside, and isoophioglonin 7- O -β- d -glucopyranoside, quercetin, luteolin, kaempferol and 3,5,7,3’,4’-pentahydroxy-8-prenylflavone etc. [ 18 , 52 ].…”
Section: Methods: Field Work and Descriptionmentioning
confidence: 99%