Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5177576 | Phytochemistry Letters | 2008 | 5 Pages |
A flavonoid glycoside, kaempferol 3-O-β-d-glucopyranosyl (1 â 2)-O-β-d-glucopyranosyl (1 â 2)-O-[α-l-rhamnopyranosyl-(1 â 6)]-β-d-glucopyranoside (1), along with two known C- and O-flavonoid glycosides (2 and 3, respectively), were isolated from carnation (Dianthus caryophyllus). The structures of the isolated compounds have been elucidated unambiguously by UV, MS, and a series of 1D and 2D NMR analyses. The isolated compounds and other flavonoid glycoside analogues exhibited antifungal activity against different Fusarium oxysporum f.sp. dianthi pathotypes.
Graphical abstractThe new kaempferol 3-O-β-d-glucopyranosyl (1 â 2)-O-β-d-glucopyranosyl (1 â 2)-O-[α-l-rhamnopyranosyl-(1 â 6)]-β-d-glucopyranoside (1) has been isolated from carnation (Dianthus caryophyllus) along with two known C- and O-flavonoid glycosides. The isolated compounds exhibited antifungal activity against different Fusarium oxysporum f.sp. dianthi pathotypes.