Flavonoid aglycones from the leaf and stem exudates of some Geraniaceae species.

Six species of Pelargonium and one species of Geranium were studied for their surface flavonoids. Some of them were found to exhibit an unexpectedly high number of methylated flavonoids, mostly flavonols. The chemotaxonomic significance of exudate flavonoid diversification is shortly addressed.

Chemodiversity of exudate flavonoids in Dionysia (Primulaceae): a comparative study.

More than 60 accessions of various Dionysia spp. were analysed for their exudate flavonoid composition. Many Dionysia spp.

Exudate flavonoids of Primula spp: structural and biogenetic chemodiversity.

Several new accessions of the genus Primula and of the closely related Cortusa matthioli have been studied for their exudate flavonoid profiles. Unsubstituted flavone, 5-hydroxy-, 2'-hydroxyflavone and 5,2'-dihydroxyflavone were found as main components. Several other rather unusual substitution patterns were also found.

Exudate flavonoids of some Juglandaceae.

Six species of Juglandaceae have been checked for the occurrence of flavonoid aglycones on their leaf and fruit surfaces. Except for one, they exhibit flavonols, mostly methyl ethers of kaempferol and quercetin, including 6-O-substituted derivatives. Apigenin and acacetin are the only flavones found so far.

Contribution of methylated exudate flavonoids to the anti-inflammatory activity of Grindelia robusta.

The flavonoid pattern of an acetonic extract of Grindelia robusta Nutt. was investigated in detail. The flavonoids were enriched by CC.

Chemodiversity of exudate flavonoids in Cassinia and Ozothamnus (Asteraceae, Gnaphalieae).

The lipophilic exudates deposited on aerial parts of four species of Cassinia and twelve species of Ozothamnus (Asteraceae, Gnaphalieae) have been analyzed for the presence of flavonoid aglycones and some other phenolics. A total of 55 flavonoids were identified, including several rare flavonols. Flavonols are prevailing over flavones, and 8-O-substitution is dominant in both groups.

Triterpenoids as major components of the insect-trapping glue of Roridula species.

Roridula dentata and R. gorgonias, two South African plants that were formerly believed to be carnivorous, exhibit an extremely sticky exudate at the tips of secretory trichomes. Unlike the trapping mucilage of Droseraceae, it does not consist of acidic polysaccharides.

Effect of Egyptian propolis on the susceptibility of LDL to oxidative modification and its antiviral activity with special emphasis on chemical composition.

The antioxidant activity of eight Egyptian propolis samples from different localities was evaluated by the antioxidative potential and capacity of the DPPH-ESR signal, superoxide anion generated in the xanthine-xanthine oxidase (XOD) system and low density lipoprotein (LDL) peroxidation assay. As, F, Is and D samples showed the highest antioxidative capacity and potential, respectively. The El, IsR, Is, D and So samples exhibited highly significant antioxidant activity in the XOD system and in LDL peroxidation assays.

Chemodiversity of exudate flavonoids in seven tribes of Cichorioideae and Asteroideae (Asteraceae).

Members of several genera of Asteraceae, belonging to the tribes Mutisieae, Cardueae, Lactuceae (all subfamily Cichorioideae), and of Astereae, Senecioneae, Helenieae and Heliantheae (all subfamily Asteroideae) have been analyzed for chemodiversity of their exudate flavonoid profiles. The majority of structures found were flavones and flavonols, sometimes with 6- and/or 8-substitution, and with a varying degree of oxidation and methylation. Flavanones were observed in exudates of some genera, and, in some cases, also flavonol- and flavone glycosides were detected.

Sequential O-methylation of tricetin by a single gene product in wheat.

Flavonoid compounds are ubiquitous in nature. They constitute an important part of the human diet and act as active principles of many medicinal plants. Their O-methylation increases their lipophilicity and hence, their compartmentation and functional diversity.

Highly oxygenated guaianolides and eudesman-12-oic acids from Balsamorhiza sagittata and Balsamorhiza macrophylla.

Investigation of lipophilic exudates from the aerial parts of Balsamorhiza sagittata and B. macrophylla afforded three new highly oxygenated guaianolides (1-3), in addition to known guaianolides, germacranolide and eudesmane acids. Their chemical structures were elucidated by spectroscopic methods and the data for the compounds are reported in Tables 1 and 2 and in Experimental.

Exudate flavonoids in some Gnaphalieae and Inuleae (Asteraceae).

Three members of the tribe Gnaphalieae and six members of the tribe Inuleae (Asteraceae) were analyzed for their exudate flavonoids. Whereas some species exhibit rather trivial flavonoids, others produce rare compounds. Spectral data of rare flavonoids are reported and their structural identification is discussed.

Chemodiversity of surface flavonoids in Solanaceae.

Several species of Nicotiana and Solanum and further members of the Solanaceae have been examined for their exudate flavonoids. Most of the aglycones are widespread flavonols, but rare and unusual flavonols were also found, e.g.

Exudate flavonoids of eight species of Ceanothus (Rhamnaceae).

Leaf glands of Ceanothus species excrete a lipophilic material that contains a variety of flavonoids. Most of these are aglycones, but some glycosides were also observed. Seven out of eight species exhibit flavonols, whereas flavones are excreted by only one species.

Biological effects of epicuticular flavonoids from Primula denticulata on human leukemia cells.

The biological effects of epicuticular substances in farinose exudates accumulated on inflorescence shafts and calyces of Primula denticulata on human acute myeloid leukemia cells (HL-60) were analyzed. The crude material possessed little antioxidative capacity but strong cytostatic properties. Some of its known components (5-hydroxyflavone, 2'-hydroxyflavone, 5,2'-dihydroxyflavone, and 5,8-dihydroxyflavone) were further tested to identify the biologically active compounds.

Externally accumulated flavonoids in three Mediterranean Ononis species.

The Mediterranean Ononis species, O. fruticosa, O. natrix subsp.

Cuticular waxes and flavonol aglycones of mistletoes.

Cuticular waxes of Viscum album subspecies and of V. cruciatum have been examined for their micromorphology and chemical composition. Wax crystalloids occur preferably as irregular platelets and rodlets, while deviant structures are found in small areas.

Flavonoids and terpenoids from the resinous exudates of Madia species (Asteraceae, Helenieae).

The resinous material accumulated on aerial parts of Madia species is shown to consist mainly of diterpenes, containing a series of flavonoid aglycones. A6- and/or 8-O-substitution is characteristic for many of these flavonoids. Three known rare diterpenes were found and the structure elucidation of a diterpene with a new carbon skeleton, named madiaol, is reported.

Taxonomic significance of flavonoid variation in temperate species of Nothofagus.

Forty-two flavonoids and a stilbene (pinosylvin) were identified in the leaf exudates of 11 temperate species of Nothofagus from South America, Australia and New Zealand. The flavonoid profiles demonstrate significant taxonomic value at the subgeneric level. Most species of subgenus Fuscospora are characterized by the presence of pinosylvin, galangin and galangin methyl ethers.

Cancer chemopreventive in vitro activities of isoflavones isolated from Iris germanica.

Six known isoflavones were isolated from the rhizomes of Iris germanica, and were established by UV, MS and NMR techniques as irisolidone (1), irisolidone 7-O-alpha-D-glucoside (1a), irigenin (2), irilone (3), iriflogenin (4), and iriskashmirianin (5). These compounds were examined for their cancer chemopreventive potential. They were shown to be potent inhibitors of cytochrome P450 1A activity with IC 50 values in the range 0.

On the occurrence of exudate flavonoids in the borage family (Boraginaceae).

Externally accumulated flavonoid aglycones have been found for the first time in Nonea species. They exhibit only flavones, one of them being the rare tricetin-4'-methyl ether. Within the subfamily Boraginoideae, exudate flavonoids appear to be a rare character.