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1.
Phytochemistry ; 68(9): 1321-6, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17399747

RESUMO

From the aerial parts of Veronica turrilliana two phenylethanoid glycosides, turrilliosides A and B and a steroidal saponin, turrillianoside were isolated and their structures elucidated as beta-(3,4-dihydroxyphenyl)ethyl-4-O-E-caffeoyl-O-[beta-glucopyranosyl-(1-->4)-alpha-rhamnopyranosyl-(1-->6)]-beta-glucopyranoside, beta-(3,4-dihydroxyphenyl)ethyl-4-O-E-caffeoyl-[6-O-E-feruloyl-beta-glucopyranosyl-(1-->4)-alpha-rhamnopyranosyl-(1-->6)]-beta-glucopyranoside and (23S,25S)-12beta,23-dihydroxyspirost-5-en-3beta-yl O-alpha-rhamnopyranosyl-(1-->4)-beta-glucopyranoside, respectively. Furthermore, eight known glucosides are reported namely, catalpol, catalposide, verproside, amphicoside, isovanilloylcatalpol, aucubin, arbutin, and 6-O-E-caffeoylarbutin, the latter two for the first time in the genus Veronica. The two phenylethanoid glycosides were found to be potent DPPH radical scavengers. All of the tested compounds were inactive against the representative species of fungi and bacteria.


Assuntos
Iridoides/química , Iridoides/isolamento & purificação , Fenóis/química , Fenóis/isolamento & purificação , Espirostanos/química , Espirostanos/isolamento & purificação , Veronica/química , Estrutura Molecular , Componentes Aéreos da Planta/química
2.
Fitoterapia ; 77(7-8): 608-10, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16962726

RESUMO

Extracts, fractions and constituents of Carthamus lanatus were tested for their mitogenic effect on bone marrow cells in mice. Most of the studied samples inhibited cell proliferation and only the flavonoid glycoside rutin caused increasing of mitotic activity.


Assuntos
Carthamus , Ciclo Celular/efeitos dos fármacos , Mitógenos/farmacologia , Fitoterapia , Extratos Vegetais/farmacologia , Animais , Células da Medula Óssea/efeitos dos fármacos , Feminino , Masculino , Camundongos , Camundongos Endogâmicos ICR , Mitógenos/administração & dosagem , Mitógenos/uso terapêutico , Extratos Vegetais/administração & dosagem , Extratos Vegetais/uso terapêutico
3.
Phytochemistry ; 64(8): 1413-7, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14630008

RESUMO

A new class of compounds for the plant family Lamiaceae, benzoxazinoids, was found in Lamium galeobdolon. From the aerial parts of the species were isolated the new 2-O-beta-D-glucopyranosyl-6-hydroxy-2H-1,4-benzoxazin-3(4H)-one (6-hydroxy blepharin) together with four known benzoxazinoids, DHBOA-Glc, blepharin, DIBOA, DIBOA-Glc, as well as harpagide, 8-O-acetyl-harpagide and salidroside. Eight known iridoid glucosides, 24-epi-pterosterone and verbascoside were isolated from Lamium amplexicaule, L. purpureum and L. garganicum. The iridoids, 5-deoxylamiol and sesamoside, as well as the phytoecdysone, 24-epi-pterosterone, were found for the first time for the genus Lamium. The phytochemical data are discussed from a systematic and evolutionary point of view.


Assuntos
Iridoides/química , Iridoides/isolamento & purificação , Lamiaceae/química , Oxazinas/química , Oxazinas/isolamento & purificação , Ecdisona/química , Ecdisona/isolamento & purificação , Lamiaceae/genética , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Filogenia , Fitosteróis/química , Fitosteróis/isolamento & purificação
4.
Z Naturforsch C J Biosci ; 57(3-4): 226-34, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12064718

RESUMO

From 19 species of Galium, members of 6 European sections of the genus, 24 compounds were isolated, namely 16 iridoid glucosides, 2 secoiridoid glucosides and 6 triterpene saponins (the later found only in G. rivale (Sibth. & Sm. Griseb.) The iridoid content was analyzed by thin layer chromatography - densitometry. An effort was made to clarify interspecies relationships, based on the obtained results and previous data. Generally, a nearly uniform iridoid pattern in the studied species was observed. Nevertheless, some distinctions gave reason the following chemical characters to be treated as taxonomic markers: iridoids, secogalioside (characteristic of G. mollugo group), iridoids V1 and V2 (G. humifusum Bieb. and G. verum L.), 6-acetylscandoside (G. incurvum group and G. verum) and the triterpene saponins, rivalioside A and rivalioside C (characteristic of G. rivale). The studied species regarding to the iridoids could be attributed to three lines of evolutionary differentiation. One line is leading to the differentiation of G. rivale. It contains specific triterpenoids as well as iridoid acids, which show parallel development of both glyceraldehyde 3-phosphate/pyruvate and mevalonate biosynthetic routes in this species. A second line includes G. mollugo and G. incurvum species groups and the species G. humifusum and G. verum. Variety of iridoid esters, hydroxy and carboxy derivatives of iridoids and secoiridoids characterised this line. Third line comprises the remaining studied species, members of different sections and species groups. They posses a nearly identical iridoid pattern, which suggests a convergent evolution regarding to the iridoids.


Assuntos
Asteraceae/classificação , Piranos/química , Asteraceae/química , Cromatografia em Camada Fina , Conformação Molecular , Estrutura Molecular , Filogenia , Piranos/isolamento & purificação , Especificidade da Espécie
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