Flavonoids from shoots and roots of Trifolium repens (white clover) grown in presence or absence of the arbuscular mycorrhizal fungus Glomus intraradices

White clover (Trifolium repens) plants were grown in the presence or absence of the arbuscular mycorrhizal fungus Glomus intraradices. Flavones, 4′,5,6,7,8-pentahydroxy-3-methoxyflavone and 5,6,7,8-tetrahydroxy-3-methoxyflavone, as well as two flavones 3,7-dihydroxy-4′-methoxyflavone and 5,6,7,8-tet...

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Autor principal: Ponce, M.A
Otros Autores: Scervino, J.M, Erra-Balsells, R., Ocampo, J.A, Godeas, A.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2004
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
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024 7 |2 scopus  |a 2-s2.0-3242811168 
024 7 |2 cas  |a acacetin, 480-44-4; quercetin, 117-39-5; rhamnetin, 90-19-7; 4',5,6,7,8-pentahydroxy-3-methoxyflavone; 5,6,7,8-tetrahydroxy-3-methoxyflavone; acacetin, 480-44-4; Flavones; Quercetin, 117-39-5; rhamnetin, 90-19-7 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a PYTCA 
100 1 |a Ponce, M.A. 
245 1 0 |a Flavonoids from shoots and roots of Trifolium repens (white clover) grown in presence or absence of the arbuscular mycorrhizal fungus Glomus intraradices 
260 |c 2004 
270 1 0 |m Ponce, M.A.; Depto. de Quím. Orgán., Fac. de Ciencias Exactas Y Naturales, CIHIDECAR-CONICET, Univ. Buenos A., Buenos Aires, Argentina; email: henryh@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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504 |a Hattori, M., Huang, X.L., Che, Q.M., Kawata, Y., Tezuka, Y., Kikuchi, T., Namba, T., 6-Hydroxykaempferol and its glycosides from Carthamus tinctorius petals (1992) Phytochemistry, 31, pp. 4001-4004 
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504 |a Jerzmanowska, Z.I., Michalska, M., Preparation of some polyhydroxy flavones (1961) Roczniki Chemii, 35, pp. 353-357 
504 |a Ma, Y.L., Van Den Heuvel, H., Claeys, M., Characterization of 3-methoxyflavones using fast-atom bombardment and collision-induced dissociation tandem mass spectrometry (1999) Rapid Communication in Mass Spectrometry, 13, pp. 1932-1942 
504 |a Mabry, T.J., Markham, K.R., Thomas, M.B., (1970) The Systematic Identification of Flavonoids, , New York: Springer 
504 |a Miyahara, M., Ohtaka, H., Katayama, H., Tatsumi, Y., Miyaichi, Y., Tomimori, T., Structure-activity relationship of flavonoids in suppressing rat liver lipid peroxidation (1993) Yakugaku Zasshi, 113, pp. 133-154 
504 |a Nagao, M., Morita, N., Yahagi, T., Shimizu, M., Kuroyanagi, M., Fukuoka, M., Yoshihara, K., Sugimura, T., Mutagenicities of 61 flavonoids and 11 related compounds (1981) Environmental Mutagenesis, 3, pp. 401-419 
504 |a Ponce, M.A., Scervino, J.M., Erra-Balsells, R., Ocampo, J.A., Godeas, A.M., Flavonoids isolated from shoots, roots and roots exudates of Brassica alba (2004) Phytochemistry, , (submitted) 
504 |a Poulin, M.J., Bel-Rhlid, R., Piche, Y., Chenevert, R., Flavonoids released by carrot (Daucus carota) seedlings stimulate hyphal development of vesicular-arbuscular mycorrhizal fungi in the presence of optimal CO2 enrichment (1993) Journal of Chemical Ecology, 19, pp. 2317-2327 
504 |a Robin, V., Irurzun, A., Amoros, M., Boustie, J., Carrasco, L., Antipoliovirus flavonoids from Psiadia dentata (2001) Antiviral Chemistry and Chemotherapy, 12, pp. 283-291 
504 |a Serra-Bonvehi, J., Ventura-Coll, F., Escola-Jorda, R., The composition, active components and bacteriostatic activity of propolis in diets (1994) Journal of the American Oil Chemists Society, 71, pp. 529-532 
504 |a Stevens, J.F., Wollenweber, E., Ivancic, M., Hsu, V.L., Sundberg, S., Deinzer, M.L., Leaf surface flavonoids of Chrysothamnus (1999) Phytochemistry, 51, pp. 771-780 
504 |a (1996) The Wiley Registry of Mass Spectral Data, 1996, Sixth Ed., , Wiley, New York 
504 |a Valant-Vetschera, K.M., Wollenweber, E., Comparative analysis of leaf exudate flavonoids in Achillea subsect. Filipendulinae (1996) Biochemical Systematics and Ecology, 24, pp. 435-446 
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504 |a Wollenweber, E., Schober, I., Dostal, P., Hradetzky, D., Arriaga-Giner, F.J., Yatskievych, G., Flavonoids and terpenoids from the exudates of some Baccharis species (1986) Zeitschrift fur Naturforschung C-A Journal of Biosciences, 41, pp. 87-93 
504 |a Wollenweber, E., Doerr, M., Exudate flavonoids in some Solanaceae (1995) Biochemical Systematics and Ecology, 23, pp. 457-458 
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504 |a Wollenweber, E., Doerr, M., Fritz, H., Valant-Vetschera, K.M., Exudate flavonoids in several Asteroideae and Cichorioideae (1998) Zeitschrift fur Naturforschung C-A Journal of Biosciences, 53, p. 937 
504 |a Zhu, H.-Y., Zhang, C.-M., Liu, F.-C., Synthesis of 3,4′-dimethoxykaempferol (2000) Hecheng Huaxue Bianjibu, 8, pp. 284-286 
520 3 |a White clover (Trifolium repens) plants were grown in the presence or absence of the arbuscular mycorrhizal fungus Glomus intraradices. Flavones, 4′,5,6,7,8-pentahydroxy-3-methoxyflavone and 5,6,7,8-tetrahydroxy-3-methoxyflavone, as well as two flavones 3,7-dihydroxy-4′-methoxyflavone and 5,6,7,8-tetrahydroxy-4 ′-methoxyflavone never previously reported in plants, were isolated. The known 3,5,6,7,8-pentahydroxy-4′-methoxyflavone, 2′,3′,4′,5 ′,6′-pentahydroxy-chalcone, 6-hydroxykaempferol, 4′,5,6,7,8-pentahydroxyflavone and 3,4′-dimethoxykaempferol were also obtained. Analysis of extracts obtained from roots and shoots revealed that the compositions of the flavonoid mixtures varied with growing conditions. Quercetin, acacetin and rhamnetin accumulated in roots of inoculated plants, whereas they were not detected in non-inoculated plants. © 2004 Published by Elsevier Ltd.  |l eng 
536 |a Detalles de la financiación: Secretaría de Ciencia y Técnica, Universidad de Buenos Aires, X028 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas, PIP 904/98 
536 |a Detalles de la financiación: We thank UBA (UBACyT X027 and X028) and CONICET (PIP 904/98) for partial financial support. R. Erra-Balsells and A.M. Godeas are research members of CIC (CONICET). 
593 |a Depto. de Quím. Orgán., Fac. de Ciencias Exactas Y Naturales, CIHIDECAR-CONICET, Univ. Buenos A., Buenos Aires, Argentina 
593 |a Depto. de Biodiversidad Y Biol. Exp., Fac. de Ciencias Exactas Y Naturales, Univ. Buenos Aires, Pabellon I., Buenos Aires, Argentina 
593 |a Estac. Experimental de Zaidin, CSIC, (18008) Granada, Spain 
690 1 0 |a 3,7-DIHYDROXY-4 ′-METHOXYFLAVONE 
690 1 0 |a 4′,5,6,7,8-PENTAHYDROXY-3- METHOXYFLAVONE 
690 1 0 |a 5,6,7,8-TETRAHYDROXY-3-METHOXYFLAVONE 
690 1 0 |a CHALCONE 
690 1 0 |a FLAVONES 
690 1 0 |a FLAVONOIDS 
690 1 0 |a GLOMUS INTRARADICES 
690 1 0 |a LEGUMINOSAE 
690 1 0 |a ROOTS 
690 1 0 |a SHOOTS 
690 1 0 |a TRIFOLIUM REPENS 
690 1 0 |a WHITE CLOVER 
690 1 0 |a 2',3',4',5',6' PENTAHYDROXYCHALCONE 
690 1 0 |a 3,4' DIMETHOXYKAEMPFEROL 
690 1 0 |a 3,5,6,7,8 PENTAHYDROXY 4' METHOXYFLAVONE 
690 1 0 |a 3,7 DIHYDROXY 2 (4 METHOXYPHENYL) 4H 1 BENZOPYRAN 4 ONE 
690 1 0 |a 4',5,6,7,8 PENTAHYDROXYFLAVONE 
690 1 0 |a 5,6,7,8 TETRAHYDROXY 2 (4 HYDROXYPHENYL) 3 METHOXY 4H 1 BENZOPYRAN 4 ONE 
690 1 0 |a 5,6,7,8 TETRAHYDROXY 2 (4 METHOXYPHENYL) 4H 1 BENZOPYRAN 4 ONE 
690 1 0 |a 5,6,7,8 TETRAHYDROXY 3 METHOXY 2 PHENYL 4H 1 BENZOPYRAN 4 ONE 
690 1 0 |a 6 HYDROXYKAEMPFEROL 
690 1 0 |a ACACETIN 
690 1 0 |a FLAVONOID 
690 1 0 |a PLANT EXTRACT 
690 1 0 |a QUERCETIN 
690 1 0 |a RHAMNETIN 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a WHITE CLOVER EXTRACT 
690 1 0 |a ARBUSCULAR MYCORRHIZA 
690 1 0 |a ARTICLE 
690 1 0 |a GLOMUS INTRARADICES 
690 1 0 |a PLANT ROOT 
690 1 0 |a WHITE CLOVER 
690 1 0 |a FLAVONES 
690 1 0 |a FUNGI 
690 1 0 |a MAGNETIC RESONANCE SPECTROSCOPY 
690 1 0 |a MOLECULAR STRUCTURE 
690 1 0 |a MYCORRHIZAE 
690 1 0 |a PLANT ROOTS 
690 1 0 |a PLANT SHOOTS 
690 1 0 |a QUERCETIN 
690 1 0 |a TRIFOLIUM 
690 1 0 |a FABACEAE 
690 1 0 |a FUNGI 
690 1 0 |a GLOMUS 
690 1 0 |a GLOMUS INTRARADICES 
690 1 0 |a TRIFOLIUM 
690 1 0 |a TRIFOLIUM REPENS 
700 1 |a Scervino, J.M. 
700 1 |a Erra-Balsells, R. 
700 1 |a Ocampo, J.A. 
700 1 |a Godeas, A.M. 
773 0 |d 2004  |g v. 65  |h pp. 1925-1930  |k n. 13  |p Phytochemistry  |x 00319422  |w (AR-BaUEN)CENRE-88  |t Phytochemistry 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00319422_v65_n13_p1925_Ponce  |y Handle 
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