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dc.contributor.authorZatout, Roukiaes_ES
dc.contributor.authorMasi, Marcoes_ES
dc.contributor.authorEvidente, Antonioes_ES
dc.contributor.authorFernández-Aparicio, Mónicaes_ES
dc.contributor.authorCimmino, Alessioes_ES
dc.date.accessioned2020-07-02T09:29:33Z-
dc.date.available2020-07-02T09:29:33Z-
dc.date.issued2019-
dc.identifier.citationAtti del XXXIX Convegno Nazionale della Divisione di Chimica Organica della Società Chimica Italiana: 277 (2019)es_ES
dc.identifier.isbn978-88-3319-066-2-
dc.identifier.urihttp://hdl.handle.net/10261/215854-
dc.descriptionTrabajo presentado en el XXXIX Convegno Nazionale della Divisione di Chimica Organica della Società Chimica Italiana, celebrado en Turín del 8 al 12 de septiembre de 2019.es_ES
dc.description.abstractA number of parasitic plants have adapted to agricultural environments becoming weedy and posing a serious threat to important crops. Available control measures rely heavily on use of synthetic herbicides. The side effects on environmental pollution and food health of chemical control prompted studies to find alternative strategies based on the use of natural products. Some sesquiterpene lactones named inuloxins A-D, belonging to different subgroup as germacrane, eudesmane and seco-eudesmane, were isolated from the aerial parts of Dittrichia viscosa (family Asteraceae) and showed to stimulate seed germination leading to suicidal germination, or inhibit germination or disrupting germling growth and haustorium development. The absolute configuration (AC) of inuloxin A was determined by chiroptical and computational methods. The same methods were successively used to assign the AC to inuloxin C, while studies are in progress to assign that of inuloxin D. Recently, considering the potential herbicidal activity of inuloxin A, it was formulated in β-cyclodextrins to overcome its low water solubility and preserving its ability to inhibit Phelipanche ramosa seed germination. In this communication, the purification of other germination stimulants and/or inhibitors of parasitic seed germination, isolated from the same plant, will be illustrated as well as the results of structureactivity relationship studies comparing the biological activity of the natural sesquiterpenoids to that of some their hemisynthetic derivatives.es_ES
dc.language.isoenges_ES
dc.publisherEdiSES Universitàes_ES
dc.rightsopenAccesses_ES
dc.titleNatural products as stimulants and inhibitors of parasitic seed germination and radical growthes_ES
dc.typepóster de congresoes_ES
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
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