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  1. Pubblicazioni

Phytotoxic Potential and Biological Activity of Three Synthetic Coumarin Derivatives as New Natural-Like Herbicides

Articolo
Data di Pubblicazione:
2015
Abstract:
Coumarin is a natural compound well known for its phytotoxic potential. In the search for new herbicidal compounds to manage weeds, three synthetic derivatives bearing the coumarin scaffold (1–3), synthesized by a carbonylative organometallic approach, were in vitro assayed on germination and root growth of two noxious weeds, Amaranthus retroflexus and Echinochloa crus-galli. Moreover, the synthetic coumarins 1–3 were also in vitro assayed on seedlings growth of the model species Arabidopsis thaliana to identify the possible physiological targets. All molecules strongly affected seed germination and root growth of both weeds. Interestingly, the effects of synthetic coumarins on weed germination were higher than template natural coumarin, pointing out ED50 values ranging from 50–115 µM. Moreover, all synthetic coumarins showed a strong phytotoxic potential on both Arabidopsis shoot and root growth, causing a strong reduction in shoot fresh weight (ED50 values ≤ 60 µM), accompanied by leaf development and a decrease in pigment content. Furthermore, they caused a strong alteration in root growth (ED50 values ≤ 170 µM) and morphology with evident alterations in root tip anatomy. Taken together, our results highlight the promising potential herbicidal activity of these compounds.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
Arabidopsis thaliana, Amaranthus retroflexus, Echinochloa crus-galli, germination, root morphology, phytotoxicity, natural-like herbicides, coumarins
Elenco autori:
Araniti, Fabrizio; Mancuso, Raffaella; Lupini, Antonio; Giofre', Salvatore Vincenzo; Sunseri, Francesco; Gabriele, Bartolo; Abenavoli, Maria
Autori di Ateneo:
GIOFRE' Salvatore Vincenzo
Link alla scheda completa:
https://iris.unime.it/handle/11570/3062795
Link al Full Text:
https://iris.unime.it//retrieve/handle/11570/3062795/49334/molecules-20-17883.pdf
Pubblicato in:
MOLECULES
Journal
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