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Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives

Three new hydrazide and five new hydrazonoyl derivatives were synthesized. The chemical structures of these compounds were confirmed by (1)H-NMR, IR spectroscopy and elemental analysis. The prepared compounds were tested for their activity to inhibit photosynthetic electron transport in spinach chlo...

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Autores principales: Šeršeň, František, Gregáň, Fridrich, Peško, Matúš, Dvoranová, Dana, Kráľová, Katarína, Matkovičová, Zuzana, Gregáň, Juraj, Donovalová, Jana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759945/
https://www.ncbi.nlm.nih.gov/pubmed/26248070
http://dx.doi.org/10.3390/molecules200814139
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author Šeršeň, František
Gregáň, Fridrich
Peško, Matúš
Dvoranová, Dana
Kráľová, Katarína
Matkovičová, Zuzana
Gregáň, Juraj
Donovalová, Jana
author_facet Šeršeň, František
Gregáň, Fridrich
Peško, Matúš
Dvoranová, Dana
Kráľová, Katarína
Matkovičová, Zuzana
Gregáň, Juraj
Donovalová, Jana
author_sort Šeršeň, František
collection PubMed
description Three new hydrazide and five new hydrazonoyl derivatives were synthesized. The chemical structures of these compounds were confirmed by (1)H-NMR, IR spectroscopy and elemental analysis. The prepared compounds were tested for their activity to inhibit photosynthetic electron transport in spinach chloroplasts and growth of the green algae Chlorella vulgaris. IC(50) values of these compounds varied in wide range, from a strong to no inhibitory effect. EPR spectroscopy showed that the active compounds interfered with intermediates Z(•)/D(•), which are localized on the donor side of photosystem II. Fluorescence spectroscopy suggested that the mechanism of inhibitory action of the prepared compounds possibly involves interactions with aromatic amino acids present in photosynthetic proteins.
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spelling pubmed-47599452016-02-19 Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives Šeršeň, František Gregáň, Fridrich Peško, Matúš Dvoranová, Dana Kráľová, Katarína Matkovičová, Zuzana Gregáň, Juraj Donovalová, Jana Molecules Communication Three new hydrazide and five new hydrazonoyl derivatives were synthesized. The chemical structures of these compounds were confirmed by (1)H-NMR, IR spectroscopy and elemental analysis. The prepared compounds were tested for their activity to inhibit photosynthetic electron transport in spinach chloroplasts and growth of the green algae Chlorella vulgaris. IC(50) values of these compounds varied in wide range, from a strong to no inhibitory effect. EPR spectroscopy showed that the active compounds interfered with intermediates Z(•)/D(•), which are localized on the donor side of photosystem II. Fluorescence spectroscopy suggested that the mechanism of inhibitory action of the prepared compounds possibly involves interactions with aromatic amino acids present in photosynthetic proteins. MDPI 2015-08-04 /pmc/articles/PMC4759945/ /pubmed/26248070 http://dx.doi.org/10.3390/molecules200814139 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Šeršeň, František
Gregáň, Fridrich
Peško, Matúš
Dvoranová, Dana
Kráľová, Katarína
Matkovičová, Zuzana
Gregáň, Juraj
Donovalová, Jana
Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
title Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
title_full Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
title_fullStr Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
title_full_unstemmed Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
title_short Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
title_sort synthesis and herbicidal activity of new hydrazide and hydrazonoyl derivatives
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759945/
https://www.ncbi.nlm.nih.gov/pubmed/26248070
http://dx.doi.org/10.3390/molecules200814139
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