期刊论文详细信息
Molecules
Synthesis and Herbicidal Activity of New Hydrazide and Hydrazonoyl Derivatives
Frantiᘞk ᘎrᘞň4  Fridrich Gregáň3  Matúš Peško1  Dana Dvoranová5  Katarína Kráľová4  Zuzana Matkovičová4  Juraj Gregáň2  Jana Donovalová4 
[1] Department of Environmental Ecology, Faculty of Natural Sciences, Comenius University in Bratislava, Mlynská dolina, Bratislava 842 15, Slovakia; E-Mail:;Department of Genetics, Faculty of Natural Sciences, Comenius University in Bratislava, Mlynská dolina, Bratislava 842 15, Slovakia;Department of Chemistry, Faculty of Natural Sciences, Matej Bell University, Tajovského 40, Banská Bystrica 974 01, Slovakia; E-Mail:;Institute of Chemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Mlynská dolina, Bratislava 842 15, Slovakia; E-Mails:;Institute of Physical Chemistry and Chemical Physics, Faculty Chemical and Food Technology, Slovak University of Technology in Bratislava, Radlinského 9, Bratislava 812 37, Slovakia; E-Mail:
关键词: green algae;    N′-[2;    6-dinitro-4-(trifluoromethyl)phenyl]hydrazides;    N′-[2;    6-dinitro-4-[trifluoromethyl)phenyl]hydrazonoyl derivatives;    photosynthesis inhibition;    spinach chloroplasts;   
DOI  :  10.3390/molecules200814139
来源: mdpi
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【 摘 要 】

Three new hydrazide and five new hydrazonoyl derivatives were synthesized. The chemical structures of these compounds were confirmed by 1H-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. IC50 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.

【 授权许可】

CC BY   
© 2015 by the authors; licensee MDPI, Basel, Switzerland.

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