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Photosynthesis-Inhibiting Activity of Fluorinated 2‑Hydroxynaphthalene-1-carboxanilides

Název česky Fluorované 2-hydroxynaftalen-1-karboxanilidy inhibující fotosyntézu
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GONĚC Tomáš ORAVEC Michal JAMPÍLEK Josef

Rok publikování 2021
Druh Konferenční abstrakty
Fakulta / Pracoviště MU

Farmaceutická fakulta

Citace
Popis 2-Hydroxy-N-phenylnaphthalene-1-carboxamide, three fluoro monosubstituted and five fluoro disubstituted 2-hydroxynaphthalene-1-carboxanilides were prepared by microwave-assisted synthesis and characterized. All the compounds were evaluated for their ability to inhibit photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. The PET inhibitory activity of the discussed compounds proved to be in a wide range, from inactive N-(2,6-difluorophenyl)-2-hydroxynaphthalene-1-carboxamide with an IC50 = 904 µM to N-(2,5-difluorophenyl)-2-hydroxynaphthalene-1-carboxamide with an IC50 of 44.2 µM, which was the most potent isomer of the series of evaluated compounds. Based on previous studies, it can be assumed that the mechanism of PET inhibition of these compounds is the inhibition of photosystem II in the thylakoid membrane.

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