Photosynthesis-Inhibiting Activity of Methoxy-Substituted 3-Hydroxynaphthalene-2-Carboxanilides

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15640%2F21%3A73612538" target="_blank" >RIV/61989592:15640/21:73612538 - isvavai.cz</a>
Result on the web
<a href="https://www.mdpi.com/2673-4583/3/1/105" target="_blank" >https://www.mdpi.com/2673-4583/3/1/105</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/ecsoc-24-08295" target="_blank" >10.3390/ecsoc-24-08295</a>

Result language
angličtina
Original language name
Photosynthesis-Inhibiting Activity of Methoxy-Substituted 3-Hydroxynaphthalene-2-Carboxanilides
Original language description
set of six 3-hydroxynaphthalene-2-carboxanilides, substituted on the anilide ring by combinations of methoxy–methoxy, methoxy–fluoro and methoxy–chloro groups at different positions, was designed. All the molecules were prepared by microwave-assisted synthesis. The compounds were tested for their ability to inhibit photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. The PET-inhibiting activity of the compounds was rather moderate. N-(3,5-Dimehoxyphenyl)-3-hydroxynaphthalene-2-carboxamide demonstrated the highest activity (IC50 = 24.5 µM) within the series. These compounds are supposed to inhibit PET in photosystem II.
Czech name
—
Czech description
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Project
<a href="/en/project/LO1305" target="_blank" >LO1305: Development of the center of advanced technologies and materials</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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