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Synthesis, Anthelmintic Activity, and Mechanism of Action of 5-Aryl-1H-indoles

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389030%3A_____%2F25%3A00644040" target="_blank" >RIV/61389030:_____/25:00644040 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15310/25:73633178 RIV/61989592:15110/25:73633178

  • Result on the web

    <a href="https://doi.org/10.1021/acs.jafc.5c14071" target="_blank" >https://doi.org/10.1021/acs.jafc.5c14071</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.jafc.5c14071" target="_blank" >10.1021/acs.jafc.5c14071</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis, Anthelmintic Activity, and Mechanism of Action of 5-Aryl-1H-indoles

  • Original language description

    Parasitic nematodes are a significant concern in human and veterinary medicine as well as agriculture. In this study, we prepared twenty-seven 5-phenyl-1H-indole derivatives bearing various substituents on the phenyl ring and assessed their efficacy against nematodes. Using Caenorhabditis elegans, we selected the most potent compounds and evaluated their toxicity on selected animal and plant-parasitic nematode species. Compounds featuring 4-chloro, 4-fluoro, and 4-trifluoromethoxy groups on the phenyl ring inhibited the motility of exsheathed L3 larvae of Hemonchus contortus while exhibiting limited cytotoxicity in mammalian cell cultures. These compounds showed similar effects against the plant-parasitic nematodes Heterodera schachtii and Ditylenchus destructor, albeit with reduced potency. We propose that the compounds might act as inhibitors of mitochondrial complex II as inferred from molecular modeling, decreased mitochondrial membrane potential, and reduced activity in C. elegans complex II mutants.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    40401 - Agricultural biotechnology and food biotechnology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Agricultural and Food Chemistry

  • ISSN

    0021-8561

  • e-ISSN

    1520-5118

  • Volume of the periodical

    73

  • Issue of the periodical within the volume

    52

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    33059-33069

  • UT code for WoS article

    001640343100001

  • EID of the result in the Scopus database

    2-s2.0-105026202968