Počet záznamů: 1  

Medicinal chemistry of viral polymerases and proteases

  1. 1.
    SYSNO ASEP0567307
    Druh ASEPA - Abstrakt
    Zařazení RIVO - Ostatní
    NázevMedicinal chemistry of viral polymerases and proteases
    Tvůrce(i) Kožíšek, Milan (UOCHB-X) RID, ORCID
    Král, Michal (UOCHB-X) ORCID
    Radilová, Kateřina (UOCHB-X) ORCID
    Gregor, Jiří (UOCHB-X)
    Kotačka, Tomáš (UOCHB-X)
    Machara, Aleš (UOCHB-X) ORCID
    Reiberger, Róbert (UOCHB-X) ORCID
    Majerová, Taťána (UOCHB-X) RID, ORCID
    Novotný, Pavel (UOCHB-X)
    Zdroj.dok.Czech Chemical Society Symposium Series - ISSN 2336-7202
    Roč. 20, č. 6 (2022), s. 350-350
    Poč.str.1 s.
    AkceAnnual meeting of the National Institute of Virology and Bacteriology (NIVB) /1./
    Datum konání30.11.2022 - 02.12.2022
    Místo konáníKutná Hora
    ZeměCZ - Česká republika
    Typ akceEUR
    Jazyk dok.eng - angličtina
    Země vyd.CZ - Česká republika
    Klíč. slovaviral protease ; viral polymerase
    Obor OECDVirology
    CEPLX22NPO5103 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaUOCHB-X - RVO:61388963
    AnotaceThe influenza virus causes severe infectious diseases that represents a serious threat to public health. There is an urgent need for the development of new anti-influenza drugs effective against resistant viral strains and different viral subtypes. In this project we plan to study endonuclease and cap-binding small molecule inhibitors, as well as peptide inhibitors targeting protein-protein interaction in viral polymerase. Furthermore, due to the functional and presumed structural similarity between influenza A polymerase and L-protein of the emerging Rift Valley Fever virus (RVFV), we plan to utilize our prior experience1–6to develop and identify novel inhibitors of the endonuclease and polymerase activity of RVFV. This project will thus allow the development of active compounds against these important pathogens.In the second part of the project, we focus on viral proteases which are key enzymes in virion maturation that contribute to viral pathogenesis. Targeting viral proteases represents a viable strategy of antiviral therapy. The main focus of this research objective involves proteases of HIV, SARS-CoV-2, Zika and Dengue viruses. Detailed understanding of regulatory steps during autoactivation of these enzymes, their role in virion maturation and pathogenesis is still lacking. We plan to combine biological, chemical and biophysical approaches to study proteases activation, regulation of maturation, intra and their interactions with low-molecular-weight ligands or other viral and host proteins.
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
    Rok sběru2023
    Elektronická adresahttp://www.ccsss.cz/index.php/ccsss/issue/view/37/67
Počet záznamů: 1  

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