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Structure-activity relationships of nucleoside analogues for inhibition of tick-borne encephalitis virus
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SYSNO ASEP 0465631 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Structure-activity relationships of nucleoside analogues for inhibition of tick-borne encephalitis virus Tvůrce(i) Eyer, L. (CZ)
Šmídková, Markéta (UOCHB-X) RID, ORCID
Nencka, Radim (UOCHB-X) RID, ORCID
Neča, J. (CZ)
Kastl, T. (CZ)
Palus, Martin (BC-A) RID, ORCID
De Clercq, E. (BE)
Růžek, Daniel (BC-A) RID, ORCIDZdroj.dok. Antiviral Research. - : Elsevier - ISSN 0166-3542
Roč. 133, Sep (2016), s. 119-129Poč.str. 11 s. Jazyk dok. eng - angličtina Země vyd. NL - Nizozemsko Klíč. slova structure-activity relationship ; tick-borne encephalitis ; nucleoside inhibitor ; antiviral activity ; cytotoxicity Vědní obor RIV CC - Organická chemie Vědní obor RIV – spolupráce Biologické centrum (od r. 2006) - Mikrobiologie, virologie CEP NV16-34238A GA MZd - Ministerstvo zdravotnictví GA16-20054S GA ČR - Grantová agentura ČR Institucionální podpora UOCHB-X - RVO:61388963 ; BC-A - RVO:60077344 UT WOS 000384856200014 EID SCOPUS 84982836748 DOI 10.1016/j.antiviral.2016.07.018 Anotace Tick-borne encephalitis (TBE) represents one of the most serious arboviral neuro-infections in Europe and northern Asia. As no specific antiviral therapy is available at present, there is an urgent need for efficient drugs to treat patients with TBE virus (TBEV) infection. Using two standardised in vitro assay systems, we evaluated a series of 29 nucleoside derivatives for their ability to inhibit TBEV replication in cell lines of neuronal as well as extraneural origin. The series of tested compounds included 2'-C- or 2'-O-methyl substituted nucleosides, 2'-C-fluoro-2'-C-methyl substituted nucleosides, 3'-O-methyl substituted nucleosides, 3'-deoxynucleosides, derivatives with 4'-C-azido substitution, heterobase modified nucleosides and neplanocins. Our data demonstrate a relatively stringent structure-activity relationship for modifications at the 2', 3', and 4' nucleoside positions. Whereas nucleoside derivatives with the methylation at the C2' position or azido modification at the C4'position exerted a strong TBEV inhibition activity (EC50 from 0.3 to 11.1 mu M) and low cytotoxicity in vitro, substitutions of the O2' and O3' positions led to a complete loss of anti-TBEV activity (EC50 > 50 mu M). Moreover, some structural modifications of the heterobase moiety resulted in a high increase of cytotoxicity in vitro. High antiviral activity and low cytotoxicity of C2' methylated or C4' azido substituted pharmacophores suggest that such compounds might represent promising candidates for further development of potential therapeutic agents in treating TBEV infection. Pracoviště Ústav organické chemie a biochemie Kontakt asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434 Rok sběru 2017
Počet záznamů: 1