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Nucleoside Inhibitors of Tick-Borne Encephalitis Virus

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F15%3A00448138" target="_blank" >RIV/60077344:_____/15:00448138 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/15:00448138 RIV/00027162:_____/15:#0001315 RIV/60076658:12310/15:43888823

  • Result on the web

    <a href="http://dx.doi.org/10.1128/AAC.00807-15" target="_blank" >http://dx.doi.org/10.1128/AAC.00807-15</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1128/AAC.00807-15" target="_blank" >10.1128/AAC.00807-15</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Nucleoside Inhibitors of Tick-Borne Encephalitis Virus

  • Original language description

    Tick-borne encephalitis virus (TBEV) is a leading cause of human neuroinfections in Europe and Northeast Asia. There are no antiviral therapies for treating TBEV infection. A series of nucleoside analogues was tested for the ability to inhibit the replication of TBEV in porcine kidney cells and human neuroblastoma cells. The interactions of three nucleoside analogues with viral polymerase were simulated using advanced computational methods. The nucleoside analogues 7-deaza-2'-C-methyladenosine (7-deaza-2'-CMA), 2'-C-methyladenosine (2'-CMA), and 2'-C-methylcytidine (2'-CMC) inhibited TBEV replication. These compounds showed dose-dependent inhibition of TBEV-induced cytopathic effects, TBEV replication (50% effective concentrations [EC50]of 5.1 0.4 muMfor 7-deaza-2'-CMA, 7.1 1.2 muM for 2'-CMA, and 14.2 1.9 muM for 2'-CMC) and viral antigen production. Notably, 2'-CMC was relatively cytotoxic to porcine kidney cells (50% cytotoxic concentration [CC50] of 50 muM). The anti-TBEV effect o

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

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

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Antimicrobial Agents and Chemotherapy

  • ISSN

    0066-4804

  • e-ISSN

  • Volume of the periodical

    59

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    5483-5493

  • UT code for WoS article

    000364343900049

  • EID of the result in the Scopus database