Antiviral activity of triazine analogues of 1- (S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (Cidofovir) and related compounds
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F07%3A00081024" target="_blank" >RIV/61388963:_____/07:00081024 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Antiviral activity of triazine analogues of 1- (S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (Cidofovir) and related compounds
Original language description
Acyclic nucleoside phosphonates containing 5-aza and 6-azacytosine base moiety were synthesized and tested for antiviral activity. The most active compound, 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]-5-azacytosine exerted strong activity against broadspectrum of DNA viruses (adenovirus, poxviruses and herpesviruses).
Czech name
Protivirová aktivita triazinových analogů 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosinu (cidofoviru) a příbuzných sloučenin
Czech description
Byly syntetizovány acyklické nukleosidové fosfonáty obsahující jako bazickou komponentu 5-aza a 6-azacytosin a testována jejich protivirová aktivita. Nejvíce aktivní látka, 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]-5-azacytosin, vykazovala silnou aktivitu proti širokému spektru DNA virů (adenoviry, poxviry a herpesviry).
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2007
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 Medicinal Chemistry
ISSN
0022-2623
e-ISSN
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Volume of the periodical
50
Issue of the periodical within the volume
5
Country of publishing house
US - UNITED STATES
Number of pages
9
Pages from-to
1069-1077
UT code for WoS article
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EID of the result in the Scopus database
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