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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1983-5-27
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pubmed:abstractText |
Various 5-substituted perfluoroalkylpyrimidine nucleoside analogues have been synthesized, and their biological activity against L1210, S-180, Vero cells, and herpes simplex virus type 1 (HSV-1) was evaluated. The 5-trifluoromethyl derivatives, 7 and 9, showed significant antiviral activity against HSV-1 with ED50 values of 7 and 5 microM, respectively. In addition, the unblocked nucleoside 9 was found to be about 64-fold less toxic to the host Vero cells and gave a favorable therapeutic index of 64 against HSV-1 in vitro.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
598-601
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6300402-Animals,
pubmed-meshheading:6300402-Cell Division,
pubmed-meshheading:6300402-Cell Line,
pubmed-meshheading:6300402-Dose-Response Relationship, Drug,
pubmed-meshheading:6300402-Haplorhini,
pubmed-meshheading:6300402-Kidney,
pubmed-meshheading:6300402-Leukemia L1210,
pubmed-meshheading:6300402-Mice,
pubmed-meshheading:6300402-Pyrimidine Nucleosides,
pubmed-meshheading:6300402-Sarcoma 180,
pubmed-meshheading:6300402-Simplexvirus
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pubmed:year |
1983
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pubmed:articleTitle |
Synthesis and biological activity of 5-(trifluoromethyl)- and 5-(pentafluoroethyl)pyrimidine nucleoside analogues.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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