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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1993-12-15
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pubmed:abstractText |
-2',3'-Seco nucleosides 5 carrying fluorine and sulfur substituents at C-3' and C-5', respectively, of acyclic sugar moiety were synthesized in enantiomerically and diastereoisomerically pure form. These products and some structurally similar 1',2'-seco-2'-nor-and 1',2'-seco-nucleosides 3 and 4 were tested in vitro for cytotoxicity and antiviral activity. At non-cytotoxic concentrations the compounds were inactive against human immunodeficiency virus and herpes simplex virus type-1.
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pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0014-827X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
48
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1113-20
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8216673-Animals,
pubmed-meshheading:8216673-Antiviral Agents,
pubmed-meshheading:8216673-Cell Line,
pubmed-meshheading:8216673-Cell Survival,
pubmed-meshheading:8216673-HIV-1,
pubmed-meshheading:8216673-Herpesvirus 1, Human,
pubmed-meshheading:8216673-Humans,
pubmed-meshheading:8216673-Nucleosides,
pubmed-meshheading:8216673-Stereoisomerism,
pubmed-meshheading:8216673-Vero Cells
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pubmed:year |
1993
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pubmed:articleTitle |
Synthesis and evaluation of the antiviral activity of acyclic nucleosides carrying fluorine and sulfur substituents.
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pubmed:affiliation |
Dipartimento di Chimica, Politecnico, Milano, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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