Source:http://linkedlifedata.com/resource/pubmed/id/11092314
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2001-2-7
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pubmed:abstractText |
A series of beta-D-2',3'-didehydro-2',3'-dideoxy-nucleosides bearing a tether attached at the C-5 position and their beta-L-counterparts was synthesized. Their inhibitory activities against human immunodeficiency virus (HIV) were investigated and compared to establish relationship(s) between compound structure and their antiviral activity. No significant activity was observed for beta-D- and beta-L-modified nucleosides respectively 7a-c and 14a-c, but 7d and 14d exhibited a weak activity against HIV-1.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1525-7770
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1441-61
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11092314-Anti-HIV Agents,
pubmed-meshheading:11092314-Cell Line,
pubmed-meshheading:11092314-Dideoxynucleosides,
pubmed-meshheading:11092314-HIV-1,
pubmed-meshheading:11092314-Humans,
pubmed-meshheading:11092314-Microbial Sensitivity Tests,
pubmed-meshheading:11092314-Molecular Structure,
pubmed-meshheading:11092314-Thymidine
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pubmed:year |
2000
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pubmed:articleTitle |
Synthesis and antiviral activity of C-5 substituted beta-D- and beta-L-D4T analogues.
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pubmed:affiliation |
Centre d'Etudes et de Recherche sur le Médicament de Normandie, UFR des Sciences Pharmaceutiques, Caen, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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