Source:http://linkedlifedata.com/resource/pubmed/id/15943470
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2005-6-9
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pubmed:abstractText |
(-)-(2R,4R)-1-(2-Hydroxymethyl-1,3-dioxolan-4-yl)thymine (DOT) is the first thymidine kinase-activated nucleoside that is significantly active against all of the clinically significant NRTI-resistant HIV-1 mutants, including AZT (D67N/K70R/T215Y/K219Q), Tenofovir (K65R), and Lamivudine (M184V). To understand the molecular mechanism of drug resistance and the antiviral activity of DOT against drug-resistant RTs, molecular modeling studies of DOT-TP complexed with the wild-type (WT) and mutated RT were conducted. The key reason for this interesting antiviral activity profile is the presence of a dioxolane ring.
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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
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pubmed:month |
Jun
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
16
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3949-52
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15943470-Anti-HIV Agents,
pubmed-meshheading:15943470-Binding Sites,
pubmed-meshheading:15943470-Drug Resistance, Viral,
pubmed-meshheading:15943470-HIV Reverse Transcriptase,
pubmed-meshheading:15943470-HIV-1,
pubmed-meshheading:15943470-Models, Molecular,
pubmed-meshheading:15943470-Mutation,
pubmed-meshheading:15943470-Reverse Transcriptase Inhibitors,
pubmed-meshheading:15943470-Stereoisomerism
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pubmed:year |
2005
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pubmed:articleTitle |
Anti-HIV activity of (-)-(2R,4R)-1- (2-hydroxymethyl-1,3-dioxolan-4-yl)-thymine against drug-resistant HIV-1 mutants and studies of its molecular mechanism.
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pubmed:affiliation |
College of Pharmacy, The University of Georgia, Athens, 30602, USA. dchu@rx.uga.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
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