Source:http://linkedlifedata.com/resource/pubmed/id/15664842
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2005-1-24
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pubmed:abstractText |
A series of 9-(2'-beta-C-methyl-beta-d-ribofuranosyl)-6-substituted purine derivatives were synthesized as potential inhibitors of HCV RNA replication. Their inhibitory activities in a cell based HCV replicon assay were reported. A prodrug approach was used to further improve the potency of these compounds by increasing the intracellular levels of 5'-monophosphate metabolites. These nucleotide prodrugs showed much improved inhibitory activities of HCV RNA replication.
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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 |
Feb
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
709-13
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pubmed:meshHeading |
pubmed-meshheading:15664842-Antiviral Agents,
pubmed-meshheading:15664842-Cell Line,
pubmed-meshheading:15664842-Hepacivirus,
pubmed-meshheading:15664842-Humans,
pubmed-meshheading:15664842-Prodrugs,
pubmed-meshheading:15664842-Purine Nucleosides,
pubmed-meshheading:15664842-RNA, Viral,
pubmed-meshheading:15664842-Replicon,
pubmed-meshheading:15664842-Structure-Activity Relationship,
pubmed-meshheading:15664842-Virus Replication
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pubmed:year |
2005
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pubmed:articleTitle |
Synthesis of 9-(2-beta-C-methyl-beta-d-ribofuranosyl)-6-substituted purine derivatives as inhibitors of HCV RNA replication.
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pubmed:affiliation |
Valeant Pharmaceuticals International, 3300 Hyland Avenue Costa Mesa, CA 92626, USA. yding@icnpharm.com
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pubmed:publicationType |
Journal Article
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