Source:http://linkedlifedata.com/resource/pubmed/id/15324882
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
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pubmed:dateCreated |
2004-8-24
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pubmed:abstractText |
HIV-1 protease inhibitors (PI's) bearing 1,3,4-oxadiazoles at the P1' position were prepared by a novel method involving the diastereoselective installation of a carboxylic acid and conversion to the P1' heterocycle. The compounds are picomolar inhibitors of native HIV-1 protease, with most of the compounds maintaining excellent antiviral activity against a panel of PI-resistant strains.
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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 |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4651-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15324882-Cell Line, Tumor,
pubmed-meshheading:15324882-Drug Resistance, Multiple, Viral,
pubmed-meshheading:15324882-HIV Protease Inhibitors,
pubmed-meshheading:15324882-HIV-1,
pubmed-meshheading:15324882-Humans,
pubmed-meshheading:15324882-Indinavir,
pubmed-meshheading:15324882-Oxadiazoles,
pubmed-meshheading:15324882-Pyridines,
pubmed-meshheading:15324882-Stereoisomerism
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pubmed:year |
2004
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pubmed:articleTitle |
P1' oxadiazole protease inhibitors with excellent activity against native and protease inhibitor-resistant HIV-1.
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pubmed:affiliation |
Department of Basic Chemistry, Merck Research Laboratories, Rahway, NJ 07065, USA. ron_kim@merck.com
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pubmed:publicationType |
Journal Article,
Comparative Study
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