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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4986
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pubmed:dateCreated |
1991-1-22
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pubmed:abstractText |
A series of dipyridodiazepinones have been shown to be potent inhibitors of human immunodeficiency virus-1 (HIV-1) reverse transcriptase (RT). One compound, BI-RG-587, had a Ki of 200 nanomolar for inhibition of HIV-1 RT that was noncompetitive with respect to deoxyguanosine triphosphate. BI-RG-587 was specific for HIV-1 RT, having no effect on feline and simian RT or any mammalian DNA polymerases. BI-RG-587 inhibited HIV-1 replication in vitro as demonstrated by in situ hybridization, inhibition of protein p24 production, and the lack of syncytia formation in cultured human T cell lines and freshly isolated human peripheral blood lymphocytes. Cytotoxicity studies of BI-RG-587 on human cells showed a high therapeutic index (greater than 8000) in culture.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0036-8075
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:volume |
250
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
N
|
pubmed:pagination |
1411-3
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1701568-Animals,
pubmed-meshheading:1701568-Antiviral Agents,
pubmed-meshheading:1701568-Cell Line,
pubmed-meshheading:1701568-DNA-Directed DNA Polymerase,
pubmed-meshheading:1701568-HIV-1,
pubmed-meshheading:1701568-Humans,
pubmed-meshheading:1701568-Kinetics,
pubmed-meshheading:1701568-Molecular Structure,
pubmed-meshheading:1701568-Nevirapine,
pubmed-meshheading:1701568-Pyridines,
pubmed-meshheading:1701568-Reverse Transcriptase Inhibitors,
pubmed-meshheading:1701568-Virus Replication
|
pubmed:year |
1990
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pubmed:articleTitle |
Inhibition of HIV-1 replication by a nonnucleoside reverse transcriptase inhibitor.
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pubmed:affiliation |
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|