Source:http://linkedlifedata.com/resource/pubmed/id/16451084
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2006-2-2
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pubmed:abstractText |
This paper describes the design and synthesis of dipeptidyl N,N-dimethyl glutaminyl fluoromethyl ketones (fmk) as severe acute respiratory syndrome coronovirus (SARS-CoV) inhibitors. The compounds were tested against SARS-CoV-induced cell death in Vero or CaCo2 cells as a measurement of the inhibiting effects of the compounds on the replication of the virus. Z-Leu-Gln(NMe(2))-fmk (6a) was found to be a potent inhibitor with low toxicity in cells, protecting cells with an EC(50) value of 2.5 microM and exhibiting a selectivity index of >40.
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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 |
Feb
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1198-201
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16451084-Animals,
pubmed-meshheading:16451084-Antiviral Agents,
pubmed-meshheading:16451084-Caco-2 Cells,
pubmed-meshheading:16451084-Cell Death,
pubmed-meshheading:16451084-Cercopithecus aethiops,
pubmed-meshheading:16451084-Dipeptides,
pubmed-meshheading:16451084-Drug Design,
pubmed-meshheading:16451084-Humans,
pubmed-meshheading:16451084-SARS Virus,
pubmed-meshheading:16451084-Vero Cells,
pubmed-meshheading:16451084-Virus Replication
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pubmed:year |
2006
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pubmed:articleTitle |
Design and synthesis of dipeptidyl glutaminyl fluoromethyl ketones as potent severe acute respiratory syndrome coronovirus (SARS-CoV) inhibitors.
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pubmed:affiliation |
Maxim Pharmaceuticals, 6650 Nancy Ridge Drive, San Diego, CA 92121, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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