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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
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pubmed:dateCreated |
1999-4-5
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pubmed:abstractText |
A novel class of CMV protease inhibitors based on a benzothiopyran-S,S-dioxide nucleus has been discovered. Enzyme kinetic data supports a reversible mode of inhibition for a representative member of this class, 2-(3-pyridyl-N-oxide)benzothiopyran-4-one-S,S-dioxide, 1. Experiments in the presence and absence of the disulfide reducing agent DTT suggest that the inhibition by 1 is not due to oxidative inactivation of the enzyme. Also presented are results of some SAR studies of the benzothiopyranone ring system.
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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 |
Dec
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3677-82
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9934494-Amino Acid Sequence,
pubmed-meshheading:9934494-Cytomegalovirus,
pubmed-meshheading:9934494-Molecular Sequence Data,
pubmed-meshheading:9934494-Oxidation-Reduction,
pubmed-meshheading:9934494-Pyrones,
pubmed-meshheading:9934494-Serine Endopeptidases,
pubmed-meshheading:9934494-Serine Proteinase Inhibitors,
pubmed-meshheading:9934494-Structure-Activity Relationship
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pubmed:year |
1998
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pubmed:articleTitle |
Benzothiopyran-4-one based reversible inhibitors of the human cytomegalovirus (HCMV) protease.
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pubmed:affiliation |
SmithKline Beecham Pharmaceuticals, Collegeville, PA 19426-0989, USA.
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pubmed:publicationType |
Journal Article
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