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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1981-9-22
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pubmed:abstractText |
(Z)-5-(2-Bromovinyl)uracil was obtained by photoisomerization of the E. isomer. Similarly, (E)-5-(2-bromovinyl)-2'-deoxyuridine gave the required Z isomer. (Z)-5-(2-Bromovinyl)-2'-deoxyuridine is much less active against herpes simplex virus type 1 (HSV-1) and somewhat less active against herpes simplex virus type 2 than is the E isomer. Both isomers show similar activity against vaccinia virus. Therefore, the highly potent and selective activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine against HSV-1 is due to its E configuration.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
759-60
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6265638-Animals,
pubmed-meshheading:6265638-Antiviral Agents,
pubmed-meshheading:6265638-Bromodeoxyuridine,
pubmed-meshheading:6265638-Rabbits,
pubmed-meshheading:6265638-Simplexvirus,
pubmed-meshheading:6265638-Stereoisomerism,
pubmed-meshheading:6265638-Structure-Activity Relationship,
pubmed-meshheading:6265638-Vaccinia virus
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pubmed:year |
1981
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pubmed:articleTitle |
Synthesis and antiviral properties of (Z)-5-(2-bromovinyl)-2'-deoxyuridine.
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pubmed:publicationType |
Journal Article,
Comparative Study
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