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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
14
|
| pubmed:dateCreated |
1999-2-4
|
| pubmed:abstractText |
Several new 6-oxiranyl-, 6-methyloxiranyluracils, and pyrimidinone derivatives, synthesized by the lithiation-alkylation sequence of 1,3,6-trimethyluracil, 1,3-dimethyl-6-chloromethyluracil, and 2-alkoxy-6-methyl-4(3H)-pyrimidinones, showed a potent and selective antiviral activity against the parainfluenza 1(Sendai) virus replication.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0960-894X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
21
|
| pubmed:volume |
8
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
1833-8
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:9873443-Animals,
pubmed-meshheading:9873443-Antiviral Agents,
pubmed-meshheading:9873443-Cell Line,
pubmed-meshheading:9873443-Dogs,
pubmed-meshheading:9873443-Pyrimidinones,
pubmed-meshheading:9873443-Respirovirus,
pubmed-meshheading:9873443-Structure-Activity Relationship,
pubmed-meshheading:9873443-Virus Replication
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
A potent and selective inhibition of parainfluenza 1 (Sendai) virus by new 6-oxiranyl-, 6-methyloxiranyluracils, and 4(3H)-pyrimidinone derivatives.
|
| pubmed:affiliation |
Dipartimento Agrochimico Agrobiologico, Università degli studi di Viterbo La Tuscia, Italy. Saladino@unitus.it
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|