Source:http://linkedlifedata.com/resource/pubmed/id/17544673
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
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pubmed:dateCreated |
2007-6-26
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pubmed:abstractText |
As part of our search for potential anticonvulsant agents, a set of compounds were designed, synthesized, and evaluated against MES and PTZ tests. Bioisosteric functional group information was used to design a new functionality, sulfamides, that complies with the requirements of the pharmacophore previously defined. Some of the molecules showed a promising anticonvulsant profile as selective anti-MES drugs, being active at low concentrations (30mg/kg). The biological data were confirmed in Phase II of the Anticonvulsant Drug Development Program of the National Institute of Health.
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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 |
Aug
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pubmed:issn |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5604-14
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pubmed:meshHeading |
pubmed-meshheading:17544673-Amides,
pubmed-meshheading:17544673-Animals,
pubmed-meshheading:17544673-Anticonvulsants,
pubmed-meshheading:17544673-Drug Design,
pubmed-meshheading:17544673-Electrons,
pubmed-meshheading:17544673-Male,
pubmed-meshheading:17544673-Mice,
pubmed-meshheading:17544673-Models, Molecular,
pubmed-meshheading:17544673-Molecular Structure,
pubmed-meshheading:17544673-Structure-Activity Relationship,
pubmed-meshheading:17544673-Sulfur
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pubmed:year |
2007
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pubmed:articleTitle |
Design, synthesis, and anticonvulsant activity of some sulfamides.
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pubmed:affiliation |
Medicinal Chemistry, Department of Biological Sciences, National University of La Plata, 47 and 115, La Plata B1900BJW, Argentina.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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