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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
24
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pubmed:dateCreated |
2003-12-3
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pubmed:abstractText |
Hydrochloride derivatives 5a-c and quaternary ammonium derivatives 6a-c of epibatidine incorporated with amino acid ester were synthesized and evaluated for their in vivo analgesic activity and toxicity. Among all tested compounds, compound 6c has the most potent analgesic activity. The quaternary ammonium salts 6a and 6c showed better analgesic activity than the corresponding hydrochlorides 5a and 5c. Both 5a-c and 6a-c showed significantly lower toxicity than epibatidine itself.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0960-894X
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4327-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14643319-Amino Acids,
pubmed-meshheading:14643319-Analgesics, Non-Narcotic,
pubmed-meshheading:14643319-Animals,
pubmed-meshheading:14643319-Bicyclo Compounds, Heterocyclic,
pubmed-meshheading:14643319-Dose-Response Relationship, Drug,
pubmed-meshheading:14643319-Hydrochloric Acid,
pubmed-meshheading:14643319-Mice,
pubmed-meshheading:14643319-Pain,
pubmed-meshheading:14643319-Pyridines,
pubmed-meshheading:14643319-Quaternary Ammonium Compounds,
pubmed-meshheading:14643319-Structure-Activity Relationship
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pubmed:year |
2003
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pubmed:articleTitle |
Synthesis and analgesic activity of hydrochlorides and quaternary ammoniums of epibatidine incorporated with amino acid ester.
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pubmed:affiliation |
School of Pharmaceutical Sciences, Peking University, Beijing 100083, PR, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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