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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1982-4-20
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pubmed:abstractText |
A group of N-(carbonylamino)-1,2,3,6-tetrahydropyridines was synthesized to investigate the effects that changes in functionality at the carbonyl group have on analgesic, antiinflammatory, and hyperglycemic activities. One of the most active analgesic compounds was N-[(ethoxycarbonyl)amino]-1,2,3,6-tetrahydropyridine (5o), which was comparable to that of morphine. Pretreatment with naloxone did not alter the activity of 5o or 5q. N-[(2-Furanylcarbonyl)amino]-1,2,3,6-tetrahydropyridine (5q) was the most potent hyperglycemic agent, elevating blood glucose 181% at 2 and 4 h after a 100 mg/kg po dose.
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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 |
Feb
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
191-5
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7057427-Analgesics,
pubmed-meshheading:7057427-Animals,
pubmed-meshheading:7057427-Anti-Inflammatory Agents,
pubmed-meshheading:7057427-Blood Glucose,
pubmed-meshheading:7057427-Chemical Phenomena,
pubmed-meshheading:7057427-Chemistry,
pubmed-meshheading:7057427-Female,
pubmed-meshheading:7057427-Male,
pubmed-meshheading:7057427-Mice,
pubmed-meshheading:7057427-Pyridines,
pubmed-meshheading:7057427-Rats,
pubmed-meshheading:7057427-Rats, Inbred Strains
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pubmed:year |
1982
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pubmed:articleTitle |
Synthesis of N-(carbonylamino)-1,2,3,6-tetrahydropyridines with analgesic, antiinflammatory, and hyperglycemic activity.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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