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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
22
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pubmed:dateCreated |
2004-10-14
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pubmed:abstractText |
Two parallel synthetic methods were developed to explore the structure-activity relationships (SAR) of a series of potent opioid agonists. This series of tropanylidene benzamides proved extremely tolerant of structural variation while maintaining excellent opioid activity. Evaluation of several representative compounds from this series in the mouse hot plate test revealed potent antinociceptive effects upon oral administration.
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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 |
Nov
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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 |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5493-8
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pubmed:meshHeading |
pubmed-meshheading:15482911-Analgesics,
pubmed-meshheading:15482911-Animals,
pubmed-meshheading:15482911-Benzamides,
pubmed-meshheading:15482911-Mice,
pubmed-meshheading:15482911-Molecular Structure,
pubmed-meshheading:15482911-Pain Measurement,
pubmed-meshheading:15482911-Receptors, Opioid, delta,
pubmed-meshheading:15482911-Receptors, Opioid, mu,
pubmed-meshheading:15482911-Structure-Activity Relationship
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pubmed:year |
2004
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pubmed:articleTitle |
Parallel methods for the preparation and SAR exploration of N-ethyl-4-[(8-alkyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-aryl-methyl]-benzamides, powerful mu and delta opioid agonists.
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pubmed:affiliation |
Drug Discovery, Johnson and Johnson Pharmaceutical Research and Development, L.L.C., Welsh and McKean Roads, PO Box 776, Spring House, PA 19477-0776, USA. scoats@prdus.jnj.com
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pubmed:publicationType |
Journal Article
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