| Literature DB >> 1495016 |
J R Carson1, R J Carmosin, J L Vaught, J F Gardocki, M J Costanzo, R B Raffa, H R Almond.
Abstract
2-Substituted 1-azabicycloalkanes (3- and 5-aryloctahydroindolizines 2 and 11, 3-cyclohexyloctahydroindolizine 12, 4-aryloctahydroquinolizines 13, and 3-arylhexahydropyrrolizines 14) constitute a new class of non-opiate antinociceptive agents. These compounds demonstrated activity in the mouse abdominal constriction test and many were active in the mouse tail-flick test. trans-3-(2-Bromophenyl)octahydroindolizine (2a) did not bind to the opiate receptor nor did it affect arachidonate metabolism. 3-Aryloctahydroindolizines were prepared by catalytic hydrogenation of 1-aryl-3-(2-pyridinyl)-2-propen-1-ones. The X-ray crystal structure of (-)-2a was determined and absolute stereochemistry assigned as 3-R,8a-R.Entities:
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Year: 1992 PMID: 1495016 DOI: 10.1021/jm00093a019
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446