Journal of Medicinal Chemistry p. 1374 - 1377 (1977)
Update date:2022-08-04
Topics:
Uwaydah
May
Harris
A series of N-substituted 9α-ethyl-2'-hydroxy-5-methyl-6,7-benzomorphans was synthesized and evaluated for their narcotic analgesic and antagonistic activities. Compounds 2a and 22 were as potent as morphine in the writhing (PPQ) and hot-plate tests, while a number of compounds demonstrated antagonistic activities greater than nalorphine. Generally, the compounds in this series show activities somewhat greater than the comparable compounds in the 5,9α- dimethyl-6,7-benzomorphan series for analgesic effect and similar or slightly less antagonistic potency.
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