| Literature DB >> 31473 |
C R Rasmussen, J F Gardocki, J N Plampin, B L Twardzik, B E Reynolds, A J Molinari, N Schwartz, W W Bennetts, B E Price, J Marakowski.
Abstract
A series of N-aryl-N'-(1-methyl-2-pyrrolidinylidene)ureas was prepared and screened for pharmacological activity. Congeners possessing either phenyl or phenyl substituted with 4-nitro, 3-bromo, 3-chloro, 3-fluoro, and 3-methyl groups were found to demonstrate anxiolytic activity. 2,6-Disubstitution of the phenyl ring with methyl, chloro, and bromo imparted potent muscle-relaxant properties which appear to be centrally mediated. A significant separation of the anxiolytic and muscle-relaxant properties from other CNS activities, e.g., anticonvulsant, sedative, and hypnotic, was achieved.Entities:
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Year: 1978 PMID: 31473 DOI: 10.1021/jm00208a008
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446