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J Med Chem ; 21(10): 1044-54, 1978 Oct.
Article in English | MEDLINE | ID: mdl-31473

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.


Subject(s)
Central Nervous System Agents/chemical synthesis , Urea/analogs & derivatives , Animals , Anti-Anxiety Agents/chemical synthesis , Anticonvulsants/chemical synthesis , Dose-Response Relationship, Drug , Hypnotics and Sedatives/chemical synthesis , Lethal Dose 50 , Mice , Muscle Relaxants, Central/chemical synthesis , Pyrrolidines/chemical synthesis , Pyrrolidines/pharmacology , Rats , Structure-Activity Relationship , Thiourea/analogs & derivatives , Thiourea/chemical synthesis , Thiourea/pharmacology , Urea/chemical synthesis , Urea/pharmacology
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