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.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jm00208a008DOI Listing

Publication Analysis

Top Keywords

muscle-relaxant properties
8
2-pyrrolidinylideneureas class
4
class central
4
central nervous
4
nervous system
4
system agents
4
agents series
4
series n-aryl-n'-1-methyl-2-pyrrolidinylideneureas
4
n-aryl-n'-1-methyl-2-pyrrolidinylideneureas prepared
4
prepared screened
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!