Rasmussen C R, Gardocki J F, Plampin J N, Twardzik B L, Reynolds B E, Molinari A J, Schwartz N, Bennetts W W, Price B E, Marakowski J
J Med Chem. 1978 Oct;21(10):1044-54. doi: 10.1021/jm00208a008.
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.
制备了一系列N-芳基-N'-(1-甲基-2-吡咯烷叉基)脲,并对其进行了药理活性筛选。发现具有苯基或被4-硝基、3-溴、3-氯、3-氟和3-甲基取代的苯基的同系物具有抗焦虑活性。苯环的2,6-位被甲基、氯和溴取代赋予了强大的肌肉松弛特性,这似乎是由中枢介导的。抗焦虑和肌肉松弛特性与其他中枢神经系统活性(如抗惊厥、镇静和催眠)有显著区别。