
Journal of Medicinal Chemistry p. 2273 - 2280 (1986)
Update date:2022-07-29
Topics:
Chapleo, Christopher B.
Myers, Malcolm
Myers, Peter L.
Saville, John F.
Smith, Alan C. B.
et al.
The synthesis and anticonvulsant activity of a series of 2-aryl-5-hydrazino-1,3,4-thiadiazoles are described.The combination of preferred aromatic substituents in the 2-position coupled with alkyl substitution on the hydrazine moiety led to a number of potent compounds lacking sedation, ataxia, or lethality. 5-(2-Biphenylyl)-2-(1-methylhydrazino)-1,3,4-thiadiazole (4m) represents a new class of anticonvulsant agent and compares favorably with the standard drugs phenytoin, phenobarbital, and carbamazepine.
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