Synthesis and anticonvulsant activities of N-benzyl-2-acetamidopropionamide derivatives
D Choi, JP Stables, H Kohn
Index: Choi, Daeock; Stables, James P.; Kohn, Harold Journal of Medicinal Chemistry, 1996 , vol. 39, # 9 p. 1907 - 1916
Full Text: HTML
Citation Number: 134
Abstract
Studies have demonstrated that 2-substituted N-benzyl-2-acetamidoacetamides (2) are potent anticonvulsants. A recent investigation has led to the hypothesis that an important structural feature in 2 for maximal anticonvulsant activity is the placement of a small, substituted heteroatom moiety one atom from the C (2) site. This paper validates this hypothesis. Twelve derivatives of N-benzyl-2-acetamidopropionamide have been ...
Related Articles:
[Takeuchi, Kumiko; Kohn, Todd J.; True, Timothy A.; Mais, Dale E.; Wikel, James H.; Utterback, Barbara G.; Wyss, Virginia L.; Jakubowski, Joseph A. Journal of Medicinal Chemistry, 1998 , vol. 41, # 27 p. 5362 - 5374]
[Takeuchi, Kumiko; Kohn, Todd J.; True, Timothy A.; Mais, Dale E.; Wikel, James H.; Utterback, Barbara G.; Wyss, Virginia L.; Jakubowski, Joseph A. Journal of Medicinal Chemistry, 1998 , vol. 41, # 27 p. 5362 - 5374]