Molecular simplification of 1, 4-diazabicyclo [4.3. 0] nonan-9-ones gives piperazine derivatives that maintain high nootropic activity

D Manetti, C Ghelardini, A Bartolini, S Dei…

Index: Manetti; Ghelardini; Bartolini; Dei; Galeotti; Gualtieri; Romanelli; Teodori Journal of Medicinal Chemistry, 2000 ,  vol. 43,  # 23  p. 4499 - 4507

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Citation Number: 35

Abstract

Several 4-substituted 1-acylpiperazines, obtained by molecular simplification of 4- substituted 1, 4-diazabicyclo [4.3. 0] nonan-9-ones, have been synthesized and tested in vivo on the mouse passive avoidance test, to evaluate their nootropic activity. The results show that, apparently, an N-acylpiperazine group can mimic the 2-pyrrolidinone ring of 1, 4- diazabicyclo [4.3. 0] nonan-9-one, as the compounds of the new series maintain high ...