Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1371024 | Bioorganic & Medicinal Chemistry Letters | 2015 | 5 Pages |
Abstract
A series of 2-phenyl- or 3-phenyl piperazines, structurally related to DM235 and DM232, two potent nootropic agents, have been prepared and tested in the mouse passive-avoidance test, to assess their ability to revert scopolamine-induced amnesia. Although the newly synthesized molecules were less potent than the parent compounds, some useful information has been obtained from structure–activity relationships. A small but significant enantioselectivity has been found for the most potent compound 5a.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Luca Guandalini, Maria Vittoria Martino, Lorenzo Di Cesare Mannelli, Gianluca Bartolucci, Fabrizio Melani, Ruchi Malik, Silvia Dei, Elisa Floriddia, Dina Manetti, Francesca Orlandi, Elisabetta Teodori, Carla Ghelardini, Maria Novella Romanelli,