Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7803316 | European Journal of Medicinal Chemistry | 2011 | 8 Pages |
Abstract
⺠new 4-aryl-5,6,7,8-tetrahydropyrido[1,2-c]pyrimidine derivatives possessing a 3-(1,2,3,6-tetrahydropyrid-4-yl)-1H-indole group or its 2-methyl derivatives were synthesized. ⺠new derivatives are considered to have a dual 5-HT1A and SERT activity. ⺠synthesized ligands possess anticipated agonistic activity toward presynaptic 5-HT1A receptors, while displaying no postsynaptic action. ⺠degree of saturation pyridine moiety bound to the indole had an influence on KiSERT values for 2-methyl-substituted indole-derivatives.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Franciszek Herold, Andrzej Chodkowski, Åukasz Izbicki, Jadwiga TurÅo, Maciej Dawidowski, Jerzy Kleps, Gabriel Nowak, Katarzyna Stachowicz, MaÅgorzata DybaÅa, Agata Siwek, Aleksander P. Mazurek, Andrzej Mazurek, Franciszek PluciÅski,