Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3918
Title: Pyrrolobenzodiazepines and related systems. 2. Synthesis and biological properties of isonoraptazepine derivatives
Authors: Silvio, Massa
Marino, Artico
Antonello, Mai
Corelli, Federico 
Botta, Maurizio 
Tafi, Andrea 
Gian Carlo, Pantaleoni
Raffaele, Giorgi
Maria Francesca, Coppolino
Issue Date: 1992
Project: None 
Journal: JOURNAL OF MEDICINAL CHEMISTRY
Abstract: 
The synthesis of some derivatives and analogues of 12,13,14,14a-tetrahydro-9H,11H-pyrazino-[2,1-c]pyrrolo[1,2-a][1,4]benzodiazepine(isonoraptazepine)is reported. The new derivatives have been subjected to pharmacological tests for evaluation of antidepressant effects. Neurobehavioral assays were also carried out to acquire data on neurotoxicity and sedative action. Isonoraptazepine analogues and derivatives lacked the pharmacological activity of mianserin and aptazepine and showed properties similar to imipramine. Molecular modeling studies revealed structural similarities between isonoraptazepine derivatives and imipramine, thus explaining the similar pharmacological profile found in some of the tests employed. Based on pharmacological data the title compounds cannot be regarded as alpha2 presynaptic adrenoceptors antagonists. In vitro studies for receptor binding gave support to this observation. The above studies lead us to conclude that isonoraptazepine derivatives are conformationally restricted analogues of imipramine, but their antidepressant activity cannot be correlated to inhibition of 5HT uptake. Among the derivatives tested, 7b and 8e show some affinity for the d-fenfluramine receptor site, a serotonin presynaptic site connected with anorectic activity.
Description: 
49325
URI: http://hdl.handle.net/20.500.12779/3918
ISSN: 0022-2623
DOI: 10.1021/jm00102a004
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