
European Journal of Medicinal Chemistry p. 237 - 244 (1998)
Update date:2022-07-29
Topics:
Costanzo, Annarella
Guerrini, Gabriella
Bruni, Fabrizio
Ciciani, Giovanna
Selleri, Silvia
Cappelletti, Silvia
Costa, Barbara
Martini, Claudia
Lucacchini, Antonio
A new series of 3-, 8-substituted pyrazolo[5,1-c][1,2,4]benzotriazine 4-oxides 3 were synthesized and their benzodiazepine receptor (BZR) affinities were evaluated in vitro in comparison with their 5-oxide isomers 2. The 4-oxide compounds 3c,m,n,o showed a better receptor affinity than their corresponding 5-oxide isomers, with an efficacy trend of antagonist/partial inverse agonist. From a structure-affinity relationship point of view some insight in the role played by N-4 and N-oxide is gained.
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