The synthesis of 3-(2-furyl)- and 3-(3-furyl)-8-chloropyrazolo[5,1-c][1,2,4]betizotriazine 5-oxides is reported. The binding affinities at the central Benzodiazepine Receptor (BZR) and the muscle relaxant, anticonvulsant and anxiolytic activities of new furyl derivatives are compared to those of the 3-heteroaryl derivatives, BZR ligands previously reported by us. The results confirm the stringent spatial requisites of the lipophilic pocket that accommodates the 3-substituent, which seems to influence both the binding and intrinsic activity of this new class of ligands.

Synthesis and pharmacological evaluation of 3-(2-furyl)- and 3-(3-furyl)-(-chloropyrazolo[5,1-c][1,2,4]benzotriazine 5-oxides, new 3-heteroaryl substituted benzodiazepine receptor ligands / A. COSTANZO; G. GUERRINI; G. CICIANI; F. BRUNI; C. COSTAGLI; S. SELLERI; B. COSTA; C. MARTINI; P. MALMBERG AIELLO. - In: MEDICINAL CHEMISTRY RESEARCH. - ISSN 1054-2523. - ELETTRONICO. - 11:(2002), pp. 87-101.

Synthesis and pharmacological evaluation of 3-(2-furyl)- and 3-(3-furyl)-(-chloropyrazolo[5,1-c][1,2,4]benzotriazine 5-oxides, new 3-heteroaryl substituted benzodiazepine receptor ligands.

COSTANZO, ANNARELLA;GUERRINI, GABRIELLA;CICIANI, GIOVANNA;BRUNI, FABRIZIO;SELLERI, SILVIA;MALMBERG, PETRA
2002

Abstract

The synthesis of 3-(2-furyl)- and 3-(3-furyl)-8-chloropyrazolo[5,1-c][1,2,4]betizotriazine 5-oxides is reported. The binding affinities at the central Benzodiazepine Receptor (BZR) and the muscle relaxant, anticonvulsant and anxiolytic activities of new furyl derivatives are compared to those of the 3-heteroaryl derivatives, BZR ligands previously reported by us. The results confirm the stringent spatial requisites of the lipophilic pocket that accommodates the 3-substituent, which seems to influence both the binding and intrinsic activity of this new class of ligands.
2002
11
87
101
A. COSTANZO; G. GUERRINI; G. CICIANI; F. BRUNI; C. COSTAGLI; S. SELLERI; B. COSTA; C. MARTINI; P. MALMBERG AIELLO
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/312364
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