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J Med Chem ; 34(1): 291-8, 1991 Jan.
Article in English | MEDLINE | ID: mdl-1992129

ABSTRACT

The synthesis and biological properties of a novel series of selective calcium-independent phosphodiesterase inhibitors are described. These compounds also inhibit the specific binding of [3H]rolipram to rat brain membranes and exhibit efficacy in preclinical models of antidepressant activity in mice, such as reducing immobility in the forced-swim test and reversing reserpine-induced hypothermia. Imidazolidinones 4 and 16 were found to be the most potent compounds studied.


Subject(s)
Antidepressive Agents/chemical synthesis , Brain/metabolism , Cerebral Cortex/enzymology , Phosphodiesterase Inhibitors/chemical synthesis , Animals , Body Temperature/drug effects , Calcium/pharmacology , Female , Indicators and Reagents , Magnetic Resonance Spectroscopy , Mice , Molecular Conformation , Molecular Structure , Motor Activity/drug effects , Phosphodiesterase Inhibitors/chemistry , Phosphodiesterase Inhibitors/pharmacology , Pyrrolidinones/pharmacology , Rats , Rats, Inbred Strains , Reserpine/pharmacology , Rolipram , Structure-Activity Relationship
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