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The development of cannabinoid antagonists.

作者信息

Barth F, Rinaldi-Carmona M

机构信息

Sanofi Recherche, 371 rue du Pr Joseph Blayac 34184, Montpellier, Cédex 04, France.

出版信息

Curr Med Chem. 1999 Aug;6(8):745-55.

PMID:10469889
Abstract

The discovery of two distinct cannabinoid receptors (CB1 and CB2) in the early 1990's has revived the research on cannabinoid antagonists. While the search for antagonists based on the structure of agonists (classical cannabinoids or aminoalkylindoles) appeared rather disappointing, the first potent cannabinoid antagonists were developed in a new chemical series: the diarylpyrazoles. Since its discovery in 1994, the selective CB1 antagonist SR 141716 has became a major pharmacological tool to elucidate the physiological role of the CB1 cannabinoid receptor and its endogenous ligand. The selective CB2 antagonist SR 144528 is expected to play the same role for the CB2 receptors, while the recent development of cannabinoid antagonists belonging to other chemical series illustrates the interest of these compounds which are now considered as interesting therapeutic targets by many pharmaceutical companies.

摘要

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