Tetrazole derivatives and methods of treatment of...

C - Chemistry – Metallurgy – 07 – D

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Details

C07D 403/04 (2006.01) A61K 31/41 (2006.01) C07D 491/04 (2006.01) C07D 495/04 (2006.01)

Patent

CA 2539985

The present invention relates to certain tetrazole derivatives of Formula (I), and pharmaceutically acceptable salts thereof, which exhibit useful pharmacological properties, for example, as agonists for the RUP25 receptor. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of metabolic-related disorders, including dyslipidemia, atherosclerosis, coronary heart disease, insulin resistance, type 2 diabetes, Syndrome-X and the like. In addition, the present invention also provides for the use of the compounds of the invention in combination with other active agents such as those belonging to the class of .alpha.-glucosidase inhibitors, aldose reductase inhibitors, biguanides, HMG- CoA reductase inhibitors, squalene synthesis inhibitors, fibrates, LDL catabolism enhancers, angiotensin converting enzyme (ACE) inhibitors, insulin secretion enhancers and the like.

La présente invention concerne certains dérivés de tétrazole de formule (I) et des sels acceptables pharmaceutiquement correspondants qui présentent des propriétés pharmacologiques utiles, par exemple, en tant qu'agonistes du récepteur RUP25. Cette invention a aussi trait à des compositions pharmaceutiques contenant des composés susmentionnés et à des méthodes d'utilisation des composés et des compositions dans le traitement de troubles liés au métabolisme, notamment, la dyslipidémie, l'athérosclérose, la coronaropathie, la résistance à l'insuline, les diabètes de type 2, le syndrome X et similaire. En outre, ladite invention a trait à l'utilisation de ces composés en combinaison avec d'autres agents actifs, tels que ceux appartenant à la classe des inhibiteurs d'.alpha.-glucosidase, des inhibiteurs de la réductase d'aldose, des biguanides, des inhibiteurs de la réductase HMG-CoA, des inhibiteurs de la synthèse du squalène, des fibrates, des activateurs du catabolisme LDL, des inhibiteurs de l'enzyme de conversion de l'angiotensine, des activateurs de sécrétion de l'insuline et similaire.

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