Hmg-coa reductase inhibitors and method

C - Chemistry – Metallurgy – 07 – D

Patent

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C07D 495/04 (2006.01) A61K 31/55 (2006.01) C07D 221/00 (2006.01) C07D 223/00 (2006.01) C07D 313/00 (2006.01) C07D 337/00 (2006.01) C07D 471/04 (2006.01) C07D 491/04 (2006.01) C07D 491/10 (2006.01)

Patent

CA 2412632

Compounds of structure (1) are HMG CoA reductase inhibitors and thus are active in inhibiting cholesterol biosynthesis, modulating blood serum lipids such as lowering LDL cholesterol and/or increasing HDl cholesterol, and treating hyperlipidemia, hypercholesterolemia, hypertriglyceridemia and atherosclerosis and pharmaceutically acceptable salts thereof, wherein X is O or S; Z is (2) or (3); n is O or 1; R1 and R2 are the same or different and are independently selected from alkyl, arylalkyl, cycloalkyl, alkenyl, cycloalkenyl, aryl, heteroaryl or cycloheteroalkyl; and R3 to R9 are as defined herein.

La présente invention concerne des composés de structure (1) qui sont des inhibiteurs de la HMG CoA réductase et qui sont par conséquent actifs pour inhiber la biosynthèse du cholestérol, moduler les lipides du sérum sanguin de manière à réduire le cholestérol LDL et/ou à augmenter le cholestérol HDl et traiter l'hyperlipidémie, l'hypercholestérolémie, l'hypertriglycéridémie et l'athérosclérose ; ainsi que les sels pharmaceutiquement acceptables de ces derniers. Dans la structure (1), X représente O ou S; Z représente (2) ou (3); n représente O ou 1; R¿1? et R¿2? sont identiques ou différents et sont indépendamment sélectionnés parmi alkyle, arylalkyle, cycloalkyle, alcényle, cycloalcényle, aryle, hétéroaryle ou cyclohétéroalkyle; et R¿3?, R¿4?, R¿5?, R¿6?, R¿7?, R¿8? et R¿9? sont tels que définis dans le descriptif. Structure (1)

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