发明名称 ANALOGS OF MEVALOLACTONE AND DERIVATIVES THEREOF, PROCESS FOR THEIR PRODUCTION, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THEIR USE AS PHARMACEUTICALS
摘要 Compounds of formula I <CHEM> and the other is primary or secondary C1-6alkyl, C3-6cycloalkyl or phenyl-(CH2)m-, wherein R4 is hydrogen, C1-4alkyl, C1-4alkoxy, (except t-butoxy), trifluoromethyl, fluoro, chloro, phenoxy or benzyloxy, R5 is hydrogen, C1-3alkyl, C1-3alkoxy, trifluoromethyl, fluoro, chloro, phenoxy or benzyloxy, R5a is hydrogen C1-2alkyl, C1-2alkoxy, fluoro or chloro, and m is 1, 2 or 3, with the provisos that both R5 and R5a must be hydrogen when R4 is hydrogen, R5a must be hydrogen when R5 is hydrogen, not more than one of R4 and R5 is trifluoromethyl, not more than one of R4 and R5 is phenoxy and not more than one of R4 and R5 is benzyloxy, R2 is hydrogen, C1-4alkyl, C3-6cycloalkyl, C1-4alkoxy, (except t-butoxy), trofluoromethyl, fluoro, chloro, phenoxy or benzyloxy, R3 is hydrogen, C1-3alkyl, C1-3alkoxy, trifluoromethyl, fluoro, chloro, phenoxy or benzyloxy, with the provisos that R3 must be hydrogen when R2 is hydrogen, not more than one of R2 and R3 is trifluoromethyl, not more than one of R2 and R3 is phenoxy, and not more than one of R2 and R3 is benzyloxy, X is -(CH2n- or -CH=CH- in (n = 0, 1, 2 or 3), <CHEM> wherein R6 is hydrogen or C1-3alkyl in free acid form or in the form of a physiologically hydrolysable and acceptable ester or a lactone thereof or in salt form. These compounds are indicated for use as pharmaceuticals particularly for inhibiting cholesterol biosynthesis and treating atherosclesoris.
申请公布号 AU2261283(A) 申请公布日期 1984.06.18
申请号 AU19830022612 申请日期 1983.11.18
申请人 SANDOZ AG 发明人 KATHAWALA, FAIZULLA GULAMHUSEIN
分类号 A61K31/40;A61K31/403;A61K31/404;A61K31/405;A61P3/06;C07D;C07D209/12;C07D209/18;C07D209/42;C07D405/04;C07D405/06;C07F7/18;C07F9/572 主分类号 A61K31/40
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