发明名称 LEUKOTRIENE ANTAGONISTS
摘要 Compounds of formula: <CHEM> in which, inter alia q is 0 to 2, R1 is (L)a-(CH2)b-(T)c-B wherein a and c are 0 or 1, b is 3 to 14, L and T are independently O, S or CH2; B is C1-4 alkyl, ethynyl, CF3, isopropenyl, furanyl, thienyl, furanyl, cyclohexyl or optionally substituted phenyl; R2 and A are H, CF3, C1-4 alkyl, C1-4 alkoxy, halogen, OH, NO2 or NH2 or R1 and A are H and R2 is (L)a-(CH2)b-(T)c as above; y is COR3 or (CHX)n(CH2)pZ wherein R3 is OH, NH2, aryloxy or alkoxy, n is 0 or 1, p is 0, 1 and 2; X is H, OH, alkyl, alkoxy or F, Z is COR3 or tetrazolyl; R is (CR4R5)mW, m is 0 to 6, R4 and R5 are alkyl and W is an optionally substituted heteroaryl group; intermediates and processes for their preparation and their use in therapy as leukotriene antagonists.
申请公布号 ZA8804239(B) 申请公布日期 1989.06.28
申请号 ZA19880004239 申请日期 1988.06.14
申请人 SMITHKLINE BECKMAN CORPORATION 发明人 JOHN GERALD GLEASON;RALPH FLOYD HALL;IRENE NIJOLE UZINSKAS
分类号 C07D249/08;A61K31/34;A61K31/341;A61K31/41;A61K31/425;A61K31/426;A61K31/433;A61P11/00;A61P37/06;A61P37/08;A61P43/00;C07D207/333;C07D233/64;C07D233/84;C07D249/04;C07D249/12;C07D257/04;C07D263/32;C07D263/46;C07D277/20;C07D277/36;C07D277/56;C07D285/12;C07D285/125;C07D307/68;C07D333/18 主分类号 C07D249/08
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