发明名称 HETEROCYCLIC AMIDE LEUKOTRIENE ANTAGONISTS
摘要 HETEROCYCLIC AMIDE LEUKOTRIENE ANTAGONISTS The invention provides a series of novel heterocyclic amides of the formula I in which the group A.CRa can be -CRb=CRa-, -CHRb-CHRa- or -N=CRa-, the amidic group Re.L can be Re.X.CO.NH, Re.X.CS.NH or Re.NH.CO attached at position 4, 5 or 6 of the benzenoid moiety, Z is an acid group selected from the group consisting of carboxy, an acylsulphonamide residue of the formula CO.NH.SOnRa and a tetrazolyl residue of the formula II, and the radicals Ra, Rb, Rc, Rd, Re, Rf, Rg, Rh, n, X, G1, Q and G2 have the meanings defined in the following specification. The compounds of formula I are leukotriene antagonists. The invention also provides pharmaceutically acceptable salts of the formula I compounds; pharmaceutical compositions containing the formula I compounds, or their salts, for use in the treatment of, for example, allergic or inflammatory diseases, or endotoxic or traumatic shock conditions; and processes for the manufacture of the formula I compounds, as well as intermediates for use in such manufacture.
申请公布号 CA1273934(A) 申请公布日期 1990.09.11
申请号 CA19850493372 申请日期 1985.10.18
申请人 ICI AMERICAN INC. 发明人 BROWN, FREDERICK J.;BERNSTEIN, PETER R.;YEE, YING K.
分类号 A61K31/395;A61K31/40;A61K31/403;A61K31/404;A61K31/41;A61K31/415;A61K31/44;A61K31/4427;A61K31/443;A61K31/4433;A61P9/08;A61P17/00;A61P29/00;A61P37/08;A61P43/00;C07D209/00;C07D209/08;C07D209/12;C07D209/18;C07D209/30;C07D209/82;C07D209/88;C07D231/54;C07D231/56;C07D333/00;C07D401/06;C07D401/12;C07D403/02;C07D403/06;C07D403/10;C07D403/12;C07D405/06;C07D405/12;C07D407/02;C07D407/14;C07D409/02;C07D409/06;C07D409/12;C07D409/14 主分类号 A61K31/395
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