Indazole compounds, pharmaceutical compositions and use

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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548371, 548372, A61K 31415, C07D23116

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active

049978446

ABSTRACT:
The invention provides a series of novel heterocyclic amides of the formula I in which the group A CRa can be --CRb.dbd.CRa--, --CHRb--CHRa-- or --N.dbd.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.SO.sub.n Rg and a tetrazolyl residue of the formula II, and the radicals Ra, Rb, Rc, Rd, Re, Rf, Rg, Rh, n, X, G.sup.1, Q and G.sup.2 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.

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Marx, J. L., Science, 1982, 215, 1380-1383.
Krell, R. D., J. Pharmacol. Exp. Ther., 1979, 211, 436.
Hannig, E., Kollmorgen, Chr. and Dressel, M., "Zur Kenntnis einiger Derivate des 1-Benzyl-6-aminoindazols", Pharmazie 29, H. 10-11 (1974), pp. 685-686.
Fleisch, Jerome H., Rinkema, Lynn E., Haisch, Klaus D., Swanson-Bean, Dorothy, Goodson, Theodore, Ho, Peter P. K., and Marshall, Winston S., "LY171883, 1-<2-Hydroxy-3-Propyl-4-<4-(1H-Tetrazol-5-yl) Butoxy>Phenyl>Ethanone, and Orally Active Leukotriene D.sub.4 Antagonist.sup.1 ", The Journal of Pharmacology and Experimental Therapeutics, vol. 233, No. 1, pp. 148-157 (1985).
J. A. Cook, et al., Pharm. Exp. Ther. (1985), 235, 470.

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