Quinolines and their therapeutic use

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

Reexamination Certificate

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Details

C514S312000, C514S313000, C546S152000, C546S153000, C546S159000

Reexamination Certificate

active

07858640

ABSTRACT:
Compounds of formula [1] are CRTH2 antagonists, useful in the treatment of conditions having an inflammatory components; in which: R1-R9are various substituents; A is —CHR10—, —C(O)—, —S(O)n—, —O—, or —NR10— wherein n is an integer from 0-1 and R10is selected from various substituents; B is a direct bond or a divalent radical; R11and R12are selected from cvarious substituents; X is a carboxylic acid, tetrazole, 3-hydroxyisoxazole, hydroxamic acid, phosphinate, phosphonate, phosphonamide, sulfonic acid group, or a group of formula C═(O)NHSO2R6or SO2NHC(═O)R6; and Y is aryl, heteroaryl, aryl-fused-heterocycloalkyl, heteroaryl-fused-cycloalkyl, heteroaryl-fused-heterocycloalkyl or aryl-fused-cycloalkyl group.

REFERENCES:
patent: 2004/0127708 (2004-07-01), Fuji et al.
patent: 0 101 330 (1984-02-01), None
patent: 0 556 060 (1993-08-01), None
patent: 1 413 306 (2004-04-01), None
patent: WO 03/066046 (2003-08-01), None
patent: WO 2004106302 (2004-05-01), None
Vippagunta et. al., Advanced Drug Delivery Reviews, 2001, Elsevier, vol. 48, pp. 3-26.
Lloyd, J. et al., “Quinoline-4-carboxylic acids as angiotensin II receptor antagonists,”Bioorganic&Medicinal Chemistry Letters, 1994, vol. 4, No. 1, pp. 195-200.

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