发明名称 PHARMACEUTICAL COMPOSITIONS BASED ON KININ B2 RECEPTOR ANTAGONISTS AND CORTICOSTEROIDS, AND THEIR USE
摘要 Disclosed is a pharmaceutical composition comprising, as active ingredients, a corticosteroid and a B2 kinin receptor antagonist, together with pharmaceutically acceptable carriers and excipients, wherein: a.) the corticosteroid, either natural or synthetic, is selected from Cortisone, Hydrocortisone, Beclomethasone, Betamethasone, Budesonide, Dexamethasone, Flumethasone, Flunisolide, Fluocortone, Fluticasone, Methylprednisolone, Methylprednisone, Paramethasone, Prednisolone, Triamcinolone, optionally in the form of an ester with acetic, benzoic, caproic, succinic, phosphoric, propionic or valeric acid, or in the form of acetonide; b.) the B2 kinin receptor antagonist is selected from: - H-D-Arg-Arg-Pro-Hyp-Gly-Igl-Ser-D-F5F-Igl-Arg-OH; - H-Arg-Arg-Pro-Hyp-Gly-Igl-Ser-D-Igl-Oic-Arg-OH; - H-D-Arg-Arg-Pro-Hyp-Gly-Thi-Ser-D-Tic-Oic-Arg-OH (Icatibant); - 4-[2-[([[3-(3-Bromo-2-methyl-imidazo[ 1.2-a]pyridine-8-yl oxymethyl)-2,4-dichloro-phenyl]-methyl-carbamoyl]-methy1)carbamoyl]-vinyl]-N,N-dimethyl-benzamide; - 3-(6-Acetylamino-pyridin-3-yl)-N-([[2,4-dichloro-3-(2-methylquinolin-8-yl oxymethyl)-phenyl]-methyl-carbamoyl]-methyl)-acrylamide; -1-[2,4-Dichloro-3-(2,4-dimethy l-quinolin-8-yl oxymethy 1)-benzene sulfonyl]-pyrrolidine-2-carboxylic acid [3-(4-carbamidoyl-benzoylamino )-propyl]-amide (Anatibant); - Bradizide; - 4-( 4-[1-[2,4-Dichloro-3 -(2,4-dimethy l-quinolin-8-y I oxymethy 1)-benzenesulfonyl]-pyrrolidine-2-carbonyl]-piperazine-1-carbonyl)-benzamidine; - 2-[5-(4-Cyano-benzoyl)-1-methyl-1H-pyrrol-2-yl]-N-[2,4-dichloro-3-(2-methly-quinoline-8-yl oxymethyl)-phenyl]-N-methyl-acetamide; -or a compound of general formula (I), wherein the substituents are as described within the specification. Further disclosed is the use of a corticosteroid and a B2 kinin receptor antagonist for the preparation of a medicament for the prevention or therapy of articular and respiratory tract inflammation, lesion and degeneration,
申请公布号 NZ590427(A) 申请公布日期 2012.09.28
申请号 NZ20090590427 申请日期 2009.07.03
申请人 ISTITUTO LUSO FARMACO D'ITALIA S.P.A. 发明人 GIULIANI, SANDRO;MAGGI, CARLO ALBERTO
分类号 A61K31/437;A61K31/4709;A61K31/496;A61K31/573;A61K38/08;A61P19/02 主分类号 A61K31/437
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