首页> 外国专利> COMBINATION COMPRISING 6-FLU0R0-N- ((1S, 4S) - 4- (6-FLUORO-2, 4-DI0X0-1- (4'- (PIPERAZIN-1- YLMETHYL) BIPHENYL- 3-YL) -1, 2-DIHYDROPYRIDO 2, 3-D PYRIMIDIN-3 (4H) - YL) CYCLOHEXYL) IMIDAZO 1,2-A PYRIDINE -2- CARBOXAMIDE OR A SALT

COMBINATION COMPRISING 6-FLU0R0-N- ((1S, 4S) - 4- (6-FLUORO-2, 4-DI0X0-1- (4'- (PIPERAZIN-1- YLMETHYL) BIPHENYL- 3-YL) -1, 2-DIHYDROPYRIDO 2, 3-D PYRIMIDIN-3 (4H) - YL) CYCLOHEXYL) IMIDAZO 1,2-A PYRIDINE -2- CARBOXAMIDE OR A SALT

机译:包含6-FLU0R0-N-((1S,4S)-4-(6-FLUORO-2,4-DI0X0-1-(4'-(哌嗪-1-甲基)联苯基-3-YL)-1)的组合2-二氢吡咯并[2,3-D]吡唑啉-3(4H)-YL)环己基)咪唑啉[1,2-A]吡啶-2-甲酰胺或盐

摘要

The invention provides a pharmaceutical product, kit or composition comprising a first active ingredient which is 6-fluoro-N-((1s,4s)-4-(6-fluoro-2,4-dioxo-1-(4'-(piperazin-1- ylmethy1)-biphenyl-3-yl)-l,2-dihydropyrido[2,3-d]pyrimidin-3(4H)- yl)cyclohexyl)imidazo[l,2-a]pyridine-2-carboxamide or a salt thereof, and a second active ingredient selected from: a non-steroidal Glucocorticoid Receptor (GR Receptor) Agonist; an antioxidant; a β2 adrenoceptor agonist; a CCR1 antagonist; a chemokine antagonist (not CCR1); a corticosteroid; a CRTh2 antagonist; a DP1 antagonist; an Histone Deacetylase Inducer; an IKK2 inhibitor; a COX inhibitor; a lipoxygenase inhibitor; a leukotriene receptor antagonist; a MABA compound; an MPO inhibitor; a muscarinic antagonist; a p38 inhibitor; a PPARγ agonist; a protease inhibitor; a Statin; a thromboxane antagonist; a vasodilator; or, an ENAC blocker (Epithelial Sodium-channel blocker); and its use in the treatment of respiratory disease.
机译:本发明提供了包含第一活性成分的药物产品,试剂盒或组合物,所述第一活性成分是6-氟-N-((1s,4s)-4-(6-氟-2,4-二氧-1-(4'-(哌嗪-1-基甲基1)-联苯-3-基)-1,2-二氢吡啶并[2,3-d]嘧啶-3(4H)-基)环己基)咪唑并[1,2-a]吡啶-2-羧酰胺或其盐,以及第二活性成分,其选自:非甾体糖皮质激素受体(GR Receptor)激动剂;抗氧化剂; β2肾上腺素受体激动剂; CCR1拮抗剂;趋化因子拮抗剂(非CCR1);皮质类固醇; CRTh2拮抗剂; DP1拮抗剂;组蛋白脱乙酰基酶诱导剂; IKK2抑制剂; COX抑制剂;脂氧合酶抑制剂;白三烯受体拮抗剂; MABA化合物; MPO抑制剂;毒蕈碱拮抗剂p38抑制剂; PPARγ激动剂;蛋白酶抑制剂;他汀血栓烷拮抗剂;血管扩张药;或ENAC阻滞剂(上皮钠通道阻滞剂);及其在呼吸系统疾病的治疗中的用途。

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