首页> 外国专利> INHALATION FORMULATION THAT INCLUDES A GLUCOCORTICOID AND A BETA 2-ADRENO-RECEIVER AGONIST.

INHALATION FORMULATION THAT INCLUDES A GLUCOCORTICOID AND A BETA 2-ADRENO-RECEIVER AGONIST.

机译:包括糖皮质激素和β2-肾上腺素受体激动剂的吸入剂。

摘要

A pharmaceutical formulation for administration by inhalation comprising a compound of formula (I), (See formula) in which the compound of formula (I) is S-fluoromethyl ester of 6alpha, 9alpha-difluoro-11beta-hydroxy-16alpha- methyl-17alpha - [(4-methyl-1,3-thiazol-5-carbonyl) oxy] -3-oxo-androsta-1,4-diene-17beta-carbothioic acid or a salt or solvate thereof together with an agonist long-acting beta 2-adrenoceptor which is salmeterol or formoterol or a compound of formula (M): (See formula) or a salt or solvate thereof, in which: m is an integer from 2 to 8; n is an integer from 3 to 11, with the proviso that m + n is from 5 to 19, R 11 is -XSO2NR 16 R 17 where X is - (CH2) p - or C2-6 alkenylene; R 16 and R 17 are independently selected from hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl, C (O) NR 18 R 19, phenyl, and phenyl (C 1-4 alkyl) -, or R 18 and R 17, together with the nitrogen to which they are attached, they form a ring containing 5, 6, or 7-membered nitrogen, and R 18 and R 17 are each optionally substituted by one or two groups selected from halo, C1-6 alkyl, C1 haloalkyl - 6, C1-6 alkoxy, hydroxy-substituted C1-6 alkoxy, -CO2R 18, -SO2NR 18 R 19, -CONR 18 R 19, -NR 18 C (O) R 19, or a 5-6 heterocyclic ring or 7 members; R 18 and R 19 are independently selected from hydrogen, C 1-6 alkyl, C 3-6 cycloalkyl, phenyl, and phenyl (C 1-4 alkyl) -; and p is an integer from 0 to 6, preferably from 0 to 4; R 12 and R 13 are independently selected from hydrogen, C 1-6 alkyl, C 1-6 alkoxy, halo, phenyl, and C 1-6 haloalkyl; and R 14 and R 15 are independently selected from hydrogen and C1-4 alkyl with the proviso that the total amount of carbon atoms in R 14 and R 15 is not more than 4, said formulation having a therapeutically useful effect in the treatment of asthma or COPD for a period of 24 hours or more.
机译:通过吸入给药的药物制剂,其包含式(I)的化合物(参见式),其中式(I)的化合物是6α,9α-二氟-11β-羟基-16α-甲基-17α的S-氟甲基酯-[[(4-甲基-1,3-噻唑-5-羰基)氧基] -3-氧代-雄烷-1,4-二烯-17β-碳硫代乙酸或其盐或溶剂化物以及激动剂长效β 2-肾上腺素能受体,其为沙美特罗或福莫特罗或式(M)的化合物:(参见式)或其盐或溶剂化物,其中:m为2至8的整数;和n为3至11的整数,条件是m + n为5至19,R 11为-XSO 2 NR 16 R 17,其中X为-(CH 2)p-或C 2-6亚烯基; R 16和R 17独立地选自氢,C 1-6烷基,C 3-7环烷基,C(O)NR 18 R 19,苯基和苯基(C 1-4烷基)-或R 18和R在图17中,R 18和R 17与它们所连接的氮一起形成包含5、6或7元氮的环,并且R 18和R 17各自任选地被选自卤素,C 1-6烷基的一个或两个基团取代。 ,C1卤代烷基-6,C1-6烷氧基,羟基取代的C1-6烷氧基,-CO2R 18,-SO2NR 18 R 19,-CONR 18 R 19,-NR 18 C(O)R 19或5-6杂环或7个成员; R 18和R 19独立地选自氢,C 1-6烷基,C 3-6环烷基,苯基和苯基(C 1-4烷基)-; p为0〜6的整数,优选0〜4。 R 12和R 13独立地选自氢,C 1-6烷基,C 1-6烷氧基,卤素,苯基和C 1-6卤代烷基; R 14和R 15独立地选自氢和C 1-4烷基,条件是R 14和R 15中的碳原子总量不超过4,所述制剂对哮喘的治疗具有治疗作用或COPD持续24小时或更长时间。

著录项

  • 公开/公告号ES2305438T3

    专利类型

  • 公开/公告日2008-11-01

    原文格式PDF

  • 申请/专利权人 GLAXO GROUP LIMITED;

    申请/专利号ES20030702732T

  • 申请日2003-02-04

  • 分类号A61K9/72;A61K9;A61K31/135;A61K31/18;A61K31/568;A61K31/573;A61K31/58;A61K45;A61K45/06;A61K47/26;A61P11/06;A61P29;A61P37/08;

  • 国家 ES

  • 入库时间 2022-08-21 20:04:11

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