首页> 外国专利> DRUGS COMPRISING COMBINATION OF TRIAZASPIRO5,5UNDECANE DERIVATIVE WITH CYTOCHROME P450 ISOZYME 3A4 INHIBITOR AND/OR P-GLYCOPROTEIN INHIBITOR

DRUGS COMPRISING COMBINATION OF TRIAZASPIRO5,5UNDECANE DERIVATIVE WITH CYTOCHROME P450 ISOZYME 3A4 INHIBITOR AND/OR P-GLYCOPROTEIN INHIBITOR

机译:包含曲氮杂螺[5,5]十一烷衍生物与细胞色素P450酶3A4抑制剂和/或P-糖蛋白抑制剂的组合的药物

摘要

A pharmaceutical composition which comprises a combination of a triazaspiroÄ5.5Üundecane derivative of the formula (I): CHEM (wherein all the symbols have the same meanings as defined hereinafter), a quaternary ammonium salt thereof, or an N-oxide thereof, or a non-toxic salt thereof with at least one cytochrome P450 isozyme 3A4 inhibitor and/or at least one P-glycoprotein inhibitor. As a result the pharmaceutical composition comprising the above-described combination, bioavailability of the compound of the formula (I) is enhanced and is able to be effectively utilized as an oral agent in the treatment of various diseases.
机译:药物组合物,其包含式(I)的三氮杂螺并-5.5-十一烷衍生物:(CHEM>,其中所有符号具有与下文定义相同的含义),其季铵盐或其N-氧化物的组合,或其与至少一种细胞色素P450同工酶3A4抑制剂和/或至少一种P-糖蛋白抑制剂的无毒盐。结果,包含上述组合的药物组合物提高了式(I)化合物的生物利用度,并且能够有效地用作治疗各种疾病的口服剂。

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