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AMINO GLYCOSIDE COMPOSITION FOR SUBSTANTIALLY DECREASING NEPHROTOXICITY INDUCED BY AMINO GLYCOSIDE

机译:氨基糖苷组合物可大大降低氨基糖苷引起的肾毒性

摘要

PURPOSE: To obtain an aminoglycoside composition capable of reducing nephrotoxicity induced by an aminoglycoside useful as an antibiotic, an antimicrobial agent, etc. CONSTITUTION: This aminoglycoside composition comprises a compound of formula I to formula II (R1 and R2 are each a 2-6C alkyl, cyclohexyl, alkoxyalkyl or hydroxyalkyl; A is a =4C hydrocarbon group substitutable with methyl; at least one of R3 and R4 is a group of formula III and the other is H or a =6C aliphatic hydrocarbon group which is interrupted with an oxygen atom having = two carbon chains or is substitutable with one oxygen atom or two hydroxyl groups; R6 is a 1-3C alkyl; (n) is an integer of 2-5), preferably one or more compounds selected from 1,3-di-n-butyl-7-(2-oxopropyl)xanthine and 7-(3-oxobutyl)-1,3-di-n-butylxanthine and is capable of reducing nephrotoxicity of an aminoglycoside such as gentamicin, amikacin, kanamycin and neomycin, especially neomycin.
机译:目的:获得能够减少由用作抗生素,抗微生物剂等的氨基糖苷诱导的肾毒性的氨基糖苷组合物。组成:该氨基糖苷组合物包含式I至式II的化合物(R 1和R 2各自为2-6C烷基,环己基,烷氧基烷基或羟烷基; A是可被甲基取代的<= 4C烃基; R3和R4中的至少一个是式III的基团,另一个是H或<= 6C的脂肪族烃基,其中具有≤2个碳链或可被一个氧原子或两个羟基取代的氧原子; R6为1-3C烷基;(n)为2-5的整数),优选一种或多种选自以下的化合物: 3-二正丁基-7-(2-氧丙基)黄嘌呤和7-(3-氧丁基)-1,3-二正丁基黄嘌呤并能够减少庆大霉素,丁胺卡那霉素,卡那霉素等氨基糖苷的肾毒性和新霉素,尤其是新霉素。

著录项

  • 公开/公告号JPH04282315A

    专利类型

  • 公开/公告日1992-10-07

    原文格式PDF

  • 申请/专利权人 HOECHST ROUSSEL PHARMACEUT INC;

    申请/专利号JP19910282770

  • 发明设计人 UIRIAMU JIEI NOBITSUKU JIYUNIA;

    申请日1991-10-29

  • 分类号A61K31/52;A61K31/70;A61P31/04;A61P39/02;A61P43/00;

  • 国家 JP

  • 入库时间 2022-08-22 05:39:55

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