首页> 外国专利> ANTIBACTERIAL SUBSTITUTED 7-ACYLAMINO-3-(METHYL-HYDRAZONO)-METHYLCEPHALOSPORINS, METHOD OF THEIR PREPARING, PHARMACEUTICAL COMPOSITIONS BASED ON THEREOF, INTERMEDIATE COMPOUNDS AND METHOD OF TREATMENT OF DISEASES CAUSED BY MICROORGANISMS

ANTIBACTERIAL SUBSTITUTED 7-ACYLAMINO-3-(METHYL-HYDRAZONO)-METHYLCEPHALOSPORINS, METHOD OF THEIR PREPARING, PHARMACEUTICAL COMPOSITIONS BASED ON THEREOF, INTERMEDIATE COMPOUNDS AND METHOD OF TREATMENT OF DISEASES CAUSED BY MICROORGANISMS

机译:抗菌药物取代的7-酰基氨基-3-(甲基-羟基偶氮)-甲基脂蛋白,其制备方法,基于其的药物组合物,中间化合物以及治疗由微生物引起的疾病的方法

摘要

FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention relates to novel derivatives of 7-acylamino-3-(methylhydrazono)-methylcephalosporin of the general formula (Is) where R5 means hydrogen atom or ester residue; R2s means alkyl, aralkyl, alkenyl or alkynyl; R3s means hydrogen atom, alkyl, aralkyl, alkenyl, alkynyl or cycloalkyl as free form, salt and/or solvate. Invention relates also to method of synthesis of compound of the formula (Is) by interaction of compound of the formula (II) with compound of the formula (III) and isolation of compounds of the formula (Is). Invention relates also to pharmaceutical composition comprising compound of the formula (Is) with at least one pharmaceutical carrier or vehicle that shows an antibacterial effect. Invention relates also to method of treatment of patients with diseases induced by microorganisms that involves administration to patient needing this treatment the effective dose of compound of the formula (Is). Invention provides synthesis of novel compounds exhibiting an antibacterial activity. EFFECT: improved method of synthesis and treatment, valuable medicinal properties of compounds. 9 cl, 3 tbl
机译:领域:有机化学,医学,药学。物质:本发明涉及通式(Is)的7-酰基氨基-3-(甲基methyl唑啉)-甲基头孢菌素的新型衍生物。<图像文件=“ 00000004.GIF” he =“ 37” wi =“ 89” />其中R 5 表示氢原子或酯残基; R 2s 是指烷基,芳烷基,烯基或炔基; R 3s 是指氢原子,烷基,芳烷基,烯基,炔基或环烷基的游离形式,盐和/或溶剂化物。本发明还涉及通过式(II)的化合物的相互作用合成式(Is)的化合物的方法。<图像文件=“ 00000005.GIF” he =“ 30” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 69” />与式(III)的化合物<图像文件=“ 00000006.GIF” he =“ 16” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 47” />并分离化合物公式(是)。本发明还涉及包含式(Is)化合物与至少一种显示抗菌作用的药物载体或媒介物的药物组合物。本发明还涉及治疗由微生物引起的疾病的患者的方法,该方法涉及向需要这种治疗的患者施用有效剂量的式(Is)化合物。本发明提供了具有抗菌活性的新型化合物的合成。效果:改进的合成和治疗方法,化合物的重要药用特性。 9厘升,3汤匙

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