antibiotic of aureolic acid group with anticancer activity by structural formula as follows, where R5 represents hydrogen, C3-C10-cycloalkyl or C1-C4-alkyl with straight or branched hydrocarbon chain, optionally substituted with one or more hydroxyls. Additionally, invention concerns method of production of the specified derivatives, consisting in selective modification of 2'-carbonyl group of olivomycin 1 by reaction with aminooxyacetic acid, followed by amidation reaction of produced intermediate 2'-(carboxymethoxime)olivomycin 1 and related amines condensing agent added.;EFFECT: method of production of antibiotic derivatives with anticancer activity.;2 cl, 5 tbl, 6 ex"/> DERIVATIVES OF OLIVOMYCIN 1, ANTIBIOTIC OF AUREOLIC ACID GROUP WITH ANTICANCER ACTIVITY, AND METHOD OF PRODUCTION THEREOF
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DERIVATIVES OF OLIVOMYCIN 1, ANTIBIOTIC OF AUREOLIC ACID GROUP WITH ANTICANCER ACTIVITY, AND METHOD OF PRODUCTION THEREOF

机译:具有抗癌活性的奥古霉素1衍生物,金葡糖酸基团的抗生素及其制备方法

摘要

FIELD: chemistry; pharmacology.;SUBSTANCE: invention refers to derivatives of olivomycin I antibiotic of aureolic acid group with anticancer activity by structural formula as follows, where R5 represents hydrogen, C3-C10-cycloalkyl or C1-C4-alkyl with straight or branched hydrocarbon chain, optionally substituted with one or more hydroxyls. Additionally, invention concerns method of production of the specified derivatives, consisting in selective modification of 2'-carbonyl group of olivomycin 1 by reaction with aminooxyacetic acid, followed by amidation reaction of produced intermediate 2'-(carboxymethoxime)olivomycin 1 and related amines condensing agent added.;EFFECT: method of production of antibiotic derivatives with anticancer activity.;2 cl, 5 tbl, 6 ex
机译:领域:化学;药理学;本发明是指寡霉素I的衍生​​物具有抗癌活性的金黄色酸的结构式如下,其中R 5 代表氢,C 3 -C 10 -环烷基或C 1 -C 4 -烷基,可任选被一个或多个羟基取代。另外,本发明涉及指定衍生物的制备方法,该方法包括通过与氨基氧乙酸反应选择性修饰寡霉素1的2'-羰基,然后使所产生的中间体2'-(羧甲肟基)寡霉素1和相关的胺缩合进行酰胺化反应。效果:具有抗癌活性的抗生素衍生物的生产方法; 2 cl,5 tbl,6 ex

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