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Novel macrolidic antibiotics having antibiotic activity, process and microorganism for their preparation, and related pharmaceutical compositions

机译:具有抗生素活性,其制备方法和微生物的新型大分子抗生素以及相关药物组合物

摘要

The fermentation of a substrate selected among erythronolide B, erythronolide A and erythronolide A oxime with a novel mutant, Streptomyces antibioticus ATCC 31771, obtained from an industrial stock for the production of oleandomycin, said novel mutant being incapable of producing the same oleandomycin, permits novel macrolide antibiotics to be produced, having not only an activity range like that of erythromycin, but characterized by a greater stability in acidic environment, whereby for the administration of the antibiotic it is no longer necessary to have recourse to esters and/or salts highly toxic for the organism.
机译:用从生产油橄榄霉素的工业原料获得的新型突变体链霉菌ATCC 31771对赤藓醇内酯B,赤藓醇内酯A和赤藓醇内酯肟的底物进行发酵,所述新颖突变体不能产生相同的橄榄桃素,从而允许产生新的突变体。待生产的大环内酯类抗生素,不仅具有类似于红霉素的活性范围,而且在酸性环境中具有更大的稳定性,从而不再需要使用具有高毒性的酯类和/或盐类来进行抗生素的给药对于有机体。

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