首页> 外国专利> A method for obtaining klavulinsäure and their pharmaceutically acceptable salts of fermentation cultures of streptomyces sp.

A method for obtaining klavulinsäure and their pharmaceutically acceptable salts of fermentation cultures of streptomyces sp.

机译:一种获得链霉菌的发酵培养物中的克拉维林素及其药学上可接受的盐的方法。

摘要

A NEW METHOD FOR OBTAINING ACID Z (2R, 5R) -3- (2-hydroxyethylidene) -7-oxo-4-OXA-1-azabicyclo (3,2,0) -heptane-2-carboxylic acid and salts and pharmaceutically acceptable esters thereof, from fermentation broths of Streptomyces SP. Comprising: (A) flocculation hotbed using as an electrolyte coagulant INORGANIC WITH ORGANIC AS polyelectrolyte flocculating aid; (B) Purification of said acid in the culture broth, flocculated and decanting ONCE, FOR FORMATION AS STABLE INTERMEDIATE PRODUCTS, salts derived from primary amines, secondary and tertiary; (C) forming pharmaceutically acceptable salts ACTIVE. Said novel process has EARNINGS PER YOUR FACE Inhibitory Activity lactamases SYNERGISTIC EFFECT AND MARKING WHEN associated with other lactam antibiotics TYPE penicillins and cephalosporins.
机译:获得酸Z(2R,5R)-3-(2-羟乙叉基)-7-氧代-4-OXA-1-氮杂双环(3,2,0)-庚烷-2-羧酸及其盐和药物的新方法其可接受的酯,来自链霉菌属SP的发酵肉汤。包括:(A)絮凝床,使用INORGANIC和ORGANIC AS聚电解质絮凝助剂作为电解质凝结剂; (B)纯化培养液中的所述酸,将其絮凝并倾析一次,以形成稳定的中间产物,衍生自仲和叔伯胺的盐; (C)形成活性的药学上可接受的盐。所述新方法具有与其他青霉素类和头孢菌素类其他内酰胺抗生素有关的内酰胺酶协同作用和标记。

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