首页> 外国专利> METHOD FOR THE SYNTHESIS OF SEMI-SYNTHETIC ANTIBIOTICS IN THERMODYNAMICALLY CONTROLLED WATER-COSOLVENT ORGANIC MISCIBLE APOLAR SYSTEMS BY USING PENICILLIN G ACYLASE

METHOD FOR THE SYNTHESIS OF SEMI-SYNTHETIC ANTIBIOTICS IN THERMODYNAMICALLY CONTROLLED WATER-COSOLVENT ORGANIC MISCIBLE APOLAR SYSTEMS BY USING PENICILLIN G ACYLASE

机译:青霉素G酰基转移酶在热力学控制的水溶性有机可溶极性体系中合成半合成抗生素的方法

摘要

Synthesis of semi-synthetic monobactamic or β-lactamic antibiotics by using derivatives stabilized by various methods of penicillin G acylase from various microbial sources according to a thermodynamically controlled strategy in monophase water/cosolvent organic apolar systems, wherein the concentration of the cosolvent varies between 30 % and 90 %, the temperature between -10 °C and 50 ° C, the pH between 4.5 and 8.5, with concentrations of the antibiotic nucleus between 0.5 and 875 mM and acyl donor between 0.2 mM and 1 M, with a relationship antibiotic ring/activated or free acyl donor, using a buffer between 0 and 1 M. Application to the pharmaceutical industry.
机译:在热相控制的单相水/共溶剂有机非极性体系中,根据热力学控制策略,使用各种青霉素G酰基转移酶从各种微生物来源稳定化的衍生物,合成半合成单细菌或β-乳酸抗生素。 %和90%,温度在-10°C和50°C之间,pH在4.5和8.5之间,抗生素核浓度在0.5和875 mM之间,酰基供体在0.2 mM和1 M之间,与抗生素环有关活化或游离的酰基供体,使用0到1 M之间的缓冲液。应用于制药工业。

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