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Process for the Preparation of Ziconotide

机译:齐考诺肽的制备方法

摘要

The present invention is a solid phase (solid phase) through the synthesis in place of the conventional ultrasound method for synthesizing a peptide (sonication) and heating treatment, the solid phase synthesis proceeds in a nitrogen gas stream conditions (SPPS method) and a liquid or solid phase synthesis (solution- phase) mixture of synthetic (convergence method), a method of producing a novel not suited Kono (Ziconotide). According to the invention, is the improved separation and purification of lactide Kono after its synthesis are available commercially mass-produced. In addition, the present invention is to improve the yield and purity than the method not suited Kono synthesized by the art to be used in the technical field there are economic benefits in terms of production cost. ;
机译:本发明是通过固相(固相)代替常规的用于合成肽的超声方法(超声处理和加热处理)的固相(固相),固相合成在氮气流条件下进行(SPPS方法)和液体。或固相合成(溶液相)合成的混合物(会聚法),一种生产不适合的新型Kono(Ziconotide)的方法。根据本发明,在工业上可大量获得丙交酯河诺的改进的分离和纯化。另外,本发明要比在技术领域中使用的不适合本领域合成的河野的方法提高产率和纯度,就生产成本而言具有经济上的好处。 ;

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