首页> 外国专利> DERIVATIVE OF INSULIN OR ITS PHYSIOLOGICALLY ACCEPTABLE SALT, PRECURSOR OF INSULIN DERIVATIVE, DNA SEQUENCE ENCODING PRECURSOR, EXPRESSION VECTOR COMPRISING MENTIONED DNA SEQUENCE, SUBSTRATE TRANSFORMED WITH MENTIONED EXPRESSION VECTOR, PHARMACEUTICAL COMPOSITION WITH REDUCING AND REGULATING BLOOD GLUCOSE LEVEL EFFECTIVENESS, RESPECTIVELY

DERIVATIVE OF INSULIN OR ITS PHYSIOLOGICALLY ACCEPTABLE SALT, PRECURSOR OF INSULIN DERIVATIVE, DNA SEQUENCE ENCODING PRECURSOR, EXPRESSION VECTOR COMPRISING MENTIONED DNA SEQUENCE, SUBSTRATE TRANSFORMED WITH MENTIONED EXPRESSION VECTOR, PHARMACEUTICAL COMPOSITION WITH REDUCING AND REGULATING BLOOD GLUCOSE LEVEL EFFECTIVENESS, RESPECTIVELY

机译:胰岛素或其生理上可接受的盐的衍生物,胰岛素衍生物的前体,编码前体的DNA序列,包括被提及的DNA序列的表达载体,经修饰的表达载体,呈球形的,呈针状的,呈针状的,呈针状的,呈针状的,呈针状的,呈晶体状的

摘要

FIELD: medicine, endocrinology, molecular biology, genetic engineering, medicinal industry. SUBSTANCE: invention relates to derivative of insulin or its physiologically acceptable salt with accelerated onset effect as compared with human insulin. In this insulin derivative asparagines (Asn) in position B3 of chain B is replaced for natural basic amino acid residue, and at least one amino acid residue in positions B27, B28 or B29 of chain B is replaced for another natural neutral or acid amino acid residue being asparagines (Asn) in position A21 of chain A can be replaced for Asp, Gly, Ser, Thr or Ala and phenylalanine (Phe) in position B1 of chain B and amino acid residue in position B30 of chain B can absent. Invention describes also DNA sequences encoding precursor of insulin derivative, expression vector comprising this DNA and also strains expressing insulin precursor and pharmaceutical composition with reducing and regulating blood glucose level effectiveness, respectively. The advantage of invention involves the development of preparation with accelerated onset of effect. EFFECT: valuable properties of composition. 23 cl, 6 tbl, 1 dwg, 8 ex
机译:领域:医学,内分泌学,分子生物学,基因工程,医药工业。物质:本发明涉及与人胰岛素相比具有加速的起效作用的胰岛素或其生理上可接受的盐的衍生物。在该胰岛素衍生物中,链B的B3位的天冬酰胺(Asn)被天然碱性氨基酸残基取代,链B的B27,B28或B29位的至少一个氨基酸残基被另一种天然中性或酸性氨基酸取代。可以用链A的A21位上的天冬酰胺(Asn)残基代替Asp,Gly,Ser,Thr或Ala,并用B链B1上的苯丙氨酸(Phe)取代,并且可以不存在B链B30上的氨基酸残基。本发明还描述了编码胰岛素衍生物前体的DNA序列,包含该DNA的表达载体以及表达胰岛素前体的菌株和分别具有降低和调节血糖水平有效性的药物组合物。本发明的优点涉及开发具有加速作用的制剂。效果:组合物的宝贵特性。 23 cl,6 tbl,1 dwg,8 ex

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