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LINEAR OR CYCLIC OLIGOPEPTIDES SHOWING AFFINITY TO OPIOID RECEPTORS, PHARMACEUTICAL COMPOSITION, TREATMENT METHOD

机译:显示对阿片样物质受体具有亲和力的线性或环状寡肽,药物组合物,治疗方法

摘要

FIELD: chemistry of peptides. SUBSTANCE: invention relates to new oligopeptides showing affinity to opioid receptors that are linear or cyclic ones at primary amino acid sequence in skeleton Tyr-X-Phe-Leu-Z where: X and Z mean amino acids or their derivatives and/or analogs and where X and Z can be bound by covalent linkage forming heterocyclic structure. In the latter Z is taken from Cys, Glu, Gly or derivatives of Glu and Gln; X is taken from amino acids or their analogs Ser, Glu, Pro, "АМЦК", D-Ala, D- or L-ornithine, D- or L-2,4-diaminobutyric acid, D- or L-Lys and D- or L-Cys. Invention also relates to pharmaceutical preparations containing above mentioned oligopeptides that can be used as analgetics for pain relieve, for depression, stress and shock treatment states. EFFECT: enhanced effectiveness of oligopeptides.
机译:领域:肽化学。本发明涉及新的寡肽,其在骨架Tyr-X-Phe-Leu-Z的一级氨基酸序列上显示对线性或环状阿片样物质受体的亲和力,其中:X和Z表示氨基酸或其衍生物和/或类似物,其中X和Z可以被形成杂环结构的共价键结合。在后者中,Z取自Cys,Glu,Gly或Glu和Gln的衍生物; X取自氨基酸或其类似物Ser,Glu,Pro,“АМЦК”,D-Ala,D-或L-鸟氨酸,D-或L-2,4-二氨基丁酸,D-或L-Lys和D -或L-半胱氨酸。本发明还涉及含有上述寡肽的药物制剂,其可用作止痛,抑郁,压力和休克治疗状态的止痛药。效果:增强寡肽的有效性。

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