首页> 外国专利> A process for isolating and purifying vasopeptidase-inhibiting peptides with specificity for the angiotensin-converting enzyme carboxylic site secreted by snake venom glands (bpps), particularly jararaca bothrops, or endogenously produced (evasins) having vasodilatory and anti- hypertensive; process of determining the starch sequence of inhibitor peptides secreted by the snake venom (bpps) or endogenous (evasin) venom; The process of determining the amino acid sequence of bpps by deducting the cdna from precursors of these molecules expressed in snake tissues, specifically bothrops jararaca. process of determining the amino acid sequence of evasins by deducing cdna from precursors of these molecules expressed in snake tissues, specifically bothrops jararaca, process of amplifying cdna from pancreatic and / or snake brain cdna libraries, specifically bothrops jararaca ; solid phase synthesis process of vasopeptidase inhibiting peptides with vasodilating and antihypertensive action, vaso

A process for isolating and purifying vasopeptidase-inhibiting peptides with specificity for the angiotensin-converting enzyme carboxylic site secreted by snake venom glands (bpps), particularly jararaca bothrops, or endogenously produced (evasins) having vasodilatory and anti- hypertensive; process of determining the starch sequence of inhibitor peptides secreted by the snake venom (bpps) or endogenous (evasin) venom; The process of determining the amino acid sequence of bpps by deducting the cdna from precursors of these molecules expressed in snake tissues, specifically bothrops jararaca. process of determining the amino acid sequence of evasins by deducing cdna from precursors of these molecules expressed in snake tissues, specifically bothrops jararaca, process of amplifying cdna from pancreatic and / or snake brain cdna libraries, specifically bothrops jararaca ; solid phase synthesis process of vasopeptidase inhibiting peptides with vasodilating and antihypertensive action, vaso

机译:一种分离和纯化具有对蛇毒腺(bpps),特别是贾拉卡双峰植物分泌的或具有血管扩张和抗高血压作用的内源性(evasins)分泌的血管紧张素转化酶羧基位点具有特异性的血管肽酶抑制肽的方法;确定蛇毒(bpps)或内源性(evasin)毒液分泌的抑制剂肽的淀粉序列的过程;通过从蛇组织中表达的这些分子的前体中减去cdna来确定bpps氨基酸序列的过程,尤其是杂种植物。通过从在蛇组织中表达的这些分子的前体推导cdna来确定evasins氨基酸序列的过程,特别是在蛇和蛇脑cdna文库中扩增cdna的过程,尤其是在蛇和草cdna文库中;血管肽酶抑制肽具有血管舒张和降压作用的固相合成方法

摘要

"PROCESS FOR INSULATING AND PURIFYING VASOPEPTIDASE INHIBITOR PEPTIDES, SPECIFIC TO THE CARBOXYLIC SITE OF ANGIOTENSIN CONVERTERING, BRODUCED BY THE VENOUS-SUGARS VENOSPHERE VENOSPHERE VENOSPHERE POISTS Process of determining the amino acid sequence of the inhibitor peptides secreted by the venom glands (BPPs) or the endogenous sequestration of the sinus sequestering SNAPS, SPECIFICALLY BOTHROPS JARARACA, PROCESS OF DETERMINING THE EVASINS AMINO ACIDS SEQUENCE BY DEDUCING THE CDNA OF THE PRECURSORS OF THESE SNAPS / SPECIFICALLY BOTH OF THE CDOTNATE OF THE SNAPSHOT Brain SNAKES, ESPECIALLY BOTHROPS JARARACA; SOLID PHASE SYNTHESIS PROCESS OF VASODILATING AND ANTIHYPERTENSIVE VASOPYDASE INHIBITORY PEPTIDES, ANTIHYPERTENSIVE VASOPEPDASE INHIBITORS; USE OF VASOPEPTIDASE INHIBITOR PEPTIDES WITH VASODILATING AND ANTIHYPERTENSIVE ACTION TO OBTAIN PHARMACEUTICAL COMPOSITIONS; PROCESS OF DETERMINING INHIBITORY ACTIVITY ON VASOPEPTIDASES AND BIOLOGICAL ACTIVITY ON SMOOTH MUSCLE, CARDIOVASCULAR SYSTEM AND MICROCIRCULATORY ". The present invention relates to the isolation of peptides secreted by the snake-venom peptide Bothropsar venom; as well as the process of producing it by genetic engineering techniques in prokaryotic and eukaryotic systems, the engineered peptide thus obtained, the production of said peptide via chemical synthesis as well as the resulting peptide from such chemical processing. said peptides obtained by different processes in different pharmaceutical compositions and introduced into the body by various routes to act as inhibitors of vasopeptidases and consequently reducing systemic blood pressure and local vasodilating action.
机译:“通过静脉糖,静脉球蛋白,静脉球蛋白肽或肽段的氨基酸序列(通过确定糖基的氨基酸序列)来建立和纯化特定于血管紧张素转换的羧基位的血管肽酶抑制剂肽的过程鼻窦隔离SNAPS的内源性螯合,特别是BOTHROPS JARARACA,通过推论这些SNAPS的前体的CDNA来确定Evasin氨基酸序列的过程/尤其是突触的椎间盘的CD状; USE血管肽酶抑制肽WITH血管舒张和抗高血压作用,以获得药物组合物;血管舒张和抗高血压VASOPYDASE抑制剂活性肽,抗高血压VASOPEPDASE抑制剂的处理确定抑制活性VASOPEPTIDASES和生物活性对平滑肌,心血管SY的干和微循环”。本发明涉及蛇毒肽Bothropsar毒液分泌的肽的分离。以及通过基因工程技术在原核和真核系统中生产它的方法,这样获得的工程化肽,通过化学合成生产所述肽,以及从这种化学加工中得到的肽。所述肽通过不同的方法在不同的药物组合物中获得,并通过各种途径引入体内,以作为血管肽酶的抑制剂,从而降低全身性血压和局部血管舒张作用。

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