CAS: 14997-58-1; N-Cbz-L-Histidine

该化合物是氨酸丁丁的衍生物,以其在蛋白合成和各种代谢过程中的作用著称.该化合物的特性是附属于其丁侧链氮的苯甲基苯丙基碳基化合物组,与未经改良的丁丁基胺相比,这增强了其稳定性和可溶性.苯氧基化合物的存在有助于其疏水特性,有可能影响其在生物系统中的互动.该化合物可能展示具体的生物活动,使其对制药和生物化学研究感兴趣.其结构允许药物设计的潜在应用,特别是在开发基于丙胺的治疗方法方面.此外,该化合物的特性,如溶性,稳定性和再活性,可能受到诸如pH和温度等因素的影响,这些因素对于其在各种化学和生物环境中的应用至关重要.

结构式图片

相似化合物

109425-51-6 123333-71-1 135610-90-1

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CAS号501-53-1 氯甲酸苄酯 | CAS号71-00-1 L-组氨酸 | CAS号13795-24-9 苄基硝苯基碳酸酯 | CAS号35016-67-2 N,1-Bis[(benzyl... | CAS号59577-41-2 1H-benzo[d][1,2... | CAS号15545-10-5 Z-L-组氨酸甲酯 | CAS号5934-29-2 L-组氨酸盐酸盐,一水 | CAS号645-35-2 L-组氨酸盐酸盐 | CAS号74058-68-7 2-硫酮-3-噻唑烷羧酸苄酯 | CAS号32926-43-5 N-B°C-N'-三苯甲基-L-组氨酸 | CAS号23640-03-1 4-(1H-imidazol-... | CAS号71-00-1 L-组氨酸 | CAS号15545-10-5 Z-L-组氨酸甲酯 | CAS号32675-94-8 2-phenylmethoxy... | CAS号62715-28-0 H-His(Trt)-OMe.HCl

合成工艺路线路线简述

    📜L-组氨酸置于氢氧化钾,Sodium Hydroxide,乙醇,水体系中,化学反应生成N-Cbz-L-组氨酸
    参考文献:Patchornik Et Al.,Journal Of The American Chemical Society,1957,Vol. 79,P. 6416,6420
    标题:Patchornik Et Al.,Journal Of The American Chemical Society,1957,Vol. 79,P. 6416,6420

    海关参考信息

    专利信息


    专利号:US-2019177392-A1
    优先权日:2014-09-23
    标 题 :Synthesis of glp-1 peptides
    发明人:PENIAS NAVON SHARON; NAVEH SHIRLY; VASILEIOU ZOI; BARLOS KONSTANTINOS
    权利人:NOVETIDE LTD
    摘要:Disclosed are processes for the synthesis of GLP-1 peptides, such as liraglutide and semaglutide, and a process for purifying liraglutide.

    专利号:US-7435791-B2
    优先权日:2001-07-19
    标题:Process for rapid solution synthesis of peptides
    发明人:EGGEN IVO FRANCI; TEN KORTENAAR PAULUS BERNARDUS; HAASNOOT CORNELIS ALBERT GRUSON
    权利人:ORGANON NV
    摘要:The present invention relates to a process for rapid solution synthesis of a peptide, the process comprising repetitive cycles of steps (a)-(d):n (a) a coupling step, using an excess of an activated carboxylic component to acylate an amino component, (b) a quenching step in which a scavenger is used to remove residual activated carboxylic functions, wherein the scavenger may also be used for deprotection of the growing peptide, (c) one or more aqueous extractions and optionally, (d) a separate deprotection step, followed by one or more aqueous extractions, characterised in that the process comprises at least one step (b), referred to as step (b′), in which an amine or a thiol comprising a free anion or a latent anion is used as a scavenger of residual activated carboxylic functions. nn During the process of this invention the growing peptide need not be isolated until the final peptide sequence has been obtained. n This highly efficient process is useful for the production of oligo- and polypeptides of high purity.

    专利号:US-3953416-A
    优先权日:1971-12-20
    标 题:Synthetic decapeptide having the activity of the luteinizing hormone releasing hormone and method for manufacturing the same
    发明人:FOLKERS KARL; CURRIE BRUCE L; CHANG JAW-KANG; SIEVERTSSON HANS; BOGENTOFT CONNY
    权利人:FOLKERS KARL; CURRIE BRUCE L; CHANG JAW KANG; SIEVERTSSON HANS; BOGENTOFT CONNY
    摘要:A synthetic decapeptide, L-pglutamyl-L-histidyl-L-tryptophanyl-L-seryl-L-tyrosyl-glycyl-L-leucy l-L-arginyl-L-prolyl-glycinamide which has the hormonal activities of the luteinizing hormone releasing hormone (LRH) of the hypothalamus gland of mammals is produced by utilizing as the key starting materials, the amino acids, glutamic acid or pyroglutamic acid, histidine, tryptophan, serine, tyrosine, glycine, leucine, arginine, and proline. Synthesis of the decapeptide is accomplished by coupling, in appropriate combinations of appropriate protected forms of the amino acids, and finally deprotecting to yield the amide, L-pglutamyl-L-histidyl-L-tryptophanyl-L-seryl-L-tyrosyl-glycyl-L-leucy l-L-arginyl-L-prolyl-glycinamide.

    专利号:BR-PI0202783-B1
    优先权日:2001-07-19
    标 题:process for the rapid synthesis of a peptide in solution in an organic solvent or a mixture of organic solvents, and methods for the combinatorial synthesis of peptide collections and for automated solution peptide synthesis

    专利号:PL-205559-B1
    优先权日:2001-07-19
    标 题 :Method of peptide synthesis in solution, method of combinatorial synthesis of a peptide library and method of automated peptide synthesis in solution

    专利号:US-6416861-B1
    优先权日:1999-02-16
    标题 :Organosilicon compounds and uses thereof
    发明人:LEE YOUNGHEE; SILVERMAN RICHARD B
    权利人:UNIV NORTHWESTERN
    摘要:A compound of the formula: n and a resin-bound compound of the formula: n and their use in combinatorial chemistry and in the synthesis of compounds comprising at least one aromatic moiety is described, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , L 1 , P, Ar 1 , and X are as herein defined.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Luckose F, Et Al. Effects Of Amino Acid Derivatives On Physical, Mental, And Physiological Activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

    合成参考文献


    参考文献:10.3109/10715760903456092
    摘要:Zheng J, Bizzozero OA. Traditional reactive carbonyl scavengers do not prevent the carbonylation of brain proteins induced by acute glutathione depletion. Free Radical Research. 2009 Dec 14;44(3):258–66. doi: 10.3109/10715760903456092.
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