CAS: 3705-26-8; Cyclo(-Phe-Pro)

该化合物是一种由氨酸苯丙氨酸苯丙氨和proline组成的循环二酸二酸酯,该化合物具有一种与线性酸相比增强稳定性的循环结构,该化合物的残留物的存在会助长其疏水特性,而其分泌残留物由于其循环结构而具有独特的僵硬性,它会影响peptide的顺质. Cyclo(L-Phe-L-Pro)因其潜在的生物活动而闻名,包括抗微生物和抗氧化性特性,使其对制药和生物化学研究感兴趣.其循环性质还可能影响其与生物受体和酶的相互作用,从而可能导致独特的药理学影响.此外,化合物的溶解性和稳定性可因pH和溶剂条件而不同,而这种条件对于其在药物配制和运载系统中的应用至关重要.

结构式图片

MSDS等安全信息

上下游产品

Z-DL-Phe-OH acetone 1-(3,4,5-tris(°Ctadecyloxy)benzyl)-2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine (1S)-methyl 2-[(S)-2-amino-3-phenylpropanoyl]cyclopentanecarboxylateN-L-prolyl-L-phenylalanineN-L-prolyl-L-phenylalanine [(S)-1-((3S,8aS)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazine-2-carbonyl)-2-methyl-propyl]-carbamic acid benzyl ester -Phe-Pro-LactamN--Phe-Pro-Lactam N-(d-Lysergyl-L-valyl)-L-phenylalanyl-L-prolin-lactam

合成工艺路线路线简述

    📜Boc-L-脯氨酸置于溶剂黄146 N-甲基吗啉,盐酸,1-羟基苯并三唑,N,N'-二环己基碳二亚胺体系中,化学反应 3.5H,反应生成环(Phe-Pro)
    参考文献:Acetic Acid-Catalyzed Diketopiperazine Synthesis.
    标题:Acetic Acid-Catalyzed Diketopiperazine Synthesis.
    摘要:当二肽酯在含有0.1 M醋酸的2-丁醇中回流3小时时,得到了光学纯的二酮哌嗪,产率非常好.当使用脯氨酰氨基酸酯作为起始材料时,1至2 M醋酸是最有效的浓度.
    Doi:10.1248/cpb.29.233

    海关参考信息

    专利信息


    专利号:DE-1795023-C2
    优先权日:1967-08-02
    标 题 :Process for the production of 2-benzyloxy-2-isopropylmalonic acid diethyl ester and its use for the production of heterocycles for the total synthesis of reptide alkaloids of ergot

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    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

    参考标题:Efficient Synthesis Of 2,5-Diketopiperazines Using Microwave Assisted Heating
    作者:Marcus Tullberg,Morten Grøtli,Kristina Luthman |发布日期:2006.7
    摘要:In This Study A General, Efficient And Environmentally Benign Solution Phase Synthesis Of 2,5-Diketopiperazines (Dkps) Using Microwave Assisted Heating In Water Is Described. A Series Of 11 Structurally Different Dkps Have Been Synthesized From Dipeptide Methyl Esters. A Range Of Common Laboratory Solvents Have Been Tested As Well As Different Reaction Times And Temperatures. Both Classic Thermal And

    合成参考文献


    参考文献:10.1021/np960095b
    摘要:Jayatilake GS, Thornton MP, Leonard AC, Grimwade JE, Baker BJ. Metabolites from an Antarctic sponge-associated bacterium, Pseudomonas aeruginosa. J Nat Prod. 1996 Mar;59(3):293–6. doi: 10.1021/np960095b.
    参考文献:10.1016/j.bmcl.2011.05.002
    摘要:Xu Z, Zhang Y, Fu H, Zhong H, Hong K, Zhu W. Antifungal quinazolinones from marine-derived Bacillus cereus and their preparation. Bioorganic & Medicinal Chemistry Letters. 2011 Jul;21(13):4005–7. doi: 10.1016/j.bmcl.2011.05.002.
    参考文献:10.1021/np50106a005
    摘要:Barrow CJ, Sun HH. Spiroquinazoline, a novel substance P inhibitor with a new carbon skeleton, isolated from Aspergillus flavipes. J Nat Prod. 1994 Apr;57(4):471–6. doi: 10.1021/np50106a005.
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