CAS: 112883-29-1; Fmoc-D-Tyr-Oh

该化合物是一种受保护的氨酸D-硫酸,通常用于peptide合成,是一种受保护的,D-tyrosine.Fmoc组是一个保护性动物,在合成过程中可以有选择性地取消保护.该组具有苯球氢氧基化合物的特点,有助于其再活性和进一步修改的潜力.Fmoc-D-Tyr-OH在外表上一般白色,在二甲基硫胺和二甲基硫氧化(DMFMF)等有机溶剂中可溶解,但在水中可溶性较少.它的分子结构包括一个氟化环,它提供了苯丙胺净化的稳定性和辅助剂.该化合物由于易于处理和与各种混合试剂兼容性,因此广泛用于固态丙基甲基合成.与许多氨基酸衍生物一样,它对于处理氟化物或氨基甲基硫化合物的适当安全性非常重要.如果能够处理氟化物,则作为安全性协议,则作为安全处理.

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合成工艺路线路线简述

    📜Fmoc-D-Tyr-Otbu置于水体系中,化学反应生成Fmoc-D-酪氨酸
    参考文献:支持的用于连续流化学的催化活性超分子水凝胶.
    标题:支持的用于连续流化学的催化活性超分子水凝胶.
    摘要:受生物学启发,超分子化学的当前目标之一是控制分子自组装产生的新功能的出现.特别地,一些肽可以自组装并产生能够支撑水凝胶的异常催化活性的纤维网络.不幸的是,这些材料的机械脆性与工艺发展是不相容的,这将这一令人兴奋的领域传递给了学术界的好奇心.在这里,我们表明可以通过支持多孔材料壁上的酶促肽自组装来克服这一缺陷.我们应用此策略在开孔聚合物泡沫中生长了酯酶样催化活性超分子水凝胶(cash),填充了整个内部空间.我们支持的cash材料对灭活的酯具有很高的效率,并能实现外消旋物的动力学拆分.这种混合材料足够坚固,可用于连续流反应器,并且可重复使用且在数月内稳定.
    Doi:10.1002/anie.201909424

    海关参考信息

    专利信息


    专利号:US-2024287106-A1
    优先权日:2021-06-09
    标题 :Method for Producing Fluorescent Probe Library Using Solid-Phase Extraction and Method of Measuring Enzyme Activity Using Same
    发明人:KOMATSU TORU; URANO YASUTERU; SAKAMOTO SHINGO; WATANABE RIKIYA; KAGAMI YU
    权利人:UNIV TOKYO; RIKEN
    摘要:To provide a synthesis scheme capable of easily synthesizing various kinds of fluorescent probes. A method for preparing a compound represented by Formula (III) below, the method including steps (1) to (5).

    专利号:US-7147856-B2
    优先权日:1996-08-28
    标题 :Stable radioiodine conjugates and methods of their synthesis
    发明人:GOVINDAN SERENGULAM V
    权利人:IMMUNOMEDICS INC
    摘要:Methods are described for conjugating radioiodinated peptides or carbohydrate structures to proteins with improved yields and qualities of conjugates. In one method, specially designed radioiodinated bifunctional peptides containing nonmetabolizable amide bonds are coupled to antibodies. In a second method, radioiodinated nonmetabolizable bifunctional peptides, which also contain aminopolycarboxylates, are coupled to antibodies. In a third method, radioiodinated bifunctional aminopolycarboxylates are coupled to antibodies. In a fourth method, a hydrazide-appended antibody is coupled to a radioiodinated carbohydrate or a thiolated antibody is coupled to a hydrazide-appended and radioiodinated carbohydrate. In a fifth method a monoderivatized cyanuric chloride is used to conjugate thiolated antibody. Radioiodinated residualizing antibody conjugates made by these methods are particularly stable in vivo and are suitable for radioimmunodetection and radioimmunotherapy.

    专利号:US-8338565-B2
    优先权日:2008-08-20
    标 题 :Macrocyclic compounds for inhibition of tumor necrosis factor alpha
    发明人:LEE JINBO; BOND JULIAN F; TERRETT NICHOLAS; FAVALORO JR FRANK G; WANG DANIEL; BRIGGS TIMOTHY F; SEIGAL BENJAMIN ADAM; SUN WEI-CHUAN; HALE STEPHEN P
    权利人:LEE JINBO; BOND JULIAN F; TERRETT NICHOLAS; FAVALORO JR FRANK G; WANG DANIEL; BRIGGS TIMOTHY F; SEIGAL BENJAMIN ADAM; SUN WEI-CHUAN; HALE STEPHEN P; ENSEMBLE THERAPEUTICS CORP
    摘要:Disclosed herein are macrocyclic compounds and methods for their synthesis and use. In particular, macrocyclic compounds are disclosed that modulate the activity of tumor necrosis factor alpha and/or are useful in the treatment of medical conditions, such as, rheumatoid arthritis, psoriasis, and asthma.

    专利号:US-6663866-B1
    优先权日:1996-08-28
    标题:Stable radioiodine conjugates and methods for their synthesis
    发明人:GOVINDAN SERENGULAM V
    权利人:IMMUNOMEDICS INC
    摘要:Methods are described for conjugating radioiodinated peptides to non-metabolizable carbohydrates with improved yields and qualities of conjugates. Radioiodinated residualizing antibody conjugates comprising a carbohydrate-appended peptide are also provided. The instant radioiodinated residualizing antibody conjugates are particularly stable in vivo and are suitable for radioimmunodetection and radioimmunotherapy.

    专利号:EP-0915710-B1
    优先权日:1996-08-28
    标 题:Stable radioiodine conjugates and methods for their synthesis
    发明人:GOVINDAN SERENGULAM V; GRIFFITHS GARY L
    权利人:IMMUNOMEDICS INC
    摘要:Methods are described for conjugating radioiodinated peptides or carbohydrate structures to proteins with improved yields and qualities of conjugates. In one method, specially designed radioiodinated bifunctional peptides containing nonmetabolizable amide bonds are coupled to antibodies. In a second method, radioiodinated nonmetabolizable bifunctional peptides, which also contain aminopolycarboxylates, are coupled to antibodies. In a third method, radioiodinated bifunctional aminopolycarboxylates are coupled to antibodies. In a fourth method, a hydrazide-appended antibody is coupled to a radioiodinated carbohydrate, or a thiolated antibody is coupled to a hydrazide-appended and radioiodinated carbohydrate. In a fifth method, a monoderivatized cyanuric chloride is used to conjugate thiolated antibody. Radioiodinated residualizing antibody conjugates made by these methods are particularly stable in vivo and are suitable for radioimmunodetection and radioimmunotherapy.

    专利号:US-2004022725-A1
    优先权日:1996-08-28
    标题:Stable radioiodine conjugates and methods of their synthesis

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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

    合成方法参考DOI号:10.1016/j.ijpharm.2011.06.007
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