CAS: 138797-71-4; (2R,3S)-2-((((9H-Fluoren-9-yl)Methoxy)Carbonyl)Amino)-3-(Tert-Butoxy)Butanoic Acid

该化合物是一种受保护的氨基酸,通常用于酸合成,其特点是:一种保护氨基氨基乙酰(Fmoc)组,作为氨基功能的保护组,允许在聚氨酯组装期间有选择性的反应.乙型丁基乙基氨酸组提供消毒障碍,保护对在合成过程中保持氨基硫化合物完整性至关重要的河面链中的氢氧基,该化合物的特点是在标准实验室条件下具有稳定性,适合各种混合反应.该化合物的结构包括一个助推其生物应用特性的手淫中心.Fmoco-O-ter-t-butyl-D-threonine通常用于固相丙基苯基合成,在基本条件下可以轻易去除氟化物组,便利依次添加氨基亚酸.该复合物因其在提高酸溶性,提高预期产品产量方面的能力而受到重视.总体而言,它是医学化学领域和pepide类研究领域的重要建筑块.

结构式图片

欧盟法规

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上下游产品

(O-tert-butyl)-L-threonine 9-fluorenylmethyl N-succinimidyl carbonate N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide O-tert-Butyl-L-threonine Methyl Ester p-Toluenesulfonate

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:US-8569452-B2
    优先权日:2011-02-17
    标题:Preparation of phalloidin and its derivatives
    发明人:LIU BAOSHENG; ZHANG JIANHENG
    权利人:LIU BAOSHENG; ZHANG JIANHENG; AMERICAN PEPTIDE COMPANY INC
    摘要:The present invention relates to novel phalloidin derivatives and their fluorescent dye conjugates. These new compounds may be used in studies of actin dynamics in living systems. The present invention also relates to methods for preparing such compounds. The synthesis routes combine solid-phase and solution phase peptide synthesis, and has great advantage for efficient preparation of a diverse library of the phalloidin derivatives, especially for the synthesis of phalloidin.

    专利号:US-11634741-B2
    优先权日:2013-11-20
    标 题:Synthesis of L-nucleic acids by means of an enzyme
    发明人:PECH ANDREAS; JAROSCH FLORIAN; JAHNZ MICHAEL; KLUSSMANN SVEN; DAVID RALF
    权利人:APTARION BIOTECH AG
    摘要:The present invention is related to a method for adding one or more L-nucleotides to the 3′end of a first L-nucleic acid, wherein the method comprises the step of reacting the one or more L-nucleotides with the first L-nucleic acid in the presence of a protein comprising a mutant enzymatic activity exhibiting moiety, wherein the enzymatic activity is capable of adding one or more L-nucleotides to the 3′ end of the first L-nucleic acid, wherein the mutant enzymatic activity exhibiting moiety comprises an amino acid sequence, wherein the amino acids of the amino acid sequence are D-amino acids, wherein the mutant enzymatic activity exhibiting moiety is a variant of an enzymatic activity exhibiting moiety, wherein the enzymatic activity exhibiting moiety consists of an amino acid sequence according to SEQ ID NO: 15 and wherein the amino acids of the amino acid sequence according to SEQ ID NO: 15 are D-amino acids, wherein the amino acid sequence of the mutant enzymatic activity exhibiting moiety differs from the amino acid sequence of the enzymatic activity exhibiting moiety consisting of an amino acid sequence according to SEQ ID NO: 15 at least at one amino acid position, preferably at three amino acid positions, and/or wherein the amino acid sequence of the mutant enzymatic activity exhibiting moiety is a truncated form of an amino acid sequence according to SEQ ID NO: 15, and wherein the amino acid sequence of the mutant enzymatic activity exhibiting moiety is different from an amino acid sequence according to any of SEQ ID NOs 15 to 22 and 51.

    专利号:US-2018208910-A1
    优先权日:2012-05-16
    标 题 :Enzymatic Synthesis of L-Nucleic Acids

    专利号:EP-3071702-B1
    优先权日:2013-11-20
    标题 :Synthesis of l-nucleic acids by means of an enzyme

    专利号:US-2016304926-A1
    优先权日:2013-11-20
    标题:Synthesis of L-Nucleic Acids by Means of an Enzyme

    专利号:EP-2850192-B1
    优先权日:2012-05-16
    标 题 :Enzymatic synthesis of l-nucleic acids
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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1038/s41551-025-01404-w
    摘要:Chen G, Zhao K, Li M, Zhang Y, Li T, Yuan J, Lu L, Valdiviezo J, Liu D, Polizzi NF, DeGrado WF, Dang B. Rapid clearance of achiral small-molecule drugs using de novo-designed proteins and their cyclic and mirror-image variants. Nat Biomed Eng. 2025 Oct;9(10):1775–87. doi: 10.1038/s41551-025-01404-w.
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