CAS: 13139-28-1; (S)-Benzyl (1-Amino-3-Methyl-1-Oxobutan-2-yl)Carbamate

该化合物是氨基酸醋的衍生物,其特点是与氨基氨基氨基酸组附属的Z保护性Z(苯丙氧碳酸基)组,该化合物通常用于浸泡合成和作为制药生产的中间体,Z组在化学反应中保护氨基体功能,允许有选择地修改其他功能组.Z-VAL-NH2是白到白的固态,在水和乙醇等极地溶剂中可溶解,在标准实验室条件下具有稳定性,其结构包括一个支流体侧链,有助于其缺水特性.该化合物在生物化学和药用化学领域,特别是在开发基于丙基酸的药物方面非常重要.安全数据表明,与许多氨基酸衍生物一样,应当谨慎处理,遵循适当的安全议定书,以避免与化学品接触有关的潜在危害.

结构式图片

相似化合物

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合成工艺路线路线简述

    📜L-缬氨酸盐酸盐置于氯甲酸乙酯,Sodium Carbonate,三乙胺体系中,用 四氢呋喃,水 用作溶剂,化学反应 19.0H,反应生成Cbz-L-缬氨酰胺
    参考文献: Peptidomimetic Compounds And Antibody-Drug Conjugates Thereof[fr] Composés Peptidomimétiques Et Conjugués Anticorps-Médicament De Ceux-Ci
    标题: Peptidomimetic Compounds And Antibody-Drug Conjugates Thereof[fr] Composés Peptidomimétiques Et Conjugués Anticorps-Médicament De Ceux-Ci

    海关参考信息

    专利信息


    专利号:US-4028315-A
    优先权日:1970-10-16
    标题:Solid phase synthesis of peptides
    发明人:BODANSZKY MIKLOS; SHEEHAN JOHN TIMOTHY
    权利人:SQUIBB & SONS INC
    摘要:A process for bonding an amino acid to an insoluble hydroxymethyl polymer by esterifying the C-terminal carboxyl group of an N-terminal protected amino acid with the hydroxyl group of an insoluble hydroxymethyl polymer. The esterifying takes place at about room temperature in the presence of a condensing agent. The insoluble hydroxymethyl polymer is a hydroxymethylated copolymer of styrene and divinylbenzene, hydroxymethylcellulose, hydroxymethylated sulfonated polystyrene or polyvinyl alcohol. The condensing agent is dicyclohexylcarbodiimide, carbonyldiimidazole, thionyl chloride, phosphorous oxychloride or ethoxyacetylene. Peptides can be formed by bonding one or more amino acids to the amino acid bonded to the insoluble hydroxymethyl polymer.

    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

    参考标题:Synthesis And Properties Of Aminoacylamido-Amp: Chemical Optimization For The Construction Of An N-Acyl Phosphoramidate Linkage
    作者:Tomohisa Moriguchi,Terukazu Yanagi,Masao Kunimori,Takeshi Wada,Mitsuo Sekine |发布日期:2000.12.1
    摘要:This Paper Describes The Design And Synthesis Of A New Type Of Aminoacyl-Adenylate Analogue (Aa-Ampn) Having An N-Acyl Phosphoramidate Linkage Where The Oxygen Atom Of The Mixed Anhydride Bond Of Aminoacyl-Adenylate (Aa-Amp) Is Replaced By An Amino Group. This New Type Of Aa-Amp Analogue Is Expected To Be Useful As Material For Studies On The Recognition Mechanism Of The Aminoacylation Of Trna And

    合成参考文献


    摘要:Li, W-R., Science of Synthesis, (2005) 21, 219.
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