CAS: 3321-03-7; (S)-2-(2-Aminoacetamido)-3-Phenylpropanoic Acid

该化合物是一种由氨基酸甘油和苯丙氨酸联结联系在一起的二酸二酸酯,由浸渍物联结组成,化学配方C11H14N2O3代表,分子重量反映其成分,该化合物的特点是能够参与各种生物化学过程,包括蛋白合成和生物活动调节.甘基苯拉尼具有浸泡物的典型特性,如水溶性,以及由于其矿泉和氨酸酸功能组而形成氢联结的潜力.它也可以与受体和酶进行具体互动,使其对药理学和生物化学研究感兴趣.此外,苯丙烯侧链的存在也助长了其水恐惧性特征,影响其在生物系统中的行为.还可能研究甘基苯丙烯九在药物设计和开发中的潜在应用,特别是在基于浸泡物的治疗中.

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合成工艺路线路线简述

    📜Trt-Gly-Phe-Oh置于盐酸体系中,化学反应生成 甘氨酰苯基丙氨酸
    参考文献:N-Tritylamino Acids And Peptides. A New Method Of Peptide Synthesis1
    标题:N-Tritylamino Acids And Peptides. A New Method Of Peptide Synthesis1
    摘要:
    DOI:10.1021/ja01588A027

    海关参考信息

    专利信息


    专利号:US-6451543-B1
    优先权日:1998-08-31
    标题:Lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides
    发明人:KOCHENDOERFER GERD G; HUNTER CHRISTIE L; KENT STEPHEN B H; BOTTI PAOLO
    权利人:GRYPHON SCIENCES
    摘要:The present invention relates to methods and compositions for lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides that are incorporated in a lipid matrix. The invention is exemplified in production of a prefolded membrane polypeptide embedded within a lipid matrix via stepwise chemoselective chemical ligation of unprotected peptide segments, where at least one peptide segment is embedded in a lipid matrix. Any chemoselective reaction chemistry amenable for ligation of unprotected peptide segments can be employed. Suitable lipid matrices include liposomes, micelles, cell membrane patches and optically isotropic cubic lipidic phase matrices. Prefolded synthetic and semi-synthetic membrane polypeptides synthesized according to the methods and compositions of the invention also permit site-specific incorporation of one or more detectable moieties, such as a chromophore, which can be conveniently introduced during synthesis. The methods and compositions of the invention have multiple uses. For example, they can be used to assay ligand binding to membrane polypeptides and domains comprising a receptor, and thus are extremely useful for structure/function studies, drug screening/selection/design, and diagnostics and the like, including high-throughput applications. The methods and compositions of the invention are particularly suited for FRET analyses of previously inaccessible membrane polypeptides.

    专利号:US-2003049619-A1
    优先权日:2001-03-21
    标题 :Methods for the synthesis of polynucleotides and combinatorial libraries of polynucleotides
    发明人:DELAGRAVE SIMON; MARRS BARRY
    摘要:Methods for the synthesis of polynucleotides and derivatives thereof are provided. Methods for the preparation of combinatorial libraries of polynucleotides are also provided. In addition, methods for the preparation and identification of polynucleotides having a predetermined property are provided.

    专利号:US-2003159164-A1
    优先权日:1998-05-29
    标 题:Compositions and methods for the synthesis of fatty acids, their derivatives and downstream products
    发明人:KOPCHICK JOHN JOSEPH; KELDER BRUCE; HUANG YUNG-SHENG; KIRCHNER STEPHEN J; MUKERJI PRADIP
    摘要:The invention generally relates to synthesis of essential fatty acids and their derivatives, long-chain polyunsaturated fatty acids (LC-PUFAs) and eicosanoids in transfected cells and in transgenic animals.

    专利号:US-2003138880-A1
    优先权日:2001-08-24
    标 题:Solid-phase synthesis of oligosaccharides and glycopeptides using glycosynthases
    发明人:WITHERS STEPHEN G; JENSEN KNUD J; PETERSEN LARS; TOLBORG JAKOB L
    权利人:UNIV BRITISH COLUMBIA
    摘要:The present invention provides materials and methods for the solid-phase synthesis of oligosaccharides and glycopeptides. Such materials and methods include mutant glycosidase enzymes, or “glycosynthases,â€? chemically-derivatized acceptor molecules, and specific solid support matrices.

    专利号:WO-9720061-A1
    优先权日:1995-11-30
    标题:Synthesis of hyaluronic acid
    发明人:WONG CHI-HUEY; DELUCA CLAUDIO
    权利人:SCRIPPS RESEARCH INST; WONG CHI HUEY; DELUCA CLAUDIO
    摘要:A preparative enzymatic synthesis of hyaluronic acid (HA) from UDP-N-acetyl-D-glucosamine (UDP-GlcNAc) and UDP-glucuronic acid (UDP-GlcA) catalyzed by hyaluronic acid synthase is coupled with regeneration of the sugar nucleotides. Polymerizing UDP-GlcA and UDP-GlcNAc to form hyaluronic acid results in the formation of released UDP. The released UDP is, in turn, employed in the regeneration of UDP-GlcA and UDP-GlcNAc. Use of the released UDP for regenerating UDP-GlcA and UDP-GlcNAc prevents a build-up of these compounds and prevents or reduces feed back inhibition of the hyaluronic acid synthase reaction that would otherwise be caused by such build-up. Accordingly, the product yield is enhanced by the recycling of these compounds.

    专利号:US-5405949-A
    优先权日:1993-03-29
    标题 :Process for the synthesis of glycosaminoglycans with heparin or heparan structure modified in position 2 of the α-L-iduronic-2-O-sulfate acid
    发明人:UNGARELLI FABRIZIO; PIANI SILVANO
    权利人:ALFA WASSERMANN SPA
    摘要:A process for the synthesis of glycosaminoglycans with heparin or heparan structure modified in position 2 of the α-L-iduronic-2-O-sulfate acid in which the sulfate group is, entirely or in part, substituted with a nucleophilic group, is described. The process is carried out by treating glycosaminoglycans having heparin or heparan structure with a nucleophilic reagent in alkaline solution.

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    📌 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:Benzotriazole-Mediated Synthesis Of Aza-Peptides: En Route To An Aza-Leuenkephalin Analogue
    作者:Nader E. Abo-Dya,Suvendu Biswas,Akash Basak,Ilker Avan,Khalid A. Alamry,Alan R. Katritzky |发布日期:2013.4.19
    摘要:With An Ester Bond 26B, And A Hybrid Azatripeptide With An Ester Bond 28. A New Protocol For The Synthesis Of N-Pg-Azatripeptides 33A,B And 35A,B, Each Containing A Natural Amino Acid At The N-Terminus, Avoids The Low Coupling Rates Of The Aza-Amino Acid Residue And Enables The Solution-Phase Synthesis Of An Azaphenylalanine Analogue Of Leu-Enkephalin 40.

    合成参考文献


    参考文献:10.1073/pnas.1114410109
    摘要:Dallmann R, Viola AU, Tarokh L, Cajochen C, Brown SA. The human circadian metabolome. Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2625–9.
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