CAS: 101555-62-8; Fmoc-D-Pro-Oh

该化合物是氨酸分泌物的一种衍生物,其特点是存在9-氟烯辛基碳氢化合物(Fmoc)保护组,该化合物通常用于peptide合成,特别是固相peptide合成(SPPS),因为它能够保护氨基组,同时允许其他氨基酸有选择地混合.Fmoc-D-proline保留了独特的proline环流结构,这种结构有助于其符合性僵硬性并影响peptides的二级结构.Fmoc组在基本条件下很容易被清除,有利于peptide合成的随后步骤.Fmoc-D-proline通常是白色到白色的固体,在二甲基芳基胺和二甲基硫氧化物等有机溶液中可溶解,但在水中可溶解性较小.其在研究和制药应用中的用途很重要,特别是在开发基于peptide的药物和研究折质功能方面.

结构式图片

相似化合物

71989-31-6 1148-11-4 147-85-3

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    专利号:US-2017320908-A1
    优先权日:2014-11-19
    标题 :Solid phase synthesis of cyclic amino acid molecules
    发明人:HICKEY JENNIFER L; MANCUSO JOHN; MARSAULT ERIC; ROUGHTON ANDREW L; TREDER ADAM P; TREMBLEY MARIE-CLAUDE J; YUDIN ANDREI K; ZARETSKY SERGE
    权利人:ENCYCLE THERAPEUTICS; GOVERNING COUNCIL OF THE UNIV OF TORONTO; UNIV SHERBROOKE
    摘要:The present invention relates to cyclic amino acid molecules and methods of preparing the same, and in particular the macrocyclization of amino acids or linear peptides bound to a solid support.

    专利号:US-2023220001-A1
    优先权日:2020-06-09
    标 题:Method for synthesis of thioether-containing peptides
    发明人:GRUSS HENDRIK; LUTZ CHRISTIAN; SÜSSMUTH RODERICH; Yao guiyang; KNITTEL CAROLINE; KOSOL SIMONE; MAINZ ANDI
    权利人:HEIDELBERG PHARMA RES GMBH
    摘要:The present invention relates to a method of formation of a sulphur bridge between tryptophan and cysteine in solid phase peptide synthesis under iodine treatment. The invention also relates to the resulting compounds of the method and their respective use.

    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-8410028-B2
    优先权日:2003-12-17
    标 题:Methods for synthesis of encoded libraries
    发明人:MORGAN BARRY; HALE STEPHEN; ARICO-MUENDEL CHRISTOPHER C; CLARK MATTHEW; WAGNER RICHARD; ISRAEL DAVID I; GEFTER MALCOLM L; BENJAMIN DENNIS; HANSEN NILS JAKOB VEST; KAVARANA MALCOLM J; CREASER STEFFAN PHILLIP; FRANKLIN GEORGE J; CENTRELLA PAOLO A; ACHARYA RAKSHA A
    权利人:MORGAN BARRY; HALE STEPHEN; ARICO-MUENDEL CHRISTOPHER C; CLARK MATTHEW; WAGNER RICHARD; ISRAEL DAVID I; GEFTER MALCOLM L; BENJAMIN DENNIS; HANSEN NILS JAKOB VEST; KAVARANA MALCOLM J; CREASER STEFFAN PHILLIP; FRANKLIN GEORGE J; CENTRELLA PAOLO A; ACHARYA RAKSHA A; GLAXOSMITHKLINE LLC
    摘要:The present invention provides a method of synthesizing libraries of molecules which include an encoding oligonucleotide tag.

    专利号:US-6281245-B1
    优先权日:1996-10-28
    标 题:Methods for solid-phase synthesis of hydroxylamine compounds and derivatives, and combinatorial libraries thereof
    发明人:PATEL DINESH V; NGU KHEHYONG
    权利人:VERSICOR INC
    摘要:A novel method for generating hydroxylamine, hydroxamic acid, hydroxyurea, and hydroxylsulfonamide compounds is disclosed. The method involves the nucleophilic attack of an alkoxyamine on a suitable solid phase support. Techniques of combinatorial chemistry can then be applied to the immobilized alkoxyamine to generate a diverse set of compounds. Cleavage of the compounds from the support yields a library of hydroxylamine or hydroxylamine derivative compounds, which can be screened for biological activity (e.g., inhibition of metalloproteinases).

    专利号:US-6541276-B2
    优先权日:1996-10-28
    标题:Methods for solid-phase synthesis of hydroxylamine compounds and derivatives and combinatorial libraries thereof
    发明人:PATEL DINESH V; NGU KHEHYONG
    权利人:VERSICOR INC
    摘要:A novel method for generating hydroxylamine, hydroxamic acid, hydroxyurea, and hydroxylsulfonamide compounds is disclosed. The method involves the nucleophilic attack of an alkoxyamine on a suitable solid phase support. Techniques of combinatorial chemistry can then be applied to the immobilized alkoxyamine to generate a diverse set of compounds. Cleavage of the compounds from the support yields a library of hydroxylamine or hydroxylamine derivative compounds, which can be screened for biological activity (e.g., inhibition of metalloproteases).
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    主要参考文献

    参考标题:Synthesis Of Combretastatin A-4 And 3′-Aminocombretastatin A-4 Derivatives With Aminoacid Containing Pendants And Study Of Their Interaction With Tubulin And As Downregulators Of The Vegf, Htert And C-Myc Gene Expression
    作者:Raül Agut,Eva Falomir,Juan Murga,Celia Martín-Beltrán,Raquel Gil-Edo,Alberto Pla,Miguel Carda,J. Alberto Marco
    摘要:Natural Product Combretastatin A-4 (Ca-4) And Its Nitrogenated Analogue 3′-Aminocombretastatin A-4 (Amca-4) Have Shown Promising Antitumor Activities. In This Study, A Range Of Ca-4 And Amca-4 Derivatives Containing Amino Acid Pendants Have Been Synthesized In Order To Compare Their Biological Actions With Those Of Their Parent Compounds. Thus, Inhibition Of Cell Proliferation On Tumor Cell Lines Ht-29

    合成参考文献


    参考文献:10.1007/978-3-031-04544-8_2
    摘要:Gauthier T, Liu D. Peptide Synthesis: Methods and Protocols. 2022. In: AAPS Advances in the Pharmaceutical Sciences Series.
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