CAS: 17470-24-5; 2-Amino-3-(Pyridin-3-yl)Propanoic Acid

该化合物是一种含有非蛋白性的非丙基氨基酸,可能用于药用化学和生化研究,其结构具有3-丙基替代成分,具有独特的电子和消毒特性,使其成为合成药用活性化合物的宝贵中间体.该化合物的手艺中心允许进行对应选择性合成,允许研究立体特异相互作用.它与peptide联动反应的兼容性进一步增强了其设计新型peptide类比的实用性.氨基和木箱功能组的存在有利于衍生,提供了化学修改的多功能.由于该化合物与...

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CAS号500-22-1 吡啶-3-甲醛 | CAS号553-53-7 烟酸酰肼 | CAS号5433-39-6 N-(3-pyridinylc... | CAS号170092-30-5 2-乙酰氨基-3-(吡啶-3-基)丙酸 | CAS号41668-18-2 (3Z,6E)-3,6-bis... | CAS号108-24-7 乙酸酐 | CAS号33560-91-7 2-(benzoylamino... | CAS号5086-43-1 2-phenyl-4-(pyr... | CAS号20173-24-4 3-(2-氨基乙基)吡啶

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    专利信息


    专利号:US-10087221-B2
    优先权日:2013-03-21
    标题 :Synthesis of hydantoin containing peptide products
    发明人:HENKEL BERND
    权利人:SANOFI AVENTIS DEUTSCHLAND
    摘要:The present invention relates to a method of synthesizing a peptide product comprising at least one hydantoin group. The peptide product may be used as a reference material for the quality control of pharmaceutical peptides, particularly for the quality control of exendin peptides. Further, the invention relates to hydantoin building blocks, a method for manufacturing such building blocks and their use for the synthesis of peptide products.

    专利号:US-9475837-B2
    优先权日:2011-12-23
    标题 :Process for the synthesis of therapeutic peptides
    发明人:HURLEY FIONN; WEGNER KATARZYNA; FOLEY PATRICK
    权利人:IPSEN MFG IRELAND LTD
    摘要:The present invention relates to a process for the large-scale synthesis of therapeutic peptides using a Sieber Amide resin, which comprises solid-phase Fmoc-chemistry.

    专利号:WO-9931124-A1
    优先权日:1997-12-12
    标 题:Cholic acid-based scaffolds for multidimensional molecular presentation of peptides
    发明人:HOEEG-JENSEN THOMAS
    权利人:NOVO NORDISK AS; HOEEG JENSEN THOMAS
    摘要:A solid phase method for the synthesis of a plurality of differently substituted cholic acid scaffolds with a wide variety of peptide chain, pseudo-peptide chain or peptoid chain substitutents, as leads or compounds of potential therapeutic interest. The substituted cholic acids are prepared by initial solution synthesis of a scaffold holding amino acids with 3 orthogonal protecting groups. Subsequent solid-phase synthesis provides the build-up of the target molecules, either as discretes or in mixture. The molecules may be screened on the resin or cleaved from the resin and then screened in solution. The method disclosed here provides an easy and fast access to highly diverse compounds, potential peptide mimetics and potential leads for compounds of therapeutic interest. The method is amenable to automatization.

    专利号:US-8378099-B2
    优先权日:1994-10-28
    标 题:Boronic ester and acid compounds, synthesis and uses
    发明人:ADAMS JULIAN; MA YU-TING; STEIN ROSS L; BAEVSKY MATTHEW; GRENIER LOUIS; PLAMONDON LOUIS
    权利人:MILLENNIUM PHARMACUETICALS INC; ADAMS JULIAN; STEIN ROSS L; BAEVSKY MATTHEW; GRENIER LOUIS; PLAMONDON LOUIS
    摘要:Disclosed herein is a method for reducing the rate of degradation of proteins in an animal, comprising contacting cells of the animal with certain boronic ester and acid compounds. Also disclosed herein are novel boronic ester and acid compounds, their synthesis and uses.

    专利号:CN-115515937-A
    优先权日:2020-05-08
    标 题:Dimers for the synthesis of peptidomimetics

    专利号:US-2015045534-A1
    优先权日:2011-12-23
    标题:Process for the Synthesis of Therapeutic Peptides

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    合成参考文献


    参考文献:10.1007/s00726-010-0829-3
    摘要:Moussa A, Meffre P, Martinez J, Rolland V. Chemoenzymatic routes to enantiomerically pure 2-azatyrosine and 2-, 3- and 4-pyridylalanine derivatives. Amino Acids. 2012 Apr;42(4):1339–48. doi: 10.1007/s00726-010-0829-3.
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