CAS: 131724-45-3; Boc-Phe(4-Cn)-Oh

该化合物是一种氨酸衍生物,其特点是存在一个丙诺组和一个丙氧基碳基(Boc)保护组,该组具有氨酸衍生物,其特点是苯丙氨基脊柱,因其在蛋白合成中的作用和作为...

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合成工艺路线路线简述

    二碳酸二叔丁酯置于三乙胺体系中,化学反应生成Boc-L-4-氰基苯丙氨酸
    参考文献:Peptide Compound And A Process For The Preparation Thereof
    标题:Peptide Compound And A Process For The Preparation Thereof
    摘要:本发明涉及公式(i)的糖蛋白iia/iiib拮抗剂和血小板聚集抑制剂:##str1## 其中r1是苯基,可以有一个或多个适当的取代基;R2是羧基(较低)烷基或保护羧基(较低)烷基;R3是羧基或保护羧基;A1是可以有一个或多个适当的取代基的烷基;A2是下列式的基团:##str2## (其中r是较低的烷基),或下列式的基团:--Nhch2Ch2Co--;A3是可以有一个或多个适当的取代基的较低烷基;L,M和n分别是0或1的整数,但前提是当l为0的整数时,A2不是下列式的基团:--Nhch2Ch2Co--.

    海关参考信息

    专利信息


    专利号:US-4977168-A
    优先权日:1986-01-24
    标 题:Derivatives of the N α-arylsulphonylaminoacyl-p-amidinophenyl-alaninamides, and their use as medicaments
    发明人:BERNAT ANDRE; DELABASSEE DENIS; FREHEL DANIEL; MAFFRAND JEAN-PIERRE; VALLEE ERIC
    权利人:SANOFI SA
    摘要:Nα-substituted derivatives of Nα-arylsulphonylaminoacyl p-amidinophenylalaninamides, their preparation, their use as medicaments and intermediates for their synthesis.

    专利号:US-9795613-B2
    优先权日:2014-12-10
    标题 :GLP-1 receptor modulators
    发明人:BOEHM MARCUS F; MARTINBOROUGH ESTHER; MOORJANI MANISHA; TAMIYA JUNKO; HUANG LIMING; YEAGER ADAM R; BRAHMACHARY ENUGURTHI; FOWLER THOMAS; NOVAK ANDREW; MEGHANI PREMJI; KNAGGS MICHAEL; GLYNN DANIEL; MILLS MARK
    权利人:CELGENE INT II SÀRL
    摘要:Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where “ â€? represents either or both the R and S form of the compound): n nwhere A, B, C, Y 1 , Y 2 , Z, R 1 , R 2 , R 3 , R 4 , R 5 , W 1 , n, p and q are as defined herein.

    专利号:US-9187522-B2
    优先权日:2011-12-12
    标题 :GLP-1 receptor modulators
    发明人:BOEHM MARCUS F; MARTINBOROUGH ESTHER; MOORJANI MANISHA; TAMIYA JUNKO; HUANG LIMING; YEAGER ADAM R; BRAHMACHARY ENUGURTHI; FOWLER THOMAS; NOVAK ANDREW; MEGHANI PREMJI; KNAGGS MICHAEL
    权利人:RECEPTOS INC
    摘要:The invention relates to compounds that modulate the glucagon-like peptide 1 (GLP-1) receptor, methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds are act as modulators or potentiators of GLP-1 receptor on their own, or with receptor ligands including GLP-1 peptides GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where “ â€? represents either or both the R and S form of the compound): n nwhere A, B, C, Y 1 , Y 2 , Z, R 1 , R 2 , R 3 , R 4 , R 5 , W 1 , n, p and q are as defined herein.

    专利号:US-9598430-B2
    优先权日:2013-06-11
    标 题 :GLP-1 receptor modulators
    发明人:BOEHM MARCUS F; MARTINBOROUGH ESTHER; MOORJANI MANISHA; TAMIYA JUNKO; HUANG LIMING; YEAGER ADAM R; BRAHMACHARY ENUGURTHI; FOWLER THOMAS; NOVAK ANDREW; MEGHANI PREMJI; KNAGGS MICHAEL
    权利人:RECEPTOS INC; CELGENE INT II SÀRL
    摘要:Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where “ â€? represents either or both the R and S form of the compound): n nwhere A, B, C, Y 1 , Y 2 , Z, R 1 , R 2 , R 3 , R 4 , R 5 , W 1 , n, p and q are as defined herein.
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    合成参考文献


    参考文献:10.1007/978-1-4939-7574-7_13
    摘要:Blizzard RJ, Gibson TE, Mehl RA. Site-Specific Protein Labeling with Tetrazine Amino Acids. Methods Mol Biol. 2018;1728():201–17. doi: 10.1007/978-1-4939-7574-7_13.
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