CAS: 101555-61-7; Boc-D-Beta-Homophenylalanine

该化合物是属于氨基酸类的合成化合物.该物质具有一个手性中心,有助于其立体化学,特别是R配置.该化合物含有苯丁基酸脊椎,该脊椎因二甲基乙氧碳基化合物组的存在而改变,增强了其亲耳性并有可能影响其生物活动.氨基化合物的存在表明,该物质可以参与浸泡物联结的形成,使其与浸泡物合成和药物开发相关.其结构复杂性表明制药业的潜在应用,特别是在针对特定生物路径的化合物设计中.此外,该化合物的溶性和稳定性对于其在各种化学和生物环境中的实际应用非常重要.

结构式图片

相似化合物

138165-77-2 193954-28-8 120378-17-8

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CAS号24424-99-5 二碳酸二叔丁酯 | CAS号131270-08-1 (R)-3-氨基-4-苯基丁酸 | CAS号115313-19-4 (s)-3-b°C-amino... | CAS号186581-53-3 重氮甲烷 | CAS号18942-49-9 N-B°C-D-苯丙氨酸 | CAS号106454-69-7 N-B°C-D-苯丙氨醇

合成工艺路线路线简述

    N-Boc-D-苯丙氨醇置于氢氧化钾体系中,用 吡啶,甲醇,二甲基亚砜 用作溶剂,化学反应 37.0H,反应生成(R)-3-叔丁氧羰基氨基-4-苯基丁酸
    参考文献:Syntheses And Biological Activities Of Bombesin Analogs Modified In The C-Terminal Dipeptide Part
    标题:Syntheses And Biological Activities Of Bombesin Analogs Modified In The C-Terminal Dipeptide Part
    摘要:Bombesin Receptor Antagonists Are Possible Therapeutic Agents Due To Their Ability To Act As Inhibitors Of Cellular Proliferation. On The Basis Of Our Hypothesis On The Mechanism Of Action Of Gastrin Associating An Activating Enzyme System To The Receptor And On The Results Reported In The Litterature,We Have Synthesized Bombesin Analogues Which Have Been Modified In The C-Terminal Leu(13)-Leu(14) Amide Part. We Have Shown That Modification In The C-Terminal Part Of The Bombesin Strongly Affected The Biological Activity In Rat Pancreatic Acini. The Most Potent Compound Which Is Described Here,H-D-Phe-Gln-Trp-Ala-Val-Gly-His-Leu-Psi(Ch2)Leu-Nh2,Was Able To Recognize The Bombesin Receptor On Rat Pancreatic Acini (Ki 4.3 Nm) And Antagonized The Bombesin Stimulated Amylase Secretion (Ki 7.7 Nm).
    Doi:10.1016/s0223-5234(99)80063-4

    海关参考信息

    专利信息


    专利号:US-2003158436-A1
    优先权日:1999-03-10
    标题:Synthesis of alpha--amino-alpha, alpha'- dihaloketones and process for the preparation of beta--amino acid derivatives by the use of the same

    专利号:US-6573399-B1
    优先权日:1999-03-10
    标题:Synthesis of α-amino-α′, α′-dihaloketones and process for the preparation of β-amino acid derivatives by the use of the same
    发明人:NISHIYAMA AKIRA; INOUE KENJI
    权利人:KANEKA CORP
    摘要:The present invention provides a commercially profitable process for producing a β-amino acid ester derivative n which comprises reacting an α-amino acid ester derivative with a base and a dihalomethane, n reacting the same with a lithium amide and an alkyllithium in succession, n and treating the reaction product with an acid in an alcohol.

    专利号:EP-1078919-A1
    优先权日:1999-03-10
    标题 :SYNTHESIS OF $g(a)-AMINO-$g(a)',$g(a)'-DIHALOKETONES AND PROCESS FOR THE PREPARATION OF $g(b)-AMINO ACID DERIVATIVES BY THE USE OF THE SAME

    专利号:EP-1078919-B1
    优先权日:1999-03-10
    标题 :Synthesis of alpha-amino-alpha',alpha'-dihaloketones and process for the preparation of beta)-amino acid derivatives by the use of the same
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    合成参考文献

    合成方法参考DOI号:10.1016/j.cclet.2016.10.005
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