CAS: 135944-09-1; Fmoc-D-Hophe-Oh

该化合物是氨基酸同苯丙胺的衍生物,其特点是存在9-氟乙酰碳酸(Fmoc)保护性组,该化合物主要用于peptide合成,特别是二甲基丙酰胺和二甲基硫氧化物等有机溶剂中的溶液,但水中的溶液较少.其分子结构包括一个苯性组,它有助于其水恐特性,使其在设计与特定苯丙胺的相互作用中有用.N-Fmoc-D-homobyaline通常为白色至非白色固体,在二甲基丙胺和二甲基硫磷合成合成物(DMF)和二甲基硫氧化物(DSO)等有机溶剂中是溶液,但水溶解程度较低.其分子结构包括一个有助于其水恐特性的苯性组,使其在设计粉化物时有用.与许多合成氨基苯基苯基化合物的处理程序非常重要.

结构式图片

相似化合物

100564-78-1 1012-05-1 127862-89-9

欧盟法规

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上下游产品

D-homophenylalanine N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

合成工艺路线路线简述

    D-苯基丁氨酸,9-芴甲基-N-琥珀酰亚胺基碳酸酯置于sodium Carbonate体系中,用 1,4-二氧六环,水 用作溶剂,以71.7%的收率获得fmoc-D-高苯丙氨酸
    参考文献:Preptin Analogues: Chemical Synthesis,Secondary Structure And Biological Studies
    标题:Preptin Analogues: Chemical Synthesis,Secondary Structure And Biological Studies
    摘要:Peptide Hormones That Modulate Insulin Secretion Have Been Recognized To Have Therapeutic Potential,With Peptides Such As Amylin (Pramlintide Acetate,Symlin) And Exendin‐4 (Exenatide,Byetta) Now Commercially Available. Preptin Is A Peptide That Has Been Shown To Increase Insulin Secretion In Vitro And In Vivo. Here,We Describe The First Chemical Synthesis And Analysis Of A Short Series Of Preptin Analogues Based On The Rat Preptin Sequence. Phe 21 In The Preptin Sequence Was Substituted With The Non‐protein Amino Acids D‐phe,D‐hphe,3‐aminobenzoic Acid And 1‐aminocyclooctane‐1‐carboxylic Acid,Which Rendered The Preptin Analogues Resistant To Chymotryptic Protease Hydrolysis At This Position. Substitution Of Phe 21 With These Non‐protein Amino Acids Did Not Abrogate The Insulin Secretory Effect Of Preptin,With Analogues Showing A Similar Dose‐dependent Effect On Insulin Secretion From βtc6‐f7 Mouse β‐cells In Both The Presence And Absence Of Glucose As Unmodified Rat Preptin. Further Studies On The Stability Of The Preptin Analogues And Their Effect On Insulin Secretion Are In Progress.
    Doi:10.1111/cbdd.12168

    海关参考信息

    专利信息


    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-2007042401-A1
    优先权日:2003-12-17
    标题 :Methods for synthesis of encoded libraries

    专利号:US-2012245040-A1
    优先权日:2003-12-17
    标题 :Methods for synthesis of encoded libraries

    专利号:US-2009062147-A1
    优先权日:2003-12-17
    标 题:Methods for synthesis of encoded libraries

    专利号:US-7972994-B2
    优先权日:2003-12-17
    标 题 :Methods for synthesis of encoded libraries

    专利号:US-7935658-B2
    优先权日:2003-12-17
    标 题 :Methods for synthesis of encoded libraries
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    主要参考文献

    [参考文献]: Luckose F, Et Al. Effects Of Amino Acid Derivatives On Physical, Mental, And Physiological Activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-850.

    合成参考文献

    合成方法参考DOI号:10.1111/cbdd.12168
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