CAS: 52031-05-7; Ethyl 2-Amino-3-(4-Chlorophenyl)Propanoate Hydrochloride

该化合物是一种化学化合物,其结构特征包括一个由叶牌位置上的氯替代物和乙酯功能组组成的苯麻拉尼脊柱,该化合物通常作为盐酸盐遇到,它能提高水溶性,使其在各种应用中更加稳定.它经常用于生物化学研究和药物配方,因为它在合成peptides和其他生物活性分子方面可能起到的作用.该氯化合物的存在可以影响该化合物的再活性和生物活动,使其对药用化学感兴趣.它与许多氨基酸衍生物一样,它可能具有诸如蛋白质的建筑块和影响...

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CAS号64-17-5 乙醇 | CAS号23633-07-0 2-amino-3-(4-ch... | CAS号6941-36-2 Propanedioic ac... | CAS号69555-14-2 二苯亚甲基甘氨酸乙酯 | CAS号104-83-6 4-氯氯苄 | CAS号7424-00-2 DL-4-氯苯基丙氨酸 | CAS号104-88-1 对氯苯甲醛 | CAS号84713-70-2 (4-chlorobenzyl... | CAS号622-95-7 4-氯溴苄 | CAS号7424-00-2 DL-4-氯苯基丙氨酸 | CAS号14173-39-8 4-氯-L-苯基丙氨酸 | CAS号166449-97-4 (R)-B-(P-CHLORO...

合成工艺路线路线简述

    📜2-Acetylamino-2-(4-Chlorobenzyl)Malonic Acid Diethyl Ester置于盐酸体系中,用 1,4-二氧六环,水 作为反应溶剂,化学反应生成 Dl-4-氯苯丙氨酸乙酯盐酸盐
    参考文献:Anthranilic Acid Based Cck1 Receptor Antagonists: Preliminary Investigation On Their Second "touch Point"
    标题:Anthranilic Acid Based Cck1 Receptor Antagonists: Preliminary Investigation On Their Second "touch Point"
    摘要:In This Phase Of Structure-Affinity Relationship Study Of Vl-0395,A New Anthranilic Acid Based Cck1 Selective Antagonist,We Propose A Series Of Unnatural Aminoacidic Derivatives. The Result Of This Work Is The Identification Of A New Cck Ligand,Which Possesses An Affinity (Ic50 = 35 Nm) One Order Of Magnitude Greater Than The Lead And,As A General Rule,It Points Out How The Hypothesized Receptorial Pocket Which Accommodates The Phe Residue Allows Much More Structural Modification Than That Interacting With The N-Terminal Group. Hence,The Modification Of The C-Terminal Pharmacophoric Group Of Our Lead Vl-0395 Can Not Only Enhance The Affinity Of Anthranific Acid Derivatives But Can Modulate The Selectivity For One Cck Receptor Subtype Or Afford Mixed Antagonists. (C) 2005 Elsevier Sas. All Rights Reserved.
    DOI:10.1016/j.Ejmech.2005.01.002

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    专利信息


    专利号:US-5552421-A
    优先权日:1991-09-24
    标 题:Leukotriene biosynthesis inhibitors
    发明人:LAZER EDWARD S; ADAMS JULIAN; MIAO CLARA K; FARINA PETER
    权利人:BOEHRINGER INGELHEIM PHARMA
    摘要:Various substituted benzoxazoles and benzothiazoles, are described and disclosed, which are potent inhibitors of leukotriene synthesis in warm-blooded animals.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Joel Putnam, Et Al. A Test To Determine The Nature And Presence Of The Memory Effect Columns Packed With The Amylose Tris(3,5-Dimethylphenylcarbamate) Stationary Phase. J Chromatogr A. 2011 Sep 16;1218(37):6302-7.
    [参考文献]: Rebeca Santos Marques De Carvalho, Et Al. Involvement Of Gabaergic Non-Benzodiazepine Sites In The Anxiolytic-Like And Sedative Effects Of The Flavonoid Baicalein In Mice. Behav Brain Res. 2011 Aug 1;221(1):75-82.

    合成参考文献


    参考文献:10.1007/s00213-013-3024-x
    摘要:Gigliucci V, O'Dowd G, Casey S, Egan D, Gibney S, Harkin A. Ketamine elicits sustained antidepressant-like activity via a serotonin-dependent mechanism. Psychopharmacology (Berl). 2013 Jul;228(1):157–66. doi: 10.1007/s00213-013-3024-x.
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