CAS: 885101-89-3; 3-(4-((3-Phenoxybenzyl)Amino)Phenyl)Propanoic Acid

该化合物是一种有机化合物,其结构复杂,包括一种与一个苯基组相连的丙胺酸细胞,该苯基组又被一个苯氧基苯基氨基组所取代.该化合物通常具有芳香和脂质系统特性,有助于其潜在的生物活动.由于其芳香成分,它有可能溶于有机溶剂中.而箱式酸组可能具有某种极分,允许极地溶解剂中出现溶解性.多种功能组的存在表明,它可能参与各种化学相互作用,使其对医药化学和药物设计感兴趣.此外,其结构特征可能会影响其药用植物基因特性,例如吸收,分布,代谢和排泄(ADME),这些特性对于评价其潜在的治疗用途至关重要.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号2393-17-1 3-(4-氨基苯基)丙酸 | CAS号39515-51-0 间苯氧基苯甲醛 | CAS号16642-79-8 3-(4-硝基苯基)丙酸

合成工艺路线路线简述

  • 39515-51-0 + 2393-17-1 = 885101-89-3
    反应条件:1.1 Reagents: Sodium Triacetoxyborohydride Catalysts: Acetic Acid Solvents: 1,2-Dichloroethane; 2 H,Rt
    标题:Bidirectional,Iterative Approach To The Structural Delineation Of The Functional "Chemoprint" In Gpr40 For Agonist Recognition
    作者:Tikhonova,Irina G.; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2007 卷标:50(13) 页码:2981-2989]

    39515-51-0 + 2393-17-1 = 885101-89-3
    反应条件:1.1 Reagents: Sodium Triacetoxyborohydride Solvents: 1,2-Dichloroethane; 1 - 16 H,Rt1.2 Reagents: Water
    标题:Synthesis And Activity Of Small Molecule Gpr40 Agonists
    作者:Garrido,Dulce M.; Et Al
    参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2006 卷标:16(7) 页码:1840-1845]

    39515-51-0 + 16642-79-8 = 885101-89-3
    反应条件:1.1 Reagents: Stannous Chloride Solvents: N-Methyl-2-Pyrrolidone; 67 H,Rt1.2 Catalysts: Acetic Acid Solvents: Dimethylformamide; 2 H,Rt1.3 Reagents: Sodium Cyanoborohydride; 20 H,Rt1.4 Reagents: Trifluoroacetic Acid Solvents: Dichloromethane,Water; 2 H,Rt
    标题:Solid Phase Synthesis And Sar Of Small Molecule Agonists For The Gpr40 Receptor
    作者:Mckeown,Stephen C.; Et Al
    参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2007 卷标:17(6) 页码:1584-1589
📜3-(4-硝基苯基)丙酸,间苯氧基苯甲醛 反应生成 3-(4-((3-苯氧基苄基)氨基)苯基)丙酸
参考文献:Solid Phase Synthesis And Sar Of Small Molecule Agonists For The Gpr40 Receptor
标题:Solid Phase Synthesis And Sar Of Small Molecule Agonists For The Gpr40 Receptor
摘要:The Discovery,Synthesis And Structure-Activity Relationship (Sar) Of Novel Carboxylic Acid Agonists For Gpr40 Are Described. Aryl Propionic Acid 1,Identified From A High Throughput Screen,Was Selected For Chemical Exploration. Compound 2 Was Identified As Our Lead Molecule Through Efficient Solid Phase Combinatorial Array Chemistry And Had An Attractive In Vitro And In Vivo Pharmacokinetic Profile In Rat. These Ligands May Prove Useful In Establishing A Role For Gpr40 In Insulin Regulation. (C) 2007 Elsevier Ltd. All Rights Reserved.
DOI:10.1016/j.Bmcl.2006.12.084

海关参考信息

专利信息


专利号:US-10125101-B2
优先权日:2016-11-28
标题:Indanylaminopyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof
发明人:ECKHARDT MATTHIAS; WAGNER HOLGER; PETERS STEFAN
权利人:BOEHRINGER INGELHEIM INT
摘要:The present invention relates to compounds of general formula I, n nwherein the groups R, R 1 , R 2 , R 3 , m and n are as defined herein, which compounds have valuable pharmacological properties, in particular their ability to bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular type 2 diabetes. Furthermore, the invention relates to novel intermediates, useful for the synthesis of compounds of formula I.

专利号:US-10538490-B2
优先权日:2016-10-25
标题:Benzylaminopyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof
发明人:ECKHARDT MATTHIAS; PETERS STEFAN; WAGNER HOLGER
权利人:BOEHRINGER INGELHEIM INT
摘要:The present invention relates to compounds of general formula I, n nwherein the groups R, R 1 , R 2 , R 3 , m and n are defined herein, which have valuable pharmacological properties, including binding to the GPR40 receptor and modulating its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2. Furthermore, the invention relates to novel intermediates, useful for the synthesis of compounds of formula I.

专利号:US-9617251-B2
优先权日:2015-08-07
标题:Indanylaminopyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof
发明人:ECKHARDT MATTHIAS; PETERS STEFAN; WAGNER HOLGER
权利人:BOEHRINGER INGELHEIM INT
摘要:The present invention relates to compounds of general formula I, n nwherein the groups R, R 1 , R 2 , R 3 , m and n are defined as in claim 1 , which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2. Furthermore, the invention relates to novel intermediates, useful for the synthesis of compounds of formula I.

专利号:CN-108434151-A
优先权日:2008-01-11
标题 :Synthesis of triterpenoids and method for treating diseases

专利号:CN-104739841-B
优先权日:2008-01-11
标题:Synthesis of triterpenoids and method for treating diseases

专利号:US-9771379-B2
优先权日:2015-09-24
标题:N-(2-(2-amino-6-substituted-4,4a,5,6-tetrahydropyrano[3,4-d][1,3]OXAZIN-8a(8H)-yl)-thiazol-4-yl) amides
发明人:BRODNEY MICHAEL AARON; BUTLER CHRISTOPHER RYAN; ZHANG LEI; O'NEILL BRIAN THOMAS
权利人:PFIZER
摘要:The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula I, n nwherein the variables R 1 , R 2 , R 3 , R 4 and X are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

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✅ COA系统入驻 | 共享模式

主要参考文献


1: Philippe C, Wauquier F, Léotoing L, Coxam V, Wittrant Y. GW9508, a free fatty acid receptor agonist, specifically induces cell death in bone resorbing precursor cells through increased oxidative stress from mitochondrial origin. Exp Cell Res. 2013 Nov 15;319(19):3035-41. doi: 10.1016/j.yexcr.2013.08.013. Epub 2013 Aug 22. doi: 10.1530/JME-13-0019. Print 2013. doi: 10.1038/jid.2011.123. Epub 2011 May 19. doi: 10.1016/j.jmgm.2011.01.006. Epub 2011 Feb 1.

合成参考文献


参考文献:10.1038/jid.2011.123
摘要:Fujita T, Matsuoka T, Honda T, Kabashima K, Hirata T, Narumiya S. A GPR40 Agonist GW9508 Suppresses CCL5, CCL17, and CXCL10 Induction in Keratinocytes and Attenuates Cutaneous Immune Inflammation. Journal of Investigative Dermatology. 2011 Aug;131(8):1660–7. doi: 10.1038/jid.2011.123.
参考文献:10.1074/jbc.m114.561449
摘要:Hudson BD, Shimpukade B, Milligan G, Ulven T. The Molecular Basis of Ligand Interaction at Free Fatty Acid Receptor 4 (FFA4/GPR120). Journal of Biological Chemistry. 2014 Jul;289(29):20345–58. doi: 10.1074/jbc.m114.561449.
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