CAS: 57469-76-8; 2,6-Diaminohexanoic Acid Compound With 2-(4-Isobutylphenyl)Propanoic Acid (1:1)

该化合物是一种化学化合物,具有含酸衍生物的酸衍生物,具有酯功能组,其特征为氨基酸脊,有助于其溶解性和再活性;芳香环上的甲基组和二甲基丙基亚基基基组的存在强化了其疏水特性,有可能影响其与生物系统的互动;苯乙基元素表明,该化合物可能具有芳香特性,可能影响其稳定性和在不同化学环境中的再活动;该化合物作为碱的衍生物,可参与丙酸合成,并可用于制药或生物化学领域;其具体特性,如熔点,沸点和溶性,将取决于分子结构及其功能组之间的相互作用;

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2,6-diamin°Caproic acid ibuprofen

合成工艺路线路线简述

    📜Dl-赖氨酸,布洛芬 以 乙醇 作为反应溶剂,化学反应 0.17H,反应生成 消旋布洛芬赖氨酸盐
    参考文献:一种赖氨洛芬的制备方法
    标题:一种赖氨洛芬的制备方法
    摘要:本发明属于医药制备技术领域,具体涉及一种赖氨洛芬的制备方法.包括以下步骤:将盐酸赖氨酸浓缩后与布洛芬反应;经活性炭脱色,乙酸乙酯析晶处理后制得.本发明制备赖氨洛芬的方法较为简单,不需要特殊设备,操作简便,工艺可控性好;且制成的成品品质好,纯度高.

    海关参考信息

    专利信息


    专利号:US-9751877-B2
    优先权日:2012-09-21
    标题 :Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders
    发明人:PETTERSSON MARTIN YOUNGJIN; JOHNSON DOUGLAS SCOTT; SUBRAMANYAM CHAKRAPANI; O'DONNELL CHRISTOPHER JOHN; AM ENDE CHRISTOPHER WILLIAM; GREEN MICHAEL ERIC; PATEL NANDINI CHATURBHAI; STIFF CORY MICHAEL; TRAN TUAN PHONG; KAUFFMAN GREGORY WAYNE; STEPAN ANTONIA FRIEDERIKE; VERHOEST PATRICK ROBERT
    权利人:PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    专利号:US-9550795-B2
    优先权日:2011-08-31
    标 题:Hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
    发明人:BRODNEY MICHAEL AARON; BUTLER CHRISTOPHER RYAN; HELAL CHRISTOPHER JOHN; O'NEILL BRIAN THOMAS
    权利人:BRODNEY MICHAEL AARON; BUTLER CHRISTOPHER RYAN; HELAL CHRISTOPHER JOHN; O'NEILL BRIAN THOMAS; PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I, n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    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.

    专利号:US-9403846-B2
    优先权日:2012-12-19
    标题:Carbocyclic- and heterocyclic-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
    发明人:BRODNEY MICHAEL AARON; O'NEILL BRIAN THOMAS; BUTLER CHRISTOPHER RYAN; LACHAPELLE ERIK ALPHIE
    权利人:PFIZER
    摘要:The present invention provides compounds of formula I, n nwherein the variables R 1 , R 2 , R 5 and b are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    专利号:WO-2012172449-A1
    优先权日:2011-06-13
    标题:Lactams as beta secretase inhibitors
    发明人:BRODNEY MICHAEL AARON
    权利人:PFIZER; BRODNEY MICHAEL AARON
    摘要:Compound and pharmaceutically acceptable salts of the compound are disclosed, wherein the compound has the structure (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed. The compound of formula I is useful as beta secretase inhibitor for use in the treatment of Alzheimer's and other neurodegenerative and/or neurological disorders.

    专利号:US-2016229847-A1
    优先权日:2013-10-04
    标 题:Novel bicyclic pyridinones as gamma-secretase modulators
    发明人:PETTERSSON MARTIN YOUNGJIN; AM ENDE CHRISTOPHER WILLIAM; GREEN MICHAEL ERIC; JOHNSON DOUGLAS SCOTT; KAUFFMAN GREGORY WAYNE; O'DONNELL CHRISTOPHER WILLIAM; PATEL NANDINI CHATURBHAI; STEPAN ANTONIA FRIEDERIKE; STIFF CORY MICHAEL; SUBRAMANYAM CHAKRAPANI; TRAN TUAN PHONG; VERHOEST PATRICK ROBERT
    权利人:PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula II as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

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    合成参考文献


    参考文献:10.1007/978-3-0348-0496-7_7
    摘要:Rainsford KD. Gastro-Intestinal Toxicity. 2012. In: Ibuprofen: Pharmacology, Therapeutics and Side Effects.
    参考文献:10.1007/s40278-025-89064-2
    摘要:Ibuprofen-lysinate. Reactions Weekly. 2025 Aug 30;2074(1):123. doi: 10.1007/s40278-025-89064-2.
    参考文献:10.1007/s40122-019-00148-1
    摘要:Kyselovič J, Koscova E, Lampert A, Weiser T. A Randomized, Double-Blind, Placebo-Controlled Trial of Ibuprofen Lysinate in Comparison to Ibuprofen Acid for Acute Postoperative Dental Pain. Pain and Therapy. 2020 Jan 07;9(1):249–59. doi: 10.1007/s40122-019-00148-1.
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