CAS: 301305-73-7; 2-(3,4-Dimethoxybenzamido)-4,5,6,7-Tetrahydrobenzo[b]Thiophene-3-Carboxamide

该化合物是合成有机化合物,其结构复杂,包括一个含有碳本沙胺和甲氧苯并基组的苯基核心,并配有碳本氧基苯并,这种化合物通常具有中等溶解性,并具有潜在的生物活性,因此对药用化学感兴趣. 甲型苯并氧苯甲醚的存在可能增强它的药理特性,而四氢苯并苯并苯并苯结构则有助于其总体稳定性和再活动性.该化合物还可能显示与生物目标的具体互动,可以用于治疗用途.其合成过程涉及多步的有机反应,并且可以使用NMR光谱学,质量光谱测定和染色学等技术加以分析,以证实其特性和纯度.

结构式图片

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ECHA物质C&L通报

上下游产品

2-氨基-4,5,6,7-四氢苯并[b]噻吩-3-甲酰胺 2-Amino-4,5,6,7-Tetrahydrobenzo[b]Thiophene-3-Carboxamide 4815-28-5

合成工艺路线路线简述

    📜3,4-二甲氧基苯甲酰氯,2-氨基-4,5,6,7-四氢苯并[b]噻吩-3-甲酰胺置于n,N-二异丙基乙胺体系中,用 四氢呋喃 用作溶剂,化学反应 2.0H,反应生成2-[(3,4-二甲氧基苯甲酰基)氨基]-4,5,6,7-四氢-苯并[b]噻吩-3-甲酰胺
    参考文献:Identification Of 2-Acylaminothiophene-3-Carboxamides As Potent Inhibitors Of Flt3
    标题:Identification Of 2-Acylaminothiophene-3-Carboxamides As Potent Inhibitors Of Flt3
    摘要:A Series Of 2-Acylaminothiophene-3-Carboxamides Has Been Identified Which Exhibit Potent Inhibitory Activity Against The Flt3 Tyrosine Kinase. Compound 44 Inhibits The Isolated Enzyme (Ic50 = 0.027 Mu M) And Blocks The Proliferation Of Mv4-11 Cells (Ic50 = 0.41 Mu M). Structure Activity Relationship Studies Within This Series Are Described In The Context Of A Proposed Binding Model Within The Atp Binding Site Of The Enzyme. (C) 2006 Elsevier Ltd. All Rights Reserved.
    Doi:10.1016/j.Bmcl.2006.03.032

    海关参考信息

    专利信息


    专利号:US-2019031650-A1
    优先权日:2016-01-29
    标 题 :Dna alkylation and cross-linking agents as compounds and payloads for targeted therapies
    发明人:HERZON SETH; HEALY ALAN; CRAWFORD JASON; VIZCAINO MARIA; NIKOLAYEVSKIY HERMAN
    权利人:UNIV YALE
    摘要:The present invention is directed to compounds related to precolibactin pharmaceutical compositions based upon these compounds and methods of synthesis which are employed to provide intermediates and final compounds, which are principally alkylating agents and anticancer compounds. The chemical synthetic approach disclosed facilitates the synthesis of numerous precolibactin analogs which can be used in the treatment of cancer.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Patch RJ, Baumann CA, Liu J, Gibbs AC, Ott H, Lattanze J, Player MR. Identification of 2-acylaminothiophene-3-carboxamides as potent inhibitors of FLT3. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3282-6. Epub 2006 Mar 31.

    合成参考文献


    参考文献:10.1124/mol.119.115964
    摘要:Lee TD, Lee OW, Brimacombe KR, Chen L, Guha R, Lusvarghi S, Tebase BG, Klumpp-Thomas C, Robey RW, Ambudkar SV, Shen M, Gottesman MM, Hall MD. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular Pharmacology. 2019 Nov;96(5):629–40. doi: 10.1124/mol.119.115964.
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