CAS: 4385-77-7; 3-Pyridin-3-Yl-Benzoic Acid

该化合物是一种环环芳烃化合物,其特点是与三角环环环相连的苯并酸义,具有独特的电子和消毒特性,使其成为制药和农用化学合成中有价值的中间体,其双重功能(碳酸和氮)允许多功能性反应,包括金属协调和参与凝结或组合反应.该化合物特别有助于发展用于催化的离心和作为生物活性分子的建筑块.高纯度能确保研究和工业应用的一贯性,同时其标准条件下的稳定性有利于处理和储存.

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4385-75-5 1264068-70-3 10177-12-5

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CAS号626-55-1 3-溴吡啶 | CAS号25487-66-5 3-羧基苯硼酸 | CAS号4385-67-5 3-(3-Methylphen... | CAS号28987-79-3 间甲苯基溴化镁

合成工艺路线路线简述

    📜3-吡啶硼酸置于(1,1'-Bis(Diphenylphosphino)Ferrocene)Palladium(II) Dichloride,Caesium Carbonate,Lithium Hydroxide体系中,用 四氢呋喃,甲醇,乙二醇二甲醚,水 作为反应溶剂,化学反应 18.0H,反应生成 3-吡啶-3-基苯甲酸
    参考文献:Start Selective And Rigidify: The Discovery Path Toward A Next Generation Of Egfr Tyrosine Kinase Inhibitors
    标题:Start Selective And Rigidify: The Discovery Path Toward A Next Generation Of Egfr Tyrosine Kinase Inhibitors
    摘要:The Epidermal Growth Factor Receptor (Egfr),When Carrying An Activating Mutation Like Del19 Or L858R,Acts As An Oncogenic Driver In A Subset Of Lung Tumors. While Tumor Responses To Tyrosine Kinase Inhibitors (Tkis) Are Accompanied By Marked Tumor Shrinkage,The Response Is Usually Not Durable. Most Patients Relapse Within Two Years Of Therapy Often Due To Acquisition Of An Additional Mutation In Egfr Kinase Domain That Confers Resistance To Tkis. Crucially,Oncogenic Egfr Harboring Both Resistance Mutations,T790M And C797S,Can No Longer Be Inhibited By Currently Approved Egfr Tkis. Here,We Describe The Discovery Of Bi-4020,Which Is A Noncovalent,Wild-Type Egfr Sparing,Macro-Cyclic Tki. Bi-4020 Potently Inhibits The Above-Described Egfr Variants And Induces Tumor Regressions In A Cross-Resistant Egfr(Del19 T790M C797S) Xenograft Model. Key Was The Identification Of A Highly Selective But Moderately Potent Benzimidazole Followed By Complete Rigidification Of The Molecule Through Macrocyclization.
    DOI:10.1021/acs.Jmedchem.9B01169

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Design, Synthesis And Stepwise Optimization Of Nitrile-Based Inhibitors Of Cathepsins B And L
    作者:Lorenzo Cianni,Fernanda Dos Reis Rocho,Vinícius Bonatto,Felipe Cardoso Prado Martins,Jerônimo Lameira,Andrei Leitão,Carlos A. Montanari,Anwar Shamim |发布日期:2021.1
    摘要:Human Cathepsin B (Catb) Is An Important Biological Target In Cancer Therapy. In This Work, We Performed A Knowledge-Based Design Approach And The Synthesis Of A New Set Of 19 Peptide-Like Nitrile-Based Cathepsin Inhibitors. Reported Compounds Were Assayed Against A Panel Of Human Cysteine Proteases: Catb, Catl, Catk, And Cats. Three Compounds (7H, 7I, And 7J) Displayed Nanomolar Inhibition Of Catb

    合成参考文献


    参考文献:10.1021/acs.jmedchem.6b00660
    摘要:Lund BA, Christopeit T, Guttormsen Y, Bayer A, Leiros HK. Screening and Design of Inhibitor Scaffolds for the Antibiotic Resistance Oxacillinase-48 (OXA-48) through Surface Plasmon Resonance Screening. J Med Chem. 2016 Jun 09;59(11):5542–54. doi: 10.1021/acs.jmedchem.6b00660.
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