CAS: 873305-35-2; (S)-5,6-Diphenyl-N-((Tetrahydrofuran-2-yl)Methyl)Furo[2,3-D]Pyrimidin-4-Amine

该化合物是一种复杂的有机化合物,其特点是其独特的引信环状结构,其中包括一个火水和松木味;该化合物通常具有与热循环化合物有关的特性,例如由于其与各种生物目标相互作用的能力而具有潜在的生物活动;多种苯基群体的存在表明,它可能具有严重的缺水性特征,影响其溶解性及其与脂质膜的相互作用;四氢氟化物的替代成分可能增强它的药效植物特性,有可能改善生物系统的吸收和分布;此外,地雷功能群体可以参与氢联结,这可能影响其与其他分子的再活动与相互作用;

结构式图片

上下游产品

4-Bromo-5,6-Diphenyl-Furo[2,3-D]Pyrimidine 873306-32-2
4-氯-5,6-二苯基呋喃并[2,3-D]嘧啶 4-Chloro-5,6-Diphenylfuro[2,3-D]Pyrimidine 65148-07-4

合成工艺路线路线简述

  • 107833-28-3 = 873305-35-2
    反应条件:1.1 Solvents: Acetic Acid; 60 Min,200 °C2.1 Reagents: Phosphorus Oxychloride; 2 H,55 °C3.1 Solvents: Ethanol; 5 H,Reflux
    标题:Effect Of Ack1 Tyrosine Kinase Inhibitor On Ligand-Independent Androgen Receptor Activity
    作者:Mahajan,Kiran; Et Al
    参考文献:Prostate (Hoboken 日期:2010 卷标:70(12) 页码:1274-1285]

    65148-07-4 + 7175-81-7 = 873305-35-2
    反应条件:1.1 Solvents: Ethanol; 5 H,Reflux
    标题:Effect Of Ack1 Tyrosine Kinase Inhibitor On Ligand-Independent Androgen Receptor Activity
    作者:Mahajan,Kiran; Et Al
    参考文献:Prostate (Hoboken 日期:2010 卷标:70(12) 页码:1274-1285]

    106561-29-9 = 873305-35-2
    反应条件:1.1 Reagents: Phosphorus Oxychloride; 2 H,55 °C2.1 Solvents: Ethanol; 5 H,Reflux
    标题:Effect Of Ack1 Tyrosine Kinase Inhibitor On Ligand-Independent Androgen Receptor Activity
    作者:Mahajan,Kiran; Et Al
    参考文献:Prostate (Hoboken 日期:2010 卷标:70(12) 页码:1274-1285
📜2-氨基-4,5-二苯基-3-呋喃甲腈置于乙酸酐,溶剂黄146,三氯氧磷体系中,用 乙醇 作为反应溶剂,化学反应 26.0H,反应生成 5,6-二苯基-N-[[(2S)-四氢-2-呋喃基]甲基]呋喃并[2,3-D]嘧啶-4-胺; Aim 100
参考文献:Methods For The Treatment Of Disorders Related To Phosphorylation Of Histones
标题:Methods For The Treatment Of Disorders Related To Phosphorylation Of Histones
摘要:用于疾病诊断,预后和治疗选择的方法.还公开了用于这些方法的组合物和选择的治疗方法.

海关参考信息

专利信息


专利号:CN-108379591-B
优先权日:2018-04-03
标 题 :Synthesis of Immune Agonist Targeting Compounds and Their Applications

专利号:US-11285169-B2
优先权日:2013-03-13
标题 :Methods for modulating chemotherapeutic cytotoxicity
发明人:ROBERTS DAVID D; SOTO PANTOJA DAVID R
权利人:US HEALTH
摘要:Methods of reducing cytotoxicity of a chemotherapeutic agent to non-cancer cells by administering to a subject with cancer an effective amount of an agent that inhibits CD47 signaling and a DNA damaging agent, such as an anthracycline, topoisomerase inhibitor, or nucleotide synthesis inhibitor, are provided. Example disclosed methods reduce cardiotoxicity. In one example, the methods include administering to a subject with cancer an effective amount of a CD47 antisense morpholino oligonucleotide and an anthracycline such as doxorubicin. Methods of increasing cytotoxicity of a chemotherapeutic agent in cancer cells by administering to a subject with a tumor an effective amount of an agent that inhibits CD47 signaling and a DNA damaging agent such as an anthracycline, topoisomerase inhibitor, or nucleotide synthesis inhibitor, are also provided. In some embodiments, the inhibitor of CD47 signaling is administered to the subject before, during, or after the administration of the DNA damaging agent.

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品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Cheng MH, Ponzoni L, Sorkina T, Lee JY, Zhang S, Sorkin A, Bahar I. Trimerization of dopamine transporter triggered by AIM-100 binding: Molecular mechanism and effect of mutations. Neuropharmacology. 2019 Dec 15;161:107676. doi: 10.1016/j.neuropharm.2019.107676. Epub 2019 Jun 20.
2: Sorkina T, Ma S, Larsen MB, Watkins SC, Sorkin A. Small molecule induced oligomerization, clustering and clathrin-independent endocytosis of the dopamine transporter. Elife. 2018 Apr 9;7:e32293. doi: 10.7554/eLife.32293.
3: Zhou A, Zhang W, Wang B. Host factor TNK2 is required for influenza virus infection. Genes Genomics. 2023 Jun;45(6):771-781. doi: 10.1007/s13258-023-01384-8. Epub 2023 May 3. 38(5):642-650. doi: 10.1002/cbf.3522. Epub 2020 Mar 12.

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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