CAS: 65678-07-1; 2-(3-Bromo-5-(Tert-Butyl)-4-Hydroxybenzylidene)Malononitrile

该化合物是一种有机化合物,其复杂结构特征包括一种苯基甲基苯基,一种溴基替代物和一种叔丁基组,其存在有助于其作为苯酚化合物的潜力,这种化合物可能具有抗氧化性特性.这种聚氨酯功能组表明,它可能表现出硝基苯的共性,包括可能参与核分裂反应.鉴于其结构特征,这种化合物在室温下很固,并可能在有机合成中或作为生产更复杂分子的中间体.其溴原子可能增强它的抗体性,并影响其在不同溶剂中的溶解性.

结构式图片

上下游产品

3-bromo-5-tert-butyl-4-hydroxybenzaldehyde malononitrile 2-tert-Butylphenol 3-(1,1-Dimethylethyl)-4-hydroxy-benzaldehyde

合成工艺路线路线简述

    📜3-(叔丁基)-4-羟基苯甲醛置于溴体系中,用 溶剂黄146 作为反应溶剂,化学反应生成 2-[[3-溴-5-叔丁基-4-羟基苯基]亚甲基]丙二腈
    参考文献:Compositions For Killing Internal Parasites Containing
    标题:Compositions For Killing Internal Parasites Containing
    摘要:通式i的化合物##str1##其中r.Sup.1是卤素,R.Sup.4是高度分支的烷基基团,R.Sup.2和r.Sup.3可以相同也可以不同,是氢或卤素原子或低烷基基团.

    海关参考信息

    专利信息


    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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    📌 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: Zhou W, Lou W, Chen J, Ding B, Chen B, Xie H, Zhou L, Zheng S, Jiang D. AG-1024 Sensitizes Sorafenib-Resistant Hepatocellular Carcinoma Cells to Sorafenib via Enhancing G1/S Arrest. Onco Targets Ther. 2021 Feb 15;14:1049-1059. doi: 10.2147/OTT.S289324.
    2: Wen B, Deutsch E, Marangoni E, Frascona V, Maggiorella L, Abdulkarim B, Chavaudra N, Bourhis J. Tyrphostin AG 1024 modulates radiosensitivity in human breast cancer cells. Br J Cancer. 2001 Dec 14;85(12):2017-21. doi: 10.1054/bjoc.2001.2171.
    3: Zhou X, Chen N, Xu H, Zhou X, Wang J, Fang X, Zhang Y, Li Y, Yang J, Wang X. Regulation of Hippo-YAP signaling by insulin-like growth factor-1 receptor in the tumorigenesis of diffuse large B-cell lymphoma. J Hematol Oncol. 2020 Jun 16;13(1):77. doi: 10.1186/s13045-020-00906-1.

    合成参考文献


    参考文献:10.1249/mss.0b013e318223b5d9
    摘要:Chang HC, Yang YR, Wang PS, Kuo CH, Wang RY. Insulin-like growth factor I signaling for brain recovery and exercise ability in brain ischemic rats. Med Sci Sports Exerc. 2011 Dec;43(12):2274–80. doi: 10.1249/mss.0b013e318223b5d9.
    参考文献:10.2478/v10042-008-0028-1
    摘要:Kisielewska J, Ligeza J, Klein A. The effect of tyrosine kinase inhibitors, tyrphostins: AG1024 and SU1498, on autocrine growth of prostate cancer cells (DU145). Folia Histochem Cytobiol. 2008;46(2):185–91. doi: 10.2478/v10042-008-0028-1.
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