CAS: 173529-46-9; (E)-4-(2-(N-((4-Methoxyphenyl)Sulfonyl)Acetamido)Styryl)Pyridine 1-Oxide

该化合物是一种合成有机化合物,其特征是其复杂的分子结构,包括一种磺酰胺功能组和一种丙烯衍生物.该化合物通常具有中等溶液和潜在生物活性等特性,因此对药物研究感兴趣.甲基氧基和丙烯组的存在表明可能与生物目标发生相互作用,有可能影响其药理学特征.其磺酰胺协会可能有助于形成氢结,增强它与其他分子的再活动性和相互作用.此外,该化合物的结构表明它可能具有特定的立体化学结构,这可能会影响其生物活动和功效.

结构式图片

合成工艺路线路线简述

    📜(Nz)-N-[(6E)-6-[2-(1-Hydroxypyridin-4-Ylidene)Ethylidene]Cyclohexa-2,4-Dien-1-Ylidene]-4-Methoxybenzenesulfonamide 反应生成(E)-4-[2-[2-[n-乙酰基-N-[(4-甲氧基苯基)磺酰]氨基]苯基]乙烯基]吡啶1-氧化物
    参考文献:Aminostilbazole Derivative And Medicine
    标题:Aminostilbazole Derivative And Medicine
    摘要:本发明涉及以下公式或其水合物和盐的氨基苯乙烯衍生物.其中,R1和r2分别表示氢等;R3,R4,R13和r14分别表示氢,C1-3酰基,卤素,羟基等;R5表示氢或羟基取代的c1-3烷基等;R6表示苯磺酰取代的c1-3烷氧基等;环y表示苯环等;环z表示4-吡啶基,其氧化物等.该化合物可用于治疗各种恶性肿瘤.

    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.

    供应商参考报价(招募中)

    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. Schoffski, Patrick. Polo-like kinase (PLK) inhibitors in preclinical and early clinical development in oncology. Oncologist (2009), 14(6), 559-570. CODEN: OCOLF6 ISSN:1083-7159. CAN
    152:421294 AN
    2009:879296 2. Low, Jonathan; Chakravartty, Arunava; Blosser, Wayne; Dowless, Michele; Chalfant, Christopher; Bragger, Patty; Stancato, Louis. Phenotypic fingerprinting of small molecule cell cycle kinase inhibitors for drug discovery. Current Chemical Genomics (2009), 3 13-21. CODEN: CCGUAQ ISSN:1875-3973. CAN
    152:254294 AN

    合成参考文献


    参考文献:10.1007/s12272-013-0111-9
    摘要:Pingaew R, Worachartcheewan A, Nantasenamat C, Prachayasittikul S, Ruchirawat S, Prachayasittikul V. Synthesis, cytotoxicity and QSAR study of N-tosyl-1,2,3,4-tetrahydroisoquinoline derivatives. Archives of Pharmacal Research. 2013 Apr 21;36(9):1066–77. doi: 10.1007/s12272-013-0111-9.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知