CAS: 931398-72-0; Iox2

该化合物是一种合成化合物,属于quinline衍生物类别.该物质具有一种quinocine核心,其特征是含有芳香环中氮原子的双环结构.与甘油相连的碳基类组的存在表明,它可能表现出与氨酸有关的性质,有可能影响其生物活动.氢和碳基功能组有助于其在各种溶剂中的再活性和溶性.该化合物可能具有药用化学作用,包括反炎或反微生物活动,尽管需要具体的生物数据来证实这种影响.其结构复杂性和功能组表明,它可以参与各种化学反应,从而有可能影响其生物活动.该化合物的功能组可能使其在药物开发或生物化学应用方面成为进一步研究的对象.

结构式图片

欧盟法规

C&L通报

上下游产品

sodium glycinate ethyl 4-hydroxy-2-oxo-1-(phenylmethyl)-1,2-dihydro-3-quinolinecarboxylate

合成工艺路线路线简述

  • 130058-54-7 + 6000-44-8 = 931398-72-0
    反应条件:1.1 Solvents: 2-Methoxyethanol; 2 H,Reflux; Cooled1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Cooled
    标题:Process For Preparation Of Iox2
    参考文献:China]

    130058-54-7 + 6000-44-8 = 931398-72-0
    反应条件:1.1 Solvents: Ethanol; 2 Min,Rt -> 200 °C; 5 Min,150 °C
    标题:Preparation Of N-[(4-Hydroxy-2-Oxo-1,2-Dihydro-3-Quinolinyl)Carbonyl]Glycine Derivatives As Prolyl Hydroxylase Inhibitors
    参考文献:World Intellectual Property Organization]

    = 931398-72-0
    反应条件:1.1 Reagents: Trifluoroacetic Acid Solvents: Dichloromethane; Rt
    标题:Selective Small Molecule Probes For The Hypoxia Inducible Factor (Hif) Prolyl Hydroxylases
    作者:Chowdhury,Rasheduzzaman; Candela-Lena,Jose Ignacio; Chan,Mun Chiang; Greenald,David Jeremy; Yeoh,Kar Kheng; Et Al
    参考文献:Acs Chemical Biology 日期:2013 卷标:8(7) 页码:1488-1496
📜Sodium Glycinate,1-苄基-4-羟基-2-氧代-1,2-二氢喹啉-3-羧酸乙酯置于盐酸体系中,用 乙二醇甲醚,水 作为反应溶剂,化学反应 2.0H,以61%的收率获得产物n-[[4-羟基-2-氧代-1-(苯基甲基)-1,2-二氢-3-喹啉基]羰基]甘氨酸
参考文献:Wo2007/38571
标题:Wo2007/38571

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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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: Deppe J, Popp T, Egea V, Steinritz D, Schmidt A, Thiermann H, Weber C, Ries C. Impairment of hypoxia-induced HIF-1α signaling in keratinocytes and fibroblasts by sulfur mustard is counteracted by a selective PHD-2 inhibitor. Arch Toxicol. 2015 Jun 17. [Epub ahead of print] doi: 10.3389/fchem.2014.00090. eCollection 2014.
3: Sen A, Ren S, Lerchenmüller C, Sun J, Weiss N, Most P, Peppel K. MicroRNA-138 regulates hypoxia-induced endothelial cell dysfunction by targeting S100A1. PLoS One. 2013 Nov 11;8(11):e78684. doi: 10.1371/journal.pone.0078684. eCollection 2013. Erratum in: PLoS One. 2013;8(12). doi:10.1371/annotation/53080a85-89cc-4a84-8fd9-0eb0c19cc05d. PLoS One. 2014;9(1). doi:10.1371/annotation/c7bddd8d-9f15-45f4-a886-740b351a39b6.

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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