CAS: 348622-88-8; (R)-5-(6-Cyclohexyl-1-(Hydroxyamino)-1-Oxohexan-3-yl)-1,2,4-Oxadiazole-3-Carboxamide

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ethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]-4-cyclohexylbutyl)-1,2,4-oxadiazole-3-carboxylate

合成工艺路线路线简述

    📜Ethyl 5-{(1R)-1-[2-(Tert-Butoxy)-2-Oxoethyl]-4-Cyclohexylbutyl)-1,2,4-Oxadiazole-3-Carboxylate置于n-甲基吗啉,N-Trimethylsilyl-Hydroxylamin,氨,三氟乙酸,氯甲酸异丁酯体系中,用 四氢呋喃,乙醇,二氯甲烷 作为反应溶剂,化学反应生成 Uk 383367; 5-[(1R)-4-环己基-1-[2-(羟基氨基)-2-氧代乙基]丁基]-1,2,4-恶二唑-3-甲酰胺
    参考文献:Procollagen C-Proteinase Inhibitors
    标题:Procollagen C-Proteinase Inhibitors
    摘要:它们及其盐,溶剂合物,前药等,其中取代基具有此处提及的值,是procollagen C-蛋白酶(pcp)抑制剂,并在由pcp介导的疾病中具有用途.

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    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

    Huang, Y., Gao, P., Qin, T., Chu, B., Xu, T., Yi, J., ... & Yin, G. (2023). Delayed inhibition of collagen deposition by targeting bone morphogenetic protein 1 promotes recovery after spinal cord injury. Matrix Biology, 118, 69-91. Bailey, S., Fish, P. V., Billotte, S., Bordner, J., Greiling, D., James, K., ... & Webster, R. (2008). Succinyl hydroxamates as potent and selective non-peptidic inhibitors of procollagen C-proteinase: design, synthesis, and evaluation as topically applied, dermal anti-scarring agents. Bioorganic & medicinal chemistry letters, 18(24), 6562-6567.

    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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