CAS: 881202-45-5; N1-(2-(1H-Indol-3-yl)Ethyl)-N4-(Pyridin-4-yl)Benzene-1,4-Diamine

该化合物是属于小分子类的化学化合物,主要因其作为某些动脉的选择性抑制剂的作用而得到承认,特别是在癌症研究方面,该化合物的潜在治疗用途已经研究,特别是针对肿瘤生长和扩散中的具体信号路径;其分子结构是一个复杂的安排,有助于其生物活动,其特点是有机溶剂溶解性以及标准实验室条件下的中度稳定性;JNJ 26854165经过各种临床前期评估,评估其功效和安全状况,使其成为药物发展的一个关注对象;与许多调查化合物一样,其药理基因学,行动机制和潜在副作用是正在进行的研究的关键领域,有助于更广泛地了解有针对性的癌症治疗.

结构式图片

上下游产品

16H17N3C16H17N3 4-bromopyridine hydr°Chloride

合成工艺路线路线简述

    📜N1-(2-(1H-Indol-3-yl)Ethyl)Benzene-1,4-Diamine,4-溴吡啶盐酸盐置于4-溴吡啶盐酸盐体系中,用32的收率获得产物n-[2-(1H-吲哚-3-基)乙基]-N'-(4-吡啶基)-1,4-苯二胺
    参考文献:Inhibitors Of The Interaction Between Mdm2 And P53
    标题:Inhibitors Of The Interaction Between Mdm2 And P53
    摘要:本发明提供了式(I)的化合物,其用作p53-Mdm2相互作用的抑制剂,以及包含该式(I)的化合物的制药组合物,其中n,M,P,S,T,R1,R2,R3,R4,R5,R6,R7,X,Y,Q和z具有定义的含义.

    海关参考信息

    专利信息


    专利号:US-2023037284-A9
    优先权日:2018-11-30
    标题:Combination therapy of peptidomimetic macrocycles
    发明人:GUERLAVAIS VINCENT; ANNIS DAVID ALLEN
    权利人:AILERON THERAPEUTICS INC
    摘要:The present disclosure describes the synthesis of peptidomimetic macrocycles and methods of using peptidomimetic macrocycles to treat a condition. The present disclosure also describes methods of using peptidomimetic macrocycles in combination with at least one additional pharmaceutically-active agent for the treatment of a condition, for example, cancer.

    专利号:US-2018371021-A1
    优先权日:2017-05-11
    标 题 :Peptidomimetic macrocycles and uses thereof
    发明人:AIVADO MANUEL; GUERLAVAIS VINCENT; OLSON KAREN
    权利人:AILERON THERAPEUTICS INC
    摘要:The present disclosure describes the synthesis of peptidomimetic macrocycles and methods of using peptidomimetic macrocycles to treat a condition. The present disclosure also describes methods of using peptidomimetic macrocycles in combination with at least one additional pharmaceutically-active agent for the treatment of a condition, for example, cancer.

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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: Park IA, Noh YK, Min KW, Kim DH, Lee JY, Son BK, Kwon MJ, Han MH, Hur JY, Pyo JS. p27 Cell Cycle Inhibitor and Survival in Luminal-Type Breast Cancer: Gene Ontology, Machine Learning, and Drug Screening Analysis. J Breast Cancer. 2024 Sep 4. doi: 10.4048/jbc.2024.0107. Epub ahead of print. 15(1):458. doi: 10.1007/s12672-024-01340-2.
    3: Kędzierski J, Jäger MC, Naeem S, Odermatt A, Smieško M. In silico and in vitro assessment of drugs potentially causing adverse effects by inhibiting CYP17A1. Toxicol Appl Pharmacol. 2024 May;486:116945. doi: 10.1016/j.taap.2024.116945. Epub 2024 Apr 28.
    243:109105. doi: 10.1016/j.clim.2022.109105. Epub 2022 Aug 31. 28(7-8):864-874. doi: 10.1038/s41417-020-0207-6. Epub 2020 Aug 6. 8(9):e74741. doi: 10.1371/journal.pone.0074741.

    合成参考文献


    摘要:S55 | ZINC15PHARMA | Pharmaceuticals from ZINC15 | DOI:10.5281/zenodo.3247749
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