CAS: 227947-06-0; 3-(4-(2-(4-(3-Chloro-2-Hydroxypropoxy)Phenyl)Propan-2-yl)Phenoxy)Propane-1,2-Diol

该化合物是一个复杂的有机化合物,具有多功能结构特征,具有丙烷基质,具有氢氧基,有助于极溶剂中的溶性以及氢联结潜力.一个氯化合物和氢丙氧基混合物的存在表明,该物质可能表现出特定的再活性和生物活动,有可能影响其药用特性.该化合物的苯丙酸成分表明它可能具有抗氧化性特性,而其总体结构则意味着它可能与各种生物目标发生相互作用.分子复杂性还可能表明其在药物或化学中间体中的潜在用途.然而,为了充分阐明其特性,包括其稳定性,再活性和在诸如药化学或材料科学等各个领域的潜在用途,有必要进行详细研究.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

18H22O4C18H22O4 3-[4-[1-[4-(2,3-dihydroxypropoxy)phenyl]-1-methylethyl]phenoxy]propane-1,2-diol 1-chloro-3-[4-[2-[4-(3-chloro-2-hydroxypropoxy)phenyl] propan-2-yl]phenoxy]propan-2-ol

合成工艺路线路线简述

    📜双酚 A 二(3-氯-2-羟丙基)醚置于sodium Hydroxide体系中,用 丙二醇甲醚,水 用作溶剂,化学反应 2.5H,反应生成双酚a(3-氯-2-羟丙基)甘油醚,2-Chloro-3-[4-[2-[4-(Oxiran-2-Ylmethoxy)Phenyl]Propan-2-Yl]Phenoxy]Propan-1-Ol,[1-Chloro-3-[4-[2-[4-(Oxiran-2-Ylmethoxy)Phenyl]Propan-2-Yl]Phenoxy]Propan-2-Yl] Acetate,[2-Hydroxy-3-[4-[2-[4-(Oxiran-2-Ylmethoxy)Phenyl]Propan-2-Yl]Phenoxy]Propyl] Acetate,3-[2-Hydroxy-3-[4-[2-[4-(Oxiran-2-Ylmethoxy)Phenyl]Propan-2-Yl]Phenoxy]Propoxy]Propane-1,2-Diol,3-[4-[1-[4-(3-氯-2-羟基丙氧基)苯基]-1-甲基乙基]苯氧基]-1,2-丙二醇,,2,2-双-(4-甘胺氧苯)丙烷,双酚 A (2,3-二羟基丙基)缩水甘油醚
    参考文献:Process For Manufacturing An Alpha-Dihydroxy Derivative And Epoxy Resins Prepared Therefrom
    标题:Process For Manufacturing An Alpha-Dihydroxy Derivative And Epoxy Resins Prepared Therefrom
    摘要:从芳基烯丙基醚制备α-二羟基衍生物的制造过程,其中该α-二羟基衍生物可用于制备α-卤代醇中间体和由此制备的环氧树脂,包括在氧化剂存在下或在氧化剂和催化剂存在下通过卤代物取代从α-二羟基衍生物脱氢反应中获得的α-卤代醇中间体的环氧化.

    海关参考信息

    专利信息


    专利号:US-2022118123-A1
    优先权日:2019-02-22
    标 题 :Combination of ar antagonists and targeted thorium conjugates
    发明人:HAMMER STEFANIE; HAGEMANN URS BEAT; HAENDLER BERNARD; LEJEUNE PASCALE; ZITZMANN-KOLBE SABINE; SCHATZ CHRISTOPH; KARLSSON JENNY
    权利人:BAYER AG; BAYER AS
    摘要:The present invention covers combinations of at least two components, component A and component B, comprising component A being PSMA-TTC, and component B being an antiandrogen selected form AR antagonists such as from cyproterone acetate, bicalutamide, flutamide, nilutamide, enzalutamide, apalutamide, darolutamide or keto-darolutamide, or an AR degrader such as ARV-110, or an ARN-terminal domain binder such as EPI-506, or an antisense oligonucleotide that reduces AR expression such as EZN-4176 or AZD-5312, or an androgen synthesis inhibitor such as abiraterone, particularly abiraterone acetate, seviteronel, galeterone, orteronel or ketoconazole, or a dual AR antagonist and androgen synthesis inhibitor such as ODM-204. Another aspect of the present invention covers the use of such combinations as described herein for the preparation of a medicament for the treatment or prophylaxis of a disease, particularly for the treatment of a hyper-proliferative disease.

    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: Kranzbühler B, Salemi S, Mortezavi A, Sulser T, Eberli D. Combined N-terminal androgen receptor and autophagy inhibition increases the antitumor effect in enzalutamide sensitive and enzalutamide resistant prostate cancer cells. Prostate. 2019 Feb;79(2):206-214. doi: 10.1002/pros.23725. Epub 2018 Oct 21. doi: 10.1016/j.yexcr.2017.07.026. Epub 2017 Jul 20. pii: E67. doi: 10.3390/cancers9060067. Review.
    4: Guo C, Yeh S, Niu Y, Li G, Zheng J, Li L, Chang C. Targeting androgen receptor versus targeting androgens to suppress castration resistant prostate cancer. Cancer Lett. 2017 Jul 1;397:133-143. doi: 10.1016/j.canlet.2017.03.022. Epub 2017 Mar 18. doi: 10.1021/acschembio.6b00182. Epub 2016 Jul 14.
    6: Monaghan AE, McEwan IJ. A sting in the tail: the N-terminal domain of the androgen receptor as a drug target. Asian J Androl. 2016 Sep-Oct;18(5):687-94. doi: 10.4103/1008-682X.181081. Review.

    合成参考文献


    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
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