CAS: 52-78-8; (8R,9S,10R,13S,14S,17S)-17-Ethyl-17-Hydroxy-13-Methyl-1,2,6,7,8,9,10,11,12,14,15,16-Dodecahydrocyclopenta[a]Phenanthren-3-One

该化合物是一种源自睾酮的合成新陈代谢类类类固醇,其特点是能够促进肌肉生长,提高体能,使其在医疗和运动环境中都受到欢迎;诺列甲酮的代谢-和诱因比率较高,这意味着它能促进肌肉发育,产生相对较低和诱因效应;该化合物经常用于荷尔蒙替代疗法,并治疗骨质疏松和某些类型贫血等条件;化学上,它被归类为19种诺尔托酮衍生物,具有增强其稳定性和有效性的改变作用;诺列多酮通常通过口服,其半衰期相对较长,允许较少发生剂量;然而,它的使用与潜在的副作用有关,包括荷尔蒙不平衡,肝毒性和心血管问题,特别是在高剂量中滥用以提升性能时.由于这些风险,它被归类为许多国家的受控物质,非医疗用途往往在竞争性体育中被禁止.

结构式图片

上下游产品

CAS号68-22-4 炔诺酮 | CAS号1042-57-5 3-methoxy-19-no... | CAS号734-32-7 甲基双酮 | CAS号6961-15-5 (3α,5α,17α)-19-...

合成工艺路线路线简述

    📜炔诺酮置于palladium 10% On Activated Carbon,氢气体系中,用 甲醇 作为反应溶剂,化学反应 6.0H,反应生成 乙诺酮
    参考文献: Compounds For Targeted Therapies Of Castration Resistant Prostate Cancer[fr] Composés Pour Thérapies Ciblées Du Cancer De La Prostate Résistant à La Castration
    标题: Compounds For Targeted Therapies Of Castration Resistant Prostate Cancer[fr] Composés Pour Thérapies Ciblées Du Cancer De La Prostate Résistant à La Castration
    摘要:本发明一般涉及用于治疗的新化合物.具体而言,本公开涉及对治疗癌症,特别是去势抵抗性前列腺癌的有用的新四环化合物.本公开范围内涉及药物组合物和通过单独或与其他治疗方法联合给予这种化合物的治疗癌症患者的方法.

    海关参考信息

    专利信息


    专利号:US-3959322-A
    优先权日:1960-09-22
    标 题:Synthesis of 13-alkyl-gon-4-ones
    发明人:HUGHES GORDON ALAN; SMITH HERCHEL
    权利人:SMITH HERCHEL
    摘要:The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

    专利号:US-2025281509-A1
    优先权日:2021-04-26
    标 题 :Sequential hormone therapy to improve survival and enhance response to immune therapy in men with prostate cancer
    发明人:DENMEADE SAMUEL R; ISAACS JOHN T; ANTONARAKIS EMMANUEL S; KACHHAP SUSHANT; MARKOWSKI MARK CHRISTOPHER
    权利人:UNIV JOHNS HOPKINS
    摘要:Disclosed are methods for treating men with castrate resistant prostate cancer with a sufficient dose of testosterone to achieve supraphysiologic serum levels of testosterone in sequence with androgen ablative treatment or androgen synthesis inhibitors for one or more cycles until evidence of radiographic progression, at which point the subject will receive immune checkpoint blockade therapy.

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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

    合成参考文献


    摘要:21 CFR Sections 1308.11-1308.15
    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
    参考文献:10.1016/s0378-4347(99)00091-2
    摘要:Van Puymbroeck M, Kuilman MEM, Maas RFM, Witkamp RF, Leyssens L, Van Miert ASJPAM, Hendriks L, Vanderzande D, Adriaensens P, Jacobs M-, Raus J. 17α-Ethyl-5β-estrane-3α,17β-diol, a biological marker for the abuse of norethandrolone and ethylestrenol in slaughter cattle. Journal of Chromatography B: Biomedical Sciences and Applications. 1999 May;728(2):217–32. doi: 10.1016/s0378-4347(99)00091-2.
    参考文献:10.1210/jcem-18-11-1308
    摘要:DOWBEN RM. EFFECT OF NORETHANDROLONE ON SERUM ENZYME LEVELS*. The Journal of Clinical Endocrinology & Metabolism. 1958 Nov;18(11):1308–9. doi: 10.1210/jcem-18-11-1308.
    参考文献:10.1016/s0140-6736(58)92309-2
    摘要:McCRACKEN BH, PARSONS FM. Use of nilevar (17-ethyl-19-nortestosterone) to suppress protein catabolism in acute renal failure. Lancet. 1958 Oct 25;2(7052):885–6. doi: 10.1016/s0140-6736(58)92309-2.
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