CAS: 2088-71-3; Testosterone 17-Benzoate

该化合物是睾丸酮的合成酯衍生物,由睾丸酮和苯甲酸的酯化形成,这种改变会增加该化合物的脂性,延长其释放时间和作用时间,与未经过改良的睾酮相比,延长其释放时间和作用时间,主要用于抗原替代疗法和研究应用,因为其具有持续的药用植物基因特征;苯甲酮酯组会延缓酯酶的水解,导致活性睾酮逐步释放到系统循环中.这种特性使得它适合需要较少频繁管理的规程.与其他睾酮酯酯一样,它具有外观和诱导和代谢效应,支持肌肉生长,体性激素和次性性特征等生理功能.适当的处理和储存对于保持稳定性至关重要.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

17β-benzoyloxy-androst-5-en-3-one 5α-hydroxy-3-oxo-5α-androstan-17β-yl benzoate testosterone benzoyl chloride17β-benzoyloxy-6β-bromo-androst-4-en-3-one 3,3-ethanediyldioxy-17β-benzoyloxy-androst-5-ene A-nor-androstan-3-oic acid17β-benzoyloxy-5-oxo-3,5-seco-A-nor-androstan-3-oic acid testosterone

合成工艺路线路线简述

    📜17β-Benzoyloxy-Androst-5-En-3-One置于硫酸体系中,化学反应生成17-安息香酸雄烯醇酮
    参考文献:Notes-The Direct Conversion Of Steroidal δ5-3β-Alcohols To δ5-And δ4-3-Ketones
    标题:Notes-The Direct Conversion Of Steroidal δ5-3β-Alcohols To δ5-And δ4-3-Ketones
    摘要:
    Doi:10.1021/jo01118A627

    海关参考信息

    专利信息


    专利号:US-4219489-A
    优先权日:1978-09-05
    标题:Synthesis of steroids
    发明人:BUNES LEONARD A; JOHNSON WILLIAM S
    权利人:STANFORD LELAND JUNIOR UNIV TR
    摘要:Method and compounds are provided for use in the synthesis of steroids wherein a polyolefin is provided having an initiating group having a chalcogen atom in juxtaposition to a double bond, so as to be capable of bond formation to close to form a ring and having a terminating group involving pi unsaturation (a double or triple bond) conjugated to an aromatic ring. Upon acid catalysis, sigma bonds are formed through the interaction of a carbocation formed at the carbon atom bonded to the chalcogen atom and the double bond intermediate the initiating group and the terminating group, which close to form rings of a steroid nucleus, the carbocation interacting with the pi unsaturation conjugated with the aromatic group and being captured by a nucleophile present in the acidic reaction medium. The resulting steroid product may then be modified in known ways to produce known steroids.

    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.

    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

    参考标题:Directing Group In Decarboxylative Cross-Coupling: Copper-Catalyzed Site-Selective C-N Bond Formation From Nonactivated Aliphatic Carboxylic Acids
    作者:Zhao-Jing Liu,Xi Lu,Guan Wang,Lei Li,Wei-Tao Jiang,Yu-Dong Wang,Bin Xiao,Yao Fu |发布日期:2016.8.3
    摘要:Copper-Catalyzed Directed Decarboxylative Amination Of Nonactivated Aliphatic Carboxylic Acids Is Described. This Intramolecular C-N Bond Formation Reaction Provides Efficient Access To The Synthesis Of Pyrrolidine And Piperidine Derivatives As Well As The Modification Of Complex Natural Products. Moreover, This Reaction Presents Excellent Site-Selectivity In The C-N Bond Formation Step Through The

    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
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知