CAS: 13103-34-9; Boldenone Undecylenate

该化合物是源自睾丸酮的合成代谢和诱变类类固醇(AAS),经过改良以延长其活性,其特征是附加一个未脱氧酯酯,该酯延长其半衰期,确保缓慢,持续地释放到血液中.该化合物具有中度的代谢效应,其活性相对较低,并具有诱变性,因此适合于促进精质肌肉质量和耐久性,降低显性及诱变副效应的风险.其稳定性和可预测的药用植物基因能允许受控剂量疗程.波尔登内酯在兽药中经常使用,在某些情况下,还在肌肉消亡条件下研究其潜在的治疗用途.

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

宝丹酮 1-Dehydrotestosterone 846-48-0
睾酮 Testosterone 58-22-0

合成工艺路线路线简述

    睾酮置于4-二甲氨基吡啶,5-甲基吩嗪硫酸甲酯,Rhodococcus Erythropolis Wy 1406 3-Ketosteroid-δ1-Dehydrogenase,I51L/i350T Double Mutant,三乙胺体系中,用 二氯甲烷,二甲基亚砜 用作溶剂,化学反应 0.42H,反应生成宝丹酮十一烯酸酯
    参考文献:通过单细胞生物催化 δ1-脱氢和 C17β-羰基还原级联合成代谢雄激素的批量和连续流不对称合成
    标题:通过单细胞生物催化 δ1-脱氢和 C17β-羰基还原级联合成代谢雄激素的批量和连续流不对称合成
    摘要:Chemoenzymatic Asymmetric Synthesis Of An Anabolic-Androgenic Steroid (+)-Boldenone (3) And Its Prodrug (+)-Boldenone Undecylenate (4) Was Accomplished Starting From Commercially Available 4-Androstene-3,17-Dione (4-Ad,1) Under Both Batch And Continuous Flow Conditions. The Key Feature Of The Current Synthesis Is The Construction Of An Enzymatic Cascade Process In A Single Escherichia Coli Cell For
    Doi:10.1039/d2Gc04894A

    海关参考信息

    专利信息


    专利号:US-9303000-B2
    优先权日:2011-01-17
    标 题 :Olefin containing nuclear transport modulators and uses thereof
    发明人:SANDANAYAKA VINCENT P; SHACHAM SHARON; SHECHTER SHARON; MCCAULEY DILARA
    权利人:SANDANAYAKA VINCENT P; SHACHAM SHARON; SHECHTER SHARON; MCCAULEY DILARA; KARYOPHARM THERAPEUTICS INC
    摘要:The invention generally relates to the field of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to new substituted-heterocyclic azole compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity such as in treating cancer and other neoplastic disorders, inflammatory diseases, disorders of abnormal tissue growth and fibrosis including cardiomyopathy, pulmonary fibrosis, hepatic fibrosis, glomerulonephritis, and other renal disorders, and for the treatment of viral infections (both acute and chronic).

    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.

    专利号:US-9550757-B2
    优先权日:2010-03-05
    标题:Nuclear transport modulators and uses thereof
    发明人:SHACHAM SHARON; KAUFFMAN MICHAEL; SANDANAYAKA VINCENT P; SHECHTER SHARON
    权利人:KARYOPHARM THERAPEUTICS INC
    摘要:The invention generally relates to the field of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to new substituted-heterocyclic azole compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity such as in treating cancer and other neoplastic disorders, inflammatory diseases, disorders of abnormal tissue growth and fibrosis including cardiomyopathy, pulmonary fibrosis, hepatic fibrosis, glomerulonephritis, and other renal disorders, and for the treatment of viral infections (both acute and chronic).

    专利号:US-2014315720-A1
    优先权日:2012-10-24
    标 题 :Polysaccharide ester microspheres and methods and articles relating thereto
    发明人:FALLON DENIS G; GARRETT THOMAS S; KIZER LAWTON E; ZAZZARA KAREN L; COMBS MICHAEL T; JOHNSON RICHARD K; DEHART GARY
    权利人:CELANESE ACETATE LLC
    摘要:A method for producing a polysaccharide ester microsphere may include forming a polysaccharide ester product from a polysaccharide synthesis, wherein the polysaccharide ester product comprises a polysaccharide ester and a solvent; diluting the polysaccharide ester product, thereby yielding a polysaccharide ester dope; and forming a plurality of polysaccharide ester microspheres from the polysaccharide ester dope. Suitable polysaccharides may include, but are not limited to, starch, cellulose, hemicellulose, algenates, chitosan, and any combination thereof. Esters thereof may be organic esters (e.g., acetate and the like), inorganic esters (e.g., sulfonates and the like), or combinations thereof. Further, the solids conent of the polysaccharide ester dope, in some instances, may be greater than about 16 wt %.
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    📌 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:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
    摘要:S72 | NTUPHTW | Pharmaceutically Active Substances from National Taiwan University | DOI:10.5281/zenodo.3955664
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