CAS: 2487-63-0; Quinbolone

该化合物是一种合成新陈代谢类固醇,产自丙酮,其特点是结构改变,在尽量减少和诱因效应的同时,强化其新陈代谢特性;昆波罗酮具有促进肌肉成长,增强体力和改善运动性能的潜力,使其在医疗和身体建设方面都感兴趣;该化合物通常具有高度亲近性和接受方的特征,从而助长了其代谢效应;此外,昆波罗酮还因其潜在的治疗用途进行了研究,特别是在与肌肉消瘦和骨质疏松有关的条件下.然而,与许多新陈代谢类固醇一样,它还可能带有副作用的风险,包括荷尔蒙不平衡和心血管问题.在竞争性体育中,由于对公平和健康影响的关切,它的使用往往受到监管或禁止.与任何代谢剂一样,认真考虑其药理学特征和潜在风险对于使用者至关重要.

结构式图片

MSDS等安全信息

上下游产品

宝丹酮 1-Dehydrotestosterone 846-48-0

合成工艺路线路线简述

    📜1,1-二乙氧基环戊烷,宝丹酮 反应生成(17B)-17-(1-环戊烯-1-基氧基)-雄甾-1,4-二烯-3-酮
    参考文献:New Classes Of Orally Active Hormonal Derivatives. Ii. 17-Cycloalk-1'-Enyl Ethers Of 17β-Hydroxy-And Rostanes And 19-Norandrostanes
    标题:New Classes Of Orally Active Hormonal Derivatives. Ii. 17-Cycloalk-1'-Enyl Ethers Of 17β-Hydroxy-And Rostanes And 19-Norandrostanes
    摘要:
    Doi:10.1016/s0039-128X(72)80029-1

    海关参考信息

    专利信息


    专利号:US-2008032964-A1
    优先权日:2006-04-10
    标题:Process for the synthesis of azetidinone
    发明人:KANSAL VINOD K; AHMAD SUHAIL; MARIAPPAN SHANMUGAVEL; TYAGI BHUPENDRA; PERLMAN NURIT; LE PAIH JACQUES; ZANOTTI-GEROSA ANTONIO
    权利人:KANSAL VINOD K; AHMAD SUHAIL; MARIAPPAN SHANMUGAVEL; TYAGI BHUPENDRA; PERLMAN NURIT; LE PAIH JACQUES; ZANOTTI-GEROSA ANTONIO
    摘要:Provided are intermediates useful for the synthesis of hydroxyl-alkyl substituted azetidinones, processes of their preparation, and processes for the synthesis of certain hydroxyl-alkyl substituted azetidinones. Also provided are processes for the synthesis of 1-(4-fluorophenyl)-3(R)-[3-(4-fluorophenyl)-3(S)-hydroxypropyl]-4(S)-(4-hydroxyphenyl)-2-azetidinone, or ezetimibe.

    专利号:US-2012165520-A1
    优先权日:2010-12-23
    标题:Process for the synthesis of prodrugs of opioids
    发明人:MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
    权利人:MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
    摘要:The present invention provides a process for the synthesis of opioid prodrugs. In particular, the present invention provides a process for the synthesis of opioid prodrugs comprising: treating an opioid, in the form of a salt or a freebase, with a carbonyl synthon to form an activated intermediate and subsequently reacting the activated intermediate with an amine, in the form of a salt or a freebase.

    专利号:US-2007259917-A1
    优先权日:2006-04-24
    标题 :Processes for the synthesis of 3-isobutylglutaric acid
    发明人:KANSAL VINOD K; CHAURASIA BRIJNATH P; PATEL HITESH K; SHELKE SHIVAJI H; MORE YOGESH P
    权利人:KANSAL VINOD K; CHAURASIA BRIJNATH P; PATEL HITESH K; SHELKE SHIVAJI H; MORE YOGESH P
    摘要:Provided are processes for the synthesis of 3-isobutylglutaric acid, an intermediate in the synthesis of (S)-Pregabalin.

    专利号:US-9376461-B2
    优先权日:2011-06-06
    标 题:Non-enzymatic synthesis of O-acetyl-ADP-ribose and analogues thereof
    发明人:KOPPETSCH KARSTEN; SZCZEPANKIEWICZ BRUCE G; PERNI ROBERT B
    权利人:KOPPETSCH KARSTEN; SZCZEPANKIEWICZ BRUCE G; PERNI ROBERT B; GLAXOSMITHKLINE LLC
    摘要:Provided herein is a simple, one-step, non-enzymatic synthesis of O-Acetyl-ADP-ribose (OAADPR) from NAD and sodium acetate in acetic acid. The extension of this reaction to other carboxylic acids, demonstrates that the reaction between NAD, and NAD analogs produces mixtures of the corresponding 2′- and 3′-carboxylic esters. Included are O-carboxyl-ADP-ribose compounds and corresponding methods of synthesis (e.g., O-propionyl-ADP-ribose, O-succinyl-ADP-ribose, O-malonyl-ADP-ribose), as well as non-adenosine nucleoside compounds.

    专利号:US-7141702-B2
    优先权日:2004-03-26
    标 题 :Process for the synthesis of α-substituted acroleins
    发明人:DESHPANDE RAJ M; DIWAKAR MAKARAND M; CHAUDHARI RAGHUNATH V
    权利人:COUNCIL SCIENT IND RES
    摘要:The present invention provides an improved process for the synthesis of α-substituted acroleins from olefins by a tandem hydroformylation and Mannich reaction sequence in the presence of syngas and formaldehyde, wherein the two catalysts are segregated into two different phases thereby preventing deactivation of the catalysts by each other, and yielding a highly selective and active catalyst.

    专利号:US-11680224-B2
    优先权日:2020-11-04
    标 题:Hydroxy fatty acid synthesis
    发明人:CERMAK STEVEN C; Isbell Terry; LOWERY BENJAMIN A
    权利人:US AGRICULTURE; THE US SECRATERY OF AGRICULTURE
    摘要:The invention relates to methods for the synthesis of hydroxy fatty acids from unsaturated fatty acids via epoxidation and catalytic hydrogenation.

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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


    参考文献:10.1007/978-3-540-79088-4_7
    摘要:Kazlauskas R. Designer steroids. Handb Exp Pharmacol. 2010;(195):155–85. doi: 10.1007/978-3-540-79088-4_7.
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