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异己酸睾酮 | 15262-86-9

中文名称
异己酸睾酮
中文别名
睾酮异己酸酯
英文名称
Testosterone isocaproate
英文别名
testosterone 17β-isocaproate;testosterone isocapronate;testosterone-(4-methylpentanoate);testosterone isocaprate;O-<4-Methyl-valeryl>-testosteron;[(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 4-methylpentanoate
异己酸睾酮化学式
CAS
15262-86-9
化学式
C25H38O3
mdl
——
分子量
386.575
InChiKey
PPYHLSBUTAPNGT-BKWLFHPQSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    79-80 °C
  • 沸点:
    487.6±45.0 °C(Predicted)
  • 密度:
    1.07±0.1 g/cm3(Predicted)
  • 溶解度:
    几乎不溶于水,极易溶于丙酮和二氯甲烷,易溶于脂肪油。

计算性质

  • 辛醇/水分配系数(LogP):
    5.5
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xn
  • 安全说明:
    S22,S36
  • 危险类别码:
    R20/21/22
  • WGK Germany:
    3
  • 海关编码:
    2942000000

SDS

SDS:cffd1cf7fd1d48eadb299ebf73fcecaa
查看

制备方法与用途

作用

异己酸睾酮属于肾上腺皮质激素类药物,具有抗炎、抗毒和抗过敏的作用。

用途

异己酸睾酮是一种天然雄激素和合成类固醇药物,也是一种睾酮酯。在临床上主要用于治疗多种男性性激素不足的情况,如隐睾症、性腺功能减退症、阳痿及男性更年期等。

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    异己酸睾酮盐酸N-羟基邻苯二甲酰亚胺 、 N,N,N,N-tetraethylammonium tetrafluoroborate 作用下, 以 乙腈 为溶剂, 以46 %的产率得到
    参考文献:
    名称:
    最小受阻叔键和苄基 C(sp3)–H 键的电化学氯化
    摘要:
    C(sp 3 )–H键的功能化将极大有利于天然产物和药物的合成。最大的挑战之一是开发新的工业适用性合成策略。在此,我们报告了一种用于叔和仲苄基 C(sp 3 )–H键氯化/溴化的电化学方法。该方法可耐受许多官能团。此外,该反应可以轻松扩大至 100 克,而不会损失其效率。
    DOI:
    10.1039/d3gc03849a
  • 作为产物:
    描述:
    3β-Hydroxy-17β-oxyisocapronyl-androsten 在 环己酮 、 aluminum isopropoxide 作用下, 以 甲苯 为溶剂, 生成 异己酸睾酮
    参考文献:
    名称:
    Zborucki,Z., Roczniki Chemii, 1973, vol. 47, p. 2247 - 2253
    摘要:
    DOI:
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文献信息

  • Small Molecule Agonists and Antagonists of NR2F6 Activity in Humans
    申请人:Regen BioPharma, Inc.
    公开号:US20180214413A1
    公开(公告)日:2018-08-02
    The present technology is directed to modulators of nuclear receptor activity, specifically to the modulation of NR2F6 activity and NR2F6 utilizing compounds, and the immune modulation and modulation of cancer stem cell activity through administration of compounds described herein to humans.
    目前的技术是针对核受体活性调节剂,具体是针对NR2F6活性的调节和利用NR2F6化合物的调节,以及通过将本文描述的化合物用于人体来进行免疫调节和调节癌症干细胞活性。
  • COMPOSITIONS AND METHODS FOR TREATMENT OF VIRAL DISEASES
    申请人:Johansen Lisa M.
    公开号:US20100009970A1
    公开(公告)日:2010-01-14
    The present invention features compositions, methods, and kits useful in the treatment of viral diseases. In certain embodiments, the viral disease is caused by a single stranded RNA virus, a flaviviridae virus, or a hepatic virus. In particular embodiments, the viral disease is viral hepatitis (e.g., hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E) and the agent or combination of agents includes sertraline, a sertraline analog, UK-416244, or a UK-416244 analog. Also featured are screening methods for identification of novel compounds that may be used to treat a viral disease.
    本发明涉及用于治疗病毒性疾病的组合物、方法和试剂盒。在某些实施方式中,病毒性疾病是由单链RNA病毒、黄病毒科病毒或肝病毒引起的。在特定实施方式中,病毒性疾病是病毒性肝炎(例如甲型肝炎、乙型肝炎、丙型肝炎、丁型肝炎、戊型肝炎),药剂或药剂组合包括舍曲林、舍曲林类似物、UK-416244或UK-416244类似物。还包括用于鉴定可用于治疗病毒性疾病的新化合物的筛选方法。
  • NEW ENZYMATIC PROCESS FOR THE PREPARATION OF TESTOSTERONE AND ESTERS THEREOF
    申请人:F.I.S.- FABBRICA ITALIANA SINTETICI S.P.A
    公开号:US20170029863A1
    公开(公告)日:2017-02-02
    The present invention relates to a new process for the preparation of testosterone by means of enzymatic hydrolysis of testosterone esters.
    本发明涉及一种通过酶解睾酮酯类物质制备睾酮的新工艺。
  • Detection of testosterone esters in human plasma
    作者:Xavier de la Torre、Jordi Segura、Aldo Polettini、Maria Montagna
    DOI:10.1002/jms.1190301004
    日期:1995.10
    The detection of testosterone misuse in sports is currently based on the urinary testosterone to epitestosterone ratio, although in some rare instances physiological or pathological conditions could compromise the application of this general criterion. The detection in the body of traces of the unchanged testosterone esters really ingested would offer unequivocal confirmation of testosterone administration. In this work, the detectability of testosterone esters in humans was studied. Liquid–liquid extraction of human blood plasma and appropriate derivatization of nine testosterone esters are described. Different acyl (trifluoroacetyl, pentafluoropropionyl and heptafluorobutyryl) and trimethylsilyl derivatives were studied. The trimethylsilyl derivatives appear to be the best for screenign purposes based on the characteristics of their mass spectra, with abundant molecular ions in the high-mass range. They also offered good conditions for tandem mass spectrometric analysis, needed to achieve the required sensitivity after oral administration of the drugs. The method was successful in the detection and determination of intramuscularly administered testosterone propionate and testosterone enanthate and orally ingested testosterone undecanoate.
    目前,检测体育运动中滥用睾酮的依据是尿液中睾酮与表睾酮的比率,但在某些罕见的情况下,生理或病理条件可能会影响这一一般标准的应用。如果能在体内检测到真正摄入的未改变的睾酮酯,就能明确证实睾酮的使用。在这项工作中,对人体中睾酮酯的可检测性进行了研究。研究描述了人体血浆的液液萃取和九种睾酮酯的适当衍生化过程。研究了不同的酰基(三氟乙酰基、五氟丙酰基和七氟丁酰)和三甲基硅基衍生物。根据其质谱特点,三甲基硅烷衍生物在高质范围内具有丰富的分子离子,似乎最适合用于筛选。它们还为串联质谱分析提供了良好的条件,而串联质谱分析是口服药物后达到所需灵敏度所必需的。该方法成功地检测和测定了肌肉注射的丙酸睾酮和庚酸睾酮以及口服的十一酸睾酮。
  • Fulvestrant formulation
    申请人:AstraZeneca AB
    公开号:EP1669073A2
    公开(公告)日:2006-06-14
    The invention relates to a novel sustained release pharmaceutical formulation adapted for administration by injection containing the compound 7α-[9-(4,4,5,5,5-pentafluoropentylsulphmyl)nonyl]oestra-1,3,5(10)-thene-3,17β-diol, more particularly to a formulation adapted for administration by injection containing the compound 7α-[9-(4,4,5,5,5-pentafluoropentylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17β-diol in solution in a ricinoleate vehicle which additionally comprises at least one alcohol and a non-aqueous ester solvent which is miscible in the ricinoleate vehicle.
    本发明涉及一种适用于注射给药的新型缓释药物制剂,该制剂含有化合物 7α-[9-(4,4,5,5,5-五氟戊基亚磺酰基)壬基]雌甾-1,3,5(10)-三烯-3,17β-二醇,特别是涉及一种适用于注射给药的制剂,该制剂含有化合物 7α-[9-(4、7α-[9-(4,5,5,5-五氟戊基亚磺酰基)壬基]雌甾-1,3,5(10)-三烯-3,17β-二醇在蓖麻油酸盐载体中的溶液。
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