摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-methoxyestra-1,3,5(10)-trien-3-ol-17-one-oxime | 431901-69-8

中文名称
——
中文别名
——
英文名称
2-methoxyestra-1,3,5(10)-trien-3-ol-17-one-oxime
英文别名
(8R,9S,13S,14S)-17-hydroxyimino-2-methoxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-ol
2-methoxyestra-1,3,5(10)-trien-3-ol-17-one-oxime化学式
CAS
431901-69-8
化学式
C19H25NO3
mdl
——
分子量
315.412
InChiKey
UMLKYOVSAWJPRN-QPWUGHHJSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    62
  • 氢给体数:
    2
  • 氢受体数:
    4

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

  • 作为产物:
    描述:
    2-甲氧基雌素酮盐酸羟胺sodium acetate 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以90%的产率得到2-methoxyestra-1,3,5(10)-trien-3-ol-17-one-oxime
    参考文献:
    名称:
    合成2-和17-取代的雌酮类似物及其与2-甲氧基雌二醇的抗增殖结构-活性关系
    摘要:
    合成和表征了一系列新的17-修饰和2,17-修饰的2-甲氧基雌二醇(2ME2)类似物。这些类似物旨在保留或增强2ME2的生物学活性,并减少了代谢功能。评价类似物对MDA-MB-231乳腺肿瘤细胞的抗增殖活性,HUVEC中的抗血管生成活性以及对MCF-7细胞增殖的雌激素活性。在大鼠盒给药模型中,评估了几种类似物在人肝微粒体中和体内的代谢稳定性。这项研究导致了2ME2的17个修饰的类似物,与2ME2相比,它们具有相似或改善的抗增殖和抗血管生成活性,缺乏雌激素特性并具有改善的代谢稳定性。
    DOI:
    10.1016/j.bmc.2009.08.038
点击查看最新优质反应信息

文献信息

  • Disturbance in sex-steroid serum profiles of cattle in response to exogenous estradiol: A screening approach to detect forbidden treatments
    作者:Patricia Regal、Carolina Nebot、Mónica Díaz-Bao、Rocio Barreiro、Alberto Cepeda、Cristina Fente
    DOI:10.1016/j.steroids.2010.12.005
    日期:2011.3
    Estradiol benzoate (EB) has been one of the most widely used estrogenic agents in animal husbandry, as a way of exogenously introducing the natural hormone estradiol-17 beta into the animal organism. Estradiol was previously employed to induce anabolic effects or reproductive improvements in cattle. However, the employment of EB in European countries has been permanently forbidden by Directive 2008/97/EC to guarantee consumers' health. Despite this prohibition, the control of estradiol-17 beta and its esters continues to be a difficult task for residue-monitoring plans in European Communities because official analyses of natural thresholds for hormones in cattle have not yet been established, leading to a lack of confirmation for any exogenous administration of natural hormones. Several researchers have worked on excretion profiles of metabolites, variation in specific hormonal ratios and metabolomic fingerprints after hormonal treatments. This research focuses on the possible existence of disturbances in the serum profile of animals treated with EB in terms of steroid sex hormones (androgens, oestrogens and progestogens), by investigating the serum levels of several of these hormones. The serum samples were collected from three groups of cows: one treated with an intramuscular injection of EB, one treated with a combination of intravaginal EB and progesterone and a control (non-treated) group. The samples have been analysed by a validated high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method, and 17 natural hormones were identified and quantified. Subsequently, data from the serum profiles were submitted for statistic and multivariate analysis, and it was possible to observe a manifest variation between animal groups. The obtained results can help in the development of a viable screening tool for monitoring purposes in cattle. (C) 2010 Elsevier Inc. All rights reserved.
  • Synthesis of 2- and 17-substituted estrone analogs and their antiproliferative structure–activity relationships compared to 2-methoxyestradiol
    作者:Jamshed H. Shah、Gregory E. Agoston、Lita Suwandi、Kimberly Hunsucker、Victor Pribluda、Xiaoguo H. Zhan、Glenn M. Swartz、Theresa M. LaVallee、Anthony M. Treston
    DOI:10.1016/j.bmc.2009.08.038
    日期:2009.10
    A novel series of 17-modified and 2,17-modified analogs of 2-methoxyestradiol (2ME2) were synthesized and characterized. These analogs were designed to retain or potentiate the biological activities of 2ME2 and have diminished metabolic liability. The analogs were evaluated for antiproliferative activity against MDA-MB-231 breast tumor cells, antiangiogenic activity in HUVEC, and estrogenic activity
    合成和表征了一系列新的17-修饰和2,17-修饰的2-甲氧基雌二醇(2ME2)类似物。这些类似物旨在保留或增强2ME2的生物学活性,并减少了代谢功能。评价类似物对MDA-MB-231乳腺肿瘤细胞的抗增殖活性,HUVEC中的抗血管生成活性以及对MCF-7细胞增殖的雌激素活性。在大鼠盒给药模型中,评估了几种类似物在人肝微粒体中和体内的代谢稳定性。这项研究导致了2ME2的17个修饰的类似物,与2ME2相比,它们具有相似或改善的抗增殖和抗血管生成活性,缺乏雌激素特性并具有改善的代谢稳定性。
查看更多