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

(13S,14S,17S)-3-methoxy-11,13-dimethyl-7,12,14,15,16,17-hexahydro-6H-cyclopenta[a]phenanthrene-11,17-diol | 1056884-64-0

中文名称
——
中文别名
——
英文名称
(13S,14S,17S)-3-methoxy-11,13-dimethyl-7,12,14,15,16,17-hexahydro-6H-cyclopenta[a]phenanthrene-11,17-diol
英文别名
——
(13S,14S,17S)-3-methoxy-11,13-dimethyl-7,12,14,15,16,17-hexahydro-6H-cyclopenta[a]phenanthrene-11,17-diol化学式
CAS
1056884-64-0
化学式
C20H26O3
mdl
——
分子量
314.425
InChiKey
STKZJBXACPQEGV-NTNVKXBTSA-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):
    2.1
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    49.7
  • 氢给体数:
    2
  • 氢受体数:
    3

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:
    参考文献:
    名称:
    Synthesis and in vivo evaluation of 11-substituted estradiol derivatives as anti-implantation agents
    摘要:
    Synthesis of 11-substituted estradiol derivatives (12-17) has been carried out by the Grignard reaction with alkyl, allyl, and benzyl halides on 17 beta-hydroxy-3-methoxy-11-oxo-estra-1,3,5(10), 8(9)-tetraene (10). The novel compounds (10 and 12-17) were evaluated for their preliminary post-coital contraceptive (anti-implantation) activity in Sprague-Dawley rats. The tested compounds were administered orally and showed significant anti-implantation activity. Compound 13 is the most potent compound in the series which showed 100% contraceptive efficacy at 1.25 mg kg (1). (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.05.093
点击查看最新优质反应信息

文献信息

  • Synthesis and in vivo evaluation of 11-substituted estradiol derivatives as anti-implantation agents
    作者:Indra Dwivedy、Atul Gupta、Arvinder Grover、Vandana Srivastava、Man Mohan Singh、Suprabhat Ray
    DOI:10.1016/j.bmcl.2008.05.093
    日期:2008.7
    Synthesis of 11-substituted estradiol derivatives (12-17) has been carried out by the Grignard reaction with alkyl, allyl, and benzyl halides on 17 beta-hydroxy-3-methoxy-11-oxo-estra-1,3,5(10), 8(9)-tetraene (10). The novel compounds (10 and 12-17) were evaluated for their preliminary post-coital contraceptive (anti-implantation) activity in Sprague-Dawley rats. The tested compounds were administered orally and showed significant anti-implantation activity. Compound 13 is the most potent compound in the series which showed 100% contraceptive efficacy at 1.25 mg kg (1). (c) 2008 Elsevier Ltd. All rights reserved.
查看更多