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2-[(17,17-dimethyl-6,7,15,16-tetrahydrocyclopenta[a]phenanthren-3-yl)oxy]-N,N-diethylethanamine | 61237-32-9

中文名称
——
中文别名
——
英文名称
2-[(17,17-dimethyl-6,7,15,16-tetrahydrocyclopenta[a]phenanthren-3-yl)oxy]-N,N-diethylethanamine
英文别名
——
2-[(17,17-dimethyl-6,7,15,16-tetrahydrocyclopenta[a]phenanthren-3-yl)oxy]-N,N-diethylethanamine化学式
CAS
61237-32-9
化学式
C25H33NO
mdl
——
分子量
363.543
InChiKey
OXMZVUCEOAMMED-UHFFFAOYSA-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):
    6.3
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    12.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    Potential hypolipidemic agents derived from 3-hydroxy-17,17-dimethylgona-1,3,5(10),8,11,13-hexaene
    摘要:
    Numerous aryloxy derivatives containing a lipophilic group have been found to possess hypolipidemic activity. This has prompted the preparation of various derivatives of 3-hydroxy-17,17-dimethylgona-1,3,5(10),8,11,13-hexaene (6a). In 6a the lipophilic biphenyl group is incorporated into the steroid nucleus. A three-step synthesis of 6a from 17beta-methylestradiol methyl ether was developed. The derivatives prepared were tested in rats made hypercholesterolemic with propylthiouracil. Several were found active in this test.
    DOI:
    10.1021/jm00212a008
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文献信息

  • Potential hypolipidemic agents derived from 3-hydroxy-17,17-dimethylgona-1,3,5(10),8,11,13-hexaene
    作者:Leland J. Chinn、Karlene W. Salamon
    DOI:10.1021/jm00212a008
    日期:1977.2
    Numerous aryloxy derivatives containing a lipophilic group have been found to possess hypolipidemic activity. This has prompted the preparation of various derivatives of 3-hydroxy-17,17-dimethylgona-1,3,5(10),8,11,13-hexaene (6a). In 6a the lipophilic biphenyl group is incorporated into the steroid nucleus. A three-step synthesis of 6a from 17beta-methylestradiol methyl ether was developed. The derivatives prepared were tested in rats made hypercholesterolemic with propylthiouracil. Several were found active in this test.
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