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(8R,9R,10R,13R,14R,17R)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

中文名称
——
中文别名
——
英文名称
(8R,9R,10R,13R,14R,17R)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
英文别名
——
(8R,9R,10R,13R,14R,17R)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one化学式
CAS
——
化学式
C21H30O2
mdl
——
分子量
314.5
InChiKey
RJKFOVLPORLFTN-ZPLOVTKXSA-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):
    3.9
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • METHOD FOR INHIBITING THE PROLIFERATION OF HEPATIC STELLATE CELLS WITH A LIGAND OF THE LOW AFFINITY GLUCOCORTICOID BINDING SITE (LAGS)
    申请人:The University Court of The University of Aberdeen
    公开号:EP1435966A2
    公开(公告)日:2004-07-14
  • [EN] COMPOSITIONS FOR THERAPY<br/>[FR] COMPOSITIONS THERAPEUTIQUES
    申请人:UNIV ABERDEEN
    公开号:WO2003026670A2
    公开(公告)日:2003-04-03
    Provided are methods of inhibiting proliferation and/or trans-differentiation of hepatic stellate cells, which method comprises the step of contacting hepatic stellate cells with a ligand of the low affinity glucocorticoid binding site (LAGS), which may be the rat p28 receptor or the human hpr6.6 receptor. The invention also provides ligands for use in such methods (e.g. pregnenolone 16-alpha carbonitrile) and methods for screening for the same (e.g. based on competition or displacement assays using LAGS ligands such as dexamethasone). Such ligands may be used in the treatment of liver disorders.
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