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(R)-7-((1R,3aR,4S,7aR)-4-Hydroxy-7a-methyl-octahydro-inden-1-yl)-2,2-dimethyl-octan-3-one | 866759-19-5

中文名称
——
中文别名
——
英文名称
(R)-7-((1R,3aR,4S,7aR)-4-Hydroxy-7a-methyl-octahydro-inden-1-yl)-2,2-dimethyl-octan-3-one
英文别名
——
(R)-7-((1R,3aR,4S,7aR)-4-Hydroxy-7a-methyl-octahydro-inden-1-yl)-2,2-dimethyl-octan-3-one化学式
CAS
866759-19-5
化学式
C20H36O2
mdl
——
分子量
308.505
InChiKey
LDGUKRHGNCPLIQ-GFAJBQDWSA-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):
    4.99
  • 重原子数:
    22.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    37.3
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    (R)-7-((1R,3aR,4S,7aR)-4-Hydroxy-7a-methyl-octahydro-inden-1-yl)-2,2-dimethyl-octan-3-one重铬酸吡啶正丁基锂四丁基氟化铵 作用下, 以 四氢呋喃正己烷二氯甲烷 为溶剂, 反应 23.0h, 生成 (R)-7-{(1R,3aS,7aR)-4-[2-((3R,5R)-3,5-Dihydroxy-cyclohexylidene)-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-2,2-dimethyl-octan-3-one
    参考文献:
    名称:
    Highly antiproliferative, low-calcemic, side-chain ketone analogs of the hormone 1α,25-dihydroxyvitamin D3
    摘要:
    A series 2a-4b of seven new side-chain ketone analogs of calcitriol (1) have been prepared. Unexpectedly, several of these 24- and 25-tert-butyl ketones, even though lacking the classical side-chain tertiary hydroxyl group, are considerably more antiproliferative in vitro than the hormone calcitriol (1) even at physiologically relevant low nanomolar concentrations and are less calcemic than calcitriol (1) in vivo. In addition, ketone analog 19-nor-2a is not significantly less calcemic in vivo than 19-methylene analog 2a. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.06.031
  • 作为产物:
    参考文献:
    名称:
    Highly antiproliferative, low-calcemic, side-chain ketone analogs of the hormone 1α,25-dihydroxyvitamin D3
    摘要:
    A series 2a-4b of seven new side-chain ketone analogs of calcitriol (1) have been prepared. Unexpectedly, several of these 24- and 25-tert-butyl ketones, even though lacking the classical side-chain tertiary hydroxyl group, are considerably more antiproliferative in vitro than the hormone calcitriol (1) even at physiologically relevant low nanomolar concentrations and are less calcemic than calcitriol (1) in vivo. In addition, ketone analog 19-nor-2a is not significantly less calcemic in vivo than 19-methylene analog 2a. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.06.031
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文献信息

  • WO2006/74227
    申请人:——
    公开号:——
    公开(公告)日:——
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