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3-Methyl-1-cyclohexyl-butandion-(1,2) | 40222-56-8

中文名称
——
中文别名
——
英文名称
3-Methyl-1-cyclohexyl-butandion-(1,2)
英文别名
1-Cyclohexyl-3-methylbutane-1,2-dione;1-cyclohexyl-3-methylbutane-1,2-dione
3-Methyl-1-cyclohexyl-butandion-(1,2)化学式
CAS
40222-56-8
化学式
C11H18O2
mdl
——
分子量
182.263
InChiKey
GAJSKTCIXRVMOR-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):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

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文献信息

  • Pipecolic esters for inhibition of the proteasome
    申请人:THE BOARD OF REGENTS OF THE UNIVERSY OF TEXAS SYSTEM
    公开号:US11345659B2
    公开(公告)日:2022-05-31
    The present disclosure relates to chemical compounds that modulate proteasome activity, pharmaceutical compositions containing such compounds, and use of these compounds and compositions for the treatment of disorders of uncontrolled cellular proliferation such as, for example, a cancer. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本公开涉及调节蛋白酶体活性的化合物、含有此类化合物的药物组合物,以及使用这些化合物和组合物治疗不受控制的细胞增殖紊乱,例如癌症。本摘要旨在作为一种扫描工具,用于在特定技术领域进行搜索,而无意限制本发明。
  • PIPECOLIC ESTERS FOR INHIBITION OF THE PROTEASOME
    申请人:THE BOARD OF REGENTS OF THE UNIVERSY OF TEXAS SYSTEM
    公开号:US20210002220A1
    公开(公告)日:2021-01-07
    The present disclosure relates to chemical compounds that modulate proteasome activity, pharmaceutical compositions containing such compounds, and use of these compounds and compositions for the treatment of disorders of uncontrolled cellular proliferation such as, for example, a cancer. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
  • Krueger,H.-R. et al., Chemische Berichte, 1973, vol. 106, p. 91 - 104
    作者:Krueger,H.-R. et al.
    DOI:——
    日期:——
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