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1-(2-Tert-butyl-2,7-diazaspiro[3.5]nonan-7-yl)ethanone

中文名称
——
中文别名
——
英文名称
1-(2-Tert-butyl-2,7-diazaspiro[3.5]nonan-7-yl)ethanone
英文别名
1-(2-tert-butyl-2,7-diazaspiro[3.5]nonan-7-yl)ethanone
1-(2-Tert-butyl-2,7-diazaspiro[3.5]nonan-7-yl)ethanone化学式
CAS
——
化学式
C13H24N2O
mdl
——
分子量
224.34
InChiKey
FIUDYWQWASSTCG-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):
    1.1
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    23.6
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • 1,3-DIARYL-SUBSTITUTED HETEROCYCLIC PESTICIDES
    申请人:E I DU PONT DE NEMOURS AND COMPANY
    公开号:US20140249025A1
    公开(公告)日:2014-09-04
    Disclosed are compounds of Formula 1, N-oxides, and salts thereof, wherein Q is and Z 1 , Z 2 , J 1 , J 2 , M, R 1a , R 1b , R 2a , R 2b , R 2c , R 2d and R 14 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.
  • CARM1 INHIBITORS AND USES THEREOF
    申请人:Epizyme, Inc.
    公开号:US20170305922A1
    公开(公告)日:2017-10-26
    Provided herein are compounds of Formula (I): and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, wherein R1, R2a, R2b, R3 and Ring B are as defined herein, and Ring A is a group of Formula (A-i), (A-ii), or (A-iii): wherein R, R, R, R, and R are as defined herein. Compounds of the present invention are useful for inhibiting CARM1 activity. Methods of using the compounds for treating CARM1-mediated disorders are also described.
  • PYRAZOLE COMPOUNDS AND METHODS OF MAKING AND USING SAME
    申请人:Abide Therapeutics, Inc.
    公开号:US20190256494A1
    公开(公告)日:2019-08-22
    Provided herein are pyrazole compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of MAGL and/or ABHD6. Furthermore, the subject compounds and compositions are useful for the treatment of, for example, pain.
  • METHODS OF TREATING DISEASE WITH MAGL INHIBITORS
    申请人:H. Lundbeck A/S
    公开号:US20220110933A1
    公开(公告)日:2022-04-14
    Provided herein are methods for the treatment of disease with monoacylglycerol lipase (MAGL) inhibitors.
  • US9113631B2
    申请人:——
    公开号:US9113631B2
    公开(公告)日:2015-08-25
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