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5-Methyl-2-oxa-5,8-diazaspiro[3.5]nonane | 1369103-58-1

中文名称
——
中文别名
——
英文名称
5-Methyl-2-oxa-5,8-diazaspiro[3.5]nonane
英文别名
——
5-Methyl-2-oxa-5,8-diazaspiro[3.5]nonane化学式
CAS
1369103-58-1
化学式
C7H14N2O
mdl
——
分子量
142.2
InChiKey
NNRYNNIIXWCPSD-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):
    -0.9
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    24.5
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Carboxamides as ubiquitin-specific protease inhibitors
    申请人:Valo Early Discovery, Inc.
    公开号:US11524966B1
    公开(公告)日:2022-12-13
    The present disclosure relates to modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25, pharmaceutical compositions comprising the inhibitors, and methods of using the inhibitors. The modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25 can be useful in the treatment of cancers, among other ailments.
    本公开涉及选自USP28和USP25的至少一种通路的调节剂(如抑制剂)、包含这些抑制剂的药物组合物以及使用这些抑制剂的方法。选自USP28和USP25的至少一种通路的调节剂(如抑制剂)可用于治疗癌症等疾病。
  • PYRAZOLE DERIVATIVES AND USES THEREOF AS INHIBITORS OF DLK
    申请人:F. Hoffmann-La Roche AG
    公开号:EP3083599B1
    公开(公告)日:2020-07-01
  • CARBOXAMIDES AS UBIQUITIN-SPECIFIC PROTEASE INHIBITORS
    申请人:Valo Early Discovery, Inc.
    公开号:US20210323975A1
    公开(公告)日:2021-10-21
    The present disclosure relates to modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25, pharmaceutical compositions comprising the inhibitors, and methods of using the inhibitors. The modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25 can be useful in the treatment of cancers, among other ailments.
  • [EN] HETEROCYCLES AND USES THEREOF<br/>[FR] HÉTÉROCYCLES ET LEURS UTILISATIONS
    申请人:[en]KUMQUAT BIOSCIENCES INC.
    公开号:WO2022081912A2
    公开(公告)日:2022-04-21
    The present disclosure provides compounds and pharmaceutically acceptable salt thereof, and methods of using the same. The compounds and methods have a range of utilities as therapeutics, diagnostics, and research tools. In particular, the subject compositions and methods are useful for reducing signaling output of oncogenic proteins.
  • WO2022271562A1
    申请人:——
    公开号:WO2022271562A1
    公开(公告)日:2022-12-29
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