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阿法替尼杂质18 | 2413212-25-4

中文名称
阿法替尼杂质18
中文别名
——
英文名称
(S,E)-4-(Dimethylamino)-N-(4-((4-fluorophenyl)amino)-7-((tetrahydrofuran-3-YL)oxy)quinazolin-6-YL)but-2-enamide
英文别名
(E)-4-(dimethylamino)-N-[4-(4-fluoroanilino)-7-[(3S)-oxolan-3-yl]oxyquinazolin-6-yl]but-2-enamide
阿法替尼杂质18化学式
CAS
2413212-25-4
化学式
C24H26FN5O3
mdl
——
分子量
451.5
InChiKey
VZZYXLOQECVTHZ-WHLIDYPQSA-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
  • 重原子数:
    33
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    88.6
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • Heterocyclic degronimers for target protein degradation
    申请人:C4 Therapeutics, Inc.
    公开号:US10646575B2
    公开(公告)日:2020-05-12
    This invention provides heterocyclic compounds that bind to E3 Ubiquitin Ligase (typically through cereblon) (“Degrons”), which can be used as is or linked to a Targeting Ligand for a selected Target Protein for therapeutic purposes and methods of use and compositions thereof as well as methods for their preparation.
    本发明提供了能与 E3 泛素连接酶(通常是通过脑龙)("Degrons")结合的杂环化合物,这些杂环化合物可用于治疗目的或与选定靶蛋白的靶向配体相连接,并提供了其使用方法和组合物及其制备方法。
  • Spirocyclic degronimers for target protein degradation
    申请人:C4 Therapeutics, Inc.
    公开号:US10660968B2
    公开(公告)日:2020-05-26
    This invention provides compounds that have spirocyclic E3 Ubiquitin Ligase targeting moieties (Degrons), which can be used as is or linked to a targeting ligand for a protein that has been selected for in vivo degradation, and methods of use and compositions thereof as well as methods for their preparation.
    本发明提供了具有螺环 E3 泛素连接酶靶向基团(Degrons)的化合物,这些化合物可单独使用,也可与用于体内降解的蛋白质的靶向配体连接,本发明还提供了其使用方法和组合物及其制备方法。
  • C3-carbon linked glutarimide degronimers for target protein degradation
    申请人:C4 Therapeutics, Inc.
    公开号:US10849982B2
    公开(公告)日:2020-12-01
    This invention provides Degronimers that have carbon-linked E3 Ubiquitin Ligase targeting moieties (Degrons), which can be linked to a targeting ligand for a protein that has been selected for in vivo degradation, and methods of use and compositions thereof as well as methods for their preparation.
    本发明提供了具有连接的 E3 泛素连接酶靶向分子(Degronimers)的 Degronimers(Degronons),这些 Degronimers 可与用于体内降解的蛋白质的靶向配体连接,本发明还提供了其使用方法和组合物及其制备方法。
  • AMINE-LINKED C3-GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN DEGRADATION
    申请人:C4 Therapeutics, Inc.
    公开号:US20190076539A1
    公开(公告)日:2019-03-14
    This invention provides amine-linked C 3 -glutarimide Degronimers and Degrons for therapeutic applications as described further herein, and methods of use and compositions thereof as well as methods for their preparation.
  • HETEROCYCLIC DEGRONIMERS FOR TARGET PROTEIN DEGRADATION
    申请人:C4 Therapeutics, Inc.
    公开号:US20190076541A1
    公开(公告)日:2019-03-14
    This invention provides heterocyclic compounds that bind to E3 Ubiquitin Ligase (typically through cereblon) (“Degrons”), which can be used as is or linked to a Targeting Ligand for a selected Target Protein for therapeutic purposes and methods of use and compositions thereof as well as methods for their preparation.
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