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N-[2-(4-ethylphenoxy)ethyl]-2-methylpropan-2-amine

中文名称
——
中文别名
——
英文名称
N-[2-(4-ethylphenoxy)ethyl]-2-methylpropan-2-amine
英文别名
——
N-[2-(4-ethylphenoxy)ethyl]-2-methylpropan-2-amine化学式
CAS
——
化学式
C14H23NO
mdl
MFCD01909172
分子量
221.34
InChiKey
SXEALRYVJDSJCL-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):
    3.2
  • 重原子数:
    16
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.571
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • Compounds and methods for the targeted degradation of androgen receptor
    申请人:Arvinas Operations, Inc.
    公开号:US10844021B2
    公开(公告)日:2020-11-24
    The present disclosure relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.
    本公开涉及双功能化合物,它们可用于降解和(抑制)雄激素受体。特别是,本公开涉及的化合物一端含有与 E3 泛素连接酶结合的脑龙配体,另一端含有与雄激素受体结合的分子,这样雄激素受体就被置于泛素连接酶附近,从而实现对雄激素受体的降解(和抑制)。本公开的化合物具有广泛的药理活性,与雄激素受体的降解/抑制作用相一致。
  • COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF ANDROGEN RECEPTOR
    申请人:Arvinas Operations, Inc.
    公开号:US20210040044A1
    公开(公告)日:2021-02-11
    The present disclosure relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.
  • INDOLE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS
    申请人:Arvinas Operations, Inc.
    公开号:US20210040081A1
    公开(公告)日:2021-02-11
    The present disclosure relates to compounds and a pharmaceutically acceptable salt thereof, compositions, combinations and medicaments containing the compounds, and processes for their preparation. The disclosure also relates to the use of the compounds, combinations, compositions and medicaments, for example as inhibitors of the activity of the estrogen receptor, including degrading the estrogen receptor, the treatment of diseases and conditions mediated by the estrogen receptor.
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