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4-(苯甲基)-1-氧杂-4,9-二氮杂螺[5.5]十一烷 | 151096-97-8

中文名称
4-(苯甲基)-1-氧杂-4,9-二氮杂螺[5.5]十一烷
中文别名
——
英文名称
4-Benzyl-1-oxa-4,9-diazaspiro[5.5]undecane
英文别名
——
4-(苯甲基)-1-氧杂-4,9-二氮杂螺[5.5]十一烷化学式
CAS
151096-97-8
化学式
C15H22N2O
mdl
——
分子量
246.35
InChiKey
AWHHKKHMEIVLFM-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

物化性质

  • 密度:
    1.11

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    24.5
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF ANDROGEN RECEPTOR
    申请人:Arvinas, Inc.
    公开号:US20180099940A1
    公开(公告)日:2018-04-12
    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,其用于降解和(抑制)雄激素受体。具体而言,本公开涉及包含一端结合到E3泛素连接酶的谷氨酰腺苷环配体,另一端结合到雄激素受体的部分的化合物,使得雄激素受体与泛素连接酶靠近,以实现雄激素受体的降解(和抑制)。本公开展示了与根据本公开涉及的化合物相关的广泛的药理活性范围,与雄激素受体的降解/抑制一致。
  • HETEROCYCLIC SPIRO COMPOUNDS AS MAGL INHIBITORS
    申请人:PFIZER INC.
    公开号:US20180208608A1
    公开(公告)日:2018-07-26
    The present invention provides, in part, heterocyclic spiro compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.
    本发明部分提供具有下式I的杂环螺化合物: 以及它们的药用盐;其制备过程;用于其制备的中间体;以及包含这些化合物或盐的药物组合物,以及它们用于治疗MAGL介导的疾病和障碍,例如疼痛、炎症性障碍、抑郁症、焦虑症、阿尔茨海默病、代谢障碍、中风或癌症的使用。
  • 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。
  • Heterocyclic spiro compounds as MAGL inhibitors
    申请人:Pfizer Inc.
    公开号:US10858373B2
    公开(公告)日:2020-12-08
    The present invention provides, in part, heterocyclic spiro compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.
    本发明部分提供了式 I 的杂环螺化合物: 及其药学上可接受的盐;制备过程;制备过程中使用的中间体;含有此类化合物或盐的组合物,以及它们在治疗 MAGL 介导的疾病和失调(包括疼痛、炎症性失调、抑郁、焦虑、阿尔茨海默病、代谢性失调、中风或癌症等)方面的用途。
  • [EN] HETEROCYCLIC SPIRO COMPOUNDS AS MAGL INHIBITORS<br/>[FR] COMPOSÉS SPIRO HÉTÉROCYCLIQUES UTILISÉS EN TANT QU'INHIBITEURS DE MAGL
    申请人:PFIZER
    公开号:WO2018134698A1
    公开(公告)日:2018-07-26
    The present invention provides, in part, heterocyclic spiro compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.
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