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(S)-4-(2-Hydroxy-3-((2-(morpholine-4-carboxamido)ethyl)amino)propoxy)phenyl 2,2-dimethyloctanoate

中文名称
——
中文别名
——
英文名称
(S)-4-(2-Hydroxy-3-((2-(morpholine-4-carboxamido)ethyl)amino)propoxy)phenyl 2,2-dimethyloctanoate
英文别名
[4-[(2S)-2-hydroxy-3-[2-(morpholine-4-carbonylamino)ethylamino]propoxy]phenyl] 2,2-dimethyloctanoate
(S)-4-(2-Hydroxy-3-((2-(morpholine-4-carboxamido)ethyl)amino)propoxy)phenyl 2,2-dimethyloctanoate化学式
CAS
——
化学式
C26H43N3O6
mdl
——
分子量
493.6
InChiKey
QNCASDDILJZBAI-NRFANRHFSA-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):
    3.5
  • 重原子数:
    35
  • 可旋转键数:
    16
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    109
  • 氢给体数:
    3
  • 氢受体数:
    7

文献信息

  • METHOD OF IMPROVING COGNITION AND SOCIAL BEHAVIOR IN HUMANS HAVING DEFICITS THEREIN DUE TO NEURODEGENERATIVE DISORDERS AND COMPOUNDS AND COMPOSITIONS THEREFOR
    申请人:Shamloo Mehrdad
    公开号:US20160184315A1
    公开(公告)日:2016-06-30
    A β 1 -ADR agonist prodrug compound, which is hydrolysable in vivo to release a β1-ADR agonist compound, and which prodrug compound contains a group which imparts greater lipophilicity and CNS bioavailability to the prodrug compound relative to the β1-ADR agonist compound.
    一种β1-ADR激动剂前药化合物,其在体内可解释放出β1-ADR激动剂化合物,该前药化合物含有一种基团,相对于β1-ADR激动剂化合物,赋予前药化合物更大的亲脂性和中枢神经系统生物利用度。
  • Adrenergic receptor modulating compounds and methods of using the same
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US11173144B2
    公开(公告)日:2021-11-16
    Adrenergic receptor modulating compounds and methods of using the same are provided. Also provided are methods of treating a subject for a disease or condition associated with an adrenergic receptor including administering a therapeutically effective amount of the subject compound. Aspects of the disclosure include a method of modulating an inflammatory pathway in a cell, such as the production of TNF-alpha in the cell. The method can include contacting a cell with β1-selective adrenergic receptor modulating compound to selectively activate a cAMP pathway over a beta-arrestin pathway in the cell. Pharmaceutical compositions and kits which include the subject compounds are provided.
    提供了肾上腺素能受体调节化合物及其使用方法。还提供了治疗与肾上腺素能受体相关的疾病或病症的方法,包括施用治疗有效量的主体化合物。本公开的各个方面包括一种调节细胞中炎症通路的方法,如细胞中 TNF-α 的产生。该方法可包括使细胞与β1选择性肾上腺素能受体调节化合物接触,以选择性地激活细胞中的cAMP通路而不是β-arrestin通路。本发明还提供了包括上述化合物的药物组合物和试剂盒。
  • ADRENERGIC RECEPTOR MODULATING COMPOUNDS AND METHODS OF USING THE SAME
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US20200237724A1
    公开(公告)日:2020-07-30
    Adrenergic receptor modulating compounds and methods of using the same are provided. Also provided are methods of treating a subject for a disease or condition associated with an adrenergic receptor including administering a therapeutically effective amount of the subject compound. Aspects of the disclosure include a method of modulating an inflammatory pathway in a cell, such as the production of TNF-alpha in the cell. The method can include contacting a cell with β1-selective adrenergic receptor modulating compound to selectively activate a cAMP pathway over a beta-arrestin pathway in the cell. Pharmaceutical compositions and kits which include the subject compounds are provided.
  • US9849134B2
    申请人:——
    公开号:US9849134B2
    公开(公告)日:2017-12-26
  • [EN] METHOD OF IMPROVING COGNITION AND SOCIAL BEHAVIOR IN HUMANS HAVING DEFICITS THEREIN DUE TO NEUROLOGICAL DISORDERS AND COMPOUNDS AND COMPOSITIONS THEREFOR<br/>[FR] PROCEDE D'AMELIORATION DE LA COGNITION ET DU COMPORTEMENT SOCIAL CHEZ DES HUMAINES QUI EN SONT DEFICIENTS CONSECUTIFS A DE TROUBLES NEUROLOGIQUES ET COMPOSES ET COMPOSITIONS A CET EFFET
    申请人:UNIV LELAND STANFORD JUNIOR
    公开号:WO2015126915A2
    公开(公告)日:2015-08-27
    A β1-ADR agonist prodrug compound, which is hydrolysable in vivo to release a β1-ADR agonist compound, and which prodrug compound contains a group which imparts greater lipophilicity and CNS bioavailability to the prodrug compound relative to the β1-ADR agonist compound.
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