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4-chloro-6-((2-(4-((3,3-difluoroazetidin-1-yl)carbonyl)-2-fluorophenyl)pyrrolidin-1-yl)carbonyl)benzene-1,3-diol | 1023885-31-5

中文名称
——
中文别名
——
英文名称
4-chloro-6-((2-(4-((3,3-difluoroazetidin-1-yl)carbonyl)-2-fluorophenyl)pyrrolidin-1-yl)carbonyl)benzene-1,3-diol
英文别名
[4-[1-(5-Chloro-2,4-dihydroxybenzoyl)pyrrolidin-2-yl]-3-fluorophenyl]-(3,3-difluoroazetidin-1-yl)methanone
4-chloro-6-((2-(4-((3,3-difluoroazetidin-1-yl)carbonyl)-2-fluorophenyl)pyrrolidin-1-yl)carbonyl)benzene-1,3-diol化学式
CAS
1023885-31-5
化学式
C21H18ClF3N2O4
mdl
——
分子量
454.833
InChiKey
RGIPRGBPJZZFNL-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):
    3.9
  • 重原子数:
    31
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    81.1
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • Methods of treating a metabolic syndrome by modulating heat shock protein (HSP) 90-beta
    申请人:Berg LLC
    公开号:US10023864B2
    公开(公告)日:2018-07-17
    The invention provides HSP90β inhibitors comprising an antisense oligonucleotide targeting HSP90β, pharmaceutical compositions comprising said inhibitors and methods of treatment of a metabolic syndrome by administering said HSP90β inhibitors to a subject in need thereof. The antisense oligonucleotides may be targeted to skeletal muscle.
    本发明提供了由靶向 HSP90β 的反义寡核苷酸组成的 HSP90β 抑制剂、由所述抑制剂组成的药物组合物以及通过向有需要的受试者施用所述 HSP90β 抑制剂来治疗代谢综合征的方法。反义寡核苷酸可靶向骨骼肌。
  • Targeted therapeutics
    申请人:Madrigal Pharmaceuticals, Inc.
    公开号:US10232049B2
    公开(公告)日:2019-03-19
    The present invention provides pharmacological compounds including an effector moiety conjugated to a binding moiety that directs the effector moiety to a biological target of interest. Likewise, the present invention provides compositions, kits, and methods (e.g., therapeutic, diagnostic, and imaging) including the compounds. The compounds can be described as a protein interacting binding moiety-drug conjugate (SDC-TRAP) compounds, which include a protein interacting binding moiety and an effector moiety. For example, in certain embodiments directed to treating cancer, the SDC-TRAP can include an Hsp90 inhibitor conjugated to a cytotoxic agent as the effector moiety.
    本发明提供的药理化合物包括与结合基团共轭的效应分子,该结合基团可将效应分子导向感兴趣的生物靶标。同样,本发明还提供了包括这些化合物的组合物、试剂盒和方法(如治疗、诊断和成像)。这些化合物可被描述为蛋白质相互作用结合分子-药物共轭物(SDC-TRAP)化合物,其中包括蛋白质相互作用结合分子和效应分子。例如,在某些用于治疗癌症的实施方案中,SDC-TRAP 可包括与细胞毒剂共轭的 Hsp90 抑制剂作为效应分子。
  • Combination therapies comprising targeted therapeutics
    申请人:MADRIGAL PHARMACEUTICALS, INC.
    公开号:US11491145B2
    公开(公告)日:2022-11-08
    The present invention provides pharmacological compounds including an effector moiety conjugated to a binding moiety that directs the effector moiety to a biological target of interest. Likewise, the present invention provides compositions, kits, and methods (e.g., therapeutic, diagnostic, and imaging) including the compounds. The compounds can be described as a protein interacting binding moiety-drug conjugate (SDC-TRAP) compounds, which include a protein interacting binding moiety and an effector moiety. For example, in certain embodiments directed to treating cancer, the SDC-TRAP can include an Hsp90 inhibitor conjugated to a cytotoxic agent as the effector moiety.
    本发明提供的药理化合物包括与结合基团共轭的效应分子,该结合基团可将效应分子导向感兴趣的生物靶标。同样,本发明还提供了包括这些化合物的组合物、试剂盒和方法(如治疗、诊断和成像)。这些化合物可被描述为蛋白质相互作用结合分子-药物共轭物(SDC-TRAP)化合物,其中包括蛋白质相互作用结合分子和效应分子。例如,在某些用于治疗癌症的实施方案中,SDC-TRAP 可包括与细胞毒剂共轭的 Hsp90 抑制剂作为效应分子。
  • METHODS OF TREATING A METABOLIC SYNDROME BY MODULATING HEAT SHOCK PROTEIN (HSP) 90-BETA
    申请人:Berg LLC
    公开号:US20150353930A1
    公开(公告)日:2015-12-10
    The invention provides HSP90β inhibitors comprising an antisense oligonucleotide targeting HSP90β, pharmaceutical compositions comprising said inhibitors and methods of treatment of a metabolic syndrome by administering said HSP90β inhibitors to a subject in need thereof. The antisense oligonucleotides may be targeted to skeletal muscle.
  • TARGETED THERAPEUTICS
    申请人:Chimmanamada Dinesh U.
    公开号:US20170056510A1
    公开(公告)日:2017-03-02
    The present invention provides pharmacological compounds including an effector moiety conjugated to a binding moiety that directs the effector moiety to a biological target of interest. Likewise, the present invention provides compositions, kits, and methods (e.g., therapeutic, diagnostic, and imaging) including the compounds. The compounds can be described as a protein interacting binding moiety-drug conjugate (SDC-TRAP) compounds, which include a protein interacting binding moiety and an effector moiety. For example, in certain embodiments directed to treating cancer, the SDC-TRAP can include an Hsp90 inhibitor conjugated to a cytotoxic agent as the effector moiety.
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