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3,6,9-Triaminoacridin | 42832-91-7

中文名称
——
中文别名
——
英文名称
3,6,9-Triaminoacridin
英文别名
acridine-3,6,9-triamine;Acridine, 3,6,9-triamino-
3,6,9-Triaminoacridin化学式
CAS
42832-91-7
化学式
C13H12N4
mdl
——
分子量
224.265
InChiKey
KHOZAFGVIMGHAD-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):
    1.1
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    91
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • [EN] NOVEL HDMX INHIBITORS AND THEIR USE FOR CANCER TREATMENT<br/>[FR] NOUVEAUX INHIBITEURS HDMX ET LEUR UTILISATION DANS LE TRAITEMENT DU CANCER
    申请人:MIRX PHARMACEUTICALS LLC
    公开号:WO2015153535A1
    公开(公告)日:2015-10-08
    The present invention provides for novel acridine-like class of compounds that have demonstrated efficiency in treating cancer. The compounds of the present invention have demonstrated efficacy in binding to and antagonizing the activity of the p53 repressor, HDMX. Once administered to a cell, the compounds of the present invention bind HDMX, thereby allowing p53 to induce apoptosis of the cancerous cell. A combination of this class of compounds along with Nutlin3 provides a novel approach to treat cancers.
    本发明提供了一种新型的类似于吖啶的化合物,已经证明可以有效地治疗癌症。本发明的化合物已经证明在结合并拮抗p53抑制剂HDMX的活性方面具有疗效。一旦这些化合物被注入细胞,它们会与HDMX结合,从而使p53诱导癌细胞凋亡。将这类化合物与Nutlin3结合使用可以提供一种治疗癌症的新方法。
  • HDMX inhibitors and their use for cancer treatment
    申请人:MIRX PHARMACEUTICALS, LLC
    公开号:US10183912B2
    公开(公告)日:2019-01-22
    The present invention provides for novel acridine-like class of compounds that have demonstrated efficiency in treating cancer. The compounds of the present invention have demonstrated efficacy in binding to and antagonizing the activity of the p53 repressor, HDMX. Once administered to a cell, the compounds of the present invention bind HDMX, thereby allowing p53 to induce apoptosis of the cancerous cell. A combination of this class of compounds along with Nutlin3 provides a novel approach to treat cancers.
    本发明提供了新型吖啶类化合物,这些化合物已证明可有效治疗癌症。本发明的化合物在与 p53 抑制剂 HDMX 结合并拮抗其活性方面具有显著疗效。一旦给细胞用药,本发明的化合物就会与 HDMX 结合,从而使 p53 能够诱导癌细胞凋亡。这类化合物与 Nutlin3 的结合提供了一种治疗癌症的新方法。
  • METHOD FOR ASSESSING VIABLE CELLS AND THE USE OF N-(7-DIMETHYLAMINO-4-METHYL-3-COUMARINYL)-MALEIMIDE (DACM) OR N-(9-ACRIDINYL)MALEIMIDE (NAM) FOR ASSESSMENT OF APOPTOSIS.
    申请人:Chemometec A/S
    公开号:EP2312943B1
    公开(公告)日:2019-11-06
  • NOVEL HDMX INHIBITORS AND THEIR USE FOR CANCER TREATMENT
    申请人:MIRX PHARMACEUTICALS, LLC
    公开号:US20170022166A1
    公开(公告)日:2017-01-26
    The present invention provides for novel acridine-like class of compounds that have demonstrated efficiency in treating cancer. The compounds of the present invention have demonstrated efficacy in binding to and antagonizing the activity of the p53 repressor, HDMX. Once administered to a cell, the compounds of the present invention bind HDMX, thereby allowing p53 to induce apoptosis of the cancerous cell. A combination of this class of compounds along with Nutlin3 provides a novel approach to treat cancers.
  • US9128097B2
    申请人:——
    公开号:US9128097B2
    公开(公告)日:2015-09-08
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