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N-{3-[4-(5-chloro-7-cyclohexyl[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy]propyl}-N,N-dimethylamine | 1021298-69-0

中文名称
——
中文别名
——
英文名称
N-{3-[4-(5-chloro-7-cyclohexyl[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy]propyl}-N,N-dimethylamine
英文别名
3-[4-(5-Chloro-7-cyclohexyl[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy]-N,N-dimethyl-1-propanamine;3-[4-(5-chloro-7-cyclohexyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy]-N,N-dimethylpropan-1-amine
N-{3-[4-(5-chloro-7-cyclohexyl[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy]propyl}-N,N-dimethylamine化学式
CAS
1021298-69-0
化学式
C22H26ClF2N5O
mdl
——
分子量
449.931
InChiKey
LNZZPSWIOUPGHV-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):
    5.5
  • 重原子数:
    31
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    55.6
  • 氢给体数:
    0
  • 氢受体数:
    7

文献信息

  • 6-[(Substituted)phenyl]triazolopyrimidines as anticancer agents
    申请人:Zhang Nan
    公开号:US20050090508A1
    公开(公告)日:2005-04-28
    This invention relates to certain 6-[(substituted)phenyl]triazolopyrimidine compounds or pharmaceutically acceptable salts thereof, and compositions containing said compounds or pharmaceutically acceptable salts thereof, wherein said compounds are anti-cancer agents useful for the treatment of cancer in mammals. This invention further relates to a method of treating or inhibiting the growth of cancerous tumor cells and associated diseases in a mammal and further provides a method for the treatment or prevention of cancerous tumors that express multiple drug resistance (MDR) or are resistant because of MDR, in a mammal in need thereof which method comprises administering to said mammal an effective amount of said compounds or pharmaceutically acceptable salts thereof. The present invention relates to a method of treating or inhibiting the growth of cancerous tumor cells and associated diseases in a mammal in need thereof by promotion of microtubule polymerization which comprises administering to said mammal an effective amount of said compounds and pharmaceutically acceptable salts thereof.
    本发明涉及某些6-[(取代)苯基]三唑嘧啶化合物或其药学上可接受的盐,以及含有该化合物或其药学上可接受的盐的组合物,其中该化合物是对哺乳动物癌症治疗有用的抗癌剂。本发明还涉及一种用于治疗或抑制哺乳动物中癌细胞肿瘤的生长和相关疾病的方法,并进一步提供了一种用于治疗或预防因多药耐药(MDR)而表达多重药物抗性的癌性肿瘤的方法,该方法包括向所述哺乳动物中需要的部位注射所述化合物或其药学上可接受的盐的有效量。本发明还涉及一种通过促进微管聚合来治疗或抑制哺乳动物中癌细胞肿瘤的生长和相关疾病的方法,该方法包括向所述哺乳动物中注射所述化合物及其药学上可接受的盐的有效量。
  • 6- [(SUBSTITUTED)PHENYL] TRIAZOLOPYRIMIDINES AS ANTICANCER AGENTS
    申请人:Wyeth Holdings Corporation
    公开号:EP1680425B1
    公开(公告)日:2007-01-10
  • US7507739B2
    申请人:——
    公开号:US7507739B2
    公开(公告)日:2009-03-24
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