摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N4-(2,3-dimethyl-2H-indazol-6-yl)-N2-(4-fluorophenyl)pyrimidine-2,4-diamine | 1572439-47-4

中文名称
——
中文别名
——
英文名称
N4-(2,3-dimethyl-2H-indazol-6-yl)-N2-(4-fluorophenyl)pyrimidine-2,4-diamine
英文别名
4-N-(2,3-dimethylindazol-6-yl)-2-N-(4-fluorophenyl)pyrimidine-2,4-diamine
N<sup>4</sup>-(2,3-dimethyl-2H-indazol-6-yl)-N<sup>2</sup>-(4-fluorophenyl)pyrimidine-2,4-diamine化学式
CAS
1572439-47-4
化学式
C19H17FN6
mdl
——
分子量
348.383
InChiKey
LVOMEPYUKJCUME-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):
    4.1
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    67.7
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    Design, Synthesis and Biological Evaluation of Pazopanib Derivatives as Antitumor Agents
    摘要:
    A novel series of pazopanib derivatives were designed, synthesized, and evaluated for their inhibitory activity against a series of kinases including VEGFR‐2, EGFR, AKT1, ALK1, and ABL1. The anti‐angiogenic activities ex vivo of some compounds were also investigated. Compounds P2d and P2e demonstrated outstanding inhibitory activity against VEGFR‐2 and ABL1 and higher anti‐angiogenic activity compared with Pazopanib, the reference standard. These two compounds (P2d and P2e) could be used as novel lead compounds for further development of anticancer agents.
    DOI:
    10.1111/cbdd.12243
点击查看最新优质反应信息

文献信息

  • Design, Synthesis and Biological Evaluation of Pazopanib Derivatives as Antitumor Agents
    作者:Yuping Jia、Jian Zhang、Jinhong Feng、Fuming Xu、Huili Pan、Wenfang Xu
    DOI:10.1111/cbdd.12243
    日期:2014.3
    A novel series of pazopanib derivatives were designed, synthesized, and evaluated for their inhibitory activity against a series of kinases including VEGFR‐2, EGFR, AKT1, ALK1, and ABL1. The anti‐angiogenic activities ex vivo of some compounds were also investigated. Compounds P2d and P2e demonstrated outstanding inhibitory activity against VEGFR‐2 and ABL1 and higher anti‐angiogenic activity compared with Pazopanib, the reference standard. These two compounds (P2d and P2e) could be used as novel lead compounds for further development of anticancer agents.
查看更多