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6-phenoxyquinazoline-2,4-diamine | 38711-03-4

中文名称
——
中文别名
——
英文名称
6-phenoxyquinazoline-2,4-diamine
英文别名
6-phenoxy-quinazoline-2,4-diamine
6-phenoxyquinazoline-2,4-diamine化学式
CAS
38711-03-4
化学式
C14H12N4O
mdl
——
分子量
252.275
InChiKey
WJNBRLBGEBNJNM-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

物化性质

  • 沸点:
    535.9±58.0 °C(Predicted)
  • 密度:
    1.362±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    87
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    参考文献:
    名称:
    Discovery and Optimization of 2,4-Diaminoquinazoline Derivatives as a New Class of Potent Dengue Virus Inhibitors
    摘要:
    The results of a high-throughput screening assay using the DENV-2 replicon showed that the 2,4-diaminoquinazoline derivative 4a has a high dengue virus inhibitory activity (EC50 = 0.15 mu M). A series of 2,4-diaminoquinazoline derivatives based on 4a as a lead compound were synthesized and subjected to structure-antidengue activity relationship studies. Among the series of 2,4-diaminoquinazoline derivative probed, 4o was observed to display both the highest antiviral potency (EC50 = 2.8 nM, SI > 1000) and an excellent pharmacokinetic profile.
    DOI:
    10.1021/jm2015952
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文献信息

  • Discovery and Optimization of 2,4-Diaminoquinazoline Derivatives as a New Class of Potent Dengue Virus Inhibitors
    作者:Bo Chao、Xian-Kun Tong、Wei Tang、De-Wen Li、Pei-Lan He、Jean-Michel Garcia、Li-Min Zeng、An-Hui Gao、Li Yang、Jia Li、Fa-Jun Nan、Michael Jacobs、Ralf Altmeyer、Jian-Ping Zuo、You-Hong Hu
    DOI:10.1021/jm2015952
    日期:2012.4.12
    The results of a high-throughput screening assay using the DENV-2 replicon showed that the 2,4-diaminoquinazoline derivative 4a has a high dengue virus inhibitory activity (EC50 = 0.15 mu M). A series of 2,4-diaminoquinazoline derivatives based on 4a as a lead compound were synthesized and subjected to structure-antidengue activity relationship studies. Among the series of 2,4-diaminoquinazoline derivative probed, 4o was observed to display both the highest antiviral potency (EC50 = 2.8 nM, SI > 1000) and an excellent pharmacokinetic profile.
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