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1-Ethyl-6-methyl-3-pyridin-2-ylpyrimido[5,4-e][1,2,4]triazine-5,7-dione

中文名称
——
中文别名
——
英文名称
1-Ethyl-6-methyl-3-pyridin-2-ylpyrimido[5,4-e][1,2,4]triazine-5,7-dione
英文别名
——
1-Ethyl-6-methyl-3-pyridin-2-ylpyrimido[5,4-e][1,2,4]triazine-5,7-dione化学式
CAS
——
化学式
C13H12N6O2
mdl
——
分子量
284.27
InChiKey
QVCYRUGIQZXLCC-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):
    0.6
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    90.6
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Inhibitors of HIV-1 integrase multimerization
    申请人:Institute for Cancer Research
    公开号:US10888564B2
    公开(公告)日:2021-01-12
    The disclosure generally relates to compounds of formulas (I) and (II)7 including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV-1 integrase, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.
    本公开一般涉及式(I)和(II)7化合物,包括治疗人类免疫缺陷病毒(HIV)感染的组合物和方法。本公开提供了 HIV-1 整合酶的新型抑制剂、含有此类化合物的药物组合物以及使用这些化合物治疗 HIV 感染的方法。
  • INHIBITORS OF HIV-1 INTEGRASE MULTIMERIZATION
    申请人:Institute for Cancer Research d/b/a The Research Institute of Fox Chase Cancer Center
    公开号:US20210113570A1
    公开(公告)日:2021-04-22
    The disclosure generally relates to compounds, compositions, and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV-1 integrase, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.
  • [EN] INHIBITORS OF HIV-1 INTEGRASE MULTIMERIZATION<br/>[FR] INHIBITEURS DE LA MULTIMÉRISATION DE L'INTÉGRASE DU VIH -1
    申请人:INSTITUTE FOR CANCER RES D B A THE RES INSTITUTE OF FOX CHASE CANCER CENTER
    公开号:WO2018140762A1
    公开(公告)日:2018-08-02
    The disclosure generally relates to compounds of formulas (I) and (ll)7 including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV-1 integrase, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.
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