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2-butoxy-9-(pyrazin-2-ylmethyl)-8-methoxyadenine | 473930-05-1

中文名称
——
中文别名
——
英文名称
2-butoxy-9-(pyrazin-2-ylmethyl)-8-methoxyadenine
英文别名
2-Butoxy-8-methoxy-9-(pyrazin-2-ylmethyl)purin-6-amine
2-butoxy-9-(pyrazin-2-ylmethyl)-8-methoxyadenine化学式
CAS
473930-05-1
化学式
C15H19N7O2
mdl
——
分子量
329.362
InChiKey
ISZCUOGGYQFEKO-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:
    24
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    114
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • Novel adenne derivatives
    申请人:——
    公开号:US20040132748A1
    公开(公告)日:2004-07-08
    This invention relates to an adenine derivative, a tautomer thereof, or a pharmaceutically acceptable salt thereof represented by general formula (I): 1 wherein X represents NR 3 (wherein R 3 represents a hydrogen atom or C 1-3 alkyl) or the like; R 1 represents substituted or unsubstituted alkyl or the like; R 2 represents hydroxyl or the like; and Y represents a substituted or unsubstituted aromatic hetero ring or the like. Also, the present invention relates to pharmaceuticals such as an interferon inducer, antiviral agent, anticancer agent, type 2 helper T cell selective immune response inhibitor, antiallergic agent, and immune response modulator comprising the above derivative as an active ingredient.
    本发明涉及一种由通式(I)表示的腺嘌呤生物、其互变异构体或其药学上可接受的盐,其中X代表NR3(其中R3代表氢原子或C1-3烷基)或类似物;R1代表取代或未取代的烷基或类似物;R2代表羟基或类似物;Y代表取代或未取代的芳香杂环或类似物。此外,本发明还涉及将上述衍生物作为活性成分的药物,例如干扰素诱导剂、抗病毒剂、抗癌剂、2型辅助T细胞选择性免疫反应抑制剂、抗过敏剂和免疫反应调节剂。
  • Novel adenine derivatives
    申请人:Isobe Yoshiaki
    公开号:US20070037832A1
    公开(公告)日:2007-02-15
    This invention relates to an adenine derivative, a tautomer thereof, or a pharmaceutically acceptable salt thereof represented by general formula (I): wherein X represents NR 3 (wherein R 3 represents a hydrogen atom or C 1-3 alkyl) or the like; R 1 represents substituted or unsubstituted alkyl or the like; R 2 represents hydroxyl or the like; and Y represents a substituted or unsubstituted aromatic hetero ring or the like. Also, the present invention relates to pharmaceuticals such as an interferon inducer, antiviral agent, anticancer agent, type 2 helper T cell selective immune response inhibitor, antiallergic agent, and immune response modulator comprising the above derivative as an active ingredient.
    本发明涉及一种腺嘌呤生物,其互变异构体或药学上可接受的盐,由下式表示:其中X代表NR3(其中R3代表氢原子或C1-3烷基)或类似物;R1代表取代或未取代的烷基或类似物;R2代表羟基或类似物;Y代表取代或未取代的芳香杂环或类似物。此外,本发明涉及上述衍生物作为活性成分的制备干扰素诱导剂、抗病毒剂、抗癌剂、选择性抑制2型辅助T细胞免疫反应抑制剂、抗过敏剂和免疫反应调节剂等药物。
  • NOVEL ADENINE DERIVATIVES
    申请人:Dainippon Sumitomo Pharma Co., Ltd.
    公开号:EP1386923B1
    公开(公告)日:2008-08-13
  • US7157465B2
    申请人:——
    公开号:US7157465B2
    公开(公告)日:2007-01-02
  • US7521454B2
    申请人:——
    公开号:US7521454B2
    公开(公告)日:2009-04-21
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