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5-(4-methoxynaphthalen-1-yl)-2H-tetrazole | 651769-45-8

中文名称
——
中文别名
——
英文名称
5-(4-methoxynaphthalen-1-yl)-2H-tetrazole
英文别名
——
5-(4-methoxynaphthalen-1-yl)-2H-tetrazole化学式
CAS
651769-45-8
化学式
C12H10N4O
mdl
——
分子量
226.238
InChiKey
HNHKYDYCJVAJHG-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):
    2.4
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    63.7
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • MACROCYCLIC HEPATITIS C SERINE PROTEASE INHIBITORS
    申请人:Miao Zhenwei
    公开号:US20090304629A1
    公开(公告)日:2009-12-10
    The present invention relates to compounds of Formula I, II or III, or a pharmaceutically acceptable salt, ester, or prodrug, thereof: wherein W is a substituted or unsubstituted heterocyclic ring system. The compounds inhibit serine protease activity, particularly the activity of hepatitis c virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis c virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
    本发明涉及I、II或III式化合物,或其药学上可接受的盐、酯或前药: 其中W是取代或未取代的杂环环系。这些化合物能够抑制丝氨酸蛋白酶活性,特别是丙型肝炎病毒(HCV)NS3-NS4A蛋白酶的活性。因此,本发明的化合物干扰了丙型肝炎病毒的生命周期,也可用作抗病毒剂。本发明还涉及包括上述化合物的制药组合物,用于治疗患有HCV感染的受试者。本发明还涉及通过给予包括本发明的化合物的制药组合物来治疗受试者的HCV感染的方法。
  • TETRAZOLYL MACROCYCLIC HEPATITIS C SERINE PROTEASE INHIBITORS
    申请人:Sun Ying
    公开号:US20090035271A1
    公开(公告)日:2009-02-05
    The present invention relates to compounds of Formula I, II, III or IV, or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising a compound of the present invention.
  • TETRAZOLYL ACYCLIC HEPATITIS C SERINE PROTEASE INHIBITORS
    申请人:Sun Ying
    公开号:US20090035268A1
    公开(公告)日:2009-02-05
    The present invention relates to compounds of Formula I, II, III or IV, or pharmaceutically acceptable salts, esters or prodrugs thereof: which can inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising a compound of the present invention.
  • US7601709B2
    申请人:——
    公开号:US7601709B2
    公开(公告)日:2009-10-13
  • US8124584B2
    申请人:——
    公开号:US8124584B2
    公开(公告)日:2012-02-28
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