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2-amino-7-propan-2-yl-3H-imidazo[2,1-f][1,2,4]triazin-4-one

中文名称
——
中文别名
——
英文名称
2-amino-7-propan-2-yl-3H-imidazo[2,1-f][1,2,4]triazin-4-one
英文别名
——
2-amino-7-propan-2-yl-3H-imidazo[2,1-f][1,2,4]triazin-4-one化学式
CAS
——
化学式
C8H11N5O
mdl
——
分子量
193.21
InChiKey
DUZZGRRLMKOYRV-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):
    0.1
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    85.3
  • 氢给体数:
    2
  • 氢受体数:
    2

文献信息

  • [EN] ACYCLIC ANTIVIRALS<br/>[FR] ANTIVIRAUX ACYCLIQUES
    申请人:ALIOS BIOPHARMA INC
    公开号:WO2017156262A1
    公开(公告)日:2017-09-14
    Disclosed herein are nucleotide analogs, methods of synthesizing nucleotide analogs and methods of treating diseases and/or conditions such as a HBV and/or HDV and/or HIV infection with one or more nucleotide analogs
    本文揭示了核苷酸类似物,合成核苷酸类似物的方法以及使用一个或多个核苷酸类似物治疗HBV、HDV和/或HIV感染等疾病和/或状况的方法。
  • 2′,4′-bridged nucleosides for HCV infection
    申请人:IDENIX PHARMACEUTICALS LLC
    公开号:US10723754B2
    公开(公告)日:2020-07-28
    Provided herein are compounds, compositions and methods for the treatment of Flaviviridae infections, including HCV infections. In certain embodiments, compounds and compositions of nucleoside derivatives are disclosed, which can be administered either alone or in combination with other anti-viral agents. In certain embodiments, the compounds are 2′,4′-bridged nucleosides which display remarkable efficacy and bioavailability for the treatment of, for example, HCV infection in a human. In certain embodiments, the 2′,4′-bridged nucleosides are of Formula 3001: or a pharmaceutically acceptable salt, solvate, stereoisomeric form, tautomeric form or polymorphic form thereof, where PD, B, W, X, RA, RB, RC and RD are as described herein.
    本文提供了用于治疗黄病毒科感染(包括 HCV 感染)的化合物、组合物和方法。在某些实施方案中,公开了核苷衍生物的化合物和组合物,可单独使用或与其他抗病毒药物联合使用。在某些实施方案中,这些化合物是2′,4′桥接核苷,在治疗人类HCV感染等方面具有显著的疗效和生物利用度。在某些实施方案中,2′,4′桥核苷为式3001: 或其药学上可接受的盐、溶液、立体异构体、同分异构体或多晶型,其中 PD、B、W、X、RA、RB、RC 和 RD 如本文所述。
  • Acyclic antivirals
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:US11472826B2
    公开(公告)日:2022-10-18
    Disclosed herein are nucleotide analogs, methods of synthesizing nucleotide analogs and methods of treating diseases and/or conditions such as a HBV and/or HDV and/or HIV infection with one or more nucleotide analogs.
    本文公开了核苷酸类似物、合成核苷酸类似物的方法以及用一种或多种核苷酸类似物治疗疾病和/或病症(如 HBV 和/或 HDV 和/或 HIV 感染)的方法。
  • ACYCLIC ANTIVIRALS
    申请人:Alios BioPharma, Inc.
    公开号:US20190055273A1
    公开(公告)日:2019-02-21
    Disclosed herein are nucleotide analogs, methods of synthesizing nucleotide analogs and methods of treating diseases and/or conditions such as a HBV and/or HDV and/or HIV infection with one or more nucleotide analogs
  • [EN] 2',4'-BRIDGED NUCLEOSIDES FOR HCV INFECTION<br/>[FR] NUCLÉOSIDES 2', 4'-PONTÉS POUR L'INFECTION PAR LE VHC
    申请人:IDENIX PHARMACEUTICALS INC
    公开号:WO2014066239A1
    公开(公告)日:2014-05-01
    Provided herein are compounds, compositions and methods for the treatment of Flaviviridae infections, including HCV infections. In certain embodiments, compounds and compositions of nucleoside derivatives are disclosed, which can be administered either alone or in combination with other anti-viral agents. In certain embodiments, the compounds are 2',4'-bridged nucleosides which display remarkable efficacy and bioavailability for the treatment of, for example, HCV infection in a human. In certain embodiments, the 2',4'-bridged nucleosides are of Formula 3001:(I) (3001); or a pharmaceutically acceptable salt, solvate, stereoisomeric form, tautomeric form or polymorphic form thereof, where PD, B, W, X, RA, RB, RC and RD are as described herein.
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