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1-[(2R,3R,4S,5R)-5-acetyl-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-aminopyrimidin-2-one

中文名称
——
中文别名
——
英文名称
1-[(2R,3R,4S,5R)-5-acetyl-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-aminopyrimidin-2-one
英文别名
——
1-[(2R,3R,4S,5R)-5-acetyl-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-aminopyrimidin-2-one化学式
CAS
——
化学式
C11H15N3O6
mdl
——
分子量
285.25
InChiKey
MTRDIPBJXPOSNU-LOKLDPHHSA-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):
    -3.1
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    146
  • 氢给体数:
    4
  • 氢受体数:
    6

文献信息

  • 4'-substituted nucleoside derivatives as inhibitors of HCV RNA replication
    申请人:——
    公开号:US20030236216A1
    公开(公告)日:2003-12-25
    The present invention relates to the use of nucleoside derivatives of formula I 1 wherein B signifies a 9-purinyl residue B1 of formula 2 or a 1-pyrimidyl residue B2 of formula 3 wherein the symbols are as defined in the specification, and of pharmaceutically acceptable salts thereof; for the treatment of diseases mediated by the Hepatitis C Virus (HCV), for the preparation of a medicament for such treatment and to pharmaceutical compositions containing such compounds.
    本发明涉及使用公式I1的核苷衍生物,其中B表示公式2的9-嘌呤基残基B1或公式3的1-嘧啶基残基B2,其中符号如规范中所定义,并且其药物可接受的盐;用于治疗由丙型肝炎病毒(HCV)介导的疾病,用于制备用于该治疗的药物以及含有这些化合物的制药组合物。
  • 4'-SUBSTITUDED NUCLEOSIDES FOR THE TREATMENT OF DISEASES MEDIATED BY THE HEPATITIS C VIRUS
    申请人:F. HOFFMANN-LA ROCHE AG
    公开号:EP1404347B1
    公开(公告)日:2006-01-18
  • 4'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AS INHIBITORS OF HCV RNA REPLICATION
    申请人:Devos Rene Robert
    公开号:US20100003213A1
    公开(公告)日:2010-01-07
    The present invention relates to the use of nucleoside derivatives of formula Ia wherein the symbols are as defined in the specification, and of pharmaceutically acceptable salts thereof and to pharmaceutical compositions containing such compounds.
  • 4'-Substituted Nucleoside Derivatives as Inhibitors of HCV RNA Replication
    申请人:Martin Joseph Armstrong
    公开号:US20100004192A1
    公开(公告)日:2010-01-07
    The present invention relates to the use of nucleoside derivatives of formula Ia wherein the symbols are as defined in the specification, and of pharmaceutically acceptable salts thereof and to pharmaceutical compositions containing such compounds.
  • US6784166B2
    申请人:——
    公开号:US6784166B2
    公开(公告)日:2004-08-31
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