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8-fluoroisoquinoline 2-oxide | 1008-23-7

中文名称
——
中文别名
——
英文名称
8-fluoroisoquinoline 2-oxide
英文别名
8-Fluoro-2-oxidoisoquinolin-2-ium
8-fluoroisoquinoline 2-oxide化学式
CAS
1008-23-7
化学式
C9H6FNO
mdl
——
分子量
163.151
InChiKey
DVJNKIMVJOJLJX-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):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    25.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Non-natural nucleotides and dinucleotides
    申请人:——
    公开号:US20040122223A1
    公开(公告)日:2004-06-24
    Nucleotide derivatives of formula (1) are described: wherein: G is a hydrogen atom or an optionally substituted aliphatic, heteroaliphatic, cycloaliphatic, polycycloaliphatic, aromatic or heteroaromatic group or a non-natural nucleoside as defined herein; G′ is a non-natural necleoside as defined herein; n is zero, or the integer 1 or 2; m is zero or the integer 1 or 2; and the salts, solvates, hydrates and N-oxides thereof. The compounds are P2Y receptor agonists and are of use in the prophylaxis and treatment of diseases and disorders involving abnormal secretory mechanisms such as inadequate functioning of mucociliary clearance mechanisms or abnormal tear secretion or in the treatment of diseases involving inappropriate cellular glucose uptake.
    公式(1)的核苷酸衍生物被描述如下:其中:G是氢原子或可选择取代的脂肪,杂脂肪,环脂肪,多环脂肪,芳香或杂芳基团或非天然核苷酸,如此处所定义;G'是如此处所定义的非天然核苷酸;n为零或整数1或2;m为零或整数1或2;以及其盐,溶剂化合物,水合物和N-氧化物。这些化合物是P2Y受体激动剂,用于预防和治疗涉及异常分泌机制的疾病和障碍,如粘液纤毛清除机制功能不足或泪液分泌异常,或用于治疗涉及不适当的细胞葡萄糖摄取的疾病。
  • NON-NATURAL NUCLEOTIDES AND DINUCLEOTIDES
    申请人:Celltech R & D Limited
    公开号:EP1368366A1
    公开(公告)日:2003-12-10
  • SUBSTITUTED ARYLMETHYLUREAS AND HETEROARYLMETHYLUREAS, ANALOGUES THEREOF, AND METHODS USING SAME
    申请人:Arbutus Biopharma Corporation
    公开号:EP3893645A1
    公开(公告)日:2021-10-20
  • [EN] NON-NATURAL NUCLEOTIDES AND DINUCLEOTIDES<br/>[FR] NUCLEOTIDES ET DINUCLEOTIDES NON NATURELS
    申请人:CELLTECH R&D LTD
    公开号:WO2002062816A1
    公开(公告)日:2002-08-15
    Nucleotide derivatives of formula (1) are described: wherein: G is a hydrogen atom or an optionally substituted aliphatic, heteroaliphatic, cycloaliphatic, polycycloaliphatic, aromatic or heteroaromatic group or a non-natural nucleoside as defined herein; G' is a non-natural necleoside as defined herein; n is zero, or the integer 1 or 2; m is zero or the integer 1 or 2; and the salts, solvates, hydrates and N-oxides thereof. The compounds are P2Y receptor agonists and are of use in the prophylaxis and treatment of diseases and disorders involving abnormal secretory mechanisms such as inadequate functioning of mucociliary clearance mechanisms or abnormal tear secretion or in the treatment of diseases involving inappropriate cellular glucose uptake.
  • [EN] SUBSTITUTED ARYLMETHYLUREAS AND HETEROARYLMETHYLUREAS, ANALOGUES THEREOF, AND METHODS USING SAME<br/>[FR] ARYLMÉTHYLURÉES ET HÉTÉROARYLMÉTHYLURÉES SUBSTITUÉES, ANALOGUES DE CES DERNIÈRES ET PROCÉDÉS D'UTILISATION DE CELLES-CI
    申请人:ARBUTUS BIOPHARMA CORP
    公开号:WO2020123674A1
    公开(公告)日:2020-06-18
    The present invention includes substituted arylmethyl ureas and heteroarylmethyl-ureas, and compositions comprising the same, that can be used to treat or prevent hepatitis B virus (HBV) infections in a patient.
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