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3-Fluoro-8-nitroquinoline | 236093-08-6

中文名称
——
中文别名
——
英文名称
3-Fluoro-8-nitroquinoline
英文别名
——
3-Fluoro-8-nitroquinoline化学式
CAS
236093-08-6
化学式
C9H5FN2O2
mdl
——
分子量
192.15
InChiKey
FTSQENVATJUJTE-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):
    1.5
  • 重原子数:
    14
  • 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:
    58.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • [1,8]naphthyridin-2-ones and related compounds for the treatment of schizophrenia
    申请人:Clark D. Jerry
    公开号:US20050043309A1
    公开(公告)日:2005-02-24
    This invention relates to compounds of the formula 1 wherein G, D, A, Z, Q, X, Y, R 1 , and R 4 through R 7 are defined as in the specification, processes for preparing the same and intermediates used in making the same, and pharmaceutical compositions containing such compounds and their use in the treatment of central nervous system disorders and other disorders.
    这项发明涉及公式1的化合物 其中G、D、A、Z、Q、X、Y、R 1 和R 4 至R 7 的定义如规范中所述,制备这些化合物的方法以及用于制备这些化合物的中间体,以及含有这些化合物的药物组合物及其在治疗中枢神经系统疾病和其他疾病中的用途。
  • [EN] INHIBITORS OF JUN N-TERMINAL KINASE<br/>[FR] INHIBITEURS DE L'ENZYME JUN N-TERMINAL KINASE
    申请人:ELAN PHARM INC
    公开号:WO2010091310A1
    公开(公告)日:2010-08-12
    The present disclosure provides inhibitors of c-Jun N-terminal kinases (JNK) having a structure according to the following formula (I): or a salt or solvate thereof, wherein ring A, Ca, Cb, Z, R5, W and Cy are defined herein. The disclosure further provides pharmaceutical compositions including the compounds of the present disclosure and methods of making and using the compounds and compositions of the present disclosure, e.g., in the treatment and prevention of various disorders, such as Alzheimer's disease.
    本公开提供了具有以下结构的c-Jun N-末端激酶(JNK)抑制剂(I)的结构,或其盐或溶剂化物,其中环A,Ca,Cb,Z,R5,W和Cy在此处定义。本公开还提供了包括本公开化合物的药物组合物,以及制备和使用本公开化合物和组合物的方法,例如在治疗和预防各种疾病,如阿尔茨海默病。
  • [EN] [1,8]NAPHTHYRIDIN-2-ONES AND RELATED COMPOUNDS FOR THE TREATMENT OF SCHIZOPHRENIA<br/>[FR] [1,8]NAPHTYRIDIN-2-ONES ET COMPOSES APPARENTES DESTINES AU TRAITEMENT DE LA SCHIZOPHRENIE
    申请人:WARNER LAMBERT CO
    公开号:WO2005019215A1
    公开(公告)日:2005-03-03
    This invention relates to compounds of the Formula (1) wherein G, A, Z, Q, X, Y, and R1 and R2 are defined as in the specification, pharmaceutical compositions containing them and their use in the treatment of central nervous system and other disorders.
    本发明涉及式(1)的化合物,其中G,A,Z,Q,X,Y和R1和R2如规范中所定义,包含它们的制药组合物以及它们在治疗中枢神经系统和其他疾病中的应用。
  • [1,8]NAPHTHYRIDIN-2-ONES AND RELATED COMPOUNDS FOR THE TREATMENT OF SCHIZOPHRENIA
    申请人:Clark D. Jerry
    公开号:US20060287310A1
    公开(公告)日:2006-12-21
    This invention relates to compounds of the formula 1 wherein G, D, A, Z, Q, X, Y, R 1 , and R 4 through R 7 are defined as in the specification, processes for preparing the same and intermediates used in making the same, and pharmaceutical compositions containing such compounds and their use in the treatment of central nervous system disorders and other disorders.
    本发明涉及式1的化合物,其中G、D、A、Z、Q、X、Y、R1和R4至R7如规范中所定义,制备该化合物的过程以及用于制备该化合物的中间体,以及含有该化合物的制药组合物及其在治疗中枢神经系统疾病和其他疾病中的应用。
  • Inhibitors of Jun N-terminal kinase
    申请人:Sham Hing L.
    公开号:US08450363B2
    公开(公告)日:2013-05-28
    The present disclosure provides inhibitors of c-Jun N-terminal kinases (JNK) having a structure according to the following formula: or a salt or solvate thereof, wherein ring A, Ca, Cb, Z, R5, W and Cy are defined herein. The disclosure further provides pharmaceutical compositions including the compounds of the present disclosure and methods of making and using the compounds and compositions of the present disclosure, e.g., in the treatment and prevention of various disorders, such as Alzheimer's disease.
    本公开提供具有以下公式结构的c-Jun N末端激酶(JNK)抑制剂:或其盐或溶剂,其中环A、Ca、Cb、Z、R5、W和Cy在此定义。本公开还提供包括本公开化合物的药物组合物以及制备和使用本公开化合物和组合物的方法,例如,在治疗和预防各种疾病,如阿尔茨海默病方面的应用。
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