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(5-Chloro-8-hydroxy-quinolin-7-yl)-trimethyl-ammonium triflate

中文名称
——
中文别名
——
英文名称
(5-Chloro-8-hydroxy-quinolin-7-yl)-trimethyl-ammonium triflate
英文别名
(5-Chloro-8-hydroxyquinolin-7-yl)-trimethylazanium;trifluoromethanesulfonate;(5-chloro-8-hydroxyquinolin-7-yl)-trimethylazanium;trifluoromethanesulfonate
(5-Chloro-8-hydroxy-quinolin-7-yl)-trimethyl-ammonium triflate化学式
CAS
——
化学式
CF3O3S*C12H14ClN2O
mdl
——
分子量
386.779
InChiKey
CVIAHOXXRLQHHL-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):
    2.84
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    98.7
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

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文献信息

  • [EN] COMPOUNDS FOR THE INHIBITION OF UNDESIRED CELL PROLIFERATION AND USE THEREOF<br/>[FR] COMPOSES POUR L'INHIBITION DE LA PROLIFERATION CELLULAIRE INDESIRABLE ET LEUR UTILISATION
    申请人:JERINI AG
    公开号:WO2005063259A1
    公开(公告)日:2005-07-14
    The present invention is related to compounds having formula (I), wherein the dashed line indicates a single or double bond or is absent and wherein A1-A9, Q, R1-R11, T, U, V, W1-W3, X1, X2, Y and Z are as defined in the claims and description, pharmaceutical compositions comprising the compounds and the use of the compounds for the manufacture of a medicament for the treatment of deseases involving abnormal cell proliferation, undesired cell proliferation, abnormal mitosis and/or undesired mitosis.
    本发明涉及具有式(I)的化合物,其中虚线表示单键或双键或不存在,A1-A9、Q、R1-R11、T、U、V、W1-W3、X1、X2、Y和Z的定义如权利要求和描述中所定义,包括这些化合物的药物组合物以及利用这些化合物制备用于治疗涉及异常细胞增殖、不良细胞增殖、异常有丝分裂和/或不良有丝分裂的药物的用途。
  • Compounds and methods for F labelled agents
    申请人:Bayer Schering Pharma Aktiengesellschaft
    公开号:EP1897885A1
    公开(公告)日:2008-03-12
    This invention relates to novel compounds suitable for or already radiolabeled with 18F, methods of making such compounds and use of such compounds for diagnostic imaging. Such labeled compounds are characterized by Formula 11, wherein the substituents G, L, U, and Q have the meaning as defined in the specification.
    这项发明涉及适用于或已经用18F标记的新型化合物,制备这种化合物的方法以及将这种化合物用于诊断成像的用途。这些标记化合物的特点是其符合式11,其中取代基G、L、U和Q的含义如规范中定义的那样。
  • Radiofluorination methods
    申请人:Bayer Schering Pharma Aktiengesellschaft
    公开号:EP1964848A1
    公开(公告)日:2008-09-03
    The present invention relates to radiolabelled substitute benzene compounds for diagnostic imaging. The present invention provides methods for preparation of such compounds, in particular, preparation of novel compounds which serve as precursors for 18F-labeling, and the use of thus 18F-labeled compounds for diagnostic imaging.
    本发明涉及用于诊断成像的放射性标记的替代苯化合物。本发明提供了制备这种化合物的方法,特别是制备作为18F标记的前体的新化合物的方法,以及利用这些18F标记化合物进行诊断成像的方法。
  • RADIOFLUORINATION METHODS
    申请人:Srinivasan Ananth
    公开号:US20090317326A1
    公开(公告)日:2009-12-24
    The present invention relates to radiolabelled substitute benzene compounds for diagnostic imaging. The present invention provides methods for preparation of such compounds, in particular, preparation of novel compounds which serve as precursors for 18 F-labeling, and the use of thus 18 F-labeled compounds for diagnostic imaging.
    本发明涉及用于诊断成像的放射性标记替代苯化合物。本发明提供了制备这种化合物的方法,特别是制备作为18F标记的前体的新化合物的方法,以及使用这样18F标记的化合物进行诊断成像的方法。
  • COMPOUNDS AND METHODS FOR 18F LABELED AGENTS
    申请人:Lehmann Lutz
    公开号:US20080292548A1
    公开(公告)日:2008-11-27
    The present invention relates to novel compounds suitable for or already radiolabeled with 18 F, methods of making such compounds and use of such compounds for diagnostic imaging. Such labeled compounds are characterized by Formula II, wherein the substituents G, Q, L, Y and U have the meaning as defined in the specification and claims.
    本发明涉及适用于或已经标记有18F的新化合物,制备这种化合物的方法以及将这种化合物用于诊断成像的用途。这些标记化合物的特征由公式II表示,其中取代基G、Q、L、Y和U的含义如规范和要求所定义。
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