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6-(4-哌啶基氧基)-1(2H)-异喹啉酮盐酸盐 | 923262-96-8

中文名称
6-(4-哌啶基氧基)-1(2H)-异喹啉酮盐酸盐
中文别名
6-(哌啶-4-氧基)异喹啉-1(2H)-酮盐酸盐
英文名称
6-(piperidin-4-yloxy)-2H-isoquinolin-1-one hydrochloride
英文别名
6-(piperidin-4-yloxy)isoquinolin-1(2H)-one hydrochloride;6-piperidin-4-yloxy-2H-isoquinolin-1-one;hydrochloride
6-(4-哌啶基氧基)-1(2H)-异喹啉酮盐酸盐化学式
CAS
923262-96-8
化学式
C14H16N2O2*ClH
mdl
——
分子量
280.754
InChiKey
KMNVOGVCCZNVNU-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

物化性质

  • 溶解度:
    H2O:50 mg/mL(178.09 mM;需要超声)DMSO:25 mg/mL(89.05 mM;需要超声)

计算性质

  • 辛醇/水分配系数(LogP):
    2.08
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    50.4
  • 氢给体数:
    3
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933990090
  • 储存条件:
    -20°C,密闭保存,置于干燥处

SDS

SDS:fb89d6fa5a1a4e95423508ec556ba4a5
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制备方法与用途

SAR407899盐酸盐是一种选择性且高效的ATP竞争性抑制剂,其IC50值为135 nM,对人和大鼠细胞的相应值分别为36 nM和41 nM。

反应信息

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文献信息

  • SUBSTITUTED PHENYL COMPOUNDS
    申请人:GESSLER Simon
    公开号:US20130012711A1
    公开(公告)日:2013-01-10
    The present invention relates to novel substituted phenyl compounds of the formula and to a process for making them. The compounds can be used as intermediates for making 6-substituted-1-(2H)-isoquinolinone derivatives.
    本发明涉及一种新型的取代苯基化合物,其化学式如下,并涉及一种制备它们的方法。这些化合物可用作制备6-取代-1-(2H)-异喹啉酮衍生物的中间体。
  • [EN] SUBSTITUTED PHENYL COMPOUNDS<br/>[FR] COMPOSÉS DE PHÉNYLE SUBSTITUÉS
    申请人:SANOFI SA
    公开号:WO2013007502A1
    公开(公告)日:2013-01-17
    The present invention relates to novel substituted phenyl compounds of the formula (VI) and to a process for making them. The compounds can be used as intermediates for making 6-substituted-1-(2H)-isoquinolinone derivatives.
    本发明涉及公式(VI)的新型取代苯基化合物以及制备它们的方法。这些化合物可用作制备6-取代-1-(2H)-异喹啉酮衍生物的中间体。
  • [EN] PROCESS FOR THE PREPARATION OF 6-SUBSTITUTED-1-(2H)-ISOQUINOLINONES<br/>[FR] PROCÉDÉ DE PRÉPARATION DE 1-(2H)-ISOQUINOLINONES 6-SUBSTITUÉES
    申请人:SANOFI AVENTIS
    公开号:WO2009080335A1
    公开(公告)日:2009-07-02
    The present invention relates to a process for making 6-substituted-1-(2H)- isoquinolinone derivatives of formula (I) wherein R1 and n are as described in the specification. The present invention further relates to novel intermediates which are used in the process according to the invention and to processes for preparing such intermediates.
    本发明涉及一种制备式(I)的6-取代-1-(2H)-异喹啉酮衍生物的方法,其中R1和n如规范中所述。本发明还涉及用于本发明方法的新型中间体,以及制备这种中间体的方法。
  • Substituted isoquinoline and isoquinolinone derivatives as inhibitors of RHO-Kinase
    申请人:PLETTENBURG Oliver
    公开号:US20100063025A1
    公开(公告)日:2010-03-11
    The invention relates to 6-substituted isoquinoline and isochinolone derivatives of the formula (I) useful for the treatment and/or prevention of diseases associated with Rho-kinase and/or Rho-kinase mediated phosphorylation of myosin light chain phosphatase, and compositions containing such compounds.
    该发明涉及公式(I)的6-取代异喹啉异喹啉生物,可用于治疗和/或预防与Rho-激酶和/或Rho-激酶介导的肌球蛋白轻链磷酸磷酸化相关的疾病,并且含有这些化合物的组合物。
  • Piperidinyl-substituted isoquinolone derivatives
    申请人:Plettenburg Oliver
    公开号:US20090093518A1
    公开(公告)日:2009-04-09
    The invention relates to 6-piperidinyl-substituted isoquinolone derivatives of the formula (I) or isoquinoline derivatives of the formula (I′) useful for the treatment and/or prevention of diseases associated with Rho-kinase and/or Rho-kinase mediated phosphorylation of myosin light chain phosphatase, and compositions containing such compounds.
    本发明涉及公式(I)的6-哌啶基取代的异喹啉生物或公式(I')的异喹啉生物,用于治疗和/或预防与Rho激酶和/或Rho激酶介导的肌球蛋白轻链磷酸磷酸化相关的疾病,以及含有这种化合物的组合物。
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