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4-Methoxy-5-[(1-methylpiperidin-4-yl)methoxy]benzene-1,2-diamine | 825619-49-6

中文名称
——
中文别名
——
英文名称
4-Methoxy-5-[(1-methylpiperidin-4-yl)methoxy]benzene-1,2-diamine
英文别名
——
4-Methoxy-5-[(1-methylpiperidin-4-yl)methoxy]benzene-1,2-diamine化学式
CAS
825619-49-6
化学式
C14H23N3O2
mdl
——
分子量
265.35
InChiKey
LBTKUEFRPZUBMK-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):
    1.3
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    73.7
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • Benzimidazole derivatives and their use as protein kinases inhibitors
    申请人:Berdini Valerio
    公开号:US20070135477A1
    公开(公告)日:2007-06-14
    The invention provides compounds of the formula (1): The compounds have activity against cyclin depdenent kinases, glycogen synthase kinase and Auroa kinases and are therefore useful to treat cancer and viral diseases.
    该发明提供了式(1)的化合物: 这些化合物具有对环素依赖性激酶、糖原合成酶激酶和Auroa激酶的活性,因此可用于治疗癌症和病毒性疾病。
  • BENZIMIDAZOLE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS
    申请人:BERDINI Valerio
    公开号:US20110224203A1
    公开(公告)日:2011-09-15
    The invention provides compounds of the formula (I): The compounds have activity against cyclin dependent kinases, glycogen synthase kinase and Aurora kinases and are therefore useful to treat cancer and viral diseases.
    该发明提供了式(I)的化合物:这些化合物对于细胞周期依赖性激酶、糖原合成酶激酶和极化激酶具有活性,因此可用于治疗癌症和病毒性疾病。
  • BENZIMIDAZOLE DERIVATIVES AND THEIR USE AS PROTEIN KINASES INHIBITORS
    申请人:Astex Therapeutics Limited
    公开号:EP2305250A1
    公开(公告)日:2011-04-06
    A combination comprising: (i) a compound of the formula (VII): or a salt, N-oxide or solvate thereof; and (ii) one or more other therapeutic agents.
    一种组合物,包括 (i) 式 (VII) 的化合物: 或其盐、N-氧化物或溶解物; 和 (ii) 一种或多种其他治疗剂。
  • US7977477B2
    申请人:——
    公开号:US7977477B2
    公开(公告)日:2011-07-12
  • [EN] PHARMACEUTICAL COMPOUNDS<br/>[FR] COMPOSES PHARMACEUTIQUES
    申请人:ASTEX TECHNOLOGY LTD
    公开号:WO2005002552A2
    公开(公告)日:2005-01-13
    The invention provides compounds having activity as inhibitors of cyclin dependent kinases, glycogen synthase kinase-3 and Aurora kinases for use in the treatment of disease states and conditions such as cancer that are mediated by the kinases. The compounds have the general formula (I). Also included within formula (I) are the salts, solvates and N-oxides of the compounds.
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