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10-((4-Methylpiperazin-1-yl)methyl)chromeno(4,3,2-de)phthalazin-3(2H)-one | 805242-85-7

中文名称
——
中文别名
——
英文名称
10-((4-Methylpiperazin-1-yl)methyl)chromeno(4,3,2-de)phthalazin-3(2H)-one
英文别名
4-[(4-methylpiperazin-1-yl)methyl]-8-oxa-15,16-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2(7),3,5,9,11,13(17)-heptaen-14-one
10-((4-Methylpiperazin-1-yl)methyl)chromeno(4,3,2-de)phthalazin-3(2H)-one化学式
CAS
805242-85-7
化学式
C20H20N4O2
mdl
——
分子量
348.4
InChiKey
DZRLVSOGARUEGQ-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):
    1.9
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    57.2
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • THERAPEUTIC KINASE MODULATORS
    申请人:PIERRE Fabrice
    公开号:US20090093465A1
    公开(公告)日:2009-04-09
    The invention relates in part to molecules having certain biological activities that include, but are not limited to, inhibiting cell proliferation, and modulating protein kinase activity. Molecules of the invention can modulate casein kinase (CK) activity. The invention also relates in part to methods for using such molecules.
    该发明涉及部分具有特定生物活性的分子,包括但不限于抑制细胞增殖和调节蛋白激酶活性。该发明的分子可以调节酪蛋白激酶(CK)活性。该发明还涉及使用这些分子的方法。
  • Compounds, methods and pharmaceutical compositions for inhibiting PARP
    申请人:Kalish J. Vincent
    公开号:US20050020595A1
    公开(公告)日:2005-01-27
    The present invention provides compounds which inhibit poly(ADP-ribose) polymerase (“PARP”), compositions containing these compounds and methods for using these PARP inhibitors to treat, prevent and/or ameliorate the effects of the conditions described herein.
    本发明提供抑制聚(ADP-核糖)聚合酶(“PARP”)的化合物,含有这些化合物的组合物以及使用这些PARP抑制剂治疗、预防和/或改善本文所述疾病的方法。
  • COMPOUNDS, METHODS AND PHARMACEUTICAL COMPOSITIONS FOR INHIBITING PARP
    申请人:Kalish J. Vincent
    公开号:US20080058325A1
    公开(公告)日:2008-03-06
    The present invention provides compounds which inhibit poly(ADP-ribose) polymerase (“PARP”) compositions containing these compounds and methods for using these PARP inhibitors to treat, prevent and/or ameliorate the effects of the conditions described herein.
    本发明提供了抑制聚(ADP核糖)聚合酶(“PARP”)的化合物,含有这些化合物的组合物以及使用这些PARP抑制剂治疗、预防和/或减轻本文所述疾病的方法。
  • SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS
    申请人:CHUA Peter
    公开号:US20090264423A2
    公开(公告)日:2009-10-22
    The invention relates in part to molecules having certain biological activities that include, but are not limited to, inhibiting cell proliferation, modulating protein kinase activity and modulating polymerase activity. Molecules of the invention can modulate casein kinase (CK) activity and/or poly(ADP-ribose)polymerase (PARP) activity. The invention also relates in part to methods for using such molecules.
    本发明涉及具有某些生物活性的分子,包括但不限于抑制细胞增殖、调节蛋白激酶活性和调节聚合酶活性。本发明的分子可以调节酪蛋白激酶(CK)活性和/或聚(ADP-核糖)聚合酶(PARP)活性。本发明还涉及使用这些分子的方法。
  • FUSED TRICYCLIC COMPOUNDS AS SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS
    申请人:CHUA Peter C.
    公开号:US20110263581A1
    公开(公告)日:2011-10-27
    The invention relates in part to molecules having certain biological activities that include, but are not limited to, inhibiting cell proliferation, modulating protein kinase activity and modulating polymerase activity. Molecules of the invention can modulate casein kinase (CK) activity and/or poly(ADP-ribose)polymerase (PARP) activity. The invention also relates in part to methods for using such molecules.
    本发明部分涉及具有某些生物活性的分子,包括但不限于抑制细胞增殖、调节蛋白激酶活性和调节聚合酶活性。本发明的分子可以调节酪氨酸激酶(CK)活性和/或聚(ADP核糖)聚合酶(PARP)活性。本发明部分还涉及使用这些分子的方法。
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