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7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydrobenzofuran-4-carboxamide | 1280665-17-9

中文名称
——
中文别名
——
英文名称
7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydrobenzofuran-4-carboxamide
英文别名
7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydro-1-benzofuran-4-carboxamide
7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydrobenzofuran-4-carboxamide化学式
CAS
1280665-17-9
化学式
C31H44N8O4
mdl
——
分子量
592.742
InChiKey
DNVPZDLDTRANOE-PXDATVDWSA-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

  • 密度:
    1.279±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    43
  • 可旋转键数:
    9
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    126
  • 氢给体数:
    3
  • 氢受体数:
    10

反应信息

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文献信息

  • CYCLIC COMPOUND, PROCESS FOR PREPARATION THEREOF, RADIATION-SENSITIVE COMPOSITION, AND METHOD FOR FORMATION OF RESIST PATTERN
    申请人:Mitsubishi Gas Chemical Company, Inc.
    公开号:EP2476662A1
    公开(公告)日:2012-07-18
    A cyclic compound represented by formula (1): wherein L, R1, R', and m are as defined in the specification. The cyclic compound of formula (1) is highly soluble to a safety solvent, highly sensitive, and capable of forming resist patterns with good profile. Therefore, the cyclic compound is useful as a component of a radiation-sensitive composition.
    式 (1) 所代表的环状化合物: 其中 L、R1、R'和 m 如说明书中所定义。式(1)的环状化合物对安全溶剂的溶解度高,灵敏度高,能形成具有良好轮廓的抗蚀图案。因此,该环状化合物可用作辐射敏感组合物的成分。
  • US8691822B2
    申请人:——
    公开号:US8691822B2
    公开(公告)日:2014-04-08
  • DIHYDROPTERIDINONE DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF
    申请人:Tang Peng Cho
    公开号:US20120184543A1
    公开(公告)日:2012-07-19
    Dihydroperidinone derivatives, preparation process and pharmaceutical use thereof are disclosed. Specially, new dihydroperidinone derivatives represented by general formula (I), wherein each substituent of the general formula (I) is defined as in the description, their preparation process, pharmaceutical compositions comprising said derivatives and their use as therapeutical agents, especially as Plk kinase inhibitors are disclosed.
    二氢吡啶酮衍生物、其制备方法及药用途被揭示。特别是,根据通用式(I)表示的新二氢吡啶酮衍生物,其中通用式(I)的每个取代基如描述中所定义,它们的制备过程,包含所述衍生物的药物组合物以及它们作为治疗剂的用途,特别是作为Plk激酶抑制剂的用途被揭示。
  • Dihydropteridinone derivatives, preparation process and pharmaceutical use thereof
    申请人:Tang Peng Cho
    公开号:US08691822B2
    公开(公告)日:2014-04-08
    Dihydroperidinone derivatives, preparation process and pharmaceutical use thereof are disclosed. Specially, new dihydroperidinone derivatives represented by general formula (I), wherein each substituent of the general formula (I) is defined as in the description, their preparation process, pharmaceutical compositions comprising said derivatives and their use as therapeutical agents, especially as Plk kinase inhibitors are disclosed.
    本发明公开了二氢吡啶酮衍生物、其制备方法和药用。具体而言,公开了由通式(I)表示的新的二氢吡啶酮衍生物,其中通式(I)的每个取代基如描述中所定义,它们的制备方法,包含所述衍生物的药物组合物以及它们作为治疗剂的用途,特别是作为Plk激酶抑制剂的用途。
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