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5-(4-Chloro-2-methoxyphenyl)-2,4-dimethylpyrazole-3-carboxylic acid | 1354408-32-4

中文名称
——
中文别名
——
英文名称
5-(4-Chloro-2-methoxyphenyl)-2,4-dimethylpyrazole-3-carboxylic acid
英文别名
——
5-(4-Chloro-2-methoxyphenyl)-2,4-dimethylpyrazole-3-carboxylic acid化学式
CAS
1354408-32-4
化学式
C13H13ClN2O3
mdl
——
分子量
280.711
InChiKey
HALJDJKWRZHRCM-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):
    2.7
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    64.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR
    申请人:Uchida Hiroshi
    公开号:US20130079306A1
    公开(公告)日:2013-03-28
    A novel heterocyclic compound or a salt thereof useful for selectively inhibiting the degradation of p27 Kip1 is provided. The compound or the salt thereof is represented by the following formula (1): wherein A represents an alkyl group, a cycloalkyl group, an aryl group or a heterocyclic group, the group A may have a substituent; the ring B represents a 5- to 8-membered monocyclic heterocyclic ring or a condensed ring containing the monocyclic heterocyclic ring, the ring B may have a substituent; the ring C represents an aromatic ring, the ring C may have a substituent; L represents a linker comprising a main chain having 3 to 5 atoms selected from the group consisting of a carbon atom, a nitrogen atom, an oxygen atom and a sulfur atom, wherein at least one atom in the main chain is a hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, the linker L may have a substituent; and n is 0 or 1.
    提供了一种新型杂环化合物或其盐,用于选择性地抑制p27Kip1的降解。该化合物或其盐由以下式(1)表示:其中A代表烷基、环烷基、芳基或杂环基,基团A可能有取代基;环B代表5至8成员的单环杂环环或包含该单环杂环环的缩合环,环B可能有取代基;环C代表芳香环,环C可能有取代基;L代表包含3至5个原子的主链的连接物,所述原子选自碳原子、氮原子、氧原子和原子组成的群,其中主链中的至少一个原子是选自氮原子、氧原子和原子组成的杂原子,连接物L可能有取代基;n为0或1。
  • HETEROCYCLIC COMPOUND, AND p27 KIP1 DEGRADATION INHIBITOR
    申请人:ASKA Pharmaceutical Co., Ltd.
    公开号:EP2594555A1
    公开(公告)日:2013-05-22
    A novel heterocyclic compound or a salt thereof useful for selectively inhibiting the degradation of p27kip1 is provided. The compound or the salt thereof is represented by the following formula (1): wherein A represents an alkyl group, a cycloalkyl group, an aryl group or a heterocyclic group, the group A may have a substituent; the ring B represents a 5- to 8-membered monocyclic heterocyclic ring or a condensed ring containing the monocyclic heterocyclic ring, the ring B may have a substituent; the ring C represents an aromatic ring, the ring C may have a substituent; L represents a linker comprising a main chain having 3 to 5 atoms selected from the group consisting of a carbon atom, a nitrogen atom, an oxygen atom and a sulfur atom, wherein at least one atom in the main chain is a hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, the linker L may have a substituent; and n is 0 or 1.
    本研究提供了一种新型杂环化合物或其盐,可用于选择性抑制 p27kip1 的降解。该化合物或其盐由下式(1)表示: 其中 A 代表烷基、环烷基、芳基或杂环基,该基团 A 可具有取代基;环 B 代表 5 至 8 元单环杂环或含有单环杂环的缩合环,该环 B 可具有取代基;环 C 代表芳香环,该环 C 可具有取代基;L 代表由主链组成的连接体,该主链具有 3 至 5 个原子,选自由碳原子、氮原子、氧原子和原子组成的组,其中主链中至少有一个原子是选自由氮原子、氧原子和原子组成的组的杂原子,连接体 L 可具有取代基;以及 n 为 0 或 1。
  • US9200008B2
    申请人:——
    公开号:US9200008B2
    公开(公告)日:2015-12-01
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