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1-(2-amino-cyclohexyl)-3-[3-(4-methoxy-phenyl)-4-oxo-2,4-dihydro-indeno[1,2-c]pyrazol-5-yl]-urea | 485820-04-0

中文名称
——
中文别名
——
英文名称
1-(2-amino-cyclohexyl)-3-[3-(4-methoxy-phenyl)-4-oxo-2,4-dihydro-indeno[1,2-c]pyrazol-5-yl]-urea
英文别名
3-(4-methoxyphenyl)-5-((cis-2-aminocyclohexylcarbamoyl)amino)indeno[1,2-c]pyrazol-4-one;3-(4-methoxyphenyl)-5-(cis-2-aminocyclohexanylcarbamoyl)aminoindeno[1,2-c]pyrazol-4-one;1-(2-aminocyclohexyl)-3-[3-(4-methoxyphenyl)-4-oxo-1H-indeno[1,2-c]pyrazol-5-yl]urea
1-(2-amino-cyclohexyl)-3-[3-(4-methoxy-phenyl)-4-oxo-2,4-dihydro-indeno[1,2-c]pyrazol-5-yl]-urea化学式
CAS
485820-04-0
化学式
C24H25N5O3
mdl
——
分子量
431.494
InChiKey
GRGDKUMEXLWRKO-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):
    3
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    122
  • 氢给体数:
    4
  • 氢受体数:
    5

文献信息

  • Indeno [1,2-c]pyrazol-4-ones and their uses
    申请人:——
    公开号:US20010027195A1
    公开(公告)日:2001-10-04
    The present invention relates to the synthesis of a new class of indeno[1,2-c]pyrazol-4-ones of formula (I): 1 that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cdk1-9 and their regulatory subunits know as cyclins A-H. This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.
    本发明涉及合成一种新类别的indeno[1,2-c]pyrazol-4-ones化合物,其化学式为(I):1,这些化合物是一类名为细胞周期依赖性激酶的酶的强效抑制剂,与催化亚基cdk1-9及其调节亚基cyclins A-H有关。本发明还提供了一种新颖的治疗癌症或其他增生性疾病的方法,即通过给予这些化合物中的一种或其药用可接受的盐形式的治疗有效剂量。另外,可以通过给予本发明化合物之一与一种或多种其他已知的抗癌或抗增生剂的治疗有效组合来治疗癌症或其他增生性疾病。
  • Acylsemicarbazides as cyclin dependent kinase inhibitors useful as anti-cancer and anti-proliferative agents
    申请人:Bristol-Myers Squibb Pharma Company
    公开号:US20040048844A1
    公开(公告)日:2004-03-11
    The present invention relates to the synthesis of a new class of indeno[1,2-c]pyrazol-4-ones of formula (I): 1 that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cdk1-7 and their regulatory subunits know as cyclins A-G. This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.
    本发明涉及合成一类新的indeno[1,2-c]pyrazol-4-ones化合物,其化学式为(I):1,它们是强效的cyclin dependent kinases酶抑制剂,这些酶与催化亚单位cdk1-7及其调节亚单位cyclin A-G有关。本发明还提供了一种新的治疗癌症或其他增生性疾病的方法,即通过给患者服用这些化合物或其药学上可接受的盐形式的治疗有效剂量来治疗。另外,可以通过给患者同时服用本发明化合物和一种或多种其他已知的抗癌或抗增生剂来治疗癌症或其他增生性疾病。
  • Semicarbazides and their uses
    申请人:——
    公开号:US20040242869A1
    公开(公告)日:2004-12-02
    The present invention relates to the synthesis of a new class of 5-substituted-3-(4-OR 1 -phenyl)-2H-indeno[1,2-c]pyrazol-4-ones of formula (I): 1 that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cdk1-7 and their regulatory subunits know as cyclins A-G. This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.
    本发明涉及一种新型5-取代-3-(4-OR1-苯基)-2H-吲哚[1,2-c]吡唑-4-酮的合成,其化合物式为(I):1,该化合物是一种有效的细胞周期蛋白依赖性激酶抑制剂,可以抑制cdk1-7催化亚基及其调节亚基cyclin A-G。本发明还提供了一种治疗癌症或其他增殖性疾病的新方法,通过给患者施用这些化合物或其药学上可接受的盐形式的治疗有效剂量。另外,也可以通过给患者施用本发明化合物和一种或多种其他已知的抗癌或抗增殖剂的治疗有效组合来治疗癌症或其他增殖性疾病。
  • 5-AMINOINDENO[1,2-C]PYRAZOL-4-ONES AS ANTI-CANCER AND ANTI-PROLIFERATIVE AGENTS
    申请人:Bristol-Myers Squibb Pharma Company
    公开号:EP1071668B1
    公开(公告)日:2009-06-03
  • ACYLSEMICARBAZIDES AS CYCLIN DEPENDENT KINASE INHIBITORS USEFUL AS ANTI-CANCER AND ANTI-PROLIFERATIVE AGENTS
    申请人:Bristol-Myers Squibb Pharma Company
    公开号:EP1417177A2
    公开(公告)日:2004-05-12
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