3-(4-Methoxyphenyl)-5-methoxycarbonylamino-2H-indeno-[1,2-c]pyrazol-4-one | 485820-05-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-(4-Methoxyphenyl)-5-methoxycarbonylamino-2H-indeno-[1,2-c]pyrazol-4-one
• 英文别名: methyl N-[3-(4-methoxyphenyl)-4-oxo-1H-indeno[1,2-c]pyrazol-5-yl]carbamate
• CAS: 485820-05-1
• 化学式: C₁₉H₁₅N₃O₄
• 分子量: 349.346
• InChiKey: VBQUTJORSQEODW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  26
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  93.3
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• Acylsemicarbazides as cyclin dependent kinase inhibitors useful as anti-cancer and anti-proliferative agents
  申请人：——

  公开号：US20030073686A1

  公开（公告）日：2003-04-17

  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吲哚并［1，2-c］吡唑-4-酮类化合物（I），它们是强效的细胞周期蛋白依赖性激酶抑制剂，与催化亚基cdk1-7及其调节亚基cyclin A-G有关。本发明还提供了一种新的治疗癌症或其他增殖性疾病的方法，即通过给患者投与这些化合物之一或其药学上可接受的盐形式的治疗有效量。或者，可以通过给患者投与本发明化合物之一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。
• 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。
• SEMICARBAZIDES AND THEIR USES
  申请人：Bristol-Myers Squibb Pharma Company

  公开号：EP1404670A1

  公开（公告）日：2004-04-07
• EP1404670A4
  申请人：——

  公开号：EP1404670A4

  公开（公告）日：2004-11-24
• 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