N-(4-chlorophenyl)-2-((2-chlorophenyl)amino)-2-oxoacetohydrazonoyl chloride | 900569-82-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(4-chlorophenyl)-2-((2-chlorophenyl)amino)-2-oxoacetohydrazonoyl chloride
• CAS: 900569-82-6
• 化学式: C₁₄H₁₀Cl₃N₃O
• 分子量: 342.612
• InChiKey: BIYBRQGPCXKBNM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  21.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  53.49
• 氢给体数：
  2.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  哌啶 、 N-(4-chlorophenyl)-2-((2-chlorophenyl)amino)-2-oxoacetohydrazonoyl chloride 以 1,4-二氧六环 为溶剂， 以92%的产率得到N-(2-chlorophenyl)-2-(2-(4-chlorophenyl)hydrazono)-2-(piperidin-1-yl)acetamide
  参考文献：
  名称：

  Synthesis and characterization of novel 1,2,4-triazine derivatives with antiproliferative activity

  摘要：

  A series of novel small molecules with a 1,2,4-triazine scaffold was obtained according to a recently published and highly efficient synthetic route. Screening for antiproliferative and cytotoxic activity revealed distinct anticancer effects against the human leukemia cell line K-562 combined with a remarkable low cytotoxicity. All compounds were in agreement with the 'rule-of-five' claims by Lipinski and calculated log P(calc) values were experimentally confirmed (log P(exp)). For the most active compounds, in vitro serum albumin binding was investigated and structure-activity relationships were established. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.01.053