2-amino-3,6-dichloroquinoxaline | 89978-28-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 2-amino-3,6-dichloroquinoxaline
• 英文别名: 3,6-dichloro-quinoxalin-2-ylamine；3,6-dichloroquinoxalin-2-amine
• CAS: 89978-28-9
• 化学式: C₈H₅Cl₂N₃
• 分子量: 214.054
• InChiKey: SQLRBNIWOMYRMG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  51.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-苯基吡啶 、 2-amino-3,6-dichloroquinoxaline 以 N,N-二甲基甲酰胺 为溶剂， 反应 48.0h， 以15%的产率得到7-Chloro-2-phenyl-4a,5,10,11-tetraaza-benzo[b]fluorene
  参考文献：
  名称：

  Tanaka, Kiyoshi; Takahashi, Hideki; Takimoto, Kozo, Journal of Heterocyclic Chemistry, 1992, vol. 29, # 4, p. 771 - 777

  摘要：

  DOI：
• 作为产物：
  描述：

  2,3,6-三氯喹喔啉 在 氨 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 0.25h， 以50%的产率得到2-amino-3,6-dichloroquinoxaline
  参考文献：
  名称：

  Tanaka, Kiyoshi; Takahashi, Hideki; Takimoto, Kozo, Journal of Heterocyclic Chemistry, 1992, vol. 29, # 4, p. 771 - 777

  摘要：

  DOI：

文献信息

• 157. Synthetic antimalarials. Part XXVII. Some derivatives of phthalazine, quinoxaline, and isoquinoline
  作者：Robert D. Haworth、Stanley Robinson

  DOI：10.1039/jr9480000777

  日期：——
• Synthesis and anticancer activity of new 1-[(5 or 6-substituted 2-alkoxyquinoxalin-3-yl)aminocarbonyl]-4-(hetero)arylpiperazine derivatives
  作者：Young Bok Lee、Young-Dae Gong、Heejeong Yoon、Chang-Ho Ahn、Moon-Kook Jeon、Jae-Yang Kong

  DOI：10.1016/j.bmc.2010.09.028

  日期：2010.11.15

  A series of novel quinoxalinyl-piperazine compounds, 1-[(5 or 6-substituted alkoxyquinoxalinyl)aminocarbonyl]-4-(hetero)arylpiperazine derivatives were synthesized and evaluated as an anticancer agent. From screening of quinoxalinyl-piperazine compound library, we identified that many compounds inhibited proliferation of various human cancer cells at nanomolar concentrations. Among them, one of the fluoro quinoxalinyl-piperazine derivatives showed its IC(50) values ranging from 11 to 21 nM in the growth inhibition of cancer cells. This compound also displayed a more potent effect than paclitaxel against paclitaxel resistant HCT-15 colorectal carcinoma cells. The potency of this novel compound was further confirmed with the synergistic cytotoxic effect with several known cancer drugs such as paclitaxel, doxorubicin, cisplatin, gemcitabine or 5-fluorouracil in cancer cells. This strong cell killing effect was derived from the induction of apoptosis. Mechanistic studies have shown that this quinoxalinyl-piperazine compound is a G2/M-specific cell cycle inhibitor and inhibits anti-apoptotic Bcl-2 protein with p21 induction. Thus the results suggest that our compound has potential use in the growth inhibition of drug resistant cancer cells and the combination therapy with other clinically approved anticancer agents as well. (C) 2010 Elsevier Ltd. All rights reserved.
• Tanaka, Kiyoshi; Takahashi, Hideki; Takimoto, Kozo, Journal of Heterocyclic Chemistry, 1992, vol. 29, # 4, p. 771 - 777
  作者：Tanaka, Kiyoshi、Takahashi, Hideki、Takimoto, Kozo、Sugita, Masahiko、Mitsuhashi, Keiryo

  DOI：——

  日期：——