8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine | 1092790-57-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine
• 英文别名: 8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide；8-(4-Methoxyphenyl)-5-oxidopyrazolo[5,1-c][1,2,4]benzotriazin-5-ium
• CAS: 1092790-57-2
• 化学式: C₁₆H₁₂N₄O₂
• 分子量: 292.297
• InChiKey: SCXGDUVFKQLSDK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  64.9
• 氢给体数：
  0
• 氢受体数：
  4

上下游信息

• 下游产品

  中文名称	英文名称	CAS号	化学式	分子量
  ——	3-iodo-8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide	1310053-43-0	C16H11IN4O2	418.193

反应信息

• 作为反应物：
  描述：

  8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine 在 ammonium cerium (IV) nitrate 、 碘 作用下， 以 乙腈 为溶剂， 反应 0.75h， 以45%的产率得到3-iodo-8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide
  参考文献：
  名称：

  New 3-, 8-disubstituted pyrazolo[5,1-c][1,2,4]benzotriazines useful for studying the interaction with the HBp-3 area (hydrogen bond point area) in the benzodiazepine site on the γ-aminobutyric acid type A (GABAA) receptor

  摘要：

  The pharmacophoric model using ADLR procedure, based on pyrazolo[5,1-c][1,2,4]benzotriazine system, studied in our laboratory, allowed us to identify the essential interaction points (HBp-1, HBp-2, and Lp-1) and the important areas for affinity modulation (HBp-3 and Lp-2) for binding recognition at benzodiazepine (Bzs) site of GABA(A) receptors (GABA(A)-Rs). In this work ADLR method is used to rationalize the affinity data of 23 new compounds and to improve the knowledge on HBp-3 area, hydrogen bond area. Among these new compounds emerge the pyrrolo derivatives (18, 25, 28, 34, and 37) for their good affinity value (14.9 > K-i(nM) > 63.0). In the orientations proposed by ADLR, the NH moiety of the pyrrole ring, independently of the position in the pyrazolobenzotriazine core, fits in HBp-3 area and points out the acceptor feature of this hydrogen bond area, already known as donor area. Unexpectedly, the oxygen atom of the furane ring does not form efficient hydrogen bond with the same area, probably for an imperfect distance. The size of substituent at position 8 is important but not necessary for the receptor recognition, in fact the interdependence between the features of the 3- and 8-substituent's is again verified, (i.e., compound 20 vs 32). (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.04.009
• 作为产物：
  描述：

  8-iodopyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide 、 4-甲氧基苯硼酸 在 四(三苯基膦)钯 、 sodium carbonate 作用下， 以 四氢呋喃 、 乙醇 、 水 为溶剂， 反应 12.0h， 以90%的产率得到8-(4-methoxyphenyl)pyrazolo[5,1-c][1,2,4]benzotriazine
  参考文献：
  名称：

  新型吡唑并[5,1-c] [1,2,4]苯并三嗪，吡唑并[5,1-c]吡啶并[4,3-e] [1,2,4]三嗪及其开放类似物的合成具有细胞毒性常氧和低氧条件下的药物。

  摘要：

  报道了一系列吡唑并[5,1-c] [1,2,4]苯并三嗪及其相关类似物在常氧和低氧条件下的合成和抗肿瘤活性。所有化合物均在人大肠腺癌细胞系HCT-8和化合物15和20上进行了测试，化合物15和20在低氧和常氧条件下分别显示出选择性的细胞毒性，测定了ROS的产生，细胞周期和DNA片段化。这项初步研究鼓励我们将15和20视为进一步优化的有趣线索。

  DOI：

  10.1016/j.bmc.2008.09.055

文献信息

• Synthesis of new pyrazolo[5,1-c][1,2,4] benzotriazines, pyrazolo[5,1-c]pyrido[4,3-e][1,2,4] triazines and their open analogues as cytotoxic agents in normoxic and hypoxic conditions
  作者：Giovanna Ciciani、Marcella Coronnello、Gabriella Guerrini、Silvia Selleri、Miriam Cantore、Paola Failli、Enrico Mini、Annarella Costanzo

  DOI：10.1016/j.bmc.2008.09.055

  日期：2008.11

  The synthesis and antitumor activity in normoxic and hypoxic conditions of a series of pyrazolo[5,1-c][1,2,4]benzotriazine and its related analogues are reported. All compounds were tested on human colorectal adenocarcinoma cell line HCT-8 and for compounds 15 and 20, which show to have selective cytotoxicity in hypoxic and in normoxic conditions respectively, ROS production, cell cycle, and DNA fragmentation

  报道了一系列吡唑并[5,1-c] [1,2,4]苯并三嗪及其相关类似物在常氧和低氧条件下的合成和抗肿瘤活性。所有化合物均在人大肠腺癌细胞系HCT-8和化合物15和20上进行了测试，化合物15和20在低氧和常氧条件下分别显示出选择性的细胞毒性，测定了ROS的产生，细胞周期和DNA片段化。这项初步研究鼓励我们将15和20视为进一步优化的有趣线索。
• New 3-, 8-disubstituted pyrazolo[5,1-c][1,2,4]benzotriazines useful for studying the interaction with the HBp-3 area (hydrogen bond point area) in the benzodiazepine site on the γ-aminobutyric acid type A (GABAA) receptor
  作者：Gabriella Guerrini、Giovanna Ciciani、Fabrizio Bruni、Silvia Selleri、Fabrizio Melani、Simona Daniele、Claudia Martini、Annarella Costanzo

  DOI：10.1016/j.bmc.2011.04.009

  日期：2011.5

  The pharmacophoric model using ADLR procedure, based on pyrazolo[5,1-c][1,2,4]benzotriazine system, studied in our laboratory, allowed us to identify the essential interaction points (HBp-1, HBp-2, and Lp-1) and the important areas for affinity modulation (HBp-3 and Lp-2) for binding recognition at benzodiazepine (Bzs) site of GABA(A) receptors (GABA(A)-Rs). In this work ADLR method is used to rationalize the affinity data of 23 new compounds and to improve the knowledge on HBp-3 area, hydrogen bond area. Among these new compounds emerge the pyrrolo derivatives (18, 25, 28, 34, and 37) for their good affinity value (14.9 > K-i(nM) > 63.0). In the orientations proposed by ADLR, the NH moiety of the pyrrole ring, independently of the position in the pyrazolobenzotriazine core, fits in HBp-3 area and points out the acceptor feature of this hydrogen bond area, already known as donor area. Unexpectedly, the oxygen atom of the furane ring does not form efficient hydrogen bond with the same area, probably for an imperfect distance. The size of substituent at position 8 is important but not necessary for the receptor recognition, in fact the interdependence between the features of the 3- and 8-substituent's is again verified, (i.e., compound 20 vs 32). (C) 2011 Elsevier Ltd. All rights reserved.