3,5-bis(3-cyanophenoxy)-2-pyrazinone | 228393-51-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3,5-bis(3-cyanophenoxy)-2-pyrazinone
• 英文别名: 3-[[5-(3-cyanophenoxy)-6-oxo-1H-pyrazin-3-yl]oxy]benzonitrile
• CAS: 228393-51-9
• 化学式: C₁₈H₁₀N₄O₃
• 分子量: 330.302
• InChiKey: VKNQPBVOCBDDPT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  108
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3,5-bis(3-cyanophenoxy)-2-pyrazinone 在 盐酸 、 氨 作用下， 以 乙醇 为溶剂， 反应 18.0h， 生成 3,3'-<(3,4-dihydro-3-oxopyrazine-2,6-diyl)bis(oxy)>bis(benzenecarboximidamide)
  参考文献：
  名称：

  Design, Synthesis, and Activity of 2,6-Diphenoxypyridine-Derived Factor Xa Inhibitors

  摘要：

  A novel series of 2,6-diphenoxypyridines has been designed to inhibit factor Xa, a serine protease strategically located in the coagulation cascade. The evolution from the photochemically unstable bisamidine (Z,Z)-BABCH to potent bisamidine compounds with a pyridine heterocycle as the core scaffold has been achieved. The most potent compound in the series, 6h, has a K-i for human factor Xa of 12 nM. The selectivity of 6h against bovine trypsin and human thrombin was greater than 90- and 1000-fold, respectively. Two proposed modes of binding of 6h Do factor Xa are made based on the crystal structures of 6h by itself and of 6h bound to bovine trypsin.

  DOI：

  10.1021/jm980667k
• 作为产物：
  描述：

  3,3'-<(2,6-pyrazinediyl 4-oxide)bis(oxy)>bis(benzonitrile) 在 三氟乙酸 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 4.0h， 以64%的产率得到3,5-bis(3-cyanophenoxy)-2-pyrazinone
  参考文献：
  名称：

  Design, Synthesis, and Activity of 2,6-Diphenoxypyridine-Derived Factor Xa Inhibitors

  摘要：

  A novel series of 2,6-diphenoxypyridines has been designed to inhibit factor Xa, a serine protease strategically located in the coagulation cascade. The evolution from the photochemically unstable bisamidine (Z,Z)-BABCH to potent bisamidine compounds with a pyridine heterocycle as the core scaffold has been achieved. The most potent compound in the series, 6h, has a K-i for human factor Xa of 12 nM. The selectivity of 6h against bovine trypsin and human thrombin was greater than 90- and 1000-fold, respectively. Two proposed modes of binding of 6h Do factor Xa are made based on the crystal structures of 6h by itself and of 6h bound to bovine trypsin.

  DOI：

  10.1021/jm980667k

文献信息

• Design, Synthesis, and Activity of 2,6-Diphenoxypyridine-Derived Factor Xa Inhibitors
  作者：Gary Phillips、David D. Davey、Keith A. Eagen、Sunil K. Koovakkat、Amy Liang、Howard P. Ng、Michael Pinkerton、Lan Trinh、Marc Whitlow、Alicia M. Beatty、Michael M. Morrissey

  DOI：10.1021/jm980667k

  日期：1999.5.1

  A novel series of 2,6-diphenoxypyridines has been designed to inhibit factor Xa, a serine protease strategically located in the coagulation cascade. The evolution from the photochemically unstable bisamidine (Z,Z)-BABCH to potent bisamidine compounds with a pyridine heterocycle as the core scaffold has been achieved. The most potent compound in the series, 6h, has a K-i for human factor Xa of 12 nM. The selectivity of 6h against bovine trypsin and human thrombin was greater than 90- and 1000-fold, respectively. Two proposed modes of binding of 6h Do factor Xa are made based on the crystal structures of 6h by itself and of 6h bound to bovine trypsin.