2-benzyl-8-methoxyquinazolin-4(3H)-one

• 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-benzyl-8-methoxyquinazolin-4(3H)-one
• 英文别名: 2-benzyl-8-methoxy-3H-quinazolin-4-one；2-Benzyl-8-methoxy-3H-chinazolin-4-on；4(1)Quinazolone,2-benzyl-8-methoxy-；2-benzyl-8-methoxy-3H-quinazolin-4-one
• 化学式: C₁₆H₁₄N₂O₂
• 分子量: 266.299
• InChiKey: KCJLPUFYGFIXFA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  50.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-氨基-5-甲基吡唑 、 2-benzyl-8-methoxyquinazolin-4(3H)-one 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate 作用下， 以 乙腈 为溶剂， 反应 0.5h， 生成 N-(5-methyl-1H-pyrazol-3-yl)-8-methoxy-2-benzylquinazolin-4-amine
  参考文献：
  名称：

  Structure-based drug design: Synthesis and biological evaluation of quinazolin-4-amine derivatives as selective Aurora A kinase inhibitors

  摘要：

  Aurora kinases play critical roles in the regulation of the cell cycle and mitotic spindle assembly. Aurora A kinase, a member of the Aurora protein family, is frequently highly expressed in tumors, and selective Aurora A inhibition serves as a significant component of anticancer therapy. However, designing highly selective Aurora A inhibitors is difficult because Aurora A and B share high homology and differ only by three residues in their ATP-binding pockets. Through structure-based drug design, we designed and synthesized a series of novel quinazolin-4-amine derivatives. These derivatives act as selective Aurora A kinase inhibitors by exploiting the structural differences between Aurora A and B. The selectivities of most compounds were improved (the best up to >757-fold) when comparing with the lead compound (3-fold). In vitro biochemical and cellular assays revealed that compound 6 potently inhibited Aurora A kinase and most human tumor cells. Furthermore, compound 6 effectively suppressed carcinoma, such as triple-negative breast cancers (TNBC) in an animal model. Therefore, compound 6 might serve as a promising anticancer drug. Moreover, through molecular dynamic (MD) analysis, we have identified that a salt bridge formed in Aurora B is key contributor for the isoform selectivity of the inhibitor. This salt bridge has not been previously detected in the reported crystal structure of Aurora B. These results might provide a crucial basis for the further development of highly potent inhibitors with high selectivity for Aurora A. (C) 2018 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2018.08.053
• 作为产物：
  描述：

  2-氨基-3-甲氧基苯甲酸 、 苯乙酰氯 在 potassium carbonate 、 乙酸酐 、 ammonium acetate 作用下， 以 乙腈 为溶剂， 反应 19.0h， 以60%的产率得到2-benzyl-8-methoxyquinazolin-4(3H)-one
  参考文献：
  名称：

  Structure-based drug design: Synthesis and biological evaluation of quinazolin-4-amine derivatives as selective Aurora A kinase inhibitors

  摘要：

  Aurora kinases play critical roles in the regulation of the cell cycle and mitotic spindle assembly. Aurora A kinase, a member of the Aurora protein family, is frequently highly expressed in tumors, and selective Aurora A inhibition serves as a significant component of anticancer therapy. However, designing highly selective Aurora A inhibitors is difficult because Aurora A and B share high homology and differ only by three residues in their ATP-binding pockets. Through structure-based drug design, we designed and synthesized a series of novel quinazolin-4-amine derivatives. These derivatives act as selective Aurora A kinase inhibitors by exploiting the structural differences between Aurora A and B. The selectivities of most compounds were improved (the best up to >757-fold) when comparing with the lead compound (3-fold). In vitro biochemical and cellular assays revealed that compound 6 potently inhibited Aurora A kinase and most human tumor cells. Furthermore, compound 6 effectively suppressed carcinoma, such as triple-negative breast cancers (TNBC) in an animal model. Therefore, compound 6 might serve as a promising anticancer drug. Moreover, through molecular dynamic (MD) analysis, we have identified that a salt bridge formed in Aurora B is key contributor for the isoform selectivity of the inhibitor. This salt bridge has not been previously detected in the reported crystal structure of Aurora B. These results might provide a crucial basis for the further development of highly potent inhibitors with high selectivity for Aurora A. (C) 2018 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2018.08.053

文献信息

• Aggarwal; Das; Ray, Journal of the Indian Chemical Society, 1929, vol. 6, p. 717,718
  作者：Aggarwal、Das、Ray

  DOI：——

  日期：——