2-phenyl-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one | 1009055-64-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: 2-phenyl-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one
• 英文别名: 2-phenyl-1H,4H,5H,6H,7H-pyrrolo[3,2-c]pyridin-4-one
• CAS: 1009055-64-4
• 化学式: C₁₃H₁₂N₂O
• 分子量: 212.251
• InChiKey: XYWBECNOAGWDMX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  44.9
• 氢给体数：
  2
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  C₁₈H₂₀N₂O₃ 在 盐酸 作用下， 以 1,4-二氧六环 、 甲醇 为溶剂， 反应 2.0h， 生成 2-phenyl-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one
  参考文献：
  名称：

  Cdc7 Kinase Inhibitors: Pyrrolopyridinones as Potential Antitumor Agents. 1. Synthesis and Structure–Activity Relationships

  摘要：

  Cdc7 kinase is an essential protein that promotes DNA replication in eukaryotic organisms. Genetic evidence indicates that Cdc7 inhibition can cause selective tumor-cell death in a p53-independent manner, supporting the rationale for developing Cdc7 small-molecule inhibitors for the treatment of cancers. In this paper, the synthesis and structure-activity relationships of 2-heteroaryl-pyrrolopyridinones, the first potent Cdc7 kinase inhibitors, are,described. Starting from 2-pyridin-4-yl-1,5,6,7-tetrahydro-pyrrolo[3,2-c]pyridin-4-one, progress toward a simple scaffold, tailored for Cdc7 inhibition, is reported.

  DOI：

  10.1021/jm700956r

文献信息

• Development of dihydropyrrolopyridinone-based PKN2/PRK2 chemical tools to enable drug discovery
  作者：Fiona Scott、Angela M. Fala、Jessica E. Takarada、Mihaela P. Ficu、Lewis E. Pennicott、Tristan D. Reuillon、Rafael M. Couñago、Katlin B. Massirer、Jonathan M. Elkins、Simon E. Ward

  DOI：10.1016/j.bmcl.2022.128588

  日期：2022.3
• Cdc7 Kinase Inhibitors: Pyrrolopyridinones as Potential Antitumor Agents. 1. Synthesis and Structure–Activity Relationships
  作者：Ermes Vanotti、Raffaella Amici、Alberto Bargiotti、Jens Berthelsen、Roberta Bosotti、Antonella Ciavolella、Alessandra Cirla、Cinzia Cristiani、Roberto D’Alessio、Barbara Forte、Antonella Isacchi、Katia Martina、Maria Menichincheri、Antonio Molinari、Alessia Montagnoli、Paolo Orsini、Antonio Pillan、Fulvia Roletto、Alessandra Scolaro、Marcellino Tibolla、Barbara Valsasina、Mario Varasi、Daniele Volpi、Corrado Santocanale

  DOI：10.1021/jm700956r

  日期：2008.2.1

  Cdc7 kinase is an essential protein that promotes DNA replication in eukaryotic organisms. Genetic evidence indicates that Cdc7 inhibition can cause selective tumor-cell death in a p53-independent manner, supporting the rationale for developing Cdc7 small-molecule inhibitors for the treatment of cancers. In this paper, the synthesis and structure-activity relationships of 2-heteroaryl-pyrrolopyridinones, the first potent Cdc7 kinase inhibitors, are,described. Starting from 2-pyridin-4-yl-1,5,6,7-tetrahydro-pyrrolo[3,2-c]pyridin-4-one, progress toward a simple scaffold, tailored for Cdc7 inhibition, is reported.