5-((4-((2-chlorophenyl)amino)pyrimidin-2-yl)amino)-1H-benzo[d]imidazol-2(3H)-one hydrochloride | 1395886-00-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: 5-((4-((2-chlorophenyl)amino)pyrimidin-2-yl)amino)-1H-benzo[d]imidazol-2(3H)-one hydrochloride
• 英文别名: 5-[[4-(2-Chloroanilino)pyrimidin-2-yl]amino]-1,3-dihydrobenzimidazol-2-one;hydrochloride
• CAS: 1395886-00-6
• 化学式: C₁₇H₁₃ClN₆O*ClH
• 分子量: 389.244
• InChiKey: XDSFCVMHYHJNLS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.21
• 重原子数：
  26
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  91
• 氢给体数：
  5
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  邻氨基苯甲酸 在 盐酸 作用下， 以 乙醇 、 水 为溶剂， 反应 72.67h， 生成 5-((4-((2-chlorophenyl)amino)pyrimidin-2-yl)amino)-1H-benzo[d]imidazol-2(3H)-one hydrochloride
  参考文献：
  名称：

  [EN] AURORA KINASE INHIBITORS AND METHODS OF MAKING AND USING THEREOF
  [FR] INHIBITEURS DE KINASE AURORA ET PROCÉDÉS POUR LES FABRIQUER ET LES UTILISER

  摘要：

  公开号：

  WO2012135641A3

文献信息

• Development of <i>o</i>-Chlorophenyl Substituted Pyrimidines as Exceptionally Potent Aurora Kinase Inhibitors
  作者：Harshani R. Lawrence、Mathew P. Martin、Yunting Luo、Roberta Pireddu、Hua Yang、Harsukh Gevariya、Sevil Ozcan、Jin-Yi Zhu、Robert Kendig、Mercedes Rodriguez、Roy Elias、Jin Q. Cheng、Saïd M. Sebti、Ernst Schonbrunn、Nicholas J. Lawrence

  DOI：10.1021/jm300334d

  日期：2012.9.13

  The o-carboxylic acid substituted bisanilinopyrimidine 1 was identified as a potent hit (Aurora A IC50 = 6.1 +/- 1.0 nM) from in-house screening. Detailed structure-activity relationship (SAR) studies indicated that polar substituents at the para position of the B-ring are critical for potent activity. X-ray crystallography studies revealed that compound 1 is a type I inhibitor that binds the Aurora kinase active site in a DFG-in conformation. Structure-activity guided replacement of the A-ring carboxylic acid with halogens and incorporation of fluorine at the pyrimidine 5-position led to highly potent inhibitors of Aurora A that bind in a DFG-out conformation. B-Ring modifications were undertaken to improve the solubility and cell permeability. Compounds such as 9m with water-solubilizing moieties at the para position of the B-ring inhibited the autophosphorylation of Aurora A in MDA-MB-468 breast cancer cells.