4-(3-Aminophenyl)-N-(3-chlorophenyl)-2-pyrimidinamine | 1026029-12-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 4-(3-Aminophenyl)-N-(3-chlorophenyl)-2-pyrimidinamine
• 英文别名: 4-(3-aminophenyl)-N-(3-chlorophenyl)pyrimidin-2-amine
• CAS: 1026029-12-8
• 化学式: C₁₆H₁₃ClN₄
• 分子量: 296.759
• InChiKey: KWPBFYVWKBJQKT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  63.8
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  3-(2-chloropyrimidin-4-yl)aniline 、 3-氯苯胺 在 palladium diacetate caesium carbonate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 作用下， 以 1,4-二氧六环 为溶剂， 反应 20.0h， 生成 4-(3-Aminophenyl)-N-(3-chlorophenyl)-2-pyrimidinamine
  参考文献：
  名称：

  Pyrimidine-based inhibitors of CaMKIIδ

  摘要：

  Non-ATP competitive pyrimidine-based inhibitors of CaMKIId were identified. Computational studies were enlisted to predict the probable mode of binding. The results of the computational studies led to the design of ATP competitive inhibitors with optimized hinge interactions. Inhibitors of this class possessed improved enzyme and cellular activity compared to early leads. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.02.056

文献信息

• [EN] AMINO - PYRIMIDINE COMPOUNDS AS INHIBITORS OF TBKL AND/OR IKK EPSILON<br/>[FR] COMPOSÉS D'AMINO-PYRIMIDINE EN TANT QU'INHIBITEURS DE TBKL ET OU D'IKK EPSILON
  申请人：MYREXIS INC

  公开号：WO2011046970A1

  公开（公告）日：2011-04-21

  The invention relates to certain amino-pyrimidine compounds which inhibit TBK1 and/or IKK epsilon and which may therefore find application in treating inflammation, cancer, septic shock and/or Primary open Angle Glaucoma (POAG).

  这项发明涉及抑制TBK1和/或IKK epsilon的某些氨基嘧啶化合物，因此可能在治疗炎症、癌症、感染性休克和/或原发性开角青光眼（POAG）中找到应用。
• Pyrimidine-based inhibitors of CaMKIIδ
  作者：Babu Mavunkel、Yong-jin Xu、Bindu Goyal、Don Lim、Qing Lu、Zheng Chen、Dan-Xiong Wang、Jeffrey Higaki、Indrani Chakraborty、Albert Liclican、Steve Sideris、Maureen Laney、Ulrike Delling、Rosanne Catalano、Linda S. Higgins、Hui Wang、Jing Wang、Ying Feng、Sundeep Dugar、Daniel E. Levy

  DOI：10.1016/j.bmcl.2008.02.056

  日期：2008.4

  Non-ATP competitive pyrimidine-based inhibitors of CaMKIId were identified. Computational studies were enlisted to predict the probable mode of binding. The results of the computational studies led to the design of ATP competitive inhibitors with optimized hinge interactions. Inhibitors of this class possessed improved enzyme and cellular activity compared to early leads. (C) 2008 Elsevier Ltd. All rights reserved.