6-methyl-N4-(tetrahydro-2H-pyran-4-yl)pyrimidine-2,4,5-triamine | 1184919-33-2

• 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: 6-methyl-N4-(tetrahydro-2H-pyran-4-yl)pyrimidine-2,4,5-triamine
• 英文别名: 6-methyl-4-N-(oxan-4-yl)pyrimidine-2,4,5-triamine
• CAS: 1184919-33-2
• 化学式: C₁₀H₁₇N₅O
• 分子量: 223.278
• InChiKey: UINMTIZRCVHMOX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  99.1
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  乙醛酸乙酯 、 6-methyl-N4-(tetrahydro-2H-pyran-4-yl)pyrimidine-2,4,5-triamine 在 溶剂黄146 作用下， 以 乙醇 为溶剂， 生成
  参考文献：
  名称：

  4-Methylpteridinones as orally active and selective PI3K/mTOR dual inhibitors

  摘要：

  Pteridinones were designed based on a non-selective kinase template. Because of the uniqueness of the PI3K and mTOR binding pockets, a methyl group was introduced to C-4 position of the peteridinone core to give compounds with excellent selectivity for PI3K and mTOR. This series of compounds were further optimized to improve their potency against PI3K alpha and mTOR. Finally, orally active compounds with improved solubility and robust in vivo efficacy in tumor growth inhibition were identified as well. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.08.045
• 作为产物：
  描述：

  6-methyl-5-nitro-4-N-(oxan-4-yl)pyrimidine-2,4-diamine 在 palladium on carbon 、 氢气 作用下， 以 甲醇 为溶剂， 生成 6-methyl-N4-(tetrahydro-2H-pyran-4-yl)pyrimidine-2,4,5-triamine
  参考文献：
  名称：

  4-Methylpteridinones as orally active and selective PI3K/mTOR dual inhibitors

  摘要：

  Pteridinones were designed based on a non-selective kinase template. Because of the uniqueness of the PI3K and mTOR binding pockets, a methyl group was introduced to C-4 position of the peteridinone core to give compounds with excellent selectivity for PI3K and mTOR. This series of compounds were further optimized to improve their potency against PI3K alpha and mTOR. Finally, orally active compounds with improved solubility and robust in vivo efficacy in tumor growth inhibition were identified as well. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.08.045

文献信息

• 4-Methylpteridinones as orally active and selective PI3K/mTOR dual inhibitors
  作者：Kevin K.-C. Liu、Shubha Bagrodia、Simon Bailey、Hengmiao Cheng、Hui Chen、Lisa Gao、Samantha Greasley、Jacqui E. Hoffman、Qiyue Hu、Ted O. Johnson、Dan Knighton、Zhengyu Liu、Matthew A. Marx、Mitchell D. Nambu、Sacha Ninkovic、Bernadette Pascual、Kristina Rafidi、Caroline M.-L. Rodgers、Graham L. Smith、Shaoxian Sun、Haitao Wang、Anle Yang、Jing Yuan、Aihua Zou

  DOI：10.1016/j.bmcl.2010.08.045

  日期：2010.10

  Pteridinones were designed based on a non-selective kinase template. Because of the uniqueness of the PI3K and mTOR binding pockets, a methyl group was introduced to C-4 position of the peteridinone core to give compounds with excellent selectivity for PI3K and mTOR. This series of compounds were further optimized to improve their potency against PI3K alpha and mTOR. Finally, orally active compounds with improved solubility and robust in vivo efficacy in tumor growth inhibition were identified as well. (C) 2010 Elsevier Ltd. All rights reserved.