2-adamantan-1-yl-3-(4,6-dimethylpyrimidin-2-yl)thiazolidin-4-one | 1118763-01-1

• 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: 2-adamantan-1-yl-3-(4,6-dimethylpyrimidin-2-yl)thiazolidin-4-one
• 英文别名: 2-(1-Adamantyl)-3-(4,6-dimethylpyrimidin-2-yl)thiazolidin-4-one；2-(1-adamantyl)-3-(4,6-dimethylpyrimidin-2-yl)-1,3-thiazolidin-4-one
• CAS: 1118763-01-1
• 化学式: C₁₉H₂₅N₃OS
• 分子量: 343.493
• InChiKey: TUJCAFHFBFZQLM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  71.4
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-氨基-4,6-二甲基嘧啶 、 1-金刚烷甲醛 、 巯基乙酸 以 甲苯 为溶剂， 以51%的产率得到2-adamantan-1-yl-3-(4,6-dimethylpyrimidin-2-yl)thiazolidin-4-one
  参考文献：
  名称：

  Synthesis and anti-HIV studies of 2- and 3-adamantyl-substituted thiazolidin-4-ones

  摘要：

  A series of novel thiazolidin-4-ones bearing a lipophilic adamantyl substituent at position 2 or 3 were synthesized. A majority of them showed a modest anti-HIV-1 activity, whereas 2-adamantan-1-yl-3-(4,6-dimethylpyrimidin-2-yl)-thiazolidin-4-one (8) was endowed with a remarkable antiviral potency (EC50 = 0.67 mu M). The new series of compounds (22-29) with an adamantyl moiety at the 3-position of the thiazolidinone ring showed good to modest anti-HIV-1 activity (EC50 = 1.0-11 mu M) but also pronounced cytostatic activity. For example 24, 26 and 29 showed an EC50 of 1.0-2.0 mu M, while the 50% effective concentrations for 23 and 28 were 7.8 and 11.0 mu M, respectively. X-ray studies and quantum chemical calculations revealed that the anti-HIV activity of the compounds strongly depends on their dipole moments and conformation of the thiazolidinones. (C) 2008 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2008.02.039

文献信息

• Synthesis and anti-HIV studies of 2- and 3-adamantyl-substituted thiazolidin-4-ones
  作者：Jan Balzarini、Barbara Orzeszko-Krzesińska、Jan K. Maurin、Andrzej Orzeszko

  DOI：10.1016/j.ejmech.2008.02.039

  日期：2009.1

  A series of novel thiazolidin-4-ones bearing a lipophilic adamantyl substituent at position 2 or 3 were synthesized. A majority of them showed a modest anti-HIV-1 activity, whereas 2-adamantan-1-yl-3-(4,6-dimethylpyrimidin-2-yl)-thiazolidin-4-one (8) was endowed with a remarkable antiviral potency (EC50 = 0.67 mu M). The new series of compounds (22-29) with an adamantyl moiety at the 3-position of the thiazolidinone ring showed good to modest anti-HIV-1 activity (EC50 = 1.0-11 mu M) but also pronounced cytostatic activity. For example 24, 26 and 29 showed an EC50 of 1.0-2.0 mu M, while the 50% effective concentrations for 23 and 28 were 7.8 and 11.0 mu M, respectively. X-ray studies and quantum chemical calculations revealed that the anti-HIV activity of the compounds strongly depends on their dipole moments and conformation of the thiazolidinones. (C) 2008 Elsevier Masson SAS. All rights reserved.