2-methoxy-5-(1-(3,4,5-trimethoxyphenyl)-1H-tetrazol-5-yl)phenol | 1355597-87-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-methoxy-5-(1-(3,4,5-trimethoxyphenyl)-1H-tetrazol-5-yl)phenol
• 英文别名: 2-Methoxy-5-[1-(3,4,5-trimethoxyphenyl)tetrazol-5-yl]phenol
• CAS: 1355597-87-3
• 化学式: C₁₇H₁₈N₄O₅
• 分子量: 358.354
• InChiKey: UPDFSBOXUUODBW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  101
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  3-羟基-4-甲氧基苯甲酸 在 劳森试剂 、 叠氮基三甲基硅烷 、 mercury(II) diacetate 、 四丁基氟化铵 、 sodium hydride 、 1-羟基苯并三唑 、 N,N'-二异丙基碳二亚胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 mineral oil 为溶剂， 反应 26.0h， 生成 2-methoxy-5-(1-(3,4,5-trimethoxyphenyl)-1H-tetrazol-5-yl)phenol
  参考文献：
  名称：

  A-Ring Dihalogenation Increases the Cellular Activity of Combretastatin-Templated Tetrazoles

  摘要：

  The combretastatins have been investigated for their antimitotic and antivascular properties, and it is widely postulated that a 3,4,5-trimethoxyaryl A-ring is essential to maintain potent activity. We have synthesized new tetrazole analogues (32-34), demonstrating that 3,5-dihalogenation can consistently increase potency by up to 5-fold when compared to the equivalent trimethoxy compound on human umbilical vein endothelial cells (HUVECs) and a range of cancer cells. Moreover, this increased potency offsets that lost by installing the tetrazole bridge into combretastatin A-4 (1), giving crystalline, soluble compounds that have low nanomolar activity, arrest cells in G(2)/M phase, and retain microtubule inhibitory activity. Molecular modeling has shown that optimized packing within the binding site resulting in increased Coulombic interaction may be responsible for this improved activity.

  DOI：

  10.1021/ml200149g