(3,4-Dichloro-phenyl)-[5-(3-methyl-5-nitro-3H-imidazol-4-yl)-[1,3,4]oxadiazol-2-yl]-amine | 876935-33-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: (3,4-Dichloro-phenyl)-[5-(3-methyl-5-nitro-3H-imidazol-4-yl)-[1,3,4]oxadiazol-2-yl]-amine
• CAS: 876935-33-0
• 化学式: C₁₂H₈Cl₂N₆O₃
• 分子量: 355.14
• InChiKey: FCRKPXNGJZNGEU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.43
• 重原子数：
  23.0
• 可旋转键数：
  4.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  111.91
• 氢给体数：
  1.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  (3,4-Dichloro-phenyl)-[5-(3-methyl-5-nitro-3H-imidazol-4-yl)-[1,3,4]oxadiazol-2-yl]-amine 在 palladium on activated charcoal 氢气 作用下， 以 甲醇 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 生成
  参考文献：
  名称：

  Hetaryl imidazoles: A novel dual inhibitors of VEGF receptors I and II

  摘要：

  A novel potent derivatives of hetaryl imidazoles were described as inhibitors of vascular endothelial growth factor receptor II (VEGFR-2). Several compounds display VEGFR-2 inhibitory activity reaching IC50 < 100 nM in both enzymatic and cellular assays, The compounds also inhibit the related tyrosine kinase, VEGFR-1. By controlling the substitution pattern on the 5-carboxamido functionality, both dual and specific VEGFR-2 thiazoles were identified. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.11.033
• 作为产物：
  描述：

  3-methyl-5-nitro-3H-imidazole-4-carboxylic acid hydrazide 在 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 6.0h， 生成 (3,4-Dichloro-phenyl)-[5-(3-methyl-5-nitro-3H-imidazol-4-yl)-[1,3,4]oxadiazol-2-yl]-amine
  参考文献：
  名称：

  Hetaryl imidazoles: A novel dual inhibitors of VEGF receptors I and II

  摘要：

  A novel potent derivatives of hetaryl imidazoles were described as inhibitors of vascular endothelial growth factor receptor II (VEGFR-2). Several compounds display VEGFR-2 inhibitory activity reaching IC50 < 100 nM in both enzymatic and cellular assays, The compounds also inhibit the related tyrosine kinase, VEGFR-1. By controlling the substitution pattern on the 5-carboxamido functionality, both dual and specific VEGFR-2 thiazoles were identified. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.11.033