1-(2-Hydroxy-ethoxymethyl)-4-nitro-2,5-diphenyl-1H-pyrrole-3-carboxylic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: 1-(2-Hydroxy-ethoxymethyl)-4-nitro-2,5-diphenyl-1H-pyrrole-3-carboxylic acid
• 英文别名: 1-[(2-Hydroxyethoxy)methyl]-4-nitro-2,5-diphenyl-1H-pyrrole-3-carboxylic acid；1-(2-hydroxyethoxymethyl)-4-nitro-2,5-diphenylpyrrole-3-carboxylic acid
• 化学式: C₂₀H₁₈N₂O₆
• 分子量: 382.373
• InChiKey: DJOWFPCMUURQMD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  28
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  118
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  ethyl 4-nitro-2,5-diphenyl-1H-pyrrole-3-carboxylate 在 氢氧化钾 、 水 、 sodium hydride 作用下， 以 乙醇 、 乙腈 为溶剂， 反应 6.0h， 生成 1-(2-Hydroxy-ethoxymethyl)-4-nitro-2,5-diphenyl-1H-pyrrole-3-carboxylic acid
  参考文献：
  名称：

  Glycosidopyrroles Part 1. Acyclic derivatives: 1-(2-hydroxyethoxy) methylpyrroles as potential anti-viral agents

  摘要：

  Acyclic glycosidopyrroles of type 1, synthesized in good overall yields, were evaluated for anti-viral activity. Compound 10i was found to inhibit the HIV-1 replication at concentrations that were very close to those cytotoxic for MT-4 cells. Compounds 10a,f,i inhibited both strains HSV-1 and HSV-2 at concentrations slightly below those cytotoxic for Vero cells. However for this series of glycosidopyrroles some relationship between calculated log P values and the observed cytotoxicity was found. (C) 1998 Elsevier Science S.A.

  DOI：

  10.1016/s0014-827x(97)00002-5