2-(1,1'-biphenyl-4-yl)ethylphosphinic acid | 860292-42-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-(1,1'-biphenyl-4-yl)ethylphosphinic acid
• CAS: 860292-42-8
• 化学式: C₁₄H₁₅O₂P
• 分子量: 246.246
• InChiKey: CFGIQBSMBGWWDF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.36
• 重原子数：
  17.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  37.3
• 氢给体数：
  1.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  2-(1,1'-biphenyl-4-yl)ethylphosphinic acid 在 1-羟基苯并三唑 、 一水合肼 、 N,N'-二环己基碳二亚胺 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 乙醇 、 二氯甲烷 、 甲苯 为溶剂， 生成 1-[(benzyloxy)carbonyl]prolyl-N¹-({[2-(1,1'-biphenyl-4-yl)ethyl](methoxy)phosphoryl}methyl)leucinamide
  参考文献：
  名称：

  Design, modelling, synthesis and biological evaluation of peptidomimetic phosphinates as inhibitors of matrix metalloproteinases MMP-2 and MMP-8

  摘要：

  Three novel peptidomimetic phosphinate inhibitors have been synthesized and evaluated as inhibitors of matrix metalloprotemases MMP-2 and MMP-8. Their IC50 values are in the micromolar range, and one of them showed to be the most effective inhibitor of MMP-2. The differences in binding affinities for MMP-2 and MMP-8 of the three phosphinates have been rationalized by means of modelling studies and molecular dynamics simulations. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.04.079
• 作为产物：
  描述：

  4-羟乙基联苯 在 咪唑 、 二(三甲基硅烷基)亚膦酸酯 、 碘 、 三苯基膦 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成 2-(1,1'-biphenyl-4-yl)ethylphosphinic acid
  参考文献：
  名称：

  Design, modelling, synthesis and biological evaluation of peptidomimetic phosphinates as inhibitors of matrix metalloproteinases MMP-2 and MMP-8

  摘要：

  Three novel peptidomimetic phosphinate inhibitors have been synthesized and evaluated as inhibitors of matrix metalloprotemases MMP-2 and MMP-8. Their IC50 values are in the micromolar range, and one of them showed to be the most effective inhibitor of MMP-2. The differences in binding affinities for MMP-2 and MMP-8 of the three phosphinates have been rationalized by means of modelling studies and molecular dynamics simulations. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.04.079