2-(Methoxy-{1-[(R)-2-(3-nitro-phenylmethanesulfonylamino)-propionylamino]-ethyl}-phosphinoylmethyl)-pentanedioic acid dimethyl ester | 874161-64-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2-(Methoxy-{1-[(R)-2-(3-nitro-phenylmethanesulfonylamino)-propionylamino]-ethyl}-phosphinoylmethyl)-pentanedioic acid dimethyl ester
• CAS: 874161-64-5
• 化学式: C₂₁H₃₂N₃O₁₁PS
• 分子量: 565.538
• InChiKey: FQLNSPDKCPZYPG-BJUFDMBDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.53
• 重原子数：
  37.0
• 可旋转键数：
  15.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  197.31
• 氢给体数：
  2.0
• 氢受体数：
  11.0

反应信息

• 作为反应物：
  描述：

  2-(Methoxy-{1-[(R)-2-(3-nitro-phenylmethanesulfonylamino)-propionylamino]-ethyl}-phosphinoylmethyl)-pentanedioic acid dimethyl ester 在 lithium hydroxide 作用下， 以 1,4-二氧六环 为溶剂， 生成 2-[[hydroxy-[1-[[(2R)-2-[(3-nitrophenyl)methylsulfonylamino]propanoyl]amino]ethyl]phosphoryl]methyl]pentanedioic acid
  参考文献：
  名称：

  Design, synthesis and structure–activity relationships of new phosphinate inhibitors of MurD

  摘要：

  A series of new phosphinate compounds were designed and synthesized as inhibitors of the D-glutamic acid-adding enzyme (MurD) involved in peptidoglycan biosynthesis. They were tested against the MurD enzyme from Escherichia coli, allowing initial structure-activity relationships to be deduced. Two compounds had IC50 values near 100 mu M and constitute a promising starting point for further development. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.09.086
• 作为产物：
  描述：

  戊二酸,2-[[甲氧基[1-[[(苯基甲氧基)羰基]氨基]乙基]氧膦基]甲基]-,二甲基酯 在 palladium on activated charcoal 氢气 、 1-羟基苯并三唑 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 生成 2-(Methoxy-{1-[(R)-2-(3-nitro-phenylmethanesulfonylamino)-propionylamino]-ethyl}-phosphinoylmethyl)-pentanedioic acid dimethyl ester
  参考文献：
  名称：

  Design, synthesis and structure–activity relationships of new phosphinate inhibitors of MurD

  摘要：

  A series of new phosphinate compounds were designed and synthesized as inhibitors of the D-glutamic acid-adding enzyme (MurD) involved in peptidoglycan biosynthesis. They were tested against the MurD enzyme from Escherichia coli, allowing initial structure-activity relationships to be deduced. Two compounds had IC50 values near 100 mu M and constitute a promising starting point for further development. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.09.086