3-[(1-Amino-2-phenyl-ethyl)-hydroxy-phosphinoyl]-2-benzyl-propionic acid | 234452-71-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 苯丙酸
• 英文名称: 3-[(1-Amino-2-phenyl-ethyl)-hydroxy-phosphinoyl]-2-benzyl-propionic acid
• 英文别名: 3-[(1-Amino-2-phenyl-ethyl)-hydroxy-phosphinoyl]-2-benzylpropionic acid；2-[[(1-amino-2-phenylethyl)-hydroxyphosphoryl]methyl]-3-phenylpropanoic acid
• CAS: 234452-71-2
• 化学式: C₁₈H₂₂NO₄P
• 分子量: 347.351
• InChiKey: PCOMAGRTKGTDAD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.7
• 重原子数：
  24
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  101
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-硝基苯基 N-(叔丁氧羰基)-L-亮氨酸酯 、 3-[(1-Amino-2-phenyl-ethyl)-hydroxy-phosphinoyl]-2-benzyl-propionic acid 在 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 生成
  参考文献：
  名称：

  Development of Potent and Selective Phosphinic Peptide Inhibitors of Angiotensin-Converting Enzyme 2

  摘要：

  Arimotensin-converting enzyme 2 (ACE2), a recently identified human homologue of angiotensin-converting enzyme, is a zinc metallocarboxypeptidase which may play a unique role in cardiovascular and renal function. Here we report the discovery of potent and selective inhibitors of ACE2, which have been identified by evaluating a series of phosphinic di- and tripeptides of the general formula: Z-Xaa(PO2-CH2)YaaOH and Ac-Zaa-Xaa(PO2-CH2)YaaOH. The most potent inhibitor in this series is a tripeptide that displays a K-i value of 0.4 nM toward ACE2 and is 3 orders of magnitude less potent toward carboxypeptidase A. Phosphinic tripeptides exhibit high potency exclusively when the Xaa position is occupied by a pseudoproline. A model of interaction between one inhibitor of this series and ACE2 suggests that the critical role played by a proline in inhibitors, but also for substrates hydrolysis, may rely on the presence of Tyr(510) in the ACE2 active site.

  DOI：

  10.1021/jm701275z
• 作为产物：
  描述：

  2-苄基丙烯酸甲酯 在 sodium hydroxide 、 N,O-双三甲硅基乙酰胺 、 三溴化硼 作用下， 生成 3-[(1-Amino-2-phenyl-ethyl)-hydroxy-phosphinoyl]-2-benzyl-propionic acid
  参考文献：
  名称：

  Design of the first highly potent and selective aminopeptidase N (EC 3.4.11.2) inhibitor

  摘要：

  A series of phosphinic compounds mimicking the transition state of substrates hydrolysed by aminopeptidase N (EC 3.4.11.2) were synthesized. These new compounds have potent inhibitory activities with Ki values in the nanomolar range. These derivatives behave as the most potent APN inhibitors designed to date.

  DOI：

  10.1016/s0960-894x(99)00219-x

文献信息

• Development of Potent and Selective Phosphinic Peptide Inhibitors of Angiotensin-Converting Enzyme 2
  作者：Andreas Mores、Magdalini Matziari、Fabrice Beau、Philippe Cuniasse、Athanasios Yiotakis、Vincent Dive

  DOI：10.1021/jm701275z

  日期：2008.4.1

  Arimotensin-converting enzyme 2 (ACE2), a recently identified human homologue of angiotensin-converting enzyme, is a zinc metallocarboxypeptidase which may play a unique role in cardiovascular and renal function. Here we report the discovery of potent and selective inhibitors of ACE2, which have been identified by evaluating a series of phosphinic di- and tripeptides of the general formula: Z-Xaa(PO2-CH2)YaaOH and Ac-Zaa-Xaa(PO2-CH2)YaaOH. The most potent inhibitor in this series is a tripeptide that displays a K-i value of 0.4 nM toward ACE2 and is 3 orders of magnitude less potent toward carboxypeptidase A. Phosphinic tripeptides exhibit high potency exclusively when the Xaa position is occupied by a pseudoproline. A model of interaction between one inhibitor of this series and ACE2 suggests that the critical role played by a proline in inhibitors, but also for substrates hydrolysis, may rely on the presence of Tyr(510) in the ACE2 active site.
• Design of the first highly potent and selective aminopeptidase N (EC 3.4.11.2) inhibitor
  作者：Huixiong Chen、Bernard P. Roques、Marie-Claude Fournié-Zaluski

  DOI：10.1016/s0960-894x(99)00219-x

  日期：1999.6

  A series of phosphinic compounds mimicking the transition state of substrates hydrolysed by aminopeptidase N (EC 3.4.11.2) were synthesized. These new compounds have potent inhibitory activities with Ki values in the nanomolar range. These derivatives behave as the most potent APN inhibitors designed to date.