(S)-2-{2-Benzyl-3-[(1-benzyloxycarbonylamino-3-methylsulfanyl-propyl)-hydroxy-phosphinoyl]-propionylamino}-3-phenyl-propionic acid methyl ester | 234452-66-5

• 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: (S)-2-{2-Benzyl-3-[(1-benzyloxycarbonylamino-3-methylsulfanyl-propyl)-hydroxy-phosphinoyl]-propionylamino}-3-phenyl-propionic acid methyl ester
• CAS: 234452-66-5
• 化学式: C₃₂H₃₉N₂O₇PS
• 分子量: 626.711
• InChiKey: GKSOXDSIFDZROK-VJPAEBCTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.02
• 重原子数：
  43.0
• 可旋转键数：
  16.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  131.03
• 氢给体数：
  3.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  (S)-2-{2-Benzyl-3-[(1-benzyloxycarbonylamino-3-methylsulfanyl-propyl)-hydroxy-phosphinoyl]-propionylamino}-3-phenyl-propionic acid methyl ester 在 sodium hydroxide 、 三溴化硼 作用下， 生成 (S)-2-{3-[(1-Amino-3-methylsulfanyl-propyl)-hydroxy-phosphinoyl]-2-benzyl-propionylamino}-3-phenyl-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
• 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 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 生成 (S)-2-{2-Benzyl-3-[(1-benzyloxycarbonylamino-3-methylsulfanyl-propyl)-hydroxy-phosphinoyl]-propionylamino}-3-phenyl-propionic acid methyl ester
  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

• Phosphinic Derivatives as New Dual Enkephalin-Degrading Enzyme Inhibitors: Synthesis, Biological Properties, and Antinociceptive Activities
  作者：Huixiong Chen、Florence Noble、Aurélie Mothé、Hervé Meudal、Pascale Coric、Sophie Danascimento、Bernard P. Roques、Pascal George、Marie-Claude Fournié-Zaluski

  DOI：10.1021/jm990483l

  日期：2000.4.6

  The development of dual inhibitors of the two zinc metallopeptidases, neprilysin (neutral endopeptidase) and aminopeptidase N involved in the inactivation of the opioid peptides, enkephalins, represents an attractive physiological approach in the search for new analgesics devoid of the major drawbacks of morphine. Phosphinic compounds, corresponding to the general formula H(3)N(+)-CH(R(1))-P(O)(OH

  涉及阿片类肽脑啡肽失活的两种锌金属肽酶，中性溶酶（中性内肽酶）和氨基肽酶N双重抑制剂的开发代表了一种寻找新的止痛药的有吸引力的生理方法，该止痛药没有吗啡的主要缺点。对应于通式H（3）N（+）-CH（R（1））-P（O）（OH）-CH（2）-CH（R（2））-CONH-CH（ R（3））-COO（-），能够充当过渡态类似物并适合两种酶的S（1），S（1）'和S（2）'亚位点。选择R（1），R（2）和R（3）残基以最佳识别这些酶，导致了首个双重竞争抑制剂，其脑啡肽酶和氨基肽酶N的K（i）值在纳摩尔范围内。