3-pyridin-4-ylpropyl (2S)-2-hydroxy-3-phenylpropanoate | 175918-13-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 3-pyridin-4-ylpropyl (2S)-2-hydroxy-3-phenylpropanoate
• CAS: 175918-13-5
• 化学式: C₁₇H₁₉NO₃
• 分子量: 285.343
• InChiKey: XZJQPMSCUPWFFM-INIZCTEOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  21
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  59.4
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-pyridin-4-ylpropyl (2S)-2-hydroxy-3-phenylpropanoate 在 palladium dihydroxide 氢气 、 三乙胺 作用下， 以 四氯化碳 、 乙醇 、 乙腈 为溶剂， 反应 19.5h， 生成 3-pyridin-4-ylpropyl (2S)-2-[methoxy-[(1R)-2-phenyl-1-[[(2R)-2-[[2-(phenylmethoxycarbonylamino)acetyl]amino]propanoyl]amino]ethyl]phosphoryl]oxy-3-phenylpropanoate
  参考文献：
  名称：

  Transition State Analogy of Phosphonic Acid Peptide Inhibitors of Pepsin

  摘要：

  A series of 11 phosphonate peptide analogs, RO(2)C-Xaa-Yaa-Phe-(PO2--O)-Phe O-(3-(4-pyridyl)propyl ester), were synthesized and evaluated as inhibitors of the aspartic peptidase pepsin. For the inhibitors with Gly or Ala at the P-2 position, the K-i values correlate with the K-m/k(cat) values of the corresponding substrates, demonstrating that these analogs mimic the transition state in the way the P-2-P-4 residues bind. Deviations from the correlation for the other inhibitor/substrate pairs imply a different binding orientation as a result of N-substitution at P-2 (Pro), contamination with the more potent diastereomer (D-Ala), or a change in rate-limiting step for turnover (lie).

  DOI：

  10.1021/jo952074c
• 作为产物：
  描述：

  4-吡啶丙醇 在 4-二甲氨基吡啶 、 四丁基氟化铵 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 14.33h， 生成 3-pyridin-4-ylpropyl (2S)-2-hydroxy-3-phenylpropanoate
  参考文献：
  名称：

  Transition State Analogy of Phosphonic Acid Peptide Inhibitors of Pepsin

  摘要：

  A series of 11 phosphonate peptide analogs, RO(2)C-Xaa-Yaa-Phe-(PO2--O)-Phe O-(3-(4-pyridyl)propyl ester), were synthesized and evaluated as inhibitors of the aspartic peptidase pepsin. For the inhibitors with Gly or Ala at the P-2 position, the K-i values correlate with the K-m/k(cat) values of the corresponding substrates, demonstrating that these analogs mimic the transition state in the way the P-2-P-4 residues bind. Deviations from the correlation for the other inhibitor/substrate pairs imply a different binding orientation as a result of N-substitution at P-2 (Pro), contamination with the more potent diastereomer (D-Ala), or a change in rate-limiting step for turnover (lie).

  DOI：

  10.1021/jo952074c

文献信息

• Transition State Analogy of Phosphonic Acid Peptide Inhibitors of Pepsin
  作者：Paul A. Bartlett、Mark A. Giangiordano

  DOI：10.1021/jo952074c

  日期：1996.1.1

  A series of 11 phosphonate peptide analogs, RO(2)C-Xaa-Yaa-Phe-(PO2--O)-Phe O-(3-(4-pyridyl)propyl ester), were synthesized and evaluated as inhibitors of the aspartic peptidase pepsin. For the inhibitors with Gly or Ala at the P-2 position, the K-i values correlate with the K-m/k(cat) values of the corresponding substrates, demonstrating that these analogs mimic the transition state in the way the P-2-P-4 residues bind. Deviations from the correlation for the other inhibitor/substrate pairs imply a different binding orientation as a result of N-substitution at P-2 (Pro), contamination with the more potent diastereomer (D-Ala), or a change in rate-limiting step for turnover (lie).