{5-amino-1-[(2-oxo-1,4-diphenyl-azetidin-3-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester | 1261613-10-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 内酰胺类
• 英文名称: {5-amino-1-[(2-oxo-1,4-diphenyl-azetidin-3-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester
• CAS: 1261613-10-8
• 化学式: C₂₇H₃₆N₄O₄
• 分子量: 480.607
• InChiKey: JUWDFCCFILNRMA-KOENEWCDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.53
• 重原子数：
  35.0
• 可旋转键数：
  10.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  113.76
• 氢给体数：
  3.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  {5-amino-1-[(2-oxo-1,4-diphenyl-azetidin-3-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester 在 溶剂黄146 、 三乙胺 作用下， 以 乙醇 为溶剂， 反应 25.0h， 以69%的产率得到[2,6-dioxo-3-(phenyl-phenylamino-methyl)-1,5diaza-cycloundec-7-yl]-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Design, synthesis and inhibition activity of novel cyclic peptides against protein tyrosine phosphatase A from Mycobacterium tuberculosis

  摘要：

  Mycobacterium tuberculosis, the causative agent for tuberculosis has employed several signalling molecules to sense the host cellular environment and act accordingly. For example, protein tyrosine phosphatase A (MPtpA) of M. tuberculosis, a signalling protein belonging to the tyrosine phosphatase superfamily, is involved in phagocytosis and is active in virulent mycobacterial form. Starting from a beta-lactam framework a new class of structure based cyclic peptide (CP) inhibitors was designed. The synthesis involves a crucial intramolecular transamidation via a ring opening reaction. All the compounds show moderate to good inhibitory activities against MPtpA in micromolar concentrations. The results of inhibition kinetics suggest mixed mode of inhibition. The binding constant determined from circular dichroism (CD) and fluorescence quenching studies shows strong binding of the hydrophilic side chain of CPs with the enzyme active site residues. All these are well supported by docking studies. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.09.052
• 作为产物：
  描述：

  {5-tert-butoxycarbonylamino-5-[(2-oxo-1,4-diphenyl-azetidin-3-ylmethyl)-carbamoyl]-pentyl}carbamic acid tert-butyl ester 在 palladium 10% on activated carbon 、 氢气 作用下， 以 乙醇 为溶剂， 反应 1.0h， 以85%的产率得到{5-amino-1-[(2-oxo-1,4-diphenyl-azetidin-3-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Design, synthesis and inhibition activity of novel cyclic peptides against protein tyrosine phosphatase A from Mycobacterium tuberculosis

  摘要：

  Mycobacterium tuberculosis, the causative agent for tuberculosis has employed several signalling molecules to sense the host cellular environment and act accordingly. For example, protein tyrosine phosphatase A (MPtpA) of M. tuberculosis, a signalling protein belonging to the tyrosine phosphatase superfamily, is involved in phagocytosis and is active in virulent mycobacterial form. Starting from a beta-lactam framework a new class of structure based cyclic peptide (CP) inhibitors was designed. The synthesis involves a crucial intramolecular transamidation via a ring opening reaction. All the compounds show moderate to good inhibitory activities against MPtpA in micromolar concentrations. The results of inhibition kinetics suggest mixed mode of inhibition. The binding constant determined from circular dichroism (CD) and fluorescence quenching studies shows strong binding of the hydrophilic side chain of CPs with the enzyme active site residues. All these are well supported by docking studies. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.09.052