N-Heptyl-oxalamic acid | 75235-41-5

• 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: N-Heptyl-oxalamic acid
• 英文别名: 2-(Heptylamino)-2-oxoacetic acid
• CAS: 75235-41-5
• 化学式: C₉H₁₇NO₃
• 分子量: 187.239
• InChiKey: AHHZPWICVXDGGE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  13
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  66.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-Heptyl-oxalamic acid 在 戴斯-马丁氧化剂 、 N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下， 以 二氯甲烷 为溶剂， 反应 2.25h， 生成 (S)-3-[(S)-2-(Heptylaminooxalyl-amino)-3-methyl-butyrylamino]-4-oxo-5-(2,3,5,6-tetrafluoro-phenoxy)-pentanoic acid tert-butyl ester
  参考文献：
  名称：

  Oxamyl dipeptide caspase inhibitors developed for the treatment of stroke

  摘要：

  Structural modifications were made to a previously described acyl dipeptide caspase inhibitor, leading to the oxamyl dipeptide series. Subsequent SAR studies directed toward the warhead, P2, and P4 regions of this novel peptidomimetic are described herein. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.106
• 作为产物：
  描述：

  庚胺 在 lithium hydroxide 、 三乙胺 作用下， 以 1,4-二氧六环 为溶剂， 生成 N-Heptyl-oxalamic acid
  参考文献：
  名称：

  Oxamyl dipeptide caspase inhibitors developed for the treatment of stroke

  摘要：

  Structural modifications were made to a previously described acyl dipeptide caspase inhibitor, leading to the oxamyl dipeptide series. Subsequent SAR studies directed toward the warhead, P2, and P4 regions of this novel peptidomimetic are described herein. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.106

文献信息

• PETYUNIN G. P., FARMATSEVTICHNIJ ZH., 1980, HO 3, 40-2
  作者：PETYUNIN G. P.

  DOI：——

  日期：——
• Oxamyl dipeptide caspase inhibitors developed for the treatment of stroke
  作者：Steven D. Linton、Teresa Aja、Peter R. Allegrini、Thomas L. Deckwerth、Jose-Luis Diaz、Bastian Hengerer、Julia Herrmann、Kathy G. Jahangiri、Joerg Kallen、Donald S. Karanewsky、Steven P. Meduna、Kip Nalley、Edward D. Robinson、Silvio Roggo、Giorgio Rovelli、Andre Sauter、Robert O. Sayers、Albert Schmitz、Robert Smidt、Robert J. Ternansky、Kevin J. Tomaselli、Brett R. Ullman、Christoph Wiessner、Joe C. Wu

  DOI：10.1016/j.bmcl.2003.12.106

  日期：2004.5

  Structural modifications were made to a previously described acyl dipeptide caspase inhibitor, leading to the oxamyl dipeptide series. Subsequent SAR studies directed toward the warhead, P2, and P4 regions of this novel peptidomimetic are described herein. (C) 2004 Elsevier Ltd. All rights reserved.