[(S)-1-(4-Hydroxy-benzooxazole-2-carbonyl)-2-methyl-propyl]-carbamic acid benzyl ester | 437755-88-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: [(S)-1-(4-Hydroxy-benzooxazole-2-carbonyl)-2-methyl-propyl]-carbamic acid benzyl ester
• 英文别名: [1-(4-Hydroxy-benzooxazole-2-carbonyl)-2-methyl-propyl]-carbamic acid benzyl ester；benzyl N-[(2S)-1-(4-hydroxy-1,3-benzoxazol-2-yl)-3-methyl-1-oxobutan-2-yl]carbamate
• CAS: 437755-88-9
• 化学式: C₂₀H₂₀N₂O₅
• 分子量: 368.389
• InChiKey: UWEQJISTSAVSHV-INIZCTEOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  27
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  102
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  [(S)-1-(4-Hydroxy-benzooxazole-2-carbonyl)-2-methyl-propyl]-carbamic acid benzyl ester 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 {(S)-1-[4-(2-Dimethylamino-ethoxy)-benzooxazole-2-carbonyl]-2-methyl-propyl}-carbamic acid benzyl ester
  参考文献：
  名称：

  Design and Synthesis of Peptide-Based Carboxylic Acid-Containing Transition-State Inhibitors of Human Neutrophil Elastase

  摘要：

  In our search for a new agent, human neutrophil elastase (HNE) inhibitor, for the treatment of acute respiratory failure, we rationally designed and synthesized a series of peptide-based carboxylic acid-containing transition-state inhibitors. The presence of valyl moiety is found to be essential for potent in vitro inhibitory activity and also prevention of an undesirable toxicity. Of these, compound 9m has the most potent in vivo effect on TINE-induced lung hemorrhage in hamsters. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(01)00797-1
• 作为产物：
  描述：

  {(S)-1-[4-(tert-Butyl-dimethyl-silanyloxy)-benzooxazole-2-carbonyl]-2-methyl-propyl}-carbamic acid benzyl ester 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 生成 [(S)-1-(4-Hydroxy-benzooxazole-2-carbonyl)-2-methyl-propyl]-carbamic acid benzyl ester
  参考文献：
  名称：

  Design and Synthesis of Peptide-Based Carboxylic Acid-Containing Transition-State Inhibitors of Human Neutrophil Elastase

  摘要：

  In our search for a new agent, human neutrophil elastase (HNE) inhibitor, for the treatment of acute respiratory failure, we rationally designed and synthesized a series of peptide-based carboxylic acid-containing transition-state inhibitors. The presence of valyl moiety is found to be essential for potent in vitro inhibitory activity and also prevention of an undesirable toxicity. Of these, compound 9m has the most potent in vivo effect on TINE-induced lung hemorrhage in hamsters. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(01)00797-1

文献信息

• Design and Synthesis of Peptide-Based Carboxylic Acid-Containing Transition-State Inhibitors of Human Neutrophil Elastase
  作者：Fuminori Sato、Yasunao Inoue、Tomoki Omodani、Kiyomi Imano、Hiroshi Okazaki、Tadashi Takemura、Masanobu Komiya

  DOI：10.1016/s0960-894x(01)00797-1

  日期：2002.2

  In our search for a new agent, human neutrophil elastase (HNE) inhibitor, for the treatment of acute respiratory failure, we rationally designed and synthesized a series of peptide-based carboxylic acid-containing transition-state inhibitors. The presence of valyl moiety is found to be essential for potent in vitro inhibitory activity and also prevention of an undesirable toxicity. Of these, compound 9m has the most potent in vivo effect on TINE-induced lung hemorrhage in hamsters. (C) 2002 Elsevier Science Ltd. All rights reserved.