(R)-N-((S)-1-cyano-3-phenylpropyl)-2-(cyclohexylmethyl)-4-morpholino-4-oxobutanamide | 939776-05-3

• 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: (R)-N-((S)-1-cyano-3-phenylpropyl)-2-(cyclohexylmethyl)-4-morpholino-4-oxobutanamide
• 英文别名: (2R)-N-[(1S)-1-cyano-3-phenylpropyl]-2-(cyclohexylmethyl)-4-morpholin-4-yl-4-oxobutanamide
• CAS: 939776-05-3
• 化学式: C₂₅H₃₅N₃O₃
• 分子量: 425.571
• InChiKey: JTOXWENSYBWYDL-PKTZIBPZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  31
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  82.4
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  在 三聚氯氰 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 (R)-N-((S)-1-cyano-3-phenylpropyl)-2-(cyclohexylmethyl)-4-morpholino-4-oxobutanamide
  参考文献：
  名称：

  Identification of a novel class of succinyl-nitrile-based Cathepsin S inhibitors

  摘要：

  The synthesis and in vitro activities of a series of suceinyl-nitrile-based inhibitors of Cathepsin S are described. Several members of this class show nanomolar inhibition of the target enzyme as well as cellular potency. The inhibitors displaying the greatest potency contain N-alkyl substituted piperidine and pyrrolidine rings spiro-fused to the alpha-carbon of the P1 residue. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.02.046

文献信息

• Identification of a novel class of succinyl-nitrile-based Cathepsin S inhibitors
  作者：Younes Bekkali、David S. Thomson、Raj Betageri、Michel J. Emmanuel、Ming-Hong Hao、Eugene Hickey、Weimin Liu、Usha Patel、Yancey D. Ward、Erick R.R. Young、Richard Nelson、Alison Kukulka、Maryanne L. Brown、Kathy Crane、Della White、Dorothy M. Freeman、Mark E. Labadia、Jessi Wildeson、Denice M. Spero

  DOI：10.1016/j.bmcl.2007.02.046

  日期：2007.5

  The synthesis and in vitro activities of a series of suceinyl-nitrile-based inhibitors of Cathepsin S are described. Several members of this class show nanomolar inhibition of the target enzyme as well as cellular potency. The inhibitors displaying the greatest potency contain N-alkyl substituted piperidine and pyrrolidine rings spiro-fused to the alpha-carbon of the P1 residue. (C) 2007 Elsevier Ltd. All rights reserved.