(2R,3S)-3-{[(S)-1-((S)-2-{(S)-2-[(S)-4-tert-Butoxycarbonyl-2-((S)-3-tert-butoxycarbonyl-2-tert-butoxycarbonylamino-propionylamino)-butyrylamino]-3-methyl-butyrylamino}-3-methyl-butyryl)-pyrrolidine-2-carbonyl]-amino}-2-hydroxy-pentanoic acid | 274918-68-2

• 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: (2R,3S)-3-{[(S)-1-((S)-2-{(S)-2-[(S)-4-tert-Butoxycarbonyl-2-((S)-3-tert-butoxycarbonyl-2-tert-butoxycarbonylamino-propionylamino)-butyrylamino]-3-methyl-butyrylamino}-3-methyl-butyryl)-pyrrolidine-2-carbonyl]-amino}-2-hydroxy-pentanoic acid
• CAS: 274918-68-2
• 化学式: C₄₂H₇₂N₆O₁₄
• 分子量: 885.065
• InChiKey: VABODAWRTHPEJW-VMIUUUFISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.83
• 重原子数：
  62.0
• 可旋转键数：
  20.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  285.17
• 氢给体数：
  7.0
• 氢受体数：
  13.0

反应信息

• 作为反应物：
  描述：

  (2R,3S)-3-{[(S)-1-((S)-2-{(S)-2-[(S)-4-tert-Butoxycarbonyl-2-((S)-3-tert-butoxycarbonyl-2-tert-butoxycarbonylamino-propionylamino)-butyrylamino]-3-methyl-butyrylamino}-3-methyl-butyryl)-pyrrolidine-2-carbonyl]-amino}-2-hydroxy-pentanoic acid 在 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 tert-butyl (4S)-5-[[(2S)-1-[[(2S)-1-[(2S)-2-[[(3S)-1,2-dioxo-1-(prop-2-enylamino)pentan-3-yl]carbamoyl]pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-4-[[(2S)-4-[(2-methylpropan-2-yl)oxy]-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoyl]amino]-5-oxopentanoate
  参考文献：
  名称：

  α-Ketoamides, α-ketoesters and α-diketones as HCV NS3 protease inhibitors

  摘要：

  Peptide-based alpha-ketoamides, alpha-ketoesters and alpha-diketones were designed, synthesized and evaluated against HCV NS3 protease. alpha-Ketoamides have the highest affinity among the three classes, with 8 being the most potent inhibitor with an IC50 Of 340 nM. (C) 2000 DuPont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(00)00074-3
• 作为产物：
  描述：

  (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-pentanoic acid methyl ester 在 palladium on activated charcoal lithium hydroxide 、 氢气 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 生成 (2R,3S)-3-{[(S)-1-((S)-2-{(S)-2-[(S)-4-tert-Butoxycarbonyl-2-((S)-3-tert-butoxycarbonyl-2-tert-butoxycarbonylamino-propionylamino)-butyrylamino]-3-methyl-butyrylamino}-3-methyl-butyryl)-pyrrolidine-2-carbonyl]-amino}-2-hydroxy-pentanoic acid
  参考文献：
  名称：

  α-Ketoamides, α-ketoesters and α-diketones as HCV NS3 protease inhibitors

  摘要：

  Peptide-based alpha-ketoamides, alpha-ketoesters and alpha-diketones were designed, synthesized and evaluated against HCV NS3 protease. alpha-Ketoamides have the highest affinity among the three classes, with 8 being the most potent inhibitor with an IC50 Of 340 nM. (C) 2000 DuPont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(00)00074-3