<2-benzyl-3-(tert-butylsulfonyl)propionyl>histidyl <(2S,3R,4R,5R,6R)-1-cyclohexyl-3,4:6,7-di-O-isopropylidene-3,4,5,6,7-pentahydroxyhept-2-yl>amide | 135902-04-4

• 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: <2-benzyl-3-(tert-butylsulfonyl)propionyl>histidyl <(2S,3R,4R,5R,6R)-1-cyclohexyl-3,4:6,7-di-O-isopropylidene-3,4,5,6,7-pentahydroxyhept-2-yl>amide
• 英文别名: [2-benzyl-3-(tert-butylsulfonyl)propionyl]histidyl ((2S,3R,4R,5R,6R)-1-cyclohexyl-3,4:6,7-di-O-isopropylidene-3,4,5,6,7-pentahydroxyhept-2-yl)amide
• CAS: 135902-04-4；138664-66-1
• 化学式: C₃₉H₆₀N₄O₉S
• 分子量: 760.993
• InChiKey: IVNLPMQOSLGZMG-FDZQTFNTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.0
• 重原子数：
  53.0
• 可旋转键数：
  15.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.72
• 拓扑面积：
  178.17
• 氢给体数：
  4.0
• 氢受体数：
  10.0

反应信息

• 作为反应物：
  描述：

  <2-benzyl-3-(tert-butylsulfonyl)propionyl>histidyl <(2S,3R,4R,5R,6R)-1-cyclohexyl-3,4:6,7-di-O-isopropylidene-3,4,5,6,7-pentahydroxyhept-2-yl>amide 在 对甲苯磺酸 作用下， 以 甲醇 、 水 为溶剂， 反应 72.0h， 以44%的产率得到<2-benzyl-3-(tert-butylsulfonyl)propionyl>histidyl <(2S,3R,4R,5R,6R)-1-cyclohexyl-3,4,5,6,7-pentahydroxyhept-2-yl>amide
  参考文献：
  名称：

  Renin inhibitory pentols showing improved enteral bioavailability

  摘要：

  Incorporation of a C-terminal pentahydroxy functionality led to potent, low molecular weight hydrophilic renin inhibitors lacking the P1' side chain. As these compounds are easy to synthesize and have sufficient water solubility, they were chosen for further study. Compound 33 was transported across rabbit intestinal brush border membrane vesicles and yielded a hypotensive effect in sodium-depleted rhesus monkeys which lasted for 90 min when dosed at 2 mg/kg id.

  DOI：

  10.1021/jm00081a019
• 作为产物：
  描述：

  N-benzhydrylmannofuranosylamine 2,3:5,6-diacetonide 在 palladium on activated charcoal 叠氮磷酸二苯酯 、 ammonium formate 、 lithium 、 三乙胺 、 N,N-二异丙基乙胺 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 70.0h， 生成 <2-benzyl-3-(tert-butylsulfonyl)propionyl>histidyl <(2S,3R,4R,5R,6R)-1-cyclohexyl-3,4:6,7-di-O-isopropylidene-3,4,5,6,7-pentahydroxyhept-2-yl>amide
  参考文献：
  名称：

  Renin inhibitory pentols showing improved enteral bioavailability

  摘要：

  Incorporation of a C-terminal pentahydroxy functionality led to potent, low molecular weight hydrophilic renin inhibitors lacking the P1' side chain. As these compounds are easy to synthesize and have sufficient water solubility, they were chosen for further study. Compound 33 was transported across rabbit intestinal brush border membrane vesicles and yielded a hypotensive effect in sodium-depleted rhesus monkeys which lasted for 90 min when dosed at 2 mg/kg id.

  DOI：

  10.1021/jm00081a019