ethyl 2-<<(2R,3S)-3-<(tert-butoxycarbonyl)amino>-4-cyclohexyl-2-hydroxy-1-butyl>thio>acetate | 142843-07-0

• 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: ethyl 2-<<(2R,3S)-3-<(tert-butoxycarbonyl)amino>-4-cyclohexyl-2-hydroxy-1-butyl>thio>acetate
• 英文别名: ethyl 2-[[(2R,3S)-3-(t-butoxycarbonylamino)-4-cyclohexyl-2-hydroxy-1-butyl]thio]acetate；ethyl 2-({(2R,3S)-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-hydroxy-1-butyl}thio)acetate；ethyl 2-[(2R,3S)-4-cyclohexyl-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]butyl]sulfanylacetate
• CAS: 142843-07-0
• 化学式: C₁₉H₃₅NO₅S
• 分子量: 389.557
• InChiKey: OLIBNBHOAVFXMS-HOTGVXAUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  26
• 可旋转键数：
  12
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  110
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  ethyl 2-<<(2R,3S)-3-<(tert-butoxycarbonyl)amino>-4-cyclohexyl-2-hydroxy-1-butyl>thio>acetate 在 间氯过氧苯甲酸 作用下， 以 二氯甲烷 为溶剂， 反应 49.5h， 生成 4-<2-<2-<<(2R,3S)-3-<(tert-butoxycarbonyl)amino>-4-cyclohexyl-2-hydroxy-1-butyl>thio>acetamido>ethyl>morpholine
  参考文献：
  名称：

  Inhibitors of human renin with C-termini derived from amides and esters of .alpha.-mercaptoalkanoic acids

  摘要：

  New transition-state analogues bearing C-termini derived from alpha-mercaptoalkanoic acids, esters, and amides were prepared and evaluated as inhibitors of human renin. Addition of alpha-mercaptoalkanoate esters to a chiral Boc-amino epoxide intermediate led ultimately to the target [(2R,3S)-3-(BocPheHis-amino)-4-cyclohexyl-2-hydroxy-1-butyl]thio derivatives. The corresponding sulfoxide and sulfone analogues were also investigated. Some of these derivatives, including one with a stable BocPhe replacement, were relatively potent inhibitors of human plasma renin, having IC50 values below 10 nM. When selected compounds were administered intravenously to sodium-deficient rhesus monkeys (Macaca mulatta) at 0.06-1 mg/kg, they reduced plasma renin activity by 87-94%. However, the accompanying drop in blood pressure was of short duration.

  DOI：

  10.1021/jm00093a009
• 作为产物：
  描述：

  (2R,3S)-3-(t-butoxycarbonylamino)-4-cyclohexyl-1,2-epoxybutane 、 巯基乙酸乙酯 在 三乙胺 作用下， 以 乙醇 、 正己烷 为溶剂， 以1.64 g (84%)的产率得到ethyl 2-<<(2R,3S)-3-<(tert-butoxycarbonyl)amino>-4-cyclohexyl-2-hydroxy-1-butyl>thio>acetate
  参考文献：
  名称：

  Renin inhibitors containing the

  摘要：

  这是一段关于某种化合物的说明，化合物的化学式为：##STR1## 这些化合物是人类肾素的强效抑制剂，可用于治疗各种形式的肾素相关高血压、高醛固酮症和充血性心力衰竭；含有这些肾素抑制剂化合物的组合物，可选搭配其他降压剂；以及使用这些新型化合物治疗高血压、高醛固酮症或充血性心力衰竭，或将肾素作为这些疾病的病因因素的方法。

  公开号：

  US05114925A1

文献信息

• US5114925A
  申请人：——

  公开号：US5114925A

  公开（公告）日：1992-05-19
• Inhibitors of human renin with C-termini derived from amides and esters of .alpha.-mercaptoalkanoic acids
  作者：Wallace T. Ashton、Christine L. Cantone、Richard L. Tolman、William J. Greenlee、Robert J. Lynch、Terry W. Schorn、John F. Strouse、Peter K. S. Siegl

  DOI：10.1021/jm00093a009

  日期：1992.7

  New transition-state analogues bearing C-termini derived from alpha-mercaptoalkanoic acids, esters, and amides were prepared and evaluated as inhibitors of human renin. Addition of alpha-mercaptoalkanoate esters to a chiral Boc-amino epoxide intermediate led ultimately to the target [(2R,3S)-3-(BocPheHis-amino)-4-cyclohexyl-2-hydroxy-1-butyl]thio derivatives. The corresponding sulfoxide and sulfone analogues were also investigated. Some of these derivatives, including one with a stable BocPhe replacement, were relatively potent inhibitors of human plasma renin, having IC50 values below 10 nM. When selected compounds were administered intravenously to sodium-deficient rhesus monkeys (Macaca mulatta) at 0.06-1 mg/kg, they reduced plasma renin activity by 87-94%. However, the accompanying drop in blood pressure was of short duration.
• Renin inhibitors containing the
  申请人：Merck & Co., Inc.

  公开号：US05114925A1

  公开（公告）日：1992-05-19

  Compounds of the formula: ##STR1## which are potent inhibitors of human renin and are useful for treating various forms of renin-associated hypertension, hyperaldosteronism and congestive heart failure; compositions containing these renin-inhibitory compounds, optionally with other antihypertensive agents; and methods of treating hypertension, hyperaldosteronism or congestive heart failure or of establishing renin as a causative factor in these conditions which employ these novel compounds.

  这是一段关于某种化合物的说明，化合物的化学式为：##STR1## 这些化合物是人类肾素的强效抑制剂，可用于治疗各种形式的肾素相关高血压、高醛固酮症和充血性心力衰竭；含有这些肾素抑制剂化合物的组合物，可选搭配其他降压剂；以及使用这些新型化合物治疗高血压、高醛固酮症或充血性心力衰竭，或将肾素作为这些疾病的病因因素的方法。