ethyl (3R)-3-[[2-amino-2-(aminohydrazinylidene)acetyl]amino]-4-[4-(3-chlorophenyl)phenyl]butanoate

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 肽模拟物
• 英文名称: ethyl (3R)-3-[[2-amino-2-(aminohydrazinylidene)acetyl]amino]-4-[4-(3-chlorophenyl)phenyl]butanoate
• 化学式: C₂₀H₂₄ClN₅O₃
• 分子量: 417.9
• InChiKey: FBHPHKXSJJYFFW-QGZVFWFLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  29
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  132
• 氢给体数：
  4
• 氢受体数：
  6

文献信息

• SUBSTITUTED AMINOPROPIONIC DERIVATIVES AS NEPRILYSIN INHIBITORS
  申请人：COPPOLA Gary Mark

  公开号：US20140296240A1

  公开（公告）日：2014-10-02

  The present invention provides a compound of formula I′; or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , R 5 , B 1 , X and n are defined herein. The invention also relates a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了式I'的化合物；或其药学上可接受的盐，其中R1、R2、R3、R5、B1、X和n在此定义。本发明还涉及制造本发明化合物的方法及其治疗用途。本发明还提供了一种药理活性剂的组合和制药组合物。
• METHOD OF TREATING CONTRAST-INDUCED NEPHROPATHY
  申请人：FOO Shi Yin

  公开号：US20140336194A1

  公开（公告）日：2014-11-13

  The present invention provides the use of a neutral endopeptidase inhibitor, in the manufacture of a medicament for the treatment, amelioration and/or prevention of contrast-induced nephropathy. The invention also relates to the use of a compound of Formula I: wherein R 1 , R 2 , R 3 , R 5 , X, A 3 , B 1 , s and n are defined herein, for the treatment, amelioration and/or prevention of contrast-induced nephropathy. The present invention further provides a combination of pharmacologically active agents for use in the treatment, amelioration and/or prevention of contrast-induced nephropathy.

  本发明提供了一种中性内肽酶抑制剂的使用，用于制造用于治疗、改善和/或预防造影剂诱导性肾病的药物。本发明还涉及使用式I的化合物：其中R1、R2、R3、R5、X、A3、B1、s和n在此被定义，用于治疗、改善和/或预防造影剂诱导性肾病。本发明进一步提供了一种药理活性剂的组合，用于治疗、改善和/或预防造影剂诱导性肾病。
• Substituted Aminopropionic Derivatives as Neprilysin inhibitors
  申请人：Coppola Gary Mark

  公开号：US20100305131A1

  公开（公告）日：2010-12-02

  The present invention provides a compound of formula I′; or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , R 5 , B 1 , X and n are defined herein. The invention also relates a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了式I'的化合物；或其药学上可接受的盐，其中R1、R2、R3、R5、B1、X和n在此定义。本发明还涉及制造该化合物的方法及其治疗用途。本发明进一步提供了一种药理活性剂的组合和制药组合物。
• Substituted aminopropionic derivatives as neprilysin inhibitors
  申请人：Novartis AG

  公开号：EP2594556A1

  公开（公告）日：2013-05-22

  The present invention provides a compound of formula I'; or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R5, B1, X and n are defined herein. The invention also relates a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了一种式 I' 的化合物； 或其药学上可接受的盐，其中 R1、R2、R3、R5、B1、X 和 n 在本文中定义。本发明还涉及一种制造本发明化合物的方法及其治疗用途。本发明进一步提供了药理活性剂和药物组合物的组合。
• US8394853B2
  申请人：——

  公开号：US8394853B2

  公开（公告）日：2013-03-12