(S)-2-Amino-1-(3-phenyl-1,2,4-oxadiazol-5-yl)-butan-1-ol | 537707-05-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: (S)-2-Amino-1-(3-phenyl-1,2,4-oxadiazol-5-yl)-butan-1-ol
• 英文别名: 2-Amino-1-(3-phenyl-1,2,4-oxadiazol-5-yl)-butan-1-ol；2-amino-1-(3-phenyl-1,2,4-oxadiazol-5-yl)butan-1-ol
• CAS: 537707-05-4
• 化学式: C₁₂H₁₅N₃O₂
• 分子量: 233.27
• InChiKey: DBAZNOUSKXILRL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  85.2
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (R)-4,4-Dimethyl-2-(2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pentanoic acid 、 (S)-2-Amino-1-(3-phenyl-1,2,4-oxadiazol-5-yl)-butan-1-ol 生成 (r)-4,4-Dimethyl-2-(2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pentanoic acid[1-(3-phenyl-1,2,4-oxadiazole-5-carbonyl)-propyl]-amide
  参考文献：
  名称：

  Compounds and compositions as cathepsin inhibitors

  摘要：

  本发明涉及新型的S型卡特普西酶抑制剂，其药用盐和N-氧化物，以及它们作为治疗剂的用途和制备方法。

  公开号：

  US07030116B2

文献信息

• [EN] AMIDINO COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS<br/>[FR] COMPOSES AMIDINO SERVANT D'INHIBITEURS DE PROTEASES A CYSTEINE
  申请人：AXYS PHARMACEUTICALS

  公开号：WO2004108661A1

  公开（公告）日：2004-12-16

  The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.

  本发明涉及一种抑制半胱氨酸蛋白酶的化合物，特别是包括B、K、L、F和S半胱氨酸蛋白酶，因此在治疗由这些蛋白酶介导的疾病方面具有用处。本发明涉及包含这些化合物的药物组合物以及其制备方法。
• [EN] CYSTEINE PROTEASE INHIBITORS<br/>[FR] INHIBITEURS DE LA CYSTEINE PROTEASE
  申请人：AXYS PHARM INC

  公开号：WO2003097617A1

  公开（公告）日：2003-11-27

  The present invention is directed to compounds that are inhibitors of cysteine protease, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.

  本发明涉及一种抑制半胱氨酸蛋白酶的化合物，特别是包括B、K、L、F和S型半胱氨酸蛋白酶，在治疗由这些蛋白酶介导的疾病中具有用途。本发明涉及包括这些化合物的药物组合物和其制备方法。
• [EN] NOVEL KETO-OXADIAZOLE DERIVATIVES AS CATHEPSIN INHIBITORS<br/>[FR] NOUVEAUX DERIVES DE CETO-OXADIAZOLE COMME INHIBITEURS DE LA CATHEPSINE
  申请人：AVENTIS PHARMA INC

  公开号：WO2005040142A1

  公开（公告）日：2005-05-06

  Novel difluorinated amide derivatives of Formula (II) as inhibitors of cathepsin S, K, B, and L, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making.

  Formula (II)的新颖二氟化酰胺衍生物作为猫hepsin S、K、B和L的抑制剂，其药用盐和N-氧化物，它们作为治疗剂的用途以及其制备方法。
• Novel compounds and compositions as cathepsin S inhibitors
  申请人：——

  公开号：US20030199506A1

  公开（公告）日：2003-10-23

  The present invention relates to novel selective cathepsin S inhibitors, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making. 1

  本发明涉及新型选择性卡特普西林S抑制剂，其药学上可接受的盐和N-氧化物，以及它们作为治疗剂的用途和制备方法。
• Novel compounds and compositions as cathepsin inhibitors
  申请人：——

  公开号：US20030105099A1

  公开（公告）日：2003-06-05

  The present invention relates to novel cathepsin S inhibitors, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making.

  本发明涉及新型卡特普西林S抑制剂、其药学上可接受的盐和N-氧化物，它们作为治疗剂的用途以及它们的制备方法。