(S)-4-氧代哌啶-2-羧酸

• 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
• 中文名称: (S)-4-氧代哌啶-2-羧酸
• 英文名称: 4-oxopiperidin-1-ium-2-carboxylate
• 化学式: C6H9NO3
• 分子量: 143.14
• InChiKey: UAISREBYDOFHJY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -2.8
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  73.8
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• PROCESS FOR THE PREPARATION OF 6-(ARYL)-4-AMINOPICOLINATES
  申请人：Renga James M.

  公开号：US20100311981A1

  公开（公告）日：2010-12-09

  3-Halo-6-(aryl)-4-iminotetrahydropicolinic acid esters are heated with polar solvents to prepare 6-(aryl)-4-aminopicolinates.

  3-卤代-6-(芳基)-4-亚胺四氢吡啶甲酸酯在极性溶剂中加热，可制备6-(芳基)-4-氨基吡啶酸酯。
• 3-HALO-(ARLY)-4-IMINOTETRAHYDROPICOLINATES AND THEIR USE AS HERBICIDES
  申请人：Renga James M.

  公开号：US20100311594A1

  公开（公告）日：2010-12-09

  3-Halo-6-(aryl)-4-iminotetrahydropicolinic acids having mono-, di- tri- and tetra-substituted aryl substituents in the 6-position, and their acid derivatives, are herbicides demonstrating a broad spectrum of weed control.

  在6-位置具有单取代、双取代、三取代和四取代芳基取代基的3-卤代-6-(芳基)-4-亚胺四氢吡啶酸及其酸衍生物是一类具有广泛杂草控制谱的除草剂。
• Substituted cyclic amine metalloprotease inhibitors
  申请人：——

  公开号：US20030105153A1

  公开（公告）日：2003-06-05

  The invention provides compounds which are useful as inhibitors of metalloproteases, and which are effective in treating conditions characterized by excess activity of these enzymes. In particular, the present invention relates to a compound having a structure according to Formula (I). 1 Also disclosed are compounds, pharmaceutical compositions and methods of treating diseases characterized by metalloprotease activity using these compounds or the pharmaceutical compositions containing them.

  该发明提供了作为金属蛋白酶抑制剂有用的化合物，对于治疗由这些酶活性过量引起的疾病具有有效性。特别是，本发明涉及具有按照式（I）的结构的化合物。还披露了利用这些化合物或含有它们的药物组合物治疗金属蛋白酶活性引起的疾病的方法。
• Bis (amino acid) molecular scaffolds
  申请人：——

  公开号：US20040077879A1

  公开（公告）日：2004-04-22

  The present invention provides molecular building blocks of rigid bis(amino acids). The molecular building blocks can be linked together through the formation of rigid diketopiperazine rings, to provide the desired three dimensional structure. Also provided is method of synthesizing macromolecules from the bis (amino acid) building blocks.

  本发明提供了刚性双(氨基酸)的分子构建模块。这些分子构建模块可以通过形成刚性二酮二肽环相互连接，以提供所需的三维结构。同时提供了一种从双(氨基酸)构建模块合成高分子的方法。
• Streptogramin antibiotics
  申请人：Koteva Kalinka

  公开号：US20050272646A1

  公开（公告）日：2005-12-08

  Disclosed is a cyclic peptide antibiotic in which an enzyme-sensitive bond is replaced by an enzyme-resistant bond.

  揭示了一种循环肽抗生素，其中一种酶敏感键被一种酶抗性键取代。