2-Indol-1-yl-2-oxoacetamide

• 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-Indol-1-yl-2-oxoacetamide
• 化学式: C₁₀H₈N₂O₂
• 分子量: 188.18
• InChiKey: ZBKZJJJGTUOACW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  65.1
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• Method for treating sepsis
  申请人：——

  公开号：US20040110825A1

  公开（公告）日：2004-06-10

  A novel method of treating and/or preventing sepsis.

  一种治疗和/或预防败血症的新方法。
• Combination therapy for the treatment of inflammatory and respiratory diseases
  申请人：——

  公开号：US20030092767A1

  公开（公告）日：2003-05-15

  A pharmaceutical composition for the treatment of Inflammatory Disease or Respiratory Disease in mammals, which comprises, as active ingredients, a neutrophil elastase inhibitor and an sPLA 2 inhibitor.

  一种用于治疗哺乳动物的炎症性疾病或呼吸道疾病的药物组合物，其包括中性粒细胞弹性蛋白酶抑制剂和sPLA2抑制剂作为活性成分。
• Diazaindole-dicarbonyl-piperazinyl antiviral agents
  申请人：Bender A. John

  公开号：US20050124623A1

  公开（公告）日：2005-06-09

  The invention comprises substituted diazaindole-dicarbonyl-piperazinyl derivatives of general Formula I wherein: Q is selected from the group consisting of — may represent a bond; T is —C(O)— or —CH(CN)—; and —Y— is selected from the group consisting of compositions thereof and their use for treating HIV infection.

  这项发明包括通式I的替代二氮杂吲哚-二羰基-哌嗪基衍生物，其中：Q选自由一组，可以表示成键；T为—C(O)—或—CH(CN)—；以及—Y—选自由一组，包括其组成物及其用于治疗HIV感染的用途。
• Indole, azaindole and related heterocyclic N-substituted piperazine derivatives
  申请人：Yeung Kap-Sun

  公开号：US20050261296A1

  公开（公告）日：2005-11-24

  This invention provides compounds of Formula I, including pharmaceutically accceptable salts thereof, having drug and bio-affecting properties, their pharmaceutical compositions and method of use. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS. The compounds of Formula I have the formula wherein: Z is Q is selected from the group consisting of m is 2; A is selected from the group consisting of cinnolinyl, napthyridinyl, quinoxalinyl, pyridinyl, pyrimidinyl, quinolinyl, isoquinolinyl, quinazolinyl, azabenzofuryl, and phthalazinyl each of which may be optionally substituted with one or two groups independently selected from methyl, methoxy, hydroxy, amino and halogen; and —W— is

  这项发明提供了具有药物和生物影响性质的Formula I化合物，包括其药用盐，以及它们的药物组合物和使用方法。这些化合物具有独特的抗病毒活性，无论是单独使用还是与其他抗病毒药物、抗感染药物、免疫调节剂或HIV进入抑制剂结合使用。更具体地，本发明涉及治疗HIV和艾滋病。Formula I化合物的结构如下：Z是Q是从以下组中选择的m为2；A是从以下组中选择的：菲啰啉基、萘啉基、喹喉基、吡啶基、嘧啶基、喹啉基、异喹啉基、喹唑啉基、氮杂苯并呋喃基和邻苯二嗪基，每种基可能被一个或两个分别选择自甲基、甲氧基、羟基、氨基和卤素的基取代；而—W—是。
• Method for the treatment of renal dysfunction with spla2 inhibitors
  申请人：——

  公开号：US20030087944A1

  公开（公告）日：2003-05-08

  A method is disclosed for the treatment of of the symptoms associated with renal dysfunction by administering to an animal in need thereof a therapeutically effective amount of a sPLA 2 inhibitor, such as a 1H-indole-3-glyoxylamide.

  本方法揭示了一种治疗与肾功能障碍相关症状的方法，通过向需要治疗的动物施用一种治疗有效量的 sPLA2 抑制剂，如 1H-吲哚-3-甘酰胺。