1-((1,1'-biphenyl)-3-ylmethyl)-2-methyl-4-hydroxy-1H-indole | 172732-89-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-((1,1'-biphenyl)-3-ylmethyl)-2-methyl-4-hydroxy-1H-indole
• 英文别名: 1-([1,1'-Biphenyl]-3-ylmethyl)-4-hydroxy-2-methyl-1H-indole；1-((1,1'-Biphenyl)-3-ylmethyl)-4-hydroxy-2-methyl-1H-indole；2-methyl-1-[(3-phenylphenyl)methyl]indol-4-ol
• CAS: 172732-89-7
• 化学式: C₂₂H₁₉NO
• 分子量: 313.399
• InChiKey: HMSMRRVYYQFEOB-UHFFFAOYSA-N

物化性质

• 沸点：
  540.7±38.0 °C(Predicted)
• 密度：
  1.11±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  24
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  25.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-((1,1'-biphenyl)-3-ylmethyl)-2-methyl-4-hydroxy-1H-indole 在 氨 、 sodium hydride 作用下， 以 二氯甲烷 为溶剂， 反应 19.0h， 生成 ((3-(2-amino-1,2-dioxoethyl)-1-((1,1'-biphenyl)-3-ylmethyl)-2-methyl-1H-indol-4-yl)oxy)acetic acid methyl ester
  参考文献：
  名称：

  Indole Inhibitors of Human Nonpancreatic Secretory Phospholipase A₂. 3. Indole-3-glyoxamides

  摘要：

  The preceding papers of this series detail the development of functionalized indole-3-acetamides as inhibitors of hnps-PLA(2). We describe here the extension of the structure-activity relationship to include a series of indole-3-glyoxamide derivatives. Functionalized indole-3-glyoxamides with an acidic substituent appended to the 4- or 5-position of the indole ring were prepared and tested as inhibitors of hnps-PLA(2). It was found that the indole-3-glyoxamides with a 4-oxyacetic acid substituent had optimal inhibitory activity. These inhibitors exhibited an improvement in potency over the best of the indole-3-acetamides, and LY315920 (6m) was selected for evaluation clinically as an hnps-PLA(2) inhibitor.

  DOI：

  10.1021/jm960487f
• 作为产物：
  描述：

  1-((1,1'-biphenyl)-3-ylmethyl)-2-methyl-4-methoxy-1H-indole 在 三溴化硼 作用下， 以87%的产率得到1-((1,1'-biphenyl)-3-ylmethyl)-2-methyl-4-hydroxy-1H-indole
  参考文献：
  名称：

  1H-indole-3-glyoxylamide SPLA.sub.2 inhibitors

  摘要：

  一种新型的1H-吲哚-3-甘氧酰胺类化合物被揭示，以及利用这类吲哚化合物抑制sPLA.sub.2介导的脂肪酸释放，用于治疗诸如感染性休克等疾病的方法。

  公开号：

  US05654326A1

文献信息

• Morpholino-N-ethyl ester prodrugs of indole sPLA2 inhibitors
  申请人：Eli Lilly and Company

  公开号：US06177426B1

  公开（公告）日：2001-01-23

  The compound, ((3(2-amino-1,2-dioxoethyl)-1-((1,1′-biphenyl)-3-ylmethyl)-2-methyl-1H-indol-4-yl)oxy)acetic acid morpholino-ethyl ester, is disclosed together with its use as a highly bioavailable indole compound for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.

  这种化合物，((3(2-氨基-1,2-二氧乙基)-1-((1,1′-联苯)-3-基甲基)-2-甲基-1H-吲哚-4-基氧基)乙酸吗啡啶乙酯)，以及其作为一种高生物利用度的吲哚化合物用于抑制sPLA2介导的脂肪酸释放，用于治疗诸如感染性休克等疾病的用途被披露。
• 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。
• Method for treatment of chronic bronchitis using indole compounds
  申请人：Eli Lilly and Company

  公开号：US05972988A1

  公开（公告）日：1999-10-26

  A method is disclosed for the treatment of chronic bronchitis by administering to a mammal in need thereof a therapeutically effective amount of a 1H-indole-3-glyoxylamide compound.

  揭示了一种治疗慢性支气管炎的方法，通过向需要的哺乳动物施用治疗有效量的1H-吲哚-3-甘氧酰胺化合物。
• N,N-diethylglycolamido ester prodrugs of indole sPLA2 inhibitors
  申请人：Eli Lilly and Company

  公开号：US06274616B1

  公开（公告）日：2001-08-14

  The compound, ((3-(2-amino-1,2-dioxoethyl)-1-((1,1′-biphenyl-3-ylmethyl)-2-methyl-1H-indol-4-yl)oxy)acetic acid N,N-diethylglycolamido ester, is disclosed together with its use as a highly bioavailable indole compound for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.

  这种化合物，((3-(2-氨基-1,2-二氧乙基)-1-((1,1′-联苯-3-基甲基)-2-甲基-1H-吲哚-4-基)氧基)乙酸N,N-二乙基甘醇酰胺酯，以及其作为一种高生物利用度的吲哚化合物用于抑制sPLA2介导的脂肪酸释放，用于治疗诸如感染性休克等疾病的用途被披露。
• 1H-indole-3-glyoxylamide sPLA.sub.2 inhibitors
  申请人：Eli Lilly and Company

  公开号：US05733923A1

  公开（公告）日：1998-03-31

  A class of novel 1H-indole-3-glyoxylamides is disclosed together with the use of such indole compounds for inhibiting sPLA.sub.2 mediated release of fatty acids for treatment of conditions such as septic shock.

  一种新型的1H-吲哚-3-甘氧酰胺类化合物被披露，以及使用这些吲哚化合物抑制sPLA.sub.2介导的脂肪酸释放，用于治疗诸如感染性休克等疾病的方法。