1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-[2-(pyridin-4-yl)thiazol-4-ylmethyl]indole

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-[2-(pyridin-4-yl)thiazol-4-ylmethyl]indole
• 英文别名: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-[2-(4-pyridyl)thiazol-4-ylmethyl]indole；(4-Chlorophenyl)-[5-methoxy-2-methyl-3-[(2-pyridin-4-yl-1,3-thiazol-4-yl)methyl]indol-1-yl]methanone
• 化学式: C₂₆H₂₀ClN₃O₂S
• 分子量: 473.983
• InChiKey: LAWDVGKULZTSDS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  33
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  85.2
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  吲哚美辛 在 氯化亚砜 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 24.0h， 生成 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-[2-(pyridin-4-yl)thiazol-4-ylmethyl]indole
  参考文献：
  名称：

  Thiazole analogues of the NSAID indomethacin as selective COX-2 Inhibitors

  摘要：

  The carboxyl group of the NSAID indomethacin was replaced with a variety of substituted thiazoles to obtain a series of potent, selective inhibitors of COX-2. Additional substitutions were made at the 1-position and 5-position of the indole of indomethacin. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(01)00212-8

文献信息

• US5811425A
  申请人：——

  公开号：US5811425A

  公开（公告）日：1998-09-22
• Thiazole analogues of the NSAID indomethacin as selective COX-2 Inhibitors
  作者：Keith W. Woods、Richard W. McCroskey、Michael R. Michaelides、Carol K. Wada、Keren I. Hulkower、Randy L. Bell

  DOI：10.1016/s0960-894x(01)00212-8

  日期：2001.5

  The carboxyl group of the NSAID indomethacin was replaced with a variety of substituted thiazoles to obtain a series of potent, selective inhibitors of COX-2. Additional substitutions were made at the 1-position and 5-position of the indole of indomethacin. (C) 2001 Elsevier Science Ltd. All rights reserved.