[2-(3-Chloro-5-oxy-6-phenyl-indolo[3,2-c]quinolin-11-yl)-ethyl]-dimethyl-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: [2-(3-Chloro-5-oxy-6-phenyl-indolo[3,2-c]quinolin-11-yl)-ethyl]-dimethyl-amine
• 英文别名: 2-(3-chloro-5-oxido-6-phenylindolo[3,2-c]quinolin-5-ium-11-yl)-N,N-dimethylethanamine
• 化学式: C₂₅H₂₂ClN₃O
• 分子量: 415.922
• InChiKey: IYZOPPBKMOGFLE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  30
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  33.6
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  [2-(4-Chloro-2-nitrophenyl)-1-[2-(dimethylamino)ethyl]-1H-indol-3-yl]phenylmethanone 在 palladium on activated charcoal 氢气 、 溶剂黄146 作用下， 以 甲醇 为溶剂， 反应 0.05h， 以36%的产率得到[2-(3-Chloro-5-oxy-6-phenyl-indolo[3,2-c]quinolin-11-yl)-ethyl]-dimethyl-amine
  参考文献：
  名称：

  Structure-activity relationships of antimalarial indolo[3,2-c]quinolines [1, 2]

  摘要：

  Structure-activity relationships have been ascertained and chemical methodology developed for a series of antimalarial 3-chloroindolo[3,2-c]quinoline-5-oxides. The basic side chain as well as the ring N-oxide are critical for antimalarial activity as is a bromine or chlorine in position 3. Substitution at positions 7, 8, 9, 10 is not essential, although the most potent analog in our studies was the 8-nitro compound 4vv.

  DOI：

  10.1016/0223-5234(93)90036-e

文献信息

• Werbel L. M., Kesten S. J., Turner W. R., Eur. J. Med. Chem, 28 (1993) N 11, S 837-852
  作者：Werbel L. M., Kesten S. J., Turner W. R.

  DOI：——

  日期：——
• Structure-activity relationships of antimalarial indolo[3,2-c]quinolines [1, 2]
  作者：LM Werbel、SJ Kesten、WR Turner

  DOI：10.1016/0223-5234(93)90036-e

  日期：1993.1

  Structure-activity relationships have been ascertained and chemical methodology developed for a series of antimalarial 3-chloroindolo[3,2-c]quinoline-5-oxides. The basic side chain as well as the ring N-oxide are critical for antimalarial activity as is a bromine or chlorine in position 3. Substitution at positions 7, 8, 9, 10 is not essential, although the most potent analog in our studies was the 8-nitro compound 4vv.