波谱学杂志 ›› 1997, Vol. 14 ›› Issue (5): 431-436.

• 研究论文 • 上一篇    下一篇

6-氨基酸取代吲哚喹嗪酮的1H NMR

彭师奇1, 郭敏1, 毛希安2, Ekkehard Winterfeldt3   

  1. 1 北京医科大学生源药物化学中德联合实验室, 北京 100083;
    2 中国科学院武汉物理与数学研究所波谱与原子分子物理国家重点实验室, 武汉 430071;
    3 Institut für Organische Chemie, Universität Hannover, Germany
  • 收稿日期:1997-04-18 修回日期:1997-06-09 出版日期:1997-10-05 发布日期:2018-01-22
  • 通讯作者: 彭师奇,男,50岁,博士,教授
  • 基金资助:
    国家自然科学基金资助项目

1H NMR OF 6-AMINO ACID SUBSTITUTED INDOLOQUINOLIZIDONES

Peng Shiqi1, Guo Ming1, Mao Xian2, Ekkehard Winterfeldt3   

  1. 1 College of Pharmaceutical Sciences, Beijing Medical University, Beijing 100083;
    2 State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute, The Chinese Academy of Sciences, Wuhan 430071;
    3 Institut für Organische Chemie, Universitatät Hannover, Germany
  • Received:1997-04-18 Revised:1997-06-09 Online:1997-10-05 Published:2018-01-22

摘要: 在抗肿瘤吲哚喹嗪酮的设计中,根据抗代谢理论,将甘氨酸、N-叔丁氧羰基甘氨酸、N-叔丁氧羰基天冬氨酸单苄酯,和N-叔丁氧羰基谷氨酰胺分别引入到3-乙酰基-1,4,6,7-四氢吲哚[2,3,-a]喹嗪-4-酮的6位.本文报道它们的1H NMR数据.

关键词: 氨基酸, 吲哚喹嗪酮, 1H NMR

Abstract: In the design of indoloquinolizidone anticancers N-butoxycarbonylglycine, monobenzyl ester of Nbutoxycarbonyl-L-asparagic acid, N-butoxycarbonyl-L-glutamine and glycine were introduced into the 6-position of the indoloquinolizidone respectively based on the antimetabolic theory. In the present paper the 1H NMR data and conformation analysis are reported.

Key words: Amino acids, Indoloquinolizidone, 1H NMR