波谱学杂志 ›› 2000, Vol. 17 ›› Issue (5): 383-388.

• 研究论文 • 上一篇    下一篇

癌基因MDM2阻断剂的分子结构的NMR研究

安东各1, 涂光忠2, 尹大力1, 贺文义1, 马立斌2, 孔漫1   

  1. 1. 中国医学科学院药物研究所, 北京 100050;
    2. 北京微量化学所, 北京 100091
  • 收稿日期:2000-07-20 修回日期:2000-09-04 出版日期:2000-10-05 发布日期:2018-01-11
  • 作者简介:安东各(1974-),女,在读硕士生
  • 基金资助:
    国家自然科学基金资助项目

STUDY ON THE STRUCTURE OF INHIBITORS OF THE MDM2 ONCOGENE

An Dong-ge1, TU Guang-zhong2, YIN Da-li1, HE Wen-yi1, MA Li-bin2, KONG Man1   

  1. 1. Institute of Materia Medica Chinese Academy of Medical Science, Beijing 100050;
    2. Beijing Institute of Microchemistry, Beijing 100091
  • Received:2000-07-20 Revised:2000-09-04 Online:2000-10-05 Published:2018-01-11

摘要: 根据P53-MDM2复合物晶体结构,设计合成了非肽类小分子作为MDM2的阻断剂.利用超导核磁共振波谱仪,测定了化合物的1H谱、13C谱、1H-1H COSY谱、HMQC和HMBC谱,确定了化合物的结构,归属了化合物的1H、13C化学位移,为筛选抗癌活性化合物提供了理论依据.

关键词: MDM2阻断剂, NMR

Abstract: The MDM2 oncoprotein is a cellular inhibitor of the P53 tumor suppressor in that it can bind the transactivation domain of P53 and downregulate its ability to activate transcription. In certain cancers, MDM2 amplification is a common event and contributes to the inactivation of P53. The crystal structure of the MDM2 bound to P53 has been analysised through x-ray crystallography. The crystal structure provides a framework for the discovery of compounds that may prevent the activation of the P53 tumor suppressor by the MDM2 oncogene in cancer. Inhibitors of the MDM2 oncogene have been synthesized on the base of this theory.
All assignments of inhibitors were obtained from 1H、13C、1H-1H COSY、HMQC and HMBC spectra. With regarded to count space distance of two benzene rings, three-bond coupling constants were utilized to determine the structure of inhibitors. Sterostructures and relative configurations were discussed, and dominant energy was computed by using Sybyl software.

Key words: Inhibitor of MDM2 oncogene, NMR

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