Chem. J. Chinese Universities ›› 2018, Vol. 39 ›› Issue (8): 1668.doi: 10.7503/cjcu20180007

• Organic Chemistry • Previous Articles     Next Articles

Cytotoxic Activity of Trichothecene Compounds and Derivatives from Myrothecium sp.

JIA Yunjing1, SHI Wensi1, HU Feiliu1, ZHU Huajie1,*(), LIU Li2,*(), MA Zhengyue1   

  1. 1. College of Pharmaceutical Sciences,2. College of Medicine, Hebei University, Baoding 071000, China
  • Received:2018-01-03 Online:2018-08-10 Published:2018-05-15
  • Contact: ZHU Huajie,LIU Li E-mail:hjzhu2017@163.com;ll1113-work@163.com
  • Supported by:
    † Supported by the Scientific Research Foundation of Hebei Educational Committee, China(No.ZD2017004), the Scientific Research Foundation of Hebei Educational Committee, China(No.QN2017021) and the Financial Support from “One Province and One School Special Project”of Hebei University, China(No.20170030).

Abstract:

Five trichothecene compounds were obtained from Myrothecium sp. KX136897 and their structures were confirmed by means of 1H NMR, 13C NMR and HRMS. Compound 1 was used for the further structural modifications and four new derivatives were synthesized. The structure of compound 6 was different from those of the other derivatives, which was identified via comparing its 13C NMR with the reported structure. Furthermore, compound 6 was confirmed by comparing the calculated data with the experimental data of 13C NMR. Compounds 1—9 were used for antibacterial and cytotoxic activity study, respectively. It was found that if the epoxy ring at positions C12 and C13 was opened and then reformed a new four-membered epoxy ring, the cytotoxic activity of compound 1 would decrease. Besides, the protection of hydroxyl at position C2' by acyl would also cause the decrease of cytotoxic activity.

Key words: Myrothecium sp., Structural modification, Antibacterial activity, Cytotoxic activity

CLC Number: 

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