Chinese Journal of Magnetic Resonance ›› 2009, Vol. 26 ›› Issue (1): 120-125.

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Assignment of 13C and 1H Chemical Shifts of Teniposide

LI Wen*; SHA Yi; ZHU Dan   

  1. (Center of Instrumental Analysis, Shenyang Pharmaceutical University, Shenyang 110016, China)
  • Received:2008-09-26 Revised:2008-10-14 Online:2009-03-05 Published:2009-12-05
  • Contact: LI Wen

Abstract: Teniposide is a semisynthetic podophyllotoxin obtainable from the extracts of the roots and the rhizomes of May apple or mandrake plant Podophyllum peltatum. As an anticancer agent, Teniposide has become a major chemotherapy drug for the treatment of intracranial malignant tumor. In this study, the 13C and 1H chemical shifts of the compound were assigned using 1D NMR and 2D NMR techniques including COSY, TOCOSY, NOESY, gHSQC and gHMBC. Its structure was determined from the NMR data.

Key words: NMR, assignments, 2D NMR, teniposide, anti-tumor drug

CLC Number: