Two new C21 steroidal glycosides isolated from Cynanchum komarovii

Chin J Nat Med. 2018 Aug;16(8):610-614. doi: 10.1016/S1875-5364(18)30098-0.

Abstract

The present study was designed to further investigate the C21 steroidal glycosides in Cynanchum plants. Two new steroidal glycosides based on a 13, 14:14, 15-disecopregnane-type aglycone, komaroside P (1) and komaroside Q (2), together with three known compounds (3-5) were isolated from the whole herbs of Cynanchum komarovii. The aglycones of compounds 1 and 2 were two new disecopregnane. Their structures were elucidated on the basis of 1D, 2D NMR spectroscopic data and acid hydrolysis. All the compounds (1-5) showed potent inhibitory activities against human leukemia cell lines (HL-60) with IC50 values ranging from 16.6 to 26.3 μmol·L-1, compared to the positive control 5-fluorouracil (6.4 μmol·L-1).

Keywords: C(21) steroidal glycosides; Cynanchum komarovii; Cytotoxic activity.

MeSH terms

  • Cell Survival / drug effects
  • Cynanchum / chemistry*
  • Drugs, Chinese Herbal / chemistry
  • Drugs, Chinese Herbal / isolation & purification
  • Drugs, Chinese Herbal / pharmacology
  • Glycosides / chemistry*
  • Glycosides / isolation & purification
  • Glycosides / pharmacology
  • HL-60 Cells
  • Humans
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Steroids / chemistry*
  • Steroids / isolation & purification
  • Steroids / pharmacology

Substances

  • Drugs, Chinese Herbal
  • Glycosides
  • Steroids