New transformation pathway and cytotoxic derivatives from the acid hydrolysis of timosaponin B III

Nat Prod Res. 2019 Oct;33(19):2755-2761. doi: 10.1080/14786419.2018.1499640. Epub 2018 Nov 20.

Abstract

Timosaponin B III is a major bioactive steroidal saponin isolated from Anemarrhena asphodeloides Bge. To potentially discover derivatives with better biological activity, timosaponin B III was structurally modified via acid hydrolysis to yield one new (2, timopregnane A I) C21 steroidal glycoside and seven known compounds. Their structures were elucidated on the basis of NMR spectroscopy and mass spectrometry. All eight compounds were evaluated for cytotoxic activity against MCF7, SW480, HepG2, and SGC7901 cell lines in vitro. As a result, compounds 6 and 7 showed significant activity (IC50 2.94-12.2 μM) against all tested cell lines. Structure-activity relationships of these compounds were investigated and the preliminary conclusions were provided. Moreover, a new transformation pathway was discovered in the acid hydrolysis of timosaponin B III for the first time.

Keywords: Acid hydrolysis; C21 steroidal glycoside; Cytotoxic activity; Steroidal saponins; Timosaponin B III.

Publication types

  • Video-Audio Media

MeSH terms

  • Anemarrhena / chemistry
  • Antineoplastic Agents, Phytogenic / chemistry*
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Humans
  • Hydrolysis
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Saponins / chemistry*
  • Spectrometry, Mass, Electrospray Ionization
  • Steroids / chemistry
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents, Phytogenic
  • Saponins
  • Steroids
  • timosaponin BIII