Cytotoxic protobassic acid saponins from the kernels of Palaquium formosanum

J Food Drug Anal. 2018 Apr;26(2):557-564. doi: 10.1016/j.jfda.2017.06.004. Epub 2017 Jul 11.

Abstract

Bioassay guided fractionation and separation of the EtOH extract of the kernels of Palaquium formosanum against PC-3 cells via Sephadex LH-20 and reverse phase C-18 columns led to the isolation of 13 protobassic saponins. One of these saponins is new and was characterized as 3‴-O-rhamnopyranosyl-arganin C, a bisdesmoside of 16α-hydroxyprotobassic acid at the C-3 and C-28 positions. The structures of these compounds were determined on the basis of 1D NMR (1H, 13C), 2D NMR (1H-1H COSY, HSQC, HMBC, and NOESY), and selectively excited 1D TOCSY spectroscopic analyses and MS data, and comparison with literature data. Bioassay of these compounds and five additional compounds, isolated from Planchonella obovata leaf, against PC-3 prostate cancer cells indicated arganin C to be the most potent one with the IC50 value of 13.8 μM. Some structure and activity relationships were also drawn.

Keywords: 1D TOCSY; Cytotoxicity; Palaquium formosanum Hayata; Protobassic acid saponins; Sapotaceae.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Humans
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Palaquium / chemistry*
  • Plant Extracts / chemistry
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Saponins / chemistry
  • Saponins / isolation & purification
  • Saponins / pharmacology*
  • Seeds / chemistry
  • Triterpenes / chemistry
  • Triterpenes / isolation & purification
  • Triterpenes / pharmacology*

Substances

  • Plant Extracts
  • Saponins
  • Triterpenes
  • protobassic acid

Grants and funding

This work was supported by the Ministry of Science and Technology, Taiwan, Republic of China, under the grants MOST 103-2320-B-002-011-MY3.