A new NMR approach for structure determination of thermally unstable biflavanones and application to phytochemicals from Garcinia buchananii

Magn Reson Chem. 2015 Oct;53(10):813-20. doi: 10.1002/mrc.4269. Epub 2015 Jul 20.

Abstract

Previous activity-guided phytochemical studies on Garcinia buchananii stem bark, which is traditionally used in Africa to treat various gastrointestinal and metabolic illnesses, revealed xanthones, polyisoprenylated benzophenones, flavanone-C-glycosides, biflavonoids, and/or biflavanones as bioactive key molecules. Unequivocal structure elucidation of biflavonoids and biflavanones by means of NMR spectroscopy is often complicated by the hindered rotation of the monomers around the C-C axis (atropisomerism), resulting in a high spectral complexity. In order to facilitate an unrestricted rotation, NMR spectra are usually recorded at elevated temperatures, commonly over 80 °C, which effects in a single set of resonance signals. However, under these conditions, one of the target compounds of this investigation, (2R,3S,2″R,3″R)-manniflavanone (1), undergoes degradation. Therefore, we demonstrated in the present study that the 1,1-ADEQUATE could be successfully used as a powerful alternative approach to confirm the C-C connectivities in 1, avoiding detrimental conditions. However, a moderate increase in temperature up to 50 °C was sufficient to deliver sharp signals in the proton NMR experiment of (2R,3S,2″R,3″R)-isomanniflavanone (2) and (2″R,3″R)-preussianone (3). In addition, two new compounds could be isolated, namely (2R,3S,2″R,3″R)-GB-2 7″-O-β-D-glucopyranoside (4) and (2R,3S,2″R,3″R)-manniflavanone-7″-O-β-D-glucopyranoside (5), and whose structures were elucidated by spectroscopic analysis including 1D and 2D NMR and mass spectrometry methods. The absolute configurations were determined by a combination of NMR and electronic circular dichroism (ECD) spectroscopy. The aforementioned compounds exhibited high anti-oxidative capacity in the H2O2 scavenging, hydrophilic Trolox equivalent antioxidant capacity (H-TEAC) and hydrophilic oxygen radical absorbance capacity (H-ORAC) assays.

Keywords: 1,1-ADEQUATE; 13C; 1H; GB2 7″-O-β-d-glucopyranoside; NMR; biflavanone glucosides; biflavanones; manniflavanone; manniflavanone-7″-O-β-d-glucopyranoside; variable temperature NMR.

MeSH terms

  • Chemistry Techniques, Analytical / methods*
  • Drug Stability
  • Flavanones / chemistry*
  • Flavones / chemistry*
  • Garcinia / chemistry*
  • Hot Temperature
  • Magnetic Resonance Spectroscopy*
  • Molecular Structure
  • Phytochemicals
  • Plant Bark / chemistry
  • Plant Extracts / chemistry*

Substances

  • Flavanones
  • Flavones
  • Phytochemicals
  • Plant Extracts
  • manniflavanone