Four new phenolics and antiparasitic secondary metabolites from Flacourtia rukam Zoll. & Mortizi

  • Nat Prod Res. 2022 Jul;36(14):3626-3637. doi: 10.1080/14786419.2021.1875462.
Naglaa I Afifi  1 Abeer S Moawad  1 Mohamed A Zaki  1 Mostafa E Rateb  1  2 Mohammed H Rashed  3 Ibrahim G Saleh  3 Mona H Hetta  4 Rabab M Mohammed  1
Affiliations
  • 1. Pharmacognosy Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt.
  • 2. School of Computing, Engineering & Physical sciences, University of the West of Scotland, Paisley, United Kingdom.
  • 3. Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.
  • 4. Pharmacognosy Department, Faculty of Pharmacy, Fayoum University, Fayoum, Egypt.
Abstract

Phytochemical investigation of Flacourtia rukam Zoll. & Mortizi (F. rukam) leaves and bark led to the isolation and characterization of seventeen compounds of which four phenolics were not previously described; 2-[(benzoyloxy)methyl]-phenyl-O-β-xylosyl-(1→2)-β-glucopyranoside (1), 2-[(benzoyloxy)methyl]-4-hydroxyphenyl-O-β-xylosyl-(1→2)-β-D-glucopyranoside (2), 2-hydroxy-5-(2-hydroxyphenoxy)phenoxy-β-glucopyranoside (3) and biphenyl-1,1',2,2'-tetraol (5). Interestingly, the later compound is known as a synthetic but this is the first report for its isolation from nature. Chemical structures were established using extensive analysis of spectroscopic data (1 D and 2 D NMR and HRESIMS). Biphenyl-1,1,2,2'-tetrol (5) exhibited a good activity against Trypanosoma brucei trypomastigotes with IC50= 6.66 ug/mL. Compounds 2, 5, 9, 10, 11 and 12 showed a good in-vitro anti-inflammatory activity using proteinase inhibitory assay. On the contrary, all tested compounds were inactive as antileishmanial or antimalarial.

Keywords
Flacourtia rukam Zoll. & Mortizi; Salicaceae; anti-inflammatory; antitrypanosomal; phenolics.
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