JOURNAL 232


Records of Natural Products
VOLUME & ISSUE
Year: 2017 Issue: 2 March-April
PAGES
p.223 - 228
STATISTICS
Viewed 2050 times.
AUTHORS
    Muhammad Imran Tousif , Naheed Riaz, Mamona Nazir, Shabir Ahmad, Muhammad Saleem, Abdul Jabbar, Muahammad Ashraf and Rasool Bakhsh Tareen
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


Ethyl acetate layer of the methanolic extract of Seriphidium quettense was subjected to silica gel column chromatography to isolate one new; seriphiloid (1), and four known compounds; ilicic acid (2), 6 a -hydroxy-8(10)-oplopen-14-one (3), 2-(4-hydroxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one (4) and 2-(3,4-dihydroxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one (5). The chemical structure of the new isolate was established with the help of 1D, 2D NMR techniques and high resolution mass spectrometry. Known compounds were identified because of 1D NMR and mass spectrometric analysis and in comparison with the literature values. Compounds 1-5 were evaluated for their acetylcholinesterase, butyrylcholinesterase, a -glucosidase and urease inhibitory activities. Most of the metabolites were found inactive; however, compounds 2 and 3 showed good antiurease activity with IC 50 value 21.5±0.1 and 20.8±0.1 µg/mL, respectively.

KEYWORDS
  • eriphidium quettense
  • secondary metabolites
  • structure elucidation
  • enzyme inhibition.