JOURNAL 476


Records of Natural Products
VOLUME & ISSUE
Year: 2012 Issue: 3 July September
PAGES
p.296 - 300
STATISTICS
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AUTHORS
    Christopher Kitalong, Ali M. El-Halawany, RihamSalah El-Dine , Chao-mei Ma and Masao Hattori
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


The methanol extract of P. nisidai leaves yielded a benzophenone rhamnoside , iriflophenone 2-O-α-L-rhamnopyranoside (1) in addition to g enkwanin 5-O-β-D-primeveroside (2) and mangiferin (3). The isolated compounds as well as the derived aglycones of 1 and 2 assigned as compounds 4 and 5, respectively, were tested for their estrogenic activity on ERα using an estrogen receptor competitive binding screen. Compounds 1 , 4 and 5 showed almost the same binding ability to ERα with IC 50 of 630 µM, 700 µM and 800 µM, respectively. Virtual docking with ERα revealed that compound 1, 4 and 5strongly hydrogen bond with amino acids Glu353, Arg349, Gly521 and His524, in the estrogen receptor ligand binding domain, similar to that of mammalian estrogen 17β-estradiol.

KEYWORDS
  • Phaleria nisidai
  • estrogenic activity
  • ER
  • benzophenone
  • mangiferin.

SUPPORTING INFORMATION


Supporting Information
Download File 41-supporting_informations-1104-586.pdf (375.28 KB)