JOURNAL 476
Records of Natural Products
Year: 2012 Issue: 3 July September
p.296 - 300
Viewed 2446 times.
-
Christopher Kitalong, Ali M. El-Halawany, RihamSalah El-Dine , Chao-mei Ma and Masao Hattori
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.