Planta Med 2010; 76(8): 796-802
DOI: 10.1055/s-0029-1240743
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Phytochemical Investigation of Cycas circinalis and Cycas revoluta Leaflets: Moderately Active Antibacterial Biflavonoids

Abeer Moawad1 , 2 , Mona Hetta2 , Jordan K. Zjawiony1 , Melissa R. Jacob3 , Mohamed Hifnawy4 , Jannie P. J. Marais1 , Daneel Ferreira1
  • 1Department of Pharmacognosy and Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS, USA
  • 2Department of Pharmacognosy, School of Pharmacy, Beni Suef University, Beni Suef, Egypt
  • 3National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS, USA
  • 4Department of Pharmacognosy, School of Pharmacy, Cairo University, Cairo, Egypt
Further Information

Publication History

received October 30, 2009 revised Dec. 6, 2009

accepted Dec. 6, 2009

Publication Date:
12 January 2010 (online)

Preview

Abstract

Chemical examination of the methanolic extract of the leaflets of Cycas circinalis L. led to the isolation of one new biflavonoid, (2S, 2′′S)-2,3,2′′,3′′-tetrahydro-4′,4′′′-di-O-methylamentoflavone (tetrahydroisoginkgetin; 2), and 15 known compounds, 11 of which are reported for the first time from C. circinalis. Chromatographic separation of the chloroform extract of C. revoluta Thunb. leaflets afforded 12 compounds, seven of which are reported for the first time from this species. The isolated compounds from both species include 14 biflavonoids, three lignans, three flavan-3-ols, two flavone-C-glucosides, two nor-isoprenoids, and one flavanone. This is the first report of NMR and CD data of 2,3,2′′,3′′-tetrahydro-4′-O-methyl- and 2,3-dihydro-4′-O-methyl-amentoflavone (6) and (7). The effect of O-methylation on the chemical shifts of the neighboring carbons in the 13C NMR spectra of the dihydro- and tetrahydro-amentoflavone skeletons provides a tool to identify the location of the methoxy groups. Compounds 2, 6, and 18 displayed moderate antibacterial activity against Staphylococcus aureus (IC50 values of 3.9, 9.7, and 8.2 µM, respectively) and methicillin-resistant S. aureus (MRSA; IC50 values of 5.9, 12.5, and 11.5 µM, respectively).

References

Dr. Daneel Ferreira

Department of Pharmacognosy
School of Pharmacy
University of Mississippi

University, MS 38677

USA

Phone: + 1 66 29 15 70 26

Fax: + 1 66 29 15 69 75

Email: dferreir@olemiss.edu