Planta Med 2014; 80 - PD121
DOI: 10.1055/s-0034-1382542

Antibacterial chromene derivatives from Psorothamnus fremontii

Q Yu 1, 3, XM Xu 1, S Ganji 1, RR Rao 1, MR Jacob 1, BY Yu 3, XC Li 1, 2
  • 1National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences
  • 2Department of Biomolecular Sciences, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, USA
  • 3State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, P. R. China

In our search for antibacterial compounds from plants, the ethanol extract of the native American plant Psorothamnus fremontii (Fabaceae) was identified as a hit due to its in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA) with an IC50 of < 8 µg/mL. Bioassay-guided fractionation of this extract was thus conducted, leading to the identification of five chromene derivatives including two new compounds. The structures of the new compounds were established by interpretation of spectroscopic data as 6-hydroxy-7-isobutyryl-3,3,5-trimethyl-2,3-dihydrooxireno[2,3-d]chromen-8(1aH)-one (1) and 6-hydroxy-7-isobutyryl-3,3-dimethyl-5-(3-methylbut-2-en-1-yl)-2,3-dihydrooxireno[2,3-d]chromen-8(1aH)-one (2). The known compound 1-(5,7-dihydroxy-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-2H-chromen-8-yl)ethanone (3) showed potent activity against MRSA with an IC50 of < 0.8 µg/mL and appeared to be responsible for the activity of the crude plant extract.