Bioassay directed isolation of secondary metabolites from the rhizomes of (Fam. ‎Zingiberaceae) led to the isolation of mono-, sesqui-, and di-terpenes. The compounds were characterized as ()-8(17),12-labdadiene-15,16-dial (), zerumbol (), zerumbone (), buddledone A (), furanodienone (), germacrone (), borneol (), and camphor () by analysing one-dimensional (1D) (¹H and C) and two-dimensional (2D) (COSY, HSQC, HMBC, and NOESY) NMR data and mass spectra. Among these terpenes, compounds and revealed potential antibacterial activity (minimum inhibitory concentrations (MIC) values 32⁻128 µg/mL; 0.145⁻0.291 mM)) against a series of clinical isolates of multi-drug resistant (MDR) and Methicillin resistant (MRSA).

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384810PMC
http://dx.doi.org/10.3390/molecules24030385DOI Listing

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