Antibacterial diterpenes from Plectranthus ernstii

M. Stavri, A. Paton, Brian Skelton, S. Gibbons

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Three new diterpenoids including two pimaranes (1 and 2) and a labdane (3) were isolated from the whole herb of Plectranthus ernstii. The structures of these compounds were determined as rel-15(ζ),16-epoxy-7α-hydroxypimar-8,14-ene (1) and rel-15(ζ),16-epoxy-7-oxopimar-8,14-ene (2), and compound 3 was elucidated as 1R,11S-dihydroxy-8R,13R-epoxylabd-14-ene on the basis of single-crystal X-ray structural analysis. Compound 1 exhibited moderate antistaphylococcal activity against a range of multidrug-resistant (MDR) and methicillin-resistant (MRSA) strains of Staphylococcus aureus with a minimum inhibitory concentration (MIC) of 32 μg/mL. All three diterpenes exhibited antimycobacterial activity against three strains of rapidly growing mycobacteria with MIC values ranging from 8 to 128 μg/mL.
Original languageEnglish
Pages (from-to)1191-1194
JournalJournal of Natural Products
Volume72
Issue number6
DOIs
Publication statusPublished - 2009

Fingerprint

Dive into the research topics of 'Antibacterial diterpenes from Plectranthus ernstii'. Together they form a unique fingerprint.

Cite this