New diterpenes from Plectranthus ernstii

The Lamiaceae herb Plectranthus ernstii L.E.Codd was phytochemically and biologically studied as part of a project to assess plants belonging to the genus Plectranthus for antibacterial activity. This genus is known to be a rich source of diterpenes, particularly of the abietane and labdane class [1...

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Hauptverfasser: Stavri, M, Gibbons, S
Format: Tagungsbericht
Sprache:eng ; ger
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Zusammenfassung:The Lamiaceae herb Plectranthus ernstii L.E.Codd was phytochemically and biologically studied as part of a project to assess plants belonging to the genus Plectranthus for antibacterial activity. This genus is known to be a rich source of diterpenes, particularly of the abietane and labdane class [1,2]. The phytochemical investigation of this herb led to the characterisation of a new pimarane ( 1 ) and a labdane diterpene with an unusual 8,13-ether moiety ( 2 ). The chemical structures were elucidated by 1D and 2D NMR experiments as 15,16-epoxy-7α-hydroxy-pimar-8,14-ene ( 1 ) and 1β,11β-dihydroxy-8,13-epoxy-labd-14-ene ( 2 ) and are reported here for the first time. Compound 1 also exhibited moderate antibacterial activity, using the broth microtitre dilution assay, with a minimum inhibitory concentration of 32µg/ml recorded against a panel of Staphylococcus aureus strains, including methicillin-resistant and multidrug resistant strains. Acknowledgement : The University of London School of Pharmacy and EPSRC are thanked for a post-doctoral scholarship to M. Stavri. References: [1] Dellar, J.E. et al. (1996) Phytochemistry 735–738. [2] Rijo, P. et al. (2005) Magn Reson Chem 595–598.
ISSN:0032-0943
1439-0221
DOI:10.1055/s-2007-986938