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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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. |
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ISSN: | 0032-0943 1439-0221 |
DOI: | 10.1055/s-2007-986938 |