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There have been only four biological studies on Plectranthus hadiensis where the<br />

antiplasmodial, insect-antifeedant, antifungal, antiradical <strong>and</strong> antibacterial properties <strong>of</strong><br />

this plant extract <strong>and</strong> the isolated compounds were evaluated for activity (van Zyl et al.,<br />

2008; Laing et al., 2006; Mothana et al., 2008; Wellsow et al., 2006). The acetone<br />

extract <strong>of</strong> this plant was found to be inactive as an insect-antifeedant (Wellsow et al.,<br />

2006). The hexane extract showed good activity against Sclerotinia sclerotiorum,<br />

Rhizoctonia solani <strong>and</strong> an unknown C<strong>and</strong>ida species while the dichloromethane extract<br />

showed moderate activity against bacterial strains, B. subtilis <strong>and</strong> X. campestris <strong>and</strong> the<br />

fungal microorganism, Sclerotinia sclerotiorum as well as an unknown C<strong>and</strong>ida species<br />

(Laing et al., 2006).<br />

Three royleanones 33, 36 <strong>and</strong> 38 were isolated previously from the dichloromethane<br />

extract <strong>of</strong> the aerial parts <strong>of</strong> P. hadienis (van Zyl et al., 2008) <strong>and</strong> the isomers <strong>of</strong> 33 <strong>and</strong><br />

36, 34 <strong>and</strong> 37 respectively, were isolated from the ethanol extract <strong>of</strong> Coleus zeylanicus (a<br />

synonym for P. hadiensis) (Mehrotra et al., 1989). Compounds 33 <strong>and</strong> 36 exhibited<br />

anticancer activity against breast, lung, renal, melanoma <strong>and</strong> central nervous system cell<br />

lines (MCF-7, NCI-H460, TK-10, UACC-62 <strong>and</strong> SF-268, respectively) with both<br />

compounds proving to be less potent than the positive control, Cyclosporin A (Cerqueira<br />

et al., 2004; Gaspar-Marques et al., 2002). These three compounds (33, 36 <strong>and</strong> 38) have<br />

also proven to be active against six strains <strong>of</strong> methicillin resistant Staphylococcus aureus,<br />

two strains <strong>of</strong> vancomycin-resistant Enterococcus faecalis, Bacillus subtilis, Vibrio<br />

cholera <strong>and</strong> Xanthomonas campestris (Laing et al., 2006; Teixera et al., 1997; Gaspar-<br />

Marques et al., 2006). Compounds 36 <strong>and</strong> 38 (van Zyl et al., 2008) exhibited<br />

antimalarial activity with 38 displaying synergistic properties when combined with<br />

quinine (Tables 11 <strong>and</strong> 13 on pages 72 <strong>and</strong> 76, respectively). There were no reports <strong>of</strong><br />

biological activity in compounds 34 <strong>and</strong> 37.<br />

95

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