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Plectranthus<br />

species<br />

Solvent <strong>of</strong><br />

Extraction<br />

P. ternifolius mixture<br />

P. verticillatus aqueouslv<br />

Other Activities Reference<br />

treat liver function<br />

impairment<br />

helps in treatment <strong>of</strong><br />

Alzheimers disease<br />

Guo et al., 2006<br />

Fale et al., 2009<br />

NB. Coleus species are also included in this table because <strong>of</strong> the uncertain relationship to the Plectranthus<br />

species<br />

* Unknown species<br />

Key: lv: leaves, rt: roots, s: stems, a: aerial parts, w: whole plant, f: flowers<br />

2.4 The phytochemistry <strong>of</strong> Plectranthus<br />

The main phytochemical constituents <strong>of</strong> Plectranthus are diterpenoids, with about one-<br />

hundred <strong>and</strong> forty-seven <strong>of</strong> these compounds being isolated from the coloured leaf-gl<strong>and</strong>s<br />

<strong>of</strong> Plectranthus species, the majority <strong>of</strong> which were highly modified abietanoids.<br />

Essential oils, monoterpenoids, sesquitepenoids <strong>and</strong> phenolics have also been isolated<br />

from Plectranthus species (Abdel-Mogib et al., 2002; Lukhoba et al., 2006).<br />

Compounds 27 to 174 are grouped into five categories, the royleoanone-type abietanes<br />

(compounds 27 to 69), the spirocoleons (compounds 70 to 108), vinylogous quinones<br />

(compounds 109 to 130), coleon-type abietanes (compounds 131 to 167) <strong>and</strong> the<br />

miscellaneous abietanes (compounds 168 to 174) which do not resemble any <strong>of</strong> the<br />

abietanes in the previous four categories.<br />

Twenty royleanone type abietanes with the presence <strong>of</strong> a hydroxybenzoquinone or p-<br />

quinoid ring C system <strong>and</strong> an isopropyl group at C-13 have been isolated from eleven<br />

known Plectranthus species <strong>and</strong> three Coleus species (Table 6a). These compounds all<br />

have methyl groups at C-4 <strong>and</strong> C-10 with the exception <strong>of</strong> compound 42 where the<br />

methyl group at C-10 is oxidized to an alcohol. Compound 45 is notably different from<br />

compounds 27 to 46, as the substituent at C-12 is an acetyl group. At C-6 <strong>and</strong> C-7 <strong>of</strong><br />

compounds 27 to 42, there are either hydroxy, aldehyde or acetyl groups attached to these<br />

positions, with the substituent at C-6 being in the beta position. In compounds 43 to 46,<br />

39

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