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The Geography of Phytochemical Races

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7.7 Larrea (Zygophyllaceae) 293<br />

Extraction <strong>of</strong> the surface <strong>of</strong> fresh leaves <strong>of</strong> creosote bush gave a rich array <strong>of</strong><br />

fl avonoid aglycones based on the fl avonols such as kaempferol, quercetin, herbacetin,<br />

and gossypetin, and on the fl avones such as apigenin and luteolin. An unusual<br />

dihydr<strong>of</strong>l avonol was also obtained. Representative members <strong>of</strong> this array are illustrated<br />

in Fig. 7.4: luteolin 7,3′-dimethyl ether [602], kaempferol 3,7-dimethyl ether<br />

[603], quercetin 7,3′,4′-trimethyl ether [604], herbacetin 3,7-dimethyl ether [605],<br />

gossypetin 3,7,3′-trimethyl ether [606], and dihydromyricetin 3′,5′-dimethyl ether<br />

[607]. <strong>The</strong> array <strong>of</strong> leaf-surface fl avonoids <strong>of</strong> L. tridentata was the most complex <strong>of</strong><br />

any <strong>of</strong> the fi ve species and, signifi cantly, there were no differences among populations<br />

that exhibit different ploidy levels. In contrast, L. divaricata exhibited two fl avonoid<br />

pr<strong>of</strong>i les, the more complex <strong>of</strong> which was observed in plants from Argentina;<br />

plants from Peru exhibited a decidedly simpler pr<strong>of</strong>i le. <strong>The</strong> distribution <strong>of</strong> nonpolar<br />

compounds identifi ed from these taxa is presented in Table 7.1.<br />

<strong>The</strong> similarity between the pr<strong>of</strong>i les <strong>of</strong> the North American and Argentinean species<br />

suggests the possibility <strong>of</strong> a closer relationship between them than between any<br />

other pair <strong>of</strong> taxa in the genus, including between the Argentinean and Peruvian<br />

Fig. 7.4 Compounds 602–607, fl avonoids from Larrea tridentata

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