The A. elgonica leaf exudate was examined for anthraquinones, and several other phytochemicals were found such as aloe emodin, aloenin, aloeresin, aloeresin B, emodin-10-C-β-glucopyranoside linked through C-10 to C-7 of the anthraquinone aloe emodin (Conner et al. 1990a,b). Similarly, four bianthraquinoid pigments (A, B, C, and D) were characterized from rhizome of A. saponaria. Besides bianthraquinoid pigments, the (+)-asphodelin; 1,1′,8,8′,10-pentahydroxy-3,3′-dimethyl-10,7′-bianthracene-9,9′,10′-trione; 1,1′,8,8′-tetrahydroxy-3,3′-dimethyl-4,7′-bianthracene (10′H, 10′H)-9,9′,10-trione; and 1,1′,8,8′,10-pentahydroxy-3,3′-dimethyl-10,7′-bianthracene (10′H, 10′H)-9,9′-dione structures were also established by analyzing the spectral data (Crosswhite and Crosswhite 1984; Reynolds and Dweck 1999; Rajasekaran et al. 2005; Loots et al. 2007; Yagi et al. 1978, 1983; Speranza et al. 1993). The geographical conditions affect the production of aloeresin A, aloesin, and aloin and distributed as major compounds in A. ferox leaf exudate. Along with major compounds, aloinoside A and aloinoside B found in western parts of the Cape and aloeresin C and 5-hydroxyaloin A aloin found in all the areas of Cape (van Wyk et al. 1995b). The levels of Barbaloin were determined in Aloe species in the Kew. The maximum concentration of barbaloin was found in exudates of young leaves but the concentration decreased in older leaves (Groom and Reynolds 1987). The littoraloside was isolated from A. littoralis leaf exudate along with littoraloin, deacetyllittoraloin, and 10-hydroxyaloin B, and their structures were confirmed by spectral analysis (Dagne et al. 1998b). The prechrysophanol, chrysophanol, helminthosporin, (R)-aloesaponol I, (R)-aloesaponol II, aloesaponarin I, aloesaponarin II, and laccaic acid D methyl ester were isolated from A. graminicola (Yenesew et al. 1993; Lakshmi and Rajlakshmi 2011).