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The chemical fractionation afforded a complex mixture of anacardic acids, which upon catalytic hydrogenation yielded anacardic acid (<jats:bold>1<\/jats:bold>). Methylation of<jats:bold>1<\/jats:bold>via reaction with diazomethane afforded an ester<jats:bold>2<\/jats:bold>. Both compounds were evaluated using polarographic approaches and fluorescence studies of chlorophyll<jats:italic>a<\/jats:italic>(ChL<jats:italic>a<\/jats:italic>). The<jats:italic>in\u2005vitro<\/jats:italic>assays informed the decision for the classification of<jats:bold>1<\/jats:bold>and<jats:bold>2<\/jats:bold>as Hill reaction inhibitors. Besides that,<jats:bold>1<\/jats:bold>inhibited the donor side of the PSII, while<jats:bold>2<\/jats:bold>acted as an energy transfer inhibitor. 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