“…For example, the metabolites of caffeic acid including reduction reaction product (M5) and glucuronic acid product (M9), the metabolic pathways of caffeic acid, and the related metabolites were displayed in Figure 3. It is worth mentioning that most constituents migrating into blood, such as (E)-p-coumaric acid and ferulic acid, exhibit various pharmacological activities such as anticancer [31,32], antidiabetic [33], antiobesity [34], anti-inflammatory [35], antiedema [36], antimicrobial [37], antihepatotoxic [38], antioxidative [39], and other effects [40][41][42]. For example, Sharma et al [32] discussed the effect of (E)-p-coumaric acid on glucose-regulated protein 78 in colon cancer and its impact on unfolded protein response: the result showed that (E)-p-coumaric acid significantly downregulated protein 78 and activated the unfolded protein response, mediated apoptosis in both in vitro and in vivo models of colon cancer, and dramatically reduced inflammation by decreasing the expression levels of cytokines COX-2, IL-6, TNF-α, PGE2, p-p65 and p-IκBα.…”