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In contrast, addition of S -substituted methyl- and hexylglutathione did not result in the formation of cyanidin ( 8 ) (Fig

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SCO also exerted antitumor effects on prostate cancer cells by inhibiting the transcription of STAT3 target genes, such as cyclin D1, c-Myc, survivin, Bcl-2 and Socs3, and decreasing the phosphorylation and nuclear accumulation of STAT3, but not JAK2 (81)