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SRO-91 is a synthetic, non-natural **ribofuranosyl-1,2,3-triazole C-nucleoside** analog structurally related to ribavirin. It is designed via C-alkynyl glycosylation mediated by metallic indium and subsequent Huisgen cycloaddition. SRO-91 acts as a cytotoxic agent with **antitumor activity**, especially in ovarian and skin cancer models. It inhibits cancer cell proliferation, migration, clonogenicity, and spheroid formation, and shows a favorable therapeutic index, being more selectively toxic to tumor cells compared to normal cells. Mechanistically, SRO-91 impairs tumor cell dissemination; its activity profile is similar to ribavirin but has reduced toxicity to non-cancer cells.
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