biostudies-literatureSong JNational Natural Science Foundation of China1131-1141https://www.ebi.ac.uk/biostudies/studies/S-EPMC6072089biostudies-literatureUnknown9(7)Twenty-four 14-sulfonamide-tetrandrine derivatives as potential anti-cancer agents were synthesized. The synthetic derivatives were investigated for their cytotoxic activity against human cancer cell lines MDA-MB-231, PC3, WM9, HEL and K562. Initially, the IC₅₀ values (50% inhibitory concentrations) of all of the compounds were determined. These derivatives exhibited potent, but distinct, inhibitory effects on the above-mentioned cell lines. Among them, compound <b>23</b>, which was modified with a 2-naphthalenesulfonyl group at the 14-amino position, showed impressive inhibition of all five cancer cell lines, and especially of MDA-MB-231 cells with an IC₅₀ value of 1.18 ± 0.14 μM. Further mechanism exploration showed that <b>23</b> induced potent apoptotic cell death on MDA-MB-231 cancer cells in a concentration-dependent manner. The results revealed that <b>23</b> might be a potential anti-cancer drug candidate.MedChemCommDesign, synthesis and bioactivity investigation of tetrandrine derivatives as potential anti-cancer agents.PMC60720898147260981360479Ben-David YPan WHu SLou HZeng XChen CSong JLan JLiu WfalseDesign, synthesis and bioactivity investigation of tetrandrine derivatives as potential anti-cancer agents.Twenty-four 14-sulfonamide-tetrandrine derivatives as potential anti-cancer agents were synthesized. The synthetic derivatives were investigated for their cytotoxic activity against human cancer cell lines MDA-MB-231, PC3, WM9, HEL and K562. Initially, the IC₅₀ values (50% inhibitory concentrations) of all of the compounds were determined. These derivatives exhibited potent, but distinct, inhibitory effects on the above-mentioned cell lines. Among them, compound <b>23</b>, which was modified with a 2-naphthalenesulfonyl group at the 14-amino position, showed impressive inhibition of all five cancer cell lines, and especially of MDA-MB-231 cells with an IC₅₀ value of 1.18 ± 0.14 μM. Further mechanism exploration showed that <b>23</b> induced potent apoptotic cell death on MDA-MB-231 cancer cells in a concentration-dependent manner. The results revealed that <b>23</b> might be a potential anti-cancer drug candidate.2018-01-01T00:00:00Z2018 Jul2025-04-19T21:01:04.862Z2019-06-06T23:04:02ZS-EPMC60720893010900010.1039/c8md00125a