Synthesis and antitumor activity of novel bis(benzylidene-benzenamine)disulfides
AssigneeKaohsiung Medical University
InventorsJeh-Jeng Wang, Wan-Ping Hu, Wei-Sheng Lo
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AssigneeKaohsiung Medical University
InventorsJeh-Jeng Wang, Wan-Ping Hu, Wei-Sheng Lo
Estimating the term…
Novel synthetic bis(benzylidene-benzenamine)disulfides and the preparation method are disclosed in the present invention. These compounds are afforded with the oxidizing reagent at low temperature and short time period via intra-molecular coupling reaction. In vitro experiments have been revealed that bis-disulfides are cytotoxic to cancer cells, especially human breast cancer cells MCF-7. Additionally, bis-disulfides arrest the cell cycle at sub-G1 phase and increase p38 phosphorylation to result in apoptosis. Bis-disulfides also inhibit growth of murine melanoma B16 cells but have no cytotoxicity to human fibroblasts. Bis-disulfides also can reduce murine melanoma size in the mouse model. The prepared compounds of the invention would be applicable in anticancer and anti-tumor therapies.
A pharmaceutical composition for treating a cancer, comprising a bis(benzylidene-benzenamine)disulfide represented by formula I:
A pharmaceutical composition for treating a cancer, comprising a bis(benzylidene-benzenamine)disulfide represented by formula III:
A preparation method of a pharmaceutical composition for treating a cancer, wherein the pharmaceutical composition comprises a bis(benzylidene-benzenamine)disulfide, the method comprising a step of:
Dependencies are inferred from the claim text.