Synthesis and cytotoxicity evaluation of naphthalimide derived N-mustards

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Abstract

A series of N-mustards, which was conjugated to mono- or bis-naphthalimides with a flexible amine link, were synthesized and evaluated for cytotoxicity against five cancer cell lines (HCT-116, PC-3, U87 MG, Hep G2 and SK-OV-3). Several compounds displayed better activities than the control compound amonafide. Further evaluations by fluorescence spectroscopy studies and DNA-interstrand cross-linking assays revealed that the derivatives showed both alkylating and intercalating properties. Among the derivatives, the bis-naphthalimide N-mustard derivative 11b was found to exhibit the highest cytotoxic activity and DNA cross-linking ability. Both 11b and 7b induce HCT-116 cell apoptosis by S phase arrest.

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Lou, Q., Ji, L., Zhong, W., Li, S., Yu, S., Li, Z., & Meng, X. (2014). Synthesis and cytotoxicity evaluation of naphthalimide derived N-mustards. Molecules, 19(7), 8803–8819. https://doi.org/10.3390/molecules19078803

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