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Synthesis and cytotoxicity evaluation of naphthalimide derived N-mustards.

Authors :
Lou Q
Ji L
Zhong W
Li S
Yu S
Li Z
Meng X
Source :
Molecules (Basel, Switzerland) [Molecules] 2014 Jun 25; Vol. 19 (7), pp. 8803-19. Date of Electronic Publication: 2014 Jun 25.
Publication Year :
2014

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.

Details

Language :
English
ISSN :
1420-3049
Volume :
19
Issue :
7
Database :
MEDLINE
Journal :
Molecules (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
24968335
Full Text :
https://doi.org/10.3390/molecules19078803