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Synthesis and cytotoxicity evaluation of naphthalimide derived N-mustards.
- 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.
- Subjects :
- Antineoplastic Agents, Alkylating pharmacology
Apoptosis drug effects
Cell Cycle Checkpoints drug effects
Drug Screening Assays, Antitumor
HCT116 Cells
Hep G2 Cells
Humans
Inhibitory Concentration 50
Naphthalimides pharmacology
Phosphoramide Mustards pharmacology
Poly (ADP-Ribose) Polymerase-1
Poly(ADP-ribose) Polymerases metabolism
Antineoplastic Agents, Alkylating chemical synthesis
Naphthalimides chemical synthesis
Phosphoramide Mustards chemical synthesis
Subjects
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