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ABSTRACT: Background
Pyridinium Schiff bases and ionic liquids have attracted increasing interest in medicinal chemistry.Results
A library of 32 cationic fluorinated pyridinium hydrazone-based amphiphiles tethering fluorinated counteranions was synthesized by alkylation of 4-fluoropyridine hydrazone with various long alkyl iodide exploiting lead quaternization and metathesis strategies. All compounds were assessed for their anticancer inhibition activity towards different cancer cell lines and the results revealed that increasing the length of the hydrophobic chain of the synthesized analogues appears to significantly enhance their anticancer activities. Substantial increase in caspase-3 activity was demonstrated upon treatment with the most potent compounds, namely 8, 28, 29 and 32
SUBMITTER: Al-Blewi FF
PROVIDER: S-EPMC6768046 | biostudies-literature | 2018 Nov
REPOSITORIES: biostudies-literature