Evaluation of Alkylating and Intercalating Properties of Mannich Bases for Cytotoxic Activity
Huseyin Istanbullu, Yalcin Erzurumlu, Petek Ballar Kirmizibayrak and Ercin Erciyas
Affiliation: Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ege University, 35100, Izmir, Turkey.
Keywords: Alkylation, cytotoxicity, ethidium bromide displacement, intercalation, mannich bases, mercaptoethanol.
A series of new “hybrid compounds”, Mannich base derivatives of planar polycyclic/heterocyclic starting materials,
was designed and synthesized. The structures of the compounds were confirmed by spectroscopic methods and elemental
analysis. Cytotoxicity of compounds was investigated in three cancer cell lines (PC3, HeLa, and MCF7) and one
non-tumoral cell line (293 HEK). We tested the DNA-intercalating capability of the molecules by ethidium bromide
(EtBr) fluorescence displacement experiment. Compounds' alkylation potency was investigated via in vitro incubation test
using 2-mercaptoethanol, a biomimetic nucleophile. The five of the compounds (7s, 9d, 10b, 11b, 12c) are reported for
first time in the literature. Our results suggest that compound 9d has a biological activity close to the reference compound
doxorubicin, an intercalating agent in clinical use.
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