Cytotoxic Activities of Mannich Bases of Chalcones and Related Compounds

Abstract

Various Mannich bases of chalcones and related compounds displayed significant cytotoxicity toward murine P388 and L1210 leukemia cells as well as a number of human tumor cell lines. The most promising lead molecule was 21 that had the highest activity toward L1210 and human tumor cells. In addition, 21 exerted preferential toxicity to human tumor lines compared to transformed human T-lymphocytes. Other compounds of interest were 38, with a huge differential in cytotoxicity between P388 and L1210 cells, and 42, with a high therapeutic index when cytotoxicity to P388 cells and Molt 4/C8 T-lymphocytes were compared. In general, the Mannich bases were more cytotoxic than the corresponding chalcones toward L1210 but not P388 cells. A ClusCor analysis of the data obtained from the in vitro human tumor screen revealed that the mode of action of certain groups of compounds was similar. For some groups of compounds, cytotoxicity was correlated with the sigma, pi, or molar refractivity constants in the aryl ring attached to the olefinic group. In addition, the IC50 values in all three screens correlated with the redox potentials of a number of Mannich bases. X-ray crystallography and molecular modeling of representative compounds revealed various structural features which were considered to contribute to cytotoxicity. While a representative compound 15 was stable and unreactive toward glutathione (GSH) in buffer, the Mannich bases 15, 18, and 21 reacted with GSH in the presence of the pi isozyme of glutathione S-transferase, suggesting that thiol alkylation may be one mechanism by which cytotoxicity was exerted in vitro. Representative compounds were shown to be nonmutagenic in an intrachromosomal recombination assay in yeast, devoid of antimicrobial properties and possessing anticonvulsant and neurotoxic properties. Thus Mannich bases of chalcones represent a new group of cytotoxic agents of which 21 in particular serves as an useful prototypic molecule.

Simple chalcones and bis-chalcones ethers as possible pleiotropic agents

“…The error limits of the e values were approximately 2%. The experiment was repeated in the presence of GSH using thiol/test compound, 2/1 and incubation at 37 C for 24 h and their UV spectra were recorded 25,27 . Inhibition of acetylocholinesterase in vitro 28 .…”

“…The nucleophilic addition of GSH to electron-deficient carbon double bonds occurs mainly in compounds with a,b-unsaturated double bonds like chalcones demonstrating preferential reactivity toward thiols in contrast to amino and hydroxyl groups 27 . In our case, we have studied the possibility of alkylation of our mono/bis-chalcones with a cellular thiol such as GSH, leading to the adducts A.…”

Niacin esters of chalcones with tumor-selective properties

“…The unsaturated ketones 1a-e and 3a have been evaluated previously against Molt4/C8, CEM and L1210 cells 10 . The average IC 50 values in these three screens of 1a-e and 3a are as follows, namely 17.1, 20.5, 22.0, 6.48, 5.16 and 18.6 mM, respectively.…”

Synthsis of flavone derivatives

“…The combined extracts were dried over anhydrous Na 2 SO 4 , the solvent was removed under vaccum. The crude product was subsequently purified by silica gel column chromatography using a mixture of ethyl acetate and petroleum ether (45-65°C) as eluent [5][6][7][8].…”