Design, Synthesis, and Anticancer and Antibacterial Activities of Quinoline-5-Sulfonamides

A series of new unique acetylene derivatives of 8-hydroxy- and 8-methoxyquinoline- 5-sulfonamide 3a–f and 6a–f were prepared by reactions of 8-hydroxy- and 8-methoxyquinoline- 5-sulfonyl chlorides with acetylene derivatives of amine. A series of new hybrid systems containing quinoline and 1,2,3-triazole systems 7a–h were obtained by reactions of acetylene derivatives of quinoline-5-sulfonamide 6a–d with organic azides. The structures of the obtained compounds were confirmed by 1H and 13C NMR spectroscopy and HR-MS spectrometry. The obtained quinoline derivatives 3a–f and 6a–f and 1,2,3-triazole derivatives 7a–h were tested for their anticancer and antimicrobial activity. Human amelanotic melanoma cells (C-32), human breast adenocarcinoma cells (MDA-MB-231), and human lung adenocarcinoma cells (A549) were selected as tested cancer lines, while cytotoxicity was investigated on normal human dermal fibroblasts (HFF-1). All the compounds were also tested against reference strains Staphylococcus aureus ATCC 29213 and Enterococcus faecalis ATCC 29212 and representatives of multidrug-resistant clinical isolates of methicillin-resistant S. aureus (MRSA) and vancomycin-resistant E. faecalis. Only the acetylene derivatives of 8-hydroxyquinoline-5-sulfonamide 3a–f were shown to be biologically active, and 8-hydroxy-N-methyl-N-(prop-2-yn-1-yl)quinoline-5-sulfonamide (3c) showed the highest activity against all three cancer lines and MRSA isolates. Its efficacies were comparable to those of cisplatin/doxorubicin and oxacillin/ciprofloxacin. In the non-cancer HFF-1 line, the compound showed no toxicity up to an IC50 of 100 µM. In additional tests, compound 3c decreased the expression of H3, increased the transcriptional activity of cell cycle regulators (P53 and P21 proteins), and altered the expression of BCL-2 and BAX genes in all cancer lines. The unsubstituted phenolic group at position 8 of the quinoline is the key structural fragment necessary for biological activity.

Based on previous experience with ring-substituted 8-HQ derivatives [12,22,[28][29][30]32,44,45] and propargyl-substituted heterocycles [67][68][69], new acetylene sulfonamides and 1,2,3-triazole hybrids of 8-HQ were designed and synthesized, and their antiproliferative and antibacterial activities were investigated.Despite the abundance of sulfonamide derivatives of 8-HQ described in the literature e.g., [18,19,44] and many scientific centers around the world engaged in the synthesis of new 8-HQ derivatives and evaluation of their biological properties, there are no reports of the synthesis of acetylene derivatives of 8-hydroxyquinoline-5-sulfonamides.In addition, the main directions of structural modifications of the 8-HQ scaffold consisted in the introduction of different pharmacophoric systems into positions 2, 5, and 7 of the quinoline core and into the oxygen atom of the hydroxyl group.
Thus, the investigation of new substituted hybrid systems combining 8-HQ, sulfonamide, acetylene, and 1,2,3-triazole expands the library of 8-HQ-based derivatives and the knowledge of their biological activities in relation to selected cancer cell lines and Gram-positive bacteria.
Molecules 2024, 29, 4044 3 of 22 properties, as mentioned above, which may cause interactions with the catalyst system used, resulting in its ineffectiveness.Thus, in the next stage of this work, we decided to protect the phenolic group by the methylation reaction and verify whether/how such a structural modification will affect the course of the cyclization reaction.
The O-methylation reaction of 8-hydroxyquinoline was carried out under anhydrous conditions in DMF solution in the presence of a stoichiometric amount of sodium hydride.Then, a sulfonation reaction (analogous to sulfonyl chloride 2) of prepared 8-methoxyquinoline (4) led to 8-methoxyquinoline-5-sulfonyl chloride (5), which, with acetylenamine derivatives, gave corresponding 8-methoxyquinoline-5-sulfonamides 6a-f in high Papers focused on the reactions of acetylenic sulfonamide derivatives with organic azides have been published, and the 1,2,3-triazole derivatives obtained in this way showed interesting biological properties [51,52].It seemed that the designed acetylenic quinoline-5sulfonamide derivatives 3a-f would be suitable substrates for obtaining hybrid systems containing a quinoline-5-sulfonamide system and a 1,2,3-triazole scaffold.We carried out a series of reactions of compounds 3a-f with organic azides.The reactions were performed in DMF/H 2 O in the presence of a copper catalyst (CuSO 4 • 5H 2 O, sodium ascorbate) at room temperature.However, the analysis of the obtained post-reaction mixtures using mass spectrometry did not reveal the presence or even trace amounts of the expected triazole derivatives of quinoline-5-sulfonamide.The 8-hydroxyquinoline system exhibits chelating properties, as mentioned above, which may cause interactions with the catalyst system used, resulting in its ineffectiveness.Thus, in the next stage of this work, we decided to protect the phenolic group by the methylation reaction and verify whether/how such a structural modification will affect the course of the cyclization reaction.
The O-methylation reaction of 8-hydroxyquinoline was carried out under anhydrous conditions in DMF solution in the presence of a stoichiometric amount of sodium hydride.Then, a sulfonation reaction (analogous to sulfonyl chloride 2) of prepared 8methoxyquinoline (4) led to 8-methoxyquinoline-5-sulfonyl chloride (5), which, with acetylenamine derivatives, gave corresponding 8-methoxyquinoline-5-sulfonamides 6a-f in high yields (Scheme 2).The reaction was performed in anhydrous acetonitrile using a two-fold molar excess of amine and triethylamine as the hydrogen chloride acceptor.
Molecules 2024, 29, 4044 3 of properties, as mentioned above, which may cause interactions with the catalyst syste used, resulting in its ineffectiveness.Thus, in the next stage of this work, we decided protect the phenolic group by the methylation reaction and verify whether/how such structural modification will affect the course of the cyclization reaction.The O-methylation reaction of 8-hydroxyquinoline was carried out under anhydrou conditions in DMF solution in the presence of a stoichiometric amount of sodium hydrid Then, a sulfonation reaction (analogous to sulfonyl chloride 2) of prepared 8-metho yquinoline (4) led to 8-methoxyquinoline-5-sulfonyl chloride (5), which, with acetylen mine derivatives, gave corresponding 8-methoxyquinoline-5-sulfonamides 6a-f in hig yields (Scheme 2).The reaction was performed in anhydrous acetonitrile using a two-fo molar excess of amine and triethylamine as the hydrogen chloride acceptor.The next stage of the work involved coupling reactions of acetylenic sulfonamid derivatives 6a-d with organic azides.The reactions were carried out in DMF/H2O in th presence of a copper catalyst (CuSO4 • 5H2O, sodium ascorbate); see Scheme 3. Comme cial azides were generally used.For the synthesis of allyl derivative 7a, allyl azide w prepared by reacting allyl bromide with sodium azide immediately prior to coupling wi propargyl derivative 6a.The synthesis was performed according to a one-pot procedu without isolating the azide from the reaction mixture.The reactions proceeded readily high yields at room temperature.An exception is the reaction of propargyl derivative with an aromatic azide (1-azido-4-chlorobenzene), which provided a very low yield room temperature.The reaction carried out in a microwave reactor at 100 °C led to corr sponding 1,2,3-triazole derivative 5d in 57% yield.The structures of the obtained com pounds were confirmed by 1 H and 13 C-NMR spectroscopy and HR-MS spectrometry (s Supplementary Materials, Figures S1-S69).In the HR-MS spectrum of compound 2, the The next stage of the work involved coupling reactions of acetylenic sulfonamide derivatives 6a-d with organic azides.The reactions were carried out in DMF/H 2 O in the presence of a copper catalyst (CuSO 4 • 5H 2 O, sodium ascorbate); see Scheme 3. Commercial azides were generally used.For the synthesis of allyl derivative 7a, allyl azide was prepared by reacting allyl bromide with sodium azide immediately prior to coupling with propargyl derivative 6a.The synthesis was performed according to a one-pot procedure without isolating the azide from the reaction mixture.The reactions proceeded readily in high yields at room temperature.An exception is the reaction of propargyl derivative 6a with an aromatic azide (1-azido-4-chlorobenzene), which provided a very low yield at room temperature.The reaction carried out in a microwave reactor at 100 • C led to corresponding 1,2,3-triazole derivative 5d in 57% yield.The structures of the obtained compounds were confirmed by 1 H and 13 C-NMR spectroscopy and HR-MS spectrometry (see Supplementary Materials, Figures S1-S69).In the HR-MS spectrum of compound 2, there is an additional signal at m/z = 226.0165.This is the effect of hydrolysis of 8-hydroxyquinoline-5-sulfonyl chloride occurring during the ionization of the sample using the ESI method.The signal corresponds to the molecular mass of 8-hydroxyquinoline-5-sulfonic acid [M+H] + .

In Vitro Cell Viability
The synthesized compounds were tested using three cancer cell lin amelanotic melanoma (C-32), human breast adenocarcinoma (MDA-MB-231), lung adenocarcinoma (A549)-and, for comparison, normal human derma (HFF-1).The WST-1 (water-soluble tetrazole salt) assay was used to evaluate the synthesized compounds on the viability of cultured cells.IC50 values for exposed to test compounds for 72 h are shown in Tables 1 and 2. The synthesized compounds were tested using three cancer cell lines-human amelanotic melanoma (C-32), human breast adenocarcinoma (MDA-MB-231), and human lung adenocarcinoma (A549)-and, for comparison, normal human dermal fibroblasts (HFF-1).The WST-1 (water-soluble tetrazole salt) assay was used to evaluate the effect of the synthesized compounds on the viability of cultured cells.IC 50 values for cell cultures exposed to test compounds for 72 h are shown in Tables 1 and 2.

Comp.
IC As can be seen from the IC 50 values in Tables 1 and 2, derivatives 3a-f, i.e., with a free 8-phenolic group, were the most effective against the tested cancer lines.Methylation of the phenolic moiety (series 6) generally resulted in a significant loss of activity, which is most evident in the effect on breast (MDA-MB-231) and lung (A549) adenocarcinoma cell lines.Compounds 3a-f showed insignificantly different activity against both C-32 and A549 lines.MDA-MB-231 cells were the least sensitive to the discussed derivatives, but compound 3c achieved excellent efficacy, comparable to that of the clinically used drugs cisplatin and doxorubicin.
Overall, it can be concluded that the inhibition of the proliferation of the non-cancerous HFF-1 line by the active compounds of series 3 was significantly worse than the growth inhibition of all three used cancer lines.For compounds 3a-c (substitution with propargyl), the disubstitution of the alpha carbon of propargyl (compound 3b) led to a significant decrease in activity, while, on the contrary, the disubstituted nitrogen of the sulfonamide group (compound 3c) resulted in the most effective derivative of the investigated compounds.Of the trio of propargyloxyanilides 3d-f, the meta-isomer was the most effective.Shifting the propargyloxy chain to the para position caused a decrease in activity, while the ortho-isomer 3f demonstrated increased general cytotoxicity, which was also observed against the non-cancer HFF-1 line.It should be noted that a similar trend, when cytotoxicity increased even for non-cancer cells in the case of spatially close substitution of the propargyloxy chain to the nitrogen atom, was reported by Kisiel-Nawrot et al. [68].As mentioned above, methylation of the 8-HQ phenolic group resulted in a significant loss of activity, with the C-32 line again being the most sensitive to these methoxy derivatives.The most active derivatives were 6d and 6e.Unfortunately, the introduction of 1,2,3-triazole into the molecule (series 7) led to a loss of activity, contrary to our expectation, when the introduction of 1,2,3-triazole onto the quinobenzothiazine scaffold resulted in a significant increase in anticancer potency [68,69].

Additional Antiproliferative Tests
Since compound 3c showed the best activity against all three cancer lines, its effects on cultured cell lines were investigated in more detail.The effect of the compound on cell viability was determined using, in addition to the WST-1 assay, the crystal violet assay and the LDH (lactate dehydrogenase) assay.Furthermore, a wound healing test (indicator of cell proliferation and migration capacity) and assessment of gene expression (in the transcription phase) of BCL-2, BAX, TP53, P21, and H3 were performed.

Violet-WST-LDH
Cell viability and cytotoxicity assays of compound 3c showed a significant decrease in cell number in cultures exposed to 3c in medium above 0.3 µM, particularly in A549 and MDA-MB-231 cells (Figure 1b,c).The differences in the results of the crystal violet and WST-1 tests indicate that some of the cells that still transform the WST-1 dye into colored products lose their adhesive abilities and are already separated from the culture vessel (they are washed away in the violet test-hence, the lower absorbance values than in WST-1), leading to their death in a short time.An increase in the number of dead cells is shown by the absorbance line in the LDH test.

Wound Healing Assay
Photographs of the cell culture (control and culture exposed to compound 3c at a concentration of 3 µM) were taken after scraping the bottom of the vessel with a pipette tip and then after 72 h of incubation (Figure 2).Image analysis of cell culture 72 h after scratching in cell culture indicates a reduction in proliferative activity and migration capacity of all cells exposed to compound 3c.In control cultures, the cell-free surface of the vessel (scraped with a pipette tip) becomes overgrown with cells, while in cultures supplemented with medium containing 3 µM of compound 3c, empty spots are visible.In the case of A549 and MDA-MB-231 cells, entire cell-free regions are clearly visible.

Transcriptional Activity
The study investigated the effect of compound 3c on the transcriptional activity of genes encoding a proliferation marker (histone H3), cell cycle regulators (P53 and P21), and genes encoding proteins involved in the mitochondrial apoptosis pathway (BCL-2 and BAX) in C-32, A549, MDA-MB-231, and HFF-1 cells.Cultures were exposed to 3c at a concentration of 36 µM in medium for 24 h. Figure 3 shows the pooled mRNA copy number results for individual genes of control compound 3c in C32, A549, MDA-MB-231, and HFF-1 cell cultures.A beneficial effect of 3c was observed in all the lines in the sense of finding an effective agent to destroy cancer cells: a) reduction in H3 expression (proliferation marker) in all the cultures with 3c, b) and c) an increase in the transcriptional activity of cell cycle regulators (P53 and P21 proteins), d) and e) changes in the expression of BCL-2 and BAX genes, leading to f) a shift in the BCL-2/BAX ratio (the ratio of the number of BCL-2 and BAX gene copies) in favor of BAX, which indicates the possibility of cells entering the path of apoptosis.

Transcriptional Activity
The study investigated the effect of compound 3c on the transcriptional activity of genes encoding a proliferation marker (histone H3), cell cycle regulators (P53 and P21), and genes encoding proteins involved in the mitochondrial apoptosis pathway (BCL-2 and BAX) in C-32, A549, MDA-MB-231, and HFF-1 cells.Cultures were exposed to 3c at a concentration of 36 µM in medium for 24 h. Figure 3 shows the pooled mRNA copy number results for individual genes of control compound 3c in C32, A549, MDA-MB-231, and HFF-1 cell cultures.A beneficial effect of 3c was observed in all the lines in the sense of finding an effective agent to destroy cancer cells: a) reduction in H3 expression (proliferation marker) in all the cultures with 3c, b) and c) an increase in the transcriptional activity of cell cycle regulators (P53 and P21 proteins), d) and e) changes in the expression of BCL-2 and BAX genes, leading to f) a shift in the BCL-2/BAX ratio (the ratio of the number of BCL-2 and BAX gene copies) in favor of BAX, which indicates the possibility of cells entering the path of apoptosis.

In Vitro Antimicrobial Activity
Since there is a general decrease in immunity during the treatment of oncological patients, i.e., patients are more susceptible to infectious diseases, it is advantageous if anticancer agents show antimicrobial properties at the same time [74,75].Therefore, the effects of the compounds were also investigated against Gram-positive bacteria.For this purpose, the susceptible collection strains of aerobic Staphylococcus aureus ATCC 29213 and facultatively aerobic Enterococcus faecalis ATCC 29212 and resistant clinical isolates of methicillin-resistant S. aureus (MRSA) SA 3202, SA 630 carrying the mecA gene [76,77], and vancomycin-resistant isolates of E. faecalis (VRE) 342B, 368, and 725B carrying the vanA gene [78] were selected.Thus, the selection of the studied bacterial strains was adopted following the CLSI (National Committee for Clinical Laboratory Standards) international reference methodologies [79].
The activities of the individual derivatives were expressed as minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) and are shown

In Vitro Antimicrobial Activity
Since there is a general decrease in immunity during the treatment of oncological patients, i.e., patients are more susceptible to infectious diseases, it is advantageous if anticancer agents show antimicrobial properties at the same time [74,75].Therefore, the effects of the compounds were also investigated against Gram-positive bacteria.For this purpose, the susceptible collection strains of aerobic Staphylococcus aureus ATCC 29213 and facultatively aerobic Enterococcus faecalis ATCC 29212 and resistant clinical isolates of methicillin-resistant S. aureus (MRSA) SA 3202, SA 630 carrying the mecA gene [76,77], and vancomycin-resistant isolates of E. faecalis (VRE) 342B, 368, and 725B carrying the vanA gene [78] were selected.Thus, the selection of the studied bacterial strains was adopted following the CLSI (National Committee for Clinical Laboratory Standards) international reference methodologies [79].
The activities of the individual derivatives were expressed as minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) and are shown in Table 3 together with the values of the antibiotics used as standards for comparison.Compounds exhibiting bactericidal activity against a particular tested strain meet the condition of MIC/MBC ≤ 4 [80].MBC values of bactericidal compounds are indicated in bold in Table 3.As in the case of anticancer activity, only series 3 was active, i.e., after blocking the phenolic group at position 8 of quinoline with methyl (series 6), there was a total loss of antibacterial activity (MIC > 256 µg/mL).Even triazine substitution (series 7) did not improve activity (MICs > 256 µg/mL).Therefore, the MIC values of series 6 and 7 are not reported as completely unimpressive.It is important to add that all the derivatives had only antistaphylococcal activity.On the other hand, all were bactericidal (see bolded MBC values in Table 3).Derivative 3c demonstrated the highest antistaphylococcal potency (although it can be rated as moderately active) as well as anticancer activity.Compound 3c had equal activity against both susceptible strains and MRSA isolates (it was more potent than clinically used antibiotics), suggesting that the presence of the mecA gene (which encodes an alternative transpeptidase and causes resistance to methicillin [76,77]) in MRSA does not affect the activity of this compound.Therefore, the specific activity against Staphylococcus sp. is a matter for speculation.The isomeric propargyloxyanilides 3d-3e showed identical activity.
The compounds were more active against aerobic staphylococci than facultatively aerobic enterococci, so an MTT assay was performed to verify whether the molecules caused inhibition of respiration.The MTT assay can be used to assess cell growth by measuring respiration.Bacterial cell respiratory activity (which is ultimately reflected in their viability) of less than 70% after exposure to the MIC values for each test compound is considered as a positive result for this test.This low level of cellular oxidative metabolism indicates inhibition of cell growth by inhibition of respiration [81,82].The lowest multiples of the MIC values by which inhibition of S. aureus ATCC 29213 viability [%] greater than 70% was achieved are shown in Table 4.The compounds showed inhibition of respiration at 1× or 2× MIC ranging from 73 to 95%, indicating that they are able to affect the respiratory chain (e.g., compared to ciprofloxacin 95% inhibition at 32× MIC), but this is not their main mechanism of action.Therefore, the antibacterial activity of the discussed compounds cannot be explained solely on the basis of respiration inhibition, so it is very difficult to draw a conclusion regarding the actual mechanism of action, since 8-HQs are multitarget agents, i.e., they affect several different targets at once (as discussed in the section dedicated to anticancer activity), which subsequently leads to the death of the treated resistant microorganisms.
As with anticancer activity, it is difficult to speculate on the structure-activity relationship for this small series of these moderately active compounds.However, it is certain that methylation of the phenolic group of 8-HQ caused a loss of antimicrobial activity that was not restored even by triazine substitution.

Chemistry
Melting points are uncorrected.NMR spectra were recorded using a Bruker Ascend 600 spectrometer (Bruker, Billerica, MA, USA).To assign the structures, the following 2D experiments were employed: 1 H/ 13 C gradient-selected HSQC and HMBC sequences.Standard experimental conditions and standard Bruker programs were used.The 1 H NMR and 13 C NMR spectral data are provided relative to the TMS signal at 0.0 ppm.HR mass spectra were recorded with a Bruker Impact II (Bruker, Billerica, MA, USA).

Synthesis of 8-Hydroxyquinoline-5-Sulfonyl Chloride (2)
A flask containing 1.450 g (10 mmol) of 8-hydroxyquinoline (1) was placed in an ice bath, and 5.850 g (50 mmol) of chlorosulfonic acid was added dropwise.The resulting reaction mixture was stirred at room temperature for 24 h.The reaction mixture was poured onto 150 g of ice and extracted with ethylene chloride (3 × 150 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporating the solvent in vacuo, the obtained product was stored under argon at a temperature of 4-8 An amount of 20 mmol of the appropriate amine was added to a suspension of 1.220 g (5 mmol) of sulfonyl chloride 2 in 15 mL of anhydrous acetonitrile.The resulting reaction mixture was stirred at room temperature for 24 h.The mixture was poured into 100 mL of water and extracted with chloroform (3 × 20 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporation of the solvent in vacuo, the crude product was purified by recrystallization from methanol.

Synthesis of 8-Methoxyquinoline (4)
A solution of 1.450 g (10 mmol) of 8-hydroxyquinoline was added dropwise to a suspension of 0.264 g (11 mmol) of sodium hydride (60% suspension in mineral oil) in 20 mL of anhydrous DMF with stirring.After 1 h, 1.562 g (11 mmol) of methyl iodide was added dropwise to the reaction mixture.The mixture was stirred at room temperature for 5 h.The mixture was poured into 150 mL of water and extracted with chloroform (3 × 15 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporation of the solvent in vacuo, the crude products were purified by silica column, using a chloroform/ethanol (v/v) 10:1 mixture as the eluent.

Synthesis of 8-Methoxyquinoline-5-Sulfochloride (5)
A flask containing 1.590 g (10 mmol) of 8-methoxyquinoline (4) was placed in an ice bath and 5.850 g (50 mmol) of chlorosulfonic acid was added dropwise.The resulting reaction mixture was stirred at room temperature for 24 h.The reaction mixture was poured onto 150 g of ice and extracted with ethylene chloride (3 × 150 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporating the solvent in vacuo, the obtained product was stored under argon at a temperature of 4-8 • C.

Synthesis of 8-Methoxyquinoline-5-Sulfonamides (6)
To a suspension of 1.290 g (5 mmol) of sulfonyl chloride (5) in 15 mL of anhydrous acetonitrile, 10 mmol of the appropriate amine and 0.3 mL of triethylamine were added.The resulting reaction mixture was stirred at room temperature for 5 h.The mixture was poured into 100 mL of water and extracted with chloroform (3 × 20 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporation of the solvent in vacuo, the crude products were purified by silica column, using a chloroform/ethanol (v/v) 10:1 mixture as the eluent.
8-Methoxy-N-(prop-2-yn-1-yl)quinoline-5-sulfonamide (6a): yield: 76%; m.p. = 161-163 To 5 mL of anhydrous DMF, 0.182 g (1.5 mmol) of allyl bromide and 0.098 g (1.5 mmol) of sodium azide were added, and the resulting suspension was stirred at room temperature for 24 h.Then, 0.276 g (1 mmol) of the 8-methoxyquinoline-5-sulfonamide (6a) was added.A solution of 40 mg of sodium ascorbate in 1 mL of distilled water and a solution of 25 mg of copper sulfate pentahydrate in 1 mL of distilled water were prepared.The resulting aqueous solutions were mixed and added to the reaction mixture.The whole mixture was stirred at room temperature for 24 h.The reaction mixture was then poured into 50 mL of water and extracted with chloroform (4 × 20 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporation of the solvent in vacuo, the crude products were purified by silica column, using a chloroform/ethanol (v/v) 10:1 mixture as the eluent.

Procedure B: Preparation of Derivatives 7b, c, and 7e-h
To 10 mL of anhydrous DMF, 1.5 mmol of the appropriate azide: benzyl azide (3 mL 0.5 M solution in dichloromethane) or (phenylthio)methyl azide 0.248 g (1.5 mmol) and 1 mmol of the appropriate 8-methoxyquinoline-5-sulfonamide (6a-f) were added.A solution of 40 mg of sodium ascorbate in 1 mL of distilled water and a solution of 25 mg of copper sulfate pentahydrate in 1 mL of distilled water were prepared.The resulting aqueous solutions were mixed and added to the reaction mixture.The whole mixture was stirred at room temperature for 24 h.The reaction mixture was then poured into 50 mL of water and extracted with chloroform (4 × 20 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporation of the solvent in a vacuum evaporator, the crude products obtained were purified by silica column chromatography, using a chloroform/ethanol (v/v) 10:1 mixture as the eluent.

Procedure C: Preparation of Derivative 7d
An amount of 10 mL of anhydrous DMF, 1.5 mmol of 4-chlorophenyl azide (3 mL of a 0.5 M solution in tert-butyl methyl ether), and 0.276 g (1 mmol) of the 8-methoxyquinoline-5-sulfonamide (6a) were placed in a microwave reactor tube.A solution of 40 mg of sodium ascorbate in 1 mL of distilled water and a solution of 25 mg of copper sulfate pentahydrate in 1 mL of distilled water were prepared.The resulting aqueous solutions were mixed and added to the reaction mixture.The reaction was carried out in a microwave reactor at 100 • C for 45 min.The solution was then cooled to room temperature and poured into 50 mL of water.The whole mixture was extracted with chloroform (4 × 20 mL).The combined extracts were dried over anhydrous sodium sulfate.After evaporation of the solvent in vacuo, the crude products were purified by silica column chromatography.Chloroform was used as an eluent, followed by chloroform/ethanol (v/v) 10:1.

Effect of Compounds on Number and Viability of Cells
Cells were seeded in 96-well plates at 5000/well in 100 µL of medium.After 24 h of incubation, the medium was replaced with a new one with the addition of the test substance.After 72 h, the following tests were performed: with crystal violet (determination of the number of adherent cells in the culture), the WST-1 test (determination of the relative number of living cells and their metabolic activity), and the LDH test (determination of the relative number of dead cells in cultures-cytotoxicity of the tested substance).
Crystal violet test: The crystal violet (Sigma-Aldrich, Darmstadt, Germany) test determines the relative number of cells based on the amount of dye bound to the DNA of cells in the culture.The absorbance measurement was performed at a wavelength of λ = 540 nm (reference wavelength λ = 690 nm).
WST-1 test: The WST-1 test (Roche Diagnostics, Mannheim, Germany) allows one to determine the relative number of cells in cultures.Absorbance is directly proportional to the number of cells and their metabolic activity.The absorbance measurement is performed at λ = 450 nm (reference wave 600 nm).
LDH test: The LDH test (Roche Diagnostics) involves measuring lactate dehydrogenase released by dead cells into the medium.It is a measure of the cytotoxic effect of an agent on cells in culture.The absorbance measurement was performed at a wavelength of λ = 490 nm (reference wave λ = 600 nm).A UVM340 microplate reader (Asys-Hitech GmbH UVM340 (Eugendorf, Austria)) was used for absorbance measurements.

Wound Healing Assay
The wound healing assay is a standard in vitro technique for examining collective cell migration in two dimensions.The test involves scratching the bottom of a vessel (wells of a culture plate) with a pipette tip and observing over time how quickly cells move to occupy a free surface under specific culture conditions.In the presented work, the observation was carried out after 72 h of culture.At t = 0, a scratch was made, the medium was replaced with fresh one with the addition of the test compound, and then the cultures were incubated for 72 h.The observation was carried out using an OLYMPUS IX 50 microscope (Tokyo, Japan) with a KERN camera (KERN & SOHN GmbH, Balingen, Germany), and an image analysis system with KERN software (BalanceConnection SCD-4.0Pro) was used to analyze the observed changes.The transcriptional activity of the following genes was assessed: H3 (a gene encoding histone H3, a proliferation marker), BCL-2 and BAX (genes encoding BCL-2 and BAX proteins, respectively; both are mitochondrial proteins associated with apoptosis), and P21 and P53 (cell cycle regulators).Activity was assessed by RT-QPCR using the CFX96 Touch Real-Time PCR Detection System (BIO-RAD Hercules, CA, USA) and a SensiFAST TM SYBR R No-ROX One-Step Kit (Meridian Bioscience, Memphis, TN, USA).Cultured cells were exposed (for 24 h) to the tested compounds (0.5 µg/mL).RNA was extracted using Quick-RNA™ MiniPrep kit columns (Zymo Research, Irvine, CA, USA).The extracted RNA was assessed qualitatively and quantitatively.The integrity of total RNA was checked by electrophoresis (1.2% agarose gel, EtBr), and the amount and purity of total RNA in the extracts was determined spectrophotometrically (HP8452A apparatus, Hewlett Packard, Waldbronn, Germany).

In Vitro Antibacterial Evaluation
The in vitro antibacterial activity of the synthesized compounds was evaluated against representatives of multidrug-resistant bacteria, three clinical isolates of methicillin-resistant S. aureus: clinical isolates of human origin, MRSA SA 3202, and MRSA SA 630 (National Institute of Public Health, Prague, Czech Republic), carrying the mecA gene [76,77].These two clinical isolates were classified as vancomycin-susceptible (but with a higher MIC of vancomycin equal to 2 µg/mL (VA2-MRSA) [76].Vancomycin-and methicillin-susceptible S. aureus ATCC 29213 and vancomycin-susceptible Enterococcus faecalis ATCC 29212, obtained from the American Type Culture Collection, were used as the reference and quality control strains.Three vanA gene-carrying vancomycin-resistant isolates of E. faecalis (VRE 342B, VRE 368, VRE 725B) (Department of Infectious Diseases and Microbiology, Faculty of Veterinary Medicine, University of Veterinary Sciences Brno, Czech Republic) were provided by Oravcova et al. [77].
The minimum inhibitory concentrations (MICs) were evaluated by the microtitration broth method according to the CLSI, with some modifications [83,84].The compounds were dissolved in DMSO (Sigma, St. Louis, MO, USA) to obtain a concentration of 10 µg/mL and diluted in a microtitration plate in an appropriate medium, i.e., Cation-Adjusted Mueller-Hinton Broth (CaMH, Oxoid, Basingstoke, UK) for staphylococci, and Brain Heart Infusion Broth (BHI, Oxoid) for enterococci to reach the final concentration of 256-0.125 µg/mL.Microtiter plates were inoculated with test microorganisms so that the final concentration of bacterial cells was 10 5 .Ampicillin, oxacillin, and ciprofloxacin (Sigma) were used as reference drugs.A drug-free control and a sterility control were included.The plates were incubated for 24 h at 37 • C for staphylococci and enterococci.After static incubation in the darkness in an aerobic atmosphere, the MIC was visually evaluated as the lowest concentration of the tested compound, which completely inhibited the growth of the microorganism.The experiments were repeated three times.The results are summarized in Table 3.

Determination of Minimum Bactericidal Concentrations
For the above-mentioned strains/isolates, the agar aliquot subculture method was used as a test for bactericidal agents [85,86].After the MIC value determination, the inocu-lum was transferred to CaMH (Oxoid) for staphylococci, and BHI (Oxoid) for enterococci medium using a multipoint inoculator.The plates were incubated in a thermostat at 37 • C for 24 h.The lowest concentration of test compound at which ≤5 colonies were obtained was then evaluated as MBC, corresponding to a 99.9% decrease in CFU relative to the original inoculum.

MTT Assay
Compounds were prepared as previously stated and diluted in CaMH broth for S. aureus to achieve the desired final concentrations.S. aureus bacterial suspension in sterile distilled water at 0.5 McFarland was diluted 1:3.Inocula were added to each well by multi-inoculator.Diluted mycobacteria in broth free from inhibiting compounds were used as the growth control.All compounds were prepared in duplicate.Plates were incubated at 37 • C for 24 h for S. aureus.After the incubation period, 10% well volume of MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) reagent (Sigma) was mixed into each well and incubated at 37 • C 1 h for S. aureus.Then, 100 µL of 17% sodium dodecyl sulphate in 40% dimethylformamide was added to each well.The plates were read at 570 nm.The absorbance readings from the cells grown in the presence of the tested compounds were compared with uninhibited cell growth to determine the relative percent inhibition.The percent inhibition was determined through MTT assay.The percent viability is calculated through the comparison of a measured value and that of the uninhibited control: % viability = OD 570E /OD 570P × 100, where OD 570E is the reading from the compound-exposed cells, while OD 570P is the reading from the uninhibited cells (positive control).Cytotoxic potential is determined by a percent viability of <70% [81,82].The results are summarized in Table 4.

Conclusions
A series of unique acetylene derivatives of 8-hydroxy and 8-methoxyquinoline-5sulfonamide 3a-f and 6a-f were prepared by reactions of 8-hydroxy and 8-methoxyquinoline-5-sulfonyl chlorides with acetylene derivatives of amine.A series of new hybrid systems containing quinoline and 1,2,3-triazole systems 7a-h were obtained by the reaction of acetylene derivatives of quinoline-5-sulfonamide 6a-d with organic azides.Biological screening performed on three cancer cell lines C-32, MDA-MB-231, and A549, reference bacterial strains S. aureus ATCC 29213 and E. faecalis ATCC 29212, and clinical isolates of MRSA and VRE demonstrated the inactivity of 8-methoxy derivatives 6a-d as well as 1,2,3-triazole derivatives 7a-h.In contrast, the acetylenic derivatives of 8-hydroxyquinoline-5-sulfonamide 3a-f were shown to be biologically active.8-Hydroxy-N-methyl-N-(prop-2-yn-1-yl)quinoline-5-sulfonamide (3c) showed the highest activity against all three cancer lines and MRSA isolates, comparable to that of cisplatin/doxorubicin and oxacillin/ciprofloxacin.In the non-cancer HFF-1 cells, derivative 3c showed no cytotoxicity up to an IC 50 of 100 µM.In further tests, compound 3c decreased the expression of H3, increased the transcriptional activity of cell cycle regulators (P53 and P21 proteins), and altered the expression of BCL-2 and BAX genes in all cancer lines.It can be assumed that both anticancer and antibacterial activities of the discussed 8-HQ derivatives are related to the presence of a free phenolic group in position 8 of the quinoline pharmacophore.Irreversible blockade (formation of methyl ether) results in the loss of biological activity, which was not restored even after the introduction of 1,2,3-triazine onto the 8-methoxyquinoline scaffold.Since 8-HQ are multi-target agents, it is very difficult to draw a conclusion regarding the exact mechanism of action.Thus, this is a challenge for future detailed investigation of the most promising agent 3c.

Figure 2 .
Figure 2. Wound healing assay.Cultures of C-32, A549, MDA-MB-231, and HFF-1 cells at times: t = 0 (moment of making a scratch and replacing the medium with fresh-control versus addition of 3c), t = 72 (72 h after making the scratch-control versus addition of 3c).

Figure 2 .
Figure 2. Wound healing assay.Cultures of C-32, A549, MDA-MB-231, and HFF-1 cells at times: t = 0 (moment of making a scratch and replacing the medium with fresh-control versus addition of 3c), t = 72 (72 h after making the scratch-control versus addition of 3c).

Table 2 .
In

Table 4 .
Lowest MIC values with at least 70% inhibition of S. aureus ATCC 29213 respiratory activity.