ABSTRACT
Improving lipophilicity for drugs to penetrate the lipid membrane and decreasing bacterial and fungal coinfections for patients with cancer pose challenges in the drug development process. Here, a series of new N-alkylated-2-(substituted phenyl)-1H-benzimidazole derivatives were synthesized and characterized by 1H and 13C NMR, FTIR, and HRMS spectrum analyses to address these difficulties. All the compounds were evaluated for their antiproliferative, antibacterial, and antifungal activities. Results indicated that compound 2g exhibited the best antiproliferative activity against the MDA-MB-231 cell line and also displayed significant inhibition at minimal inhibitory concentration (MIC) values of 8, 4, and 4 µg mL-1 against Streptococcus faecalis, Staphylococcus aureus, and methicillin-resistant Staphylococcus aureus compared with amikacin. The antifungal data of compounds 1b, 1c, 2e, and 2g revealed their moderate activities toward Candida albicans and Aspergillus niger, with MIC values of 64 µg mL-1 for both strains. Finally, the molecular docking study found that 2g interacted with crucial amino acids in the binding site of complex dihydrofolate reductase with nicotinamide adenine dinucleotide phosphate.
ABSTRACT
Microwave-solvothermal synthesized MIL-101(Fe) was successfully loaded by silver halides (AgCl and AgBr) by simple precipitation method. The XRD, FESEM mapping, XPS and DRS measurements reveal the successful fabrication of composite photocatalyst. The results suggested that silver halides altered surface charge, surface area and pore size distribution of MIL-101(Fe). The 20%AgBr@MIL-101(Fe) composite has strong tendency to remove the cationic/anionic dyes (96% of rhodamine B, 100% of malachite green and 92% of methyl orange) from wastewater after 30 min of adsorption and 90 min under visible light irradiation. The composite photocatalyst revealed the photodegradation stability up to four cycles. The formation of mesopores improves the adsorption ability of the composites for large organic molecules, while loaded silver halides might inhibit the recombination of electron-hole pairs; those were responsible for enhancing the photocatalytic degradation of organic pollutants. ESR suggested O 2 · - , · OH were responsible for dye degradation in visible light by composite photocatalysts. The photocatalytic mechanism of the composite was also explained in this work.
