| Title |
Synthesis and antibacterial activity of new azole, diazole and triazole derivatives based on p-aminobenzoic acid / |
| Authors |
Sapijanskaitė-Banevič, Birutė ; Palskys, Vykintas ; Vaickelionienė, Rita ; Šiugždaitė, Jūratė ; Kavaliauskas, Povilas ; Grybaitė, Birutė ; Mickevičius, Vytautas |
| DOI |
10.3390/molecules26092597 |
| Full Text |
|
| Is Part of |
Molecules.. Basel : MDPI. 2021, vol. 26, iss. 9, art. no. 2597, p. 1-23.. ISSN 1420-3049 |
| Keywords [eng] |
hydrazides ; 2-pyrrolidinone ; azoles ; benzimidazole ; antimicrobial activity |
| Abstract [eng] |
The p-aminobenzoic acid was applied for the synthesis of substituted 1-phenyl-5-oxopyrrolidine derivatives containing benzimidazole, azole, oxadiazole, triazole, dihydrazone, and dithiosemicarbazide moieties in the structure. All the obtained compounds were evaluated for their in vitro antimicrobial activity against Staphylococcus aureus, Bacillus cereus, Listeria monocytogenes, Salmonella enteritidis, Escherichia coli, and Pseudomonas aeruginosa by using MIC and MBC assays. This study showed a good bactericidal activity of γ-amino acid and benzimidazoles derivatives. The antimicrobial activity of the most promising compounds was higher than ampicillin. Furthermore, two benzimidazoles demonstrated good antimicrobial activity against L. monocytogenes (MIC 15.62 µg/mL) that was four times more potent than ampicillin (MIC 65 µg/mL). Further studies are needed to better understand the mechanism of the antimicrobial activity as well as to generate antimicrobial compounds based on the 1-phenyl-5-oxopyrrolidine scaffold. |
| Published |
Basel : MDPI |
| Type |
Journal article |
| Language |
English |
| Publication date |
2021 |
| CC license |
|
