A series of novel 3-aryl-5-pyrrolo[1,2-]imidazole and 5-imidazo[1,2-]azepine quaternary salts were synthesized in 58-85% yields via the reaction of 3-aryl-6, 7-dihydro-5-pyrrolo[1,2-]imidazoles or 3-aryl-6,7,8,9-tetrahydro-5-imidazo[1,2-]azepines and various alkylating reagents. All compounds were characterized by H NMR, C NMR, and LC-MS. The conducted screening studies of the in vitro antimicrobial activity of the new quaternary salts derivatives established that 15 of the 18 newly synthesized compounds show antibacterial and antifungal activity. Synthesized 3-(3,4-dichlorohenyl)-1-[(4-phenoxyphenylcarbamoyl)-methyl]-6,7-dihydro-5-pyrrolo[1,2-]imidazol-1-ium chloride possessed a broad activity spectrum towards , , , , and with a high hemolytic activity against human red blood cells and cytotoxicity against . However, compound is characterized by a low in vivo toxicity in mice (LD > 2000 mg/kg).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305969 | PMC |
http://dx.doi.org/10.3390/molecules26144253 | DOI Listing |
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