Turkish Journal of Chemistry
DOI
10.3906/kim-1512-12
Abstract
Several novel thiazolylpyrazoline derivatives were synthesized by reacting substituted 3,5-diaryl-1-thiocarba\-moyl-2-pyrazolines with phenacylbromides. The structures of the synthesized compounds were confirmed by IR, $^{1}$H NMR, $^{13}$C NMR, and MS spectral data. Their antimicrobial activities against Staphylococcus aureus(ATCC-25923), Enterococcus faecalis} (ATCC-29212), Enterococcus faecalis (ATCC-51922), Listeria monocytogenes (ATCC-1911), Klebsiella pneumoniae (ATCC-700603), Pseudomonas aeruginosa (ATCC-27853), Escherichia coli (ATCC-35218), Escherichia coli (ATCC-25922), Candida albicans (ATCC-90028), Candida glabrata (ATCC-90030), Candida krusei (ATCC-6258), and Candida parapsilosis (ATCC-22019) were investigated. The compounds were also studied for their cytotoxic effects using a MTT assay. Compound 7c showed the highest antimicrobial activity, possessing the same potential as chloramphenicol against K. pneumonia, P. aeruginosa, and E. coli (ATCC-25923).
Keywords
2-Pyrazoline, thiazole, thiazolylpyrazoline, antimicrobial activity, cytotoxicity
First Page
641
Last Page
654
Recommended Citation
TABBI, AOUATEF; KAPLANCIKLI, ZAFER ASIM; TEBBANI, DAHMANE; YURTTAŞ, LEYLA; CANTÜRK, ZERRİN; ATLI, ÖZLEM; BAYSAL, MERVE; and ZITOUNI, GÜLHAN TURAN
(2016)
"Synthesis of novel thiazolylpyrazoline derivatives and evaluation of their antimicrobial activities and cytotoxicities,"
Turkish Journal of Chemistry: Vol. 40:
No.
4, Article 10.
https://doi.org/10.3906/kim-1512-12
Available at:
https://journals.tubitak.gov.tr/chem/vol40/iss4/10