Antimicrobial, antioxidant and antiproliferative activities of novel quinolones
Yükleniyor...
Dosyalar
Tarih
2020
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Wiley-VCH GmbH
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
The compound (2) formed by esterification of dimethyl morpholine (1) was converted to acetohydrazide (3). Subsequently Schiff bases (4 a-d) and carboxy(thio)amide derivatives (5 a-e) were synthesized. Then 1,2,4-triazole (6 a-e), thia(oxa)zolidine (7 c,e) and thia(oxa)zol (8 c,e) derivatives were obtained by ring closure from carboxy(thio)amides. Mannich bases, which are containing quinolone were synthesized from 1,2,4-triazoles. The structures of newly synthesized compounds were illuminated by spectroscopic methods. Their antimicrobial (MIC method), antioxidant (DPPH, FRAP, and CUPRAC methods), and anticancer activities (MTT method) were examined. Results showed that most of the compounds exhibited good antimicrobial (<0.03-31.25 mu g/mL with MIC values) and antioxidant activities (IC50=0.001-0.004 with DPPH values). Also, some of the compounds have been found to have antiproliferative effects on the prostate (PC-3), liver (Hep3B), and breast (MCF-7) human cancer cells, and also these compounds did not have a cytotoxic effect on a normal cell.
Açıklama
Anahtar Kelimeler
1; 2; 4-triazole, Quinolone, Antioxidant, Antimicrobial, Anticancer activity
Kaynak
ChemistrySelect
WoS Q Değeri
Q3
Scopus Q Değeri
Q3
Cilt
5
Sayı
36
Künye
Ceylan, Ş., Cebeci, Y. U., Demirbaş, N., Batur, Ö. Ö., & Özakpınar, Ö. B. (2020). Antimicrobial, Antioxidant and Antiproliferative Activities of Novel Quinolones. ChemistrySelect, 5(36), 11340-11346.
