Pregled bibliografske jedinice broj: 921510
Insights into biological activity of ureidoamides with primaquine and amino acid moieties
Insights into biological activity of ureidoamides with primaquine and amino acid moieties // Journal of enzyme inhibition and medicinal chemistry, 33 (2018), 1; 376-382 doi:10.1080/14756366.2017.1423067 (međunarodna recenzija, članak, znanstveni)
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Naslov
Insights into biological activity of ureidoamides with primaquine and amino acid moieties
Autori
Vlainić, Josipa ; Kosalec, Ivan ; Pavić, Kristina ; Hadjipavlou-Litina, Dimitra ; Pontiki, Eleni ; Zorc, Branka
Izvornik
Journal of enzyme inhibition and medicinal chemistry (1475-6366) 33
(2018), 1;
376-382
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
primaquine, ureidoamide, biofilm eradication, antibacterial activity, antioxidative activity
Sažetak
Primaquine (PQ) ureidoamides 5a–f were screened for antimicrobial, biofilm eradication and antioxidative activities. Susceptibility of the tested microbial species towards tested compounds showed species- and compound-dependent activity. N-(diphenylmethyl)-2-[({; ; ; 4-[(6-methoxyquinolin-8-yl)amino]pentyl}; ; ; carbamoyl)amino]-4-methylpentanamide (5a) and 2-(4-chlorophenyl)-N-(diphenylmethyl)-2-[({; ; ; 4-[(6-methoxyquinolin-8-yl)amino]pentyl}; ; ; carbamoyl)amino]acetamide (5d) showed antibacterial activity against S. aureus strains (MIC = 6.5 µg/ml). Further, compounds 5c and 5d had weak antibacterial activity against Escherichia coli and Pseudomonas aeruginosa. None of the tested compounds showed a wide spectrum of antifungal activity. In contrast, most of the compounds exerted strong activity in a biofilm eradication assay against E. coli, P. aeruginosa and Candida albicans, comparable to or even higher than gentamycin, amphotericin B or parent PQ. The most active compounds were 5a and 5b. Tested compounds were inactive against biofilm formation by C. parapsylosis, Enterococcus faecalis, C. tropicalis and C. krusei. Compounds 5b–f significantly inhibited lipid peroxidation (80–99%), whereas compound 5c presented interesting LOX inhibition.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
HRZZ-IP-2014-09-1501 - Dizajniranje, sinteza i evaluacija derivata primakina, vorinostata i sorafeniba kao potencijalnih citostatika (PVSderivatives) (HRZZ - 2014-09) ( CroRIS)
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE