Napredna pretraga

Pregled bibliografske jedinice broj: 900697

Quaternary salts derived from 3-substituted quinuclidine as potential antioxidative and antimicrobial agents


Odžak, Renata; Šprung, Matilda, Soldo, Barbara; Skočibušić, Mirjana; Gudelj, Martina; Muić, Anita; Primožič, Ines
Quaternary salts derived from 3-substituted quinuclidine as potential antioxidative and antimicrobial agents // Open Chemistry, 15 (2017), 320-331 doi:10.1515/chem-2017-0031 (međunarodna recenzija, članak, znanstveni)


Naslov
Quaternary salts derived from 3-substituted quinuclidine as potential antioxidative and antimicrobial agents

Autori
Odžak, Renata ; Šprung, Matilda, Soldo, Barbara ; Skočibušić, Mirjana ; Gudelj, Martina ; Muić, Anita ; Primožič, Ines

Izvornik
Open Chemistry (2391-5420) 15 (2017); 320-331

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Quaternary ammonium salts, ORAC assay, DNA damage protection activity, antioxidative and antimicrobial activity

Sažetak
Two series of novel ammonium salts containing the quinuclidine moiety were prepared in order to evaluate their antioxidative, antibacterial and antifungal potential. The synthesized homologues of 3-hydroxy (QOH) and 3-chloroquinuclidine (QCl) with the different N-benzyl substituents at the para- position (bromo, chloro or nitro group) were obtained in very good yields and characterized by IR and NMR spectroscopies and elemental analysis. All compounds were tested for antioxidative activity using the oxygen radical absorbance capacity (ORAC) assay and among tested samples, N-p-nitrobenzyl-3- hydroxyquinuclidinium bromide (QOH-4) exhibited the highest antioxidative potential (293.80 nmol (TE) mL- 1), which was further investigated by the DNA nicking assay. The biological activity of selected compounds was evaluated by measuring the zone of inhibition and by determining the minimal inhibitory concentration (MIC) against three Gram-positive bacteria (B. cereus, E. faecalis and S. aureus), three Gram- negative bacteria (E. coli, P. aeruginosa and C. sakazakii) and three fungi species (C. albicans, A. niger and P. notatum). The bioactivity assay showed that some newly synthetized quaternary quinuclidinium compounds display a comparable or even better antibacterial and antifungal activity then the reference drugs such as gentamicin (GEN), cefotaxime (CTX) and amphotericin B (AMPHB). Among the tested compounds, N-p-chlorobenzyl-3-hydroxyquinuclidinium bromide (QOH-3) exhibited a considerable antibacterial efficiency against P. aeruginosa (MIC=0.39 mg mL-1) and QOH-4 displayed a potent antifungal activity against C. albicans (MIC=1.56 mg mL-1).

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove
Prirodoslovno-matematički fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Split

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


Citati