Pregled bibliografske jedinice broj: 1010122
Synthesis and biological activity of quaternary salts of 3-N-dodecylaminoquinuclidine
Synthesis and biological activity of quaternary salts of 3-N-dodecylaminoquinuclidine // Book of abstracts JMMC 2019 –Joint Meeting on Medicinal Chemistry 2019
Prag: GUARANT International spol. s r.o., 2019. str. 100-100 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Synthesis and biological activity of quaternary
salts of 3-N-dodecylaminoquinuclidine
Autori
Odžak, Renata ; Šprung, Matilda ; Soldo, Barbara ; Maravić, Ana ; Bazina, Linda ; Radman Kastelić, Andreja ; Hrenar, Tomica ; Primožič, Ines
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstracts JMMC 2019 –Joint Meeting on Medicinal Chemistry 2019
/ - Prag : GUARANT International spol. s r.o., 2019, 100-100
ISBN
978-80-907442-0-2
Skup
11th Joint Meeting on Medicinal Chemistry 2019
Mjesto i datum
Prag, Češka Republika, 27.06.2019. - 30.06.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
quaternary salts, quinuclidine-3-yl(dodec-1-yl)amine, antimicrobial activity, cytotoxicity
Sažetak
In an attempt to identify a new class of antimicrobial agents, the antimicrobial potential of quaternary quinuclidinium derivativeswith N-alkyl substituent on the position 3 of quinuclidine was evaluated.We were guided bythe results of our previouswork which showedthatquaternary derivatives of 3- substituted quinuclidineshavevery good biological activity.1Therefore, newseriesof quaternary quinuclidiniumsalts were designed and synthetized by the quaternization of quinuclidin-3-yl(dodec-1-yl)aminewith different benzyl bromides. All compounds were obtained in very good yields after which they were further characterized by physico-chemical methods includingFTIR, 1H and 13C NMR spectroscopies.The antibacterial activities of all compounds were evaluated against series of recent clinical isolates of antibiotic susceptible Gram-positive and resistant Gram- negative pathogens by determining their minimum inhibitory concentrations. All compounds showed good to strong broad-spectrum activity displaying MIC values between1.95-3.9 μg/mL.Cytotoxicity of compounds with different cell lines in human cell culture was determinedand it was determined that HaCat cell line is less tolerant that RPE1 displaying IC50values between 0.97-24.3 μM/mL. Based on these results, quaternary quinuclidine with long alkyl chain can be considered as promising new class of antimicrobials and further investigations should be performed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
IP-2016-06-3775 ADESIRE
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Split
Profili:
Ana Maravić
(autor)
Barbara Soldo
(autor)
Ines Primožič
(autor)
Tomica Hrenar
(autor)
Linda Mastelić
(autor)
Renata Odžak
(autor)
Matilda Šprung
(autor)