KUSHKEVYCH, Ivan, Petr KOLLÁR, Ana Luísa FERREIRA a Diogo PALMA. Antimicrobial effect of salicylamide derivatives against intestinal sulfate-reducing bacteria. Journal of Applied Biomedicine. 2016, roč. 2016, 14(2), s. 125-130. ISSN 1214-021X. Dostupné z: https://dx.doi.org/10.1016/j.jab.2016.01.005.
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Základní údaje
Originální název Antimicrobial effect of salicylamide derivatives against intestinal sulfate-reducing bacteria
Autoři KUSHKEVYCH, Ivan, Petr KOLLÁR, Ana Luísa FERREIRA a Diogo PALMA.
Vydání Journal of Applied Biomedicine, 2016, 1214-021X.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10600 1.6 Biological sciences
Stát vydavatele Česká republika
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 1.433
Organizační jednotka Přírodovědecká fakulta
Doi http://dx.doi.org/10.1016/j.jab.2016.01.005
UT WoS 000373608500007
Klíčová slova anglicky Sulfate-reducing bacteria; Desulfovibrio piger; Desulfomicrobium sp.; Salicylamides; Bowel disease; Lipophilicity; Structure–activity relationships
Štítky NZ
Změnil Změnila: Ing. Nicole Zrilić, učo 240776. Změněno: 13. 4. 2018 10:43.
Anotace
Sulfate-reducing bacteria (SRB) are most likely involved in both the initiation and maintenance of inflammatory bowel disease (IBD); unfortunately present antibacterial chemotherapeutics used in the treatment of IBD have been ineffective. Thus, the antimicrobial activity of salicylamide derivatives against two different genera of intestinal SRB, Desulfovibrio and Desulfomicrobium, was investigated. Six 2-(phenylcarbamoyl)phenyl N-[(benzyloxy)carbonyl]alkanoates and three 2-hydroxy-N-[(2S)-1-oxo-1-(phenylamino)alkan-2-yl]benzamides showed MIC values in the range from 0.22 to 0.35 microM against Desulfovibrio piger Vib-7 and in the range from 0.27 to 8.52 microM against Desulfomicrobium sp. Rod-9, while MIC values of ciprofloxacin were 41.2 microM and 39.3 microM. The highest potency against the two strains was observed for 4-chloro-N-{(2S)-1-[(3,4-dichlorophenyl)amino]-3-methyl-1-oxobutan-2-yl}-2-hydroxybenzamide (MIC 0.22 microM and 0.27 microM). 4-Chloro-2-[(4-nitrophenyl)carbamoyl]phenyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-methylbutanoate showed high activity against D. piger Vib-7 (MIC = 0.26 microM), while 4-chloro-2-[(4-methylphenyl)carbamoyl]phenyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-(1H-indol-2-yl)propanoate expressed high activity against Desulfomicrobium sp. Rod-9 (MIC = 0.31 microM). Structure–activity relationships are discussed.
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