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Pregled bibliografske jedinice broj: 650347

Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria


Odžak, Renata; Skočibušić, Mirjana; Maravić, Ana
Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria // Bioorganic & medicinal chemistry, 21 (2013), 23; 7499-7506 doi:10.1016/j.bmc.2013.09.041 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 650347 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria

Autori
Odžak, Renata ; Skočibušić, Mirjana ; Maravić, Ana

Izvornik
Bioorganic & medicinal chemistry (0968-0896) 21 (2013), 23; 7499-7506

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

Ključne riječi
imidazolium oximes; monoquaternary salts; synthesis; Aantimicrobial activity; β-lactamase; multidrug resistance; ESBL

Sažetak
Two different series of N-substituted imidazolium oximes and their monoquaternary salts were synthesized and biologically tested with respect to their ability to inhibit growth a diverse panel of antibiotic susceptible Gram-positive and antibiotic resistant Gram-negative bacteria as well fungal strains. The newly synthesized compounds were analyzed by spectral studies to confirm their structure. The preliminary results showed that all compounds tested possess promising antimicrobial potential against both susceptible Gram-positive and antibiotic resistant Gram-negative isolates, exhibiting a wide range of MIC values from 0.14 to 100.0 µg/mL. The structure–activity relationship demonstrates that the p-methylphenyl and p-fluorophenyl groups in monoquaternary salts 6 and 7 attached directly to the imidazolium ring could be essential for observed remarkable inhibitory profiles against clinically important pathogens Pseudomonas aeruginosa (MIC = 0.14 µg/mL) and Klebsiella pneumoniae (MIC = 1.56 µg/mL). Furthermore, the broth microdilution assay was then used to investigate the antiresistance efficacy of compound 7 against fourteen extended-spectrum β-lactamase (ESBL)-producing strains in comparison to eight clinically relevant antibiotics. Compound 7 exhibited a remarkable antiresistance profiles ranging between 0.39 and 12.50 µg/mL against all of ESBL-producing strains, which leads to the suggestion that may be interesting candidate for development of new antimicrobials to combat multidrug resistant Gram-negative bacteria.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija



POVEZANOST RADA


Projekti:
119-1191344-3121 - Sinteze i enzimske transformacije biološki aktivnih spojeva (Tomić-Pisarović, Srđanka, MZOS ) ( CroRIS)
177-0000000-3182 - Indikatori fekalnog onečišćenja i moguće patogene bakterije u obalnom moru (Skočibušić, Mirjana, MZOS ) ( CroRIS)

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

Profili:

Avatar Url Mirjana Skočibušić (autor)

Avatar Url Ana Maravić (autor)

Avatar Url Renata Odžak (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com ac.els-cdn.com

Citiraj ovu publikaciju:

Odžak, Renata; Skočibušić, Mirjana; Maravić, Ana
Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria // Bioorganic & medicinal chemistry, 21 (2013), 23; 7499-7506 doi:10.1016/j.bmc.2013.09.041 (međunarodna recenzija, članak, znanstveni)
Odžak, R., Skočibušić, M. & Maravić, A. (2013) Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria. Bioorganic & medicinal chemistry, 21 (23), 7499-7506 doi:10.1016/j.bmc.2013.09.041.
@article{article, author = {Od\v{z}ak, Renata and Sko\v{c}ibu\v{s}i\'{c}, Mirjana and Maravi\'{c}, Ana}, year = {2013}, pages = {7499-7506}, DOI = {10.1016/j.bmc.2013.09.041}, keywords = {imidazolium oximes, monoquaternary salts, synthesis, Aantimicrobial activity, β-lactamase, multidrug resistance, ESBL}, journal = {Bioorganic and medicinal chemistry}, doi = {10.1016/j.bmc.2013.09.041}, volume = {21}, number = {23}, issn = {0968-0896}, title = {Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria}, keyword = {imidazolium oximes, monoquaternary salts, synthesis, Aantimicrobial activity, β-lactamase, multidrug resistance, ESBL} }
@article{article, author = {Od\v{z}ak, Renata and Sko\v{c}ibu\v{s}i\'{c}, Mirjana and Maravi\'{c}, Ana}, year = {2013}, pages = {7499-7506}, DOI = {10.1016/j.bmc.2013.09.041}, keywords = {imidazolium oximes, monoquaternary salts, synthesis, Aantimicrobial activity, β-lactamase, multidrug resistance, ESBL}, journal = {Bioorganic and medicinal chemistry}, doi = {10.1016/j.bmc.2013.09.041}, volume = {21}, number = {23}, issn = {0968-0896}, title = {Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria}, keyword = {imidazolium oximes, monoquaternary salts, synthesis, Aantimicrobial activity, β-lactamase, multidrug resistance, ESBL} }

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


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