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Pregled bibliografske jedinice broj: 1267970

Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation


(KU Leuven, Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute) Beč, Anja; Cindrić, Maja; Persoons, Leentje; Banjanac, Mihailo; Radovanović, Vedrana; Daelemans, Dirk; Hranjec, Marijana
Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation // Molecules, 28 (2023), 3720-3737 doi:10.3390/molecules28093720 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1267970 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation

Autori
Beč, Anja ; Cindrić, Maja ; Persoons, Leentje ; Banjanac, Mihailo ; Radovanović, Vedrana ; Daelemans, Dirk ; Hranjec, Marijana

Kolaboracija
KU Leuven, Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute

Izvornik
Molecules (1420-3049) 28 (2023); 3720-3737

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

Ključne riječi
Schiff bases ; antibacterial activity ; antiproliferative activity in vitro ; benzimidazoles

Sažetak
Herein, we present the design and synthesis of novel N-substituted benzimidazole-derived Schiff bases, and the evaluation of their antiviral, antibacterial, and antiproliferative activity. The impact on the biological activity of substituents placed at the N atom of the benzimidazole nuclei and the type of substituents attached at the phenyl ring were examined. All of the synthesized Schiff bases were evaluated in vitro for their antiviral activity against different viruses, antibacterial activity against a panel of bacterial strains, and antiproliferative activity on several human cancer cell lines, thus enabling the study of the structure−activity relationships. Some mild antiviral effects were noted, although at higher concentrations in comparison with the included reference drugs. Additionally, some derivatives showed a moderate antibacterial activity, with precursor 23 being broadly active against most of the tested bacterial strains. Lastly, Schiff base 40, a 4- N, N-diethylamino-2-hydroxy-substituted derivative bearing a phenyl ring at the N atom on the benzimidazole nuclei, displayed a strong antiproliferative activity against several cancer cell lines (IC50 1.1–4.4 μM). The strongest antitumoral effect was observed towards acute myeloid leukemia (HL-60).

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija



POVEZANOST RADA


Projekti:
HRZZ-IP-2018-01-4379 - Istraživanje antioksidativnog djelovanja benzazolskog skeleta u dizajnu novih antitumorskih agensa (AntioxPot) (Hranjec, Marijana, HRZZ - 2018-01) ( CroRIS)

Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
Fidelta d.o.o.

Profili:

Avatar Url Mihailo Banjanac (autor)

Avatar Url Anja Beč (autor)

Avatar Url Marijana Hranjec (autor)

Avatar Url Maja Cindrić (autor)

Poveznice na cjeloviti tekst rada:

Pristup cjelovitom tekstu rada doi www.mdpi.com

Citiraj ovu publikaciju:

(KU Leuven, Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute) Beč, Anja; Cindrić, Maja; Persoons, Leentje; Banjanac, Mihailo; Radovanović, Vedrana; Daelemans, Dirk; Hranjec, Marijana
Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation // Molecules, 28 (2023), 3720-3737 doi:10.3390/molecules28093720 (međunarodna recenzija, članak, znanstveni)
(KU Leuven, Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute) (KU Leuven, Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute) Beč, Anja, Cindrić, M., Persoons, L., Banjanac, M., Radovanović, V., Daelemans, D. & Hranjec, M. (2023) Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation. Molecules, 28, 3720-3737 doi:10.3390/molecules28093720.
@article{article, author = {Be\v{c}, Anja and Cindri\'{c}, Maja and Persoons, Leentje and Banjanac, Mihailo and Radovanovi\'{c}, Vedrana and Daelemans, Dirk and Hranjec, Marijana}, year = {2023}, pages = {3720-3737}, DOI = {10.3390/molecules28093720}, keywords = {Schiff bases, antibacterial activity, antiproliferative activity in vitro, benzimidazoles}, journal = {Molecules}, doi = {10.3390/molecules28093720}, volume = {28}, issn = {1420-3049}, title = {Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation}, keyword = {Schiff bases, antibacterial activity, antiproliferative activity in vitro, benzimidazoles} }
@article{article, author = {Be\v{c}, Anja and Cindri\'{c}, Maja and Persoons, Leentje and Banjanac, Mihailo and Radovanovi\'{c}, Vedrana and Daelemans, Dirk and Hranjec, Marijana}, year = {2023}, pages = {3720-3737}, DOI = {10.3390/molecules28093720}, keywords = {Schiff bases, antibacterial activity, antiproliferative activity in vitro, benzimidazoles}, journal = {Molecules}, doi = {10.3390/molecules28093720}, volume = {28}, issn = {1420-3049}, title = {Novel biologically active N-substituted benzimidazole derived Schiff bases: design, synthesis and biological evaluation}, keyword = {Schiff bases, antibacterial activity, antiproliferative activity in vitro, benzimidazoles} }

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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