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Pregled bibliografske jedinice broj: 1237560

Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling


Rep, Valentina; Štulić, Rebeka; Koštrun, Sanja; Kuridža, Bojan; Crnolatac, Ivo; Radić Stojković, Marijana; Čipčić Paljetak, Hana; Perić, Mihaela; Matijašić, Mario; Raić-Malić, Silvana
Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling // RSC Medicinal Chemistry, 13 (2022), 12; 1504-1525 doi:10.1039/d2md00143h (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1237560 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling

Autori
Rep, Valentina ; Štulić, Rebeka ; Koštrun, Sanja ; Kuridža, Bojan ; Crnolatac, Ivo ; Radić Stojković, Marijana ; Čipčić Paljetak, Hana ; Perić, Mihaela ; Matijašić, Mario ; Raić-Malić, Silvana

Izvornik
RSC Medicinal Chemistry (2632-8682) 13 (2022), 12; 1504-1525

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

Ključne riječi
benzimidazole ; benzothiazole ; antibacterial activity ; ADME ; DNA interaction

Sažetak
A series of tetrahydropyrimidinyl-substituted benzimidazoles attached to various aliphatic or aromatic residues via phenoxymethylene were synthesised to investigate their antibacterial activities against selected gram-positive and gram-negative bacteria. The influence of the type of substituent at the C-3 and C-4 positions of phenoxymethylene linker on antibacterial activity was observed, showing that aromatic moiety improved the antibacterial potency. Of all the evaluated compounds, benzoyl-substituted benzimidazole derivative 15a was the most active compound, particularly against the gram-negative pathogen E. coli (MIC = 1 µg/mL) and M. catrrhalis (MIC = 2 µg/mL). Compound 15a also exhibited the most promising antibacterial activity against sensitive and resistant strains of S. pyogenes (MIC = 2 µg/mL). Significant stabilization effects and positive induced CD bands strongly support binding of biologically most active benzimidazoles inside minor grooves of AT-rich DNA, in line with docking studies. Predicted physico-chemical and ADME properties lie within drug-like space except for low membrane permeability, which needs further optimization. Our findings encourage further development of novel structurally related 5(6)- tetrahydropyrimidinyl substituted benzimidazoles in order to optimize their antibacterial effect against common respiratory pathogens.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
HRZZ-IP-2018-01-4682 - Novi spojevi temeljeni na bioizosterima purina za ispitivanje njihovih antitumorskih i antipatogenih djelovanja (PurBioCaPa) (Raić-Malić, Silvana, HRZZ - 2018-01) ( CroRIS)
--IP-2018-01-4694 - Molekularno prepoznavanje DNA:RNA hibridnih i višelančanih struktura u bioanalitičkim i in vitro sustavima (DNARNAHyB-MolBio) (Radić Stojković, Marijana) ( CroRIS)

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
Fidelta d.o.o.

Poveznice na cjeloviti tekst rada:

doi dx.doi.org pubs.rsc.org

Citiraj ovu publikaciju:

Rep, Valentina; Štulić, Rebeka; Koštrun, Sanja; Kuridža, Bojan; Crnolatac, Ivo; Radić Stojković, Marijana; Čipčić Paljetak, Hana; Perić, Mihaela; Matijašić, Mario; Raić-Malić, Silvana
Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling // RSC Medicinal Chemistry, 13 (2022), 12; 1504-1525 doi:10.1039/d2md00143h (međunarodna recenzija, članak, znanstveni)
Rep, V., Štulić, R., Koštrun, S., Kuridža, B., Crnolatac, I., Radić Stojković, M., Čipčić Paljetak, H., Perić, M., Matijašić, M. & Raić-Malić, S. (2022) Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling. RSC Medicinal Chemistry, 13 (12), 1504-1525 doi:10.1039/d2md00143h.
@article{article, author = {Rep, Valentina and \v{S}tuli\'{c}, Rebeka and Ko\v{s}trun, Sanja and Kurid\v{z}a, Bojan and Crnolatac, Ivo and Radi\'{c} Stojkovi\'{c}, Marijana and \v{C}ip\v{c}i\'{c} Paljetak, Hana and Peri\'{c}, Mihaela and Matija\v{s}i\'{c}, Mario and Rai\'{c}-Mali\'{c}, Silvana}, year = {2022}, pages = {1504-1525}, DOI = {10.1039/d2md00143h}, keywords = {benzimidazole, benzothiazole, antibacterial activity, ADME, DNA interaction}, journal = {RSC Medicinal Chemistry}, doi = {10.1039/d2md00143h}, volume = {13}, number = {12}, issn = {2632-8682}, title = {Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling}, keyword = {benzimidazole, benzothiazole, antibacterial activity, ADME, DNA interaction} }
@article{article, author = {Rep, Valentina and \v{S}tuli\'{c}, Rebeka and Ko\v{s}trun, Sanja and Kurid\v{z}a, Bojan and Crnolatac, Ivo and Radi\'{c} Stojkovi\'{c}, Marijana and \v{C}ip\v{c}i\'{c} Paljetak, Hana and Peri\'{c}, Mihaela and Matija\v{s}i\'{c}, Mario and Rai\'{c}-Mali\'{c}, Silvana}, year = {2022}, pages = {1504-1525}, DOI = {10.1039/d2md00143h}, keywords = {benzimidazole, benzothiazole, antibacterial activity, ADME, DNA interaction}, journal = {RSC Medicinal Chemistry}, doi = {10.1039/d2md00143h}, volume = {13}, number = {12}, issn = {2632-8682}, title = {Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling}, keyword = {benzimidazole, benzothiazole, antibacterial activity, ADME, DNA interaction} }

Časopis indeksira:


  • 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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  • CA Search (Chemical Abstracts)


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