Pregled bibliografske jedinice broj: 1237560
Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling
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.
Profili:
Hana Čipčić Paljetak (autor)
Sanja Koštrun (autor)
Mihaela Perić (autor)
Mario Matijašić (autor)
Ivo Crnolatac (autor)
Valentina Rep Kaulić (autor)
Marijana Radić Stojković (autor)
Rebeka Štulić (autor)
Silvana Raić-Malić (autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- BIOSIS Previews (Biological Abstracts)
- CA Search (Chemical Abstracts)