Pregled bibliografske jedinice broj: 1119692
Amidino substituted 2-aminophenols: biologically important building blocks for the amidino- functionalization of 2-substituted benzoxazoles
Amidino substituted 2-aminophenols: biologically important building blocks for the amidino- functionalization of 2-substituted benzoxazoles // Organic & biomolecular chemistry, 19 (2021), 2784-2793 doi:10.1039/d1ob00235j (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1119692 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Amidino substituted 2-aminophenols:
biologically
important building blocks for the amidino-
functionalization of 2-substituted benzoxazoles
Autori
Ptiček, Lucija ; Hok, Lucija ; Grbčić, Petra ; Topić, Filip ; Cetina, Mario ; Rissanen, Kari ; Kraljević Pavelić, Sandra ; Vianello, Robert ; Racané, Livio
Izvornik
Organic & biomolecular chemistry (1477-0520) 19
(2021);
2784-2793
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
benzoxazoles ; amidino-functionalization ; Pinner reaction ; organic synthesis ; X-ray analysis ; antiproliferative activity ; DFT calculations
Sažetak
Unlike the closely related and widely investigated amidino-substituted benzimidazoles and benzothiazoles with a range of demonstrated biological activities, the matching benzoxazole analogues still remain a largely understudied and not systematically evaluated class of compounds. To address this challenge, we utilized the Pinner reaction to convert isomeric cyano-substituted 2- aminophenols into their amidine derivatives, which were isolated as hydrochlorides and/or zwitterions, and whose structure was confirmed by single crystal X-ray diffraction. The key step during the Pinner synthesis of the crucial carboximidate intermediates was characterized through mechanistic DFT calculations, with the obtained kinetic and thermodynamic parameters indicating full agreement with the experimental observations. The obtained amidines were subjected to a condensation reaction with aryl carboxylic acids that allowed the synthesis of a new library of 5- and 6-amidino substituted 2- arylbenzoxazoles. Their antiproliferative features against four human tumour cell lines (SW620, HepG2, CFPAC-1, HeLa) revealed sub- micromolar activities on SW620 for several cyclic amidino 2- naphthyl benzoxazoles, thus demonstrating the usefulness of the proposed synthetic strategy and promoting amidino substituted 2-aminophenols as important building blocks towards biologically active systems.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
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:
Institut "Ruđer Bošković", Zagreb,
Tekstilno-tehnološki fakultet, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju,
Fakultet zdravstvenih studija u Rijeci
Profili:
Lucija Ptiček
(autor)
Robert Vianello
(autor)
Mario Cetina
(autor)
Lucija Hok
(autor)
Livio Racane
(autor)
Petra Grbčić
(autor)
Sandra Kraljević Pavelić
(autor)
Citiraj ovu publikaciju:
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