Pregled bibliografske jedinice broj: 1127653
Structural, antioxidant, antiproliferative, and in-silico study of pyridine-based hydrazonyl- selenazoles and their sulphur isosteres
Structural, antioxidant, antiproliferative, and in-silico study of pyridine-based hydrazonyl- selenazoles and their sulphur isosteres // Journal of molecular structure, 1240 (2021), 130512, 13 doi:10.1016/j.molstruc.2021.130512 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1127653 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Structural, antioxidant, antiproliferative, and
in-silico study of pyridine-based hydrazonyl-
selenazoles and their sulphur isosteres
Autori
Araškov, Jovana ; Nikolić, Milan ; Armaković, Stevan ; Rodić, Marko ; Višnjevac, Aleksandar ; Padron, Jose ; Todorović, Tamara ; Filipović, Nenad
Izvornik
Journal of molecular structure (0022-2860) 1240
(2021);
130512, 13
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Hydrazonyl–thiazoles ; Single crystal X-ray analysis ; Antiproliferative activity ; Antioxidant activity ; Drug likeness parameters ; DFT
Sažetak
To evaluate the impact of chalcogen atom type, we performed a comparative study of antioxidant capacity and antiproliferative activity of a focused library of three pyridine-based hydrazonyl-1, 3-selenazoles and their sulfur isosteres in five antioxidant assays and in six human solid tumor cell lines, respectively. Insilico calculations were further used to check pharmacokinetic profiles of investigated compounds such as drug-likeness parameters and interaction with water. Generally, selenium compounds appear to be more potent in comparison to sulfur isosteres in the performed essays.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
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