Pregled bibliografske jedinice broj: 1180946
Synthesis, photochemistry and computational study of novel 1,2,3-triazole heterostilbenes: expressed biological activity of their electrocyclization photoproducts
Synthesis, photochemistry and computational study of novel 1,2,3-triazole heterostilbenes: expressed biological activity of their electrocyclization photoproducts // Bioorganic chemistry, 121 (2022), 105701, 21 doi:10.1016/j.bioorg.2022.105701 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1180946 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis, photochemistry and computational study
of novel 1,2,3-triazole heterostilbenes: expressed
biological activity of their electrocyclization
photoproducts
Autori
Mlakić, Milena ; Faraho, Ivan ; Odak, Ilijana ; Talić, Stanislava ; Vukovinski, Ana ; Raspudić, Anamarija ; Bosnar, Martina ; Zadravec, Rahela ; Ratković, Ana ; Lasić, Kornelija ; Marinić, Željko ; Barić, Danijela ; Škorić, Irena
Izvornik
Bioorganic chemistry (0045-2068) 121
(2022);
105701, 21
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
anti-inflammatory activity ; cholinesterase inhibition ; density functional theory ; docking
Sažetak
New 1, 2, 3-triazolostilbenes were synthesized and photochemically transformed to substituted naphthotriazoles as electrocyclization products in high isolated yields for studying the acetyl- and butyrylcholinesterase inhibitory and anti- inflammatory activity. The best experimental results showed the naphthotriazole photoproducts providing interesting observation on cholinesterase inhibition associated with the inhibition of TNFα cytokine production. The geometries of synthesized triazolostilbenes were computationally examined using Density Functional Theory (DFT), followed by time-dependent DFT calculations to obtain insight into electronic properties observed by UV-Vis spectroscopy. The complexes between selected compounds with the active site of AChE are assessed by docking. A quantum mechanical cluster approach was utilized to optimize their structures, thus providing insight into the stabilizing interactions between the potential inhibitor and the active site.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
PLIVA HRVATSKA d.o.o.,
Fidelta d.o.o.
Profili:
Ana Grgičević
(autor)
Ivan Faraho
(autor)
Danijela Barić
(autor)
Irena Škorić
(autor)
Željko Marinić
(autor)
Martina Bosnar
(autor)
Milena Mlakić
(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
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)