Pregled bibliografske jedinice broj: 1088290
Vitamin B3-Based Biologically Active Compounds as Inhibitors of Human Cholinesterases
Vitamin B3-Based Biologically Active Compounds as Inhibitors of Human Cholinesterases // International journal of molecular sciences, 21 (2020), 21; 8088, 19 doi:10.3390/ijms21218088 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1088290 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Vitamin B3-Based Biologically Active Compounds as
Inhibitors of Human Cholinesterases
Autori
Zandona, Antonio ; Lihtar, Gabriela ; Maraković, Nikola ; Miš, Katarina ; Bušić, Valentina ; Gašo- Sokač, Dajana ; Pirkmajer, Segej ; Katalinić, Maja
Izvornik
International journal of molecular sciences (1422-0067) 21
(2020), 21;
8088, 19
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
AChE ; BChE ; neurodegenerative ; Alzheimer’s ; nicotinamide ; cytotoxicity
Sažetak
We evaluated the potential of nine vitamin B3 scaffold-based derivatives as acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors, as a starting point for the development of novel drugs for treating disorders with cholinergic neurotransmission- linked pathology. As the results indicate, all compounds reversibly inhibited both enzymes in the micromolar range pointing to the preference of AChE over BChE for binding the tested derivatives. Molecular docking studies revealed the importance of interactions with AChE active site residues Tyr337 and Tyr124, which dictated most of the observed differences. The most potent inhibitor of both enzymes with Ki of 4 µM for AChE and 8 µM for BChE was the nicotinamide derivative 1-(4 0 - phenylphenacyl)-3-carbamoylpyridinium bromide. Such a result places it within the range of several currently studied novel cholinesterase inhibitors. Cytotoxicity profiling did not classify this compound as highly toxic, but the induced effects on cells should not be neglected in any future detailed studies and when considering this scaffold for drug development.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Projekti:
UIP-2017-05-7260 - MOLEKULARNI MEHANIZMI TOKSIČNOSTI PROTUOTROVA I POTENCIJALNIH LIJEKOVA (CellToxTargets) (Katalinić, Maja, HRZZ - 2017-05) ( CroRIS)
IP-2018-01-7683 - Analiza interakcija butirilkolinesteraze s novim inhibitorima i reaktivatorima (AnalyseBChE) (Kovarik, Zrinka, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb,
Prehrambeno-tehnološki fakultet, Osijek
Profili:
Nikola Maraković (autor)
Valentina Bušić (autor)
Maja Katalinić (autor)
Dajana Gašo-Sokač (autor)
Antonio Zandona (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