Pregled bibliografske jedinice broj: 1274744
Development of bioactive molecules for treatment of Alzheimer’s diseases
Development of bioactive molecules for treatment of Alzheimer’s diseases // Arhiv za higijenu rada i toksikologiju
Zagreb, 2023. str. A17-A17 (pozvano predavanje, podatak o recenziji nije dostupan, sažetak, znanstveni)
CROSBI ID: 1274744 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Development of bioactive molecules for treatment of
Alzheimer’s diseases
Autori
Bosak, Anita ; Matošević, Ana ; Primožič, Ines ; Opsenica, Dejan ; Komatović, Katarina ; Zandona, Antonio ; Bartolić, Marija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Arhiv za higijenu rada i toksikologiju
/ - Zagreb, 2023, A17-A17
Skup
Cell-Based Research in Toxicology and Drug Design
Mjesto i datum
Zagreb, Hrvatska, 26.01.2023
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Podatak o recenziji nije dostupan
Ključne riječi
cholinesterase ; inhibition ; Alzheimer’s disease ; multitarget-directed ligand
Sažetak
The primary goal of the project is to develop molecules with the potential to alleviate the symptoms and slow down the progression of neurodegenerative diseases that primarily affect the neurons in the human brain that causes problems with movement and/or mental functioning. As the best results in restoration of cognitive functions of patients and alleviating the symptoms of the disease are done using drugs that targets cholinesterases (ChE), the project aims to rationally design dual site binding ChE inhibitors (acting on improving the acetylcholine level in the brain and on Aβ aggregation) and use them as starting points for multitarget-directed ligand (MTDL) design. We focused our study on butyrylcholinesterase (BChE) selective inhibitors due to the role of the BChE in the regulation of brain ACh levels in late AD and the fact that selective inhibition of BChE reduces the occurrence of side effects seen with the acetylcholinesterase (AChE) or nonselective ChE inhibitors currently in use. In design of potential bioactive molecules, we chosen two structural scaffolds, each with different mode of action with ChE’s. A carbamate functionality was chosen due to the similarity of mechanism of their interaction with choliesterases with the mechanism of AChE hydrolysis of its physiological substrate ACh. Aminoquinoline, as a structural motive, gained our attention due to their similarity to tacrine, the first centrally acting cholinesterase inhibitor approved for the treatment of Alzheimer’s disease.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Farmacija
POVEZANOST RADA
Projekti:
HRZZ-IP-2020-02-9343 - Razvoj bioaktivnih molekula za tretman neurodegenerativnih bolesti (BioMol4ND) (Bosak, Anita, HRZZ - 2020-02) ( 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,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Marija Bartolić
(autor)
Antonio Zandona
(autor)
Ines Primožič
(autor)
Ana Matošević
(autor)
Anita Bosak
(autor)