Naslov
Benzobicyclo[3.2.1]octene derivatives as a new class of cholinesterase inhibitors

Autori
Čadež, Tena ; Grgičević, Ana ; Ahmetović, Ramiza ; Barić, Danijela ; Maček Hrvat, Nikolina ; Kovarik, Zrinka ; Škorić, Irena

Izvornik
Molecules (1420-3049) 25 (2020), 21; 4872, 24

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
acylation ; benzobicyclo[3.2.1]octane/octene ; benzylamines ; cholinesterase ; epoxidation ; oximes

Sažetak
A library of amine, oxime, ether, epoxy and acyl derivatives of the benzobicyclo[3.2.1]octene were synthesized and evaluated as inhibitors of both human acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). The majority of the tested compounds exhibited higher selectivity for BChE. Structural adjustment for AChE seems to have been achieved by acylation, and the furan ring opening of furo- benzobicyclo[3.2.1]octadiene results for compound 51 with the highest AChE affinity (IC50=8.3 µM). Interestingly, its analogue, an oxime ether with a benzobicyclo[3.2.1]- skeleton, compound 32 was one of the most potent BChE inhibitors in this study (IC50=31 µM), but not as potent as endo-43, an ether derivative of the benzobicyclo[3.2.1]octene with an additional phenyl substituent (IC50=17 µM). Therefore, we identified several cholinesterase inhibitors with a potential for further development as potential drugs for treatment of neurodegenerative diseases.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Interdisciplinarne prirodne znanosti

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