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Pursuing the Complexity of Alzheimer's Disease: Discovery of Fluoren-9-Amines as Selective Butyrylcholinesterase Inhibitors and N-Methyl-d-Aspartate Receptor Antagonists

J. Konecny, A. Misiachna, M. Hrabinova, L. Pulkrabkova, M. Benkova, L. Prchal, T. Kucera, T. Kobrlova, V. Finger, M. Kolcheva, S. Kortus, D. Jun, M. Valko, M. Horak, O. Soukup, J. Korabecny

. 2020 ; 11 (1) : . [pub] 20201222

Jazyk angličtina Země Švýcarsko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc21019624

Grantová podpora
NU20-08-00296 Agentura Pro Zdravotnický Výzkum České Republiky - International
FVZ201803 Faculty of Military Health Sciences, University of Defence - International
Long-term development plan Faculty of Military Health Sciences, University of Defence - International
00179906 MH CZ - DRO - International
CZ.02.1.01/0.0/0.0/16_025/0007444 European Regional Development Fund: Project "PharmaBrain" - International
INFRA LM2018140 "e-Infrastruktura CZ" - International
SVV 260 547 Charles University - International

Alzheimer's disease (AD) is a complex disorder with unknown etiology. Currently, only symptomatic therapy of AD is available, comprising cholinesterase inhibitors and N-methyl-d-aspartate (NMDA) receptor antagonists. Drugs targeting only one pathological condition have generated only limited efficacy. Thus, combining two or more therapeutic interventions into one molecule is believed to provide higher benefit for the treatment of AD. In the presented study, we designed, synthesized, and biologically evaluated 15 novel fluoren-9-amine derivatives. The in silico prediction suggested both the oral availability and permeation through the blood-brain barrier (BBB). An initial assessment of the biological profile included determination of the cholinesterase inhibition and NMDA receptor antagonism at the GluN1/GluN2A and GluN1/GluN2B subunits, along with a low cytotoxicity profile in the CHO-K1 cell line. Interestingly, compounds revealed a selective butyrylcholinesterase (BChE) inhibition pattern with antagonistic activity on the NMDARs. Their interaction with butyrylcholinesterase was elucidated by studying enzyme kinetics for compound 3c in tandem with the in silico docking simulation. The docking study showed the interaction of the tricyclic core of new derivatives with Trp82 within the anionic site of the enzyme in a similar way as the template drug tacrine. From the kinetic analysis, it is apparent that 3c is a competitive inhibitor of BChE.

Citace poskytuje Crossref.org

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