Front. Chem. Frontiers in Chemistry Front. Chem. 2296-2646 Frontiers Media S.A. 882191 10.3389/fchem.2022.882191 Chemistry Original Research Novel 3-aminobenzofuran derivatives as multifunctional agents for the treatment of Alzheimer’s disease Hasanvand et al. 10.3389/fchem.2022.882191 Hasanvand Zaman 1 Motahari Rasoul 1 Nadri Hamid 2 Moghimi Setareh 3 Foroumadi Roham 4 Ayati Adileh 3 Akbarzadeh Tahmineh 1 Bukhari Syed Nasir Abbas 5 Foroumadi Alireza 1 3 * 1 Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran 2 Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran 3 Drug Design and Development Research Center, The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, Iran 4 Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran 5 Department of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Saudi Arabia

Edited by: Simone Brogi, University of Pisa, Italy

Reviewed by: Lhassane Ismaili, Université Bourgogne Franche-Comté, France

Konstantin Petrov, A. E. Arbuzov Institute of Organic and Physical Chemistry (RAS), Russia

Adriano Mollica, University “G. d’Annunzio” of Chieti-Pescara, Italy

 *Correspondence: Alireza Foroumadi, aforoumadi@yahoo.com

This article was submitted to Medicinal and Pharmaceutical Chemistry, a section of the journal Frontiers in Chemistry

 09 08 2022 2022 10 882191 23 02 2022 05 07 2022 Copyright © 2022 Hasanvand, Motahari, Nadri, Moghimi, Foroumadi, Ayati, Akbarzadeh, Bukhari and Foroumadi. 2022 Hasanvand, Motahari, Nadri, Moghimi, Foroumadi, Ayati, Akbarzadeh, Bukhari and Foroumadi

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

A novel multifunctional series of 3-aminobenzofuran derivatives 5a-p were designed and synthesized as potent inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). The target compounds 5a-p were prepared via a three-step reaction, starting from 2-hydroxy benzonitrile. In vitro anti-cholinesterase activity exhibited that most of the compounds had potent acetyl- and butyrylcholinesterase inhibitory activity. In particular, compound 5f containing 2-fluorobenzyl moiety showed the best inhibitory activity. Furthermore, this compound showed activity on self- and AChE-induced Aβ-aggregation and MTT assay against PC12 cells. The kinetic study revealed that compound 5f showed mixed-type inhibition on AChE. Based on these results, compound 5f can be considered as a novel multifunctional structural unit against Alzheimer’s disease.

 Alzheheimer’s disease acetylcholinesterase neuroprotection docking studies ab-aggregation 3-amino benzofuran Tehran University of Medical Sciences and Health Services10.13039/501100004484 1 Introduction

Alzheimer’s disease (AD) is the most prominent neurodegenerative illness of the Central Nervous System (CNS) progressed by abnormal cholinergic neurons loss, and deposition of extracellular amyloid-β and tau-proteins into plaques and neurofibrillary tangles (Scarpini et al., 2003; McKhann et al., 2011; Li et al., 2017). This debilitating disease is mainly characterized by a deterioration of memory, and changes in learning and personality (Lai et al., 2012). Despite the implications of many factors, still there are unclear points in the pathogenesis and etiology of AD (Gauthier et al., 2006; Poprac et al., 2017; Talesa, 2021).

Acetylcholine (ACh), is a cholinergic neurotransmitter and its deficiency is responsible for the cognitive decline in AD patients which has been considered a target to designing novel agent with an AChE-inhibition profile to increase the cerebral acetylcholine level (Lane et al., 2004; Marco-Contelles et al., 2006). Cholinesterase has two types involving acetylcholinesterase (AChE, EC 3.1.1.7) and butyrylcholinesterase (BuChE, EC 3.1.1.8) catalyzing the hydrolysis of ACh to choline and acetate (Mesulam and Asunction, 1987; Weinstock, 1999). Due to the evidence about the activity of BuChE in the pathogenesis of AD, the use of nonselective inhibitors targeting both BuChE and AChE would be more beneficial in AD patients compared to selective ones. Quite a few selective and reversible anti-AChE drugs (donepezil, rivastigmine, and galantamine) have been approved for the treatment of AD. However, these drugs suffer from severe side effects including vomiting, nausea, diarrhea, bradycardia, abnormal dreams, and fatigue (Smith et al., 1997; Forette et al., 1999; Schneider 2000; Cummings et al., 2014). Considering the complex pathophysiology of this disease, there is a high demand for the discovery and development of efficient new therapeutic agents with minimal side effects to effectively combat AD.

The development of multifunctional molecules which are capable of influencing a number of targets has represented considerable attention for the treatment of AD (Cavalli et al., 2008; Camps et al., 2008; León et al., 2013; Rosini et al., 2014). Previous studies revealed that the crystal structure of AChE consists of two binding sites, the peripheral anionic site (PAS) at the entrance and the catalytic active site (CAS) at the bottom of the gorge (Muñoz-Ruiz et al., 2005). It is proposed that the peripheral anionic site of AChE could play an important role in the aggregation of insoluble forms of Aβ plaques in the brain. So, inhibition of the self-assembled Aβ peptide formation would be a promising therapeutic strategy for AD treatment (Inestrosa et al., 1996; Castro and Martinez 2001). In addition, considerable evidence implicated the important role of oxidative stress in the development and progression of AD pathogenesis. Therefore, the neuroprotection approach against oxidative stress has beneficial effects on AD (Longo and Massa 2004; Greenough et al., 2013). In order to explain the pathogenesis of AD, the cholinergic hypothesis was first proposed and is relatively accepted, indicating that the decreased levels of ACh are related to the pathogenesis of AD. As the main cholinesterase (ChE), 80% of hydrolytic activity in the brain is performed by acetylcholinesterase (AChE), so inhibiting AChE which will result in increased levels of ACh in the brain has been considered as a good strategy to treat AD. While inhibition of BuChE might be considered a promising strategy for the treatment of AD, the development of AChE inhibitors is still the most important strategy to treat AD.

Benzofuran derivatives have attracted considerable attention in numerous natural products and therapeutic agents due to their interesting biological and pharmacological properties, including anti-Alzheimer’s, anti-inflammatory, analgesic, anti-hyperlipidemic, antiviral, antimicrobial, anti-inflammatory, and antitumor (Alper-Hayta et al., 2008; Choi et al., 2011; Al-Qirim et al., 2012; Rizzo et al., 2013; Nevagi et al., 2015). Synthesis and evaluation of different benzofuran derivatives have been considered by our research group for many years (Pouramiri et al., 2016; Mehrabi et al., 2017). In terms of the AD research, we intend to design and develop multifunctional small molecules, based on this valuable pharmacophore which can be regarded as a mimic of the indanone part of donepezil (Choi et al., 2004). The Aβ antiaggregants and site interactions with Aβ were recognized in the literature. Substitution of the C-2 position of benzofuran was done to increase the inhibitory activity towards AChE (Goyal et al., 2018). Moreover, many reports in the literature with substitution at the C-3 position of benzofuran were done to evaluate their activity as anti-Alzheimer’s agents exhibiting increased inhibitory activity towards Aβ (Howlett et al., 1999; Byun et al., 2008). Donepezil is an FDA-approved drug showing dual-binding site interactions. Docking studies indicated the interactions of N-benzyl piperidine residue with the catalytic active site (CAS) and interactions of hydrophobic aromatic part of the molecule with the peripheral anionic site (PAS) of AChE (Koellner et al., 2000; Saxena et al., 2003; Kapková et al., 2006). Up to now, quite a few numbers of aromatic rings have been reported as PAS binding scaffolds. In the light of the aforementioned and following our previous attempts (Nadri et al., 2010; Baharloo et al., 2015), in this study, we describe the design, synthesis, and biological evaluation of a novel series of 3-aminobenzofuran-based derivatives as multifunctional ligands targeting acetylcholinesterase, butyrycholinesterase, and β-Amyloid aggregation (Figure 1).

Structures of donepezil hydrochloride-based cholinesterase inhibitors, benzofuran-based compounds reported as anticholinesterase inhibitors, and newly designed benzofuran-based derivatives (Baharloo et al., 2015).

 2 Results and discussion 2.1 Chemistry

The 3-aminobenzofuran derivatives 5a-p were prepared according to Scheme 1. The pathway was started from the reaction of commercially available 2-hydroxybenzonitrile 1 with 4-(bromomethyl) pyridine 2 in the presence of K2CO3, afforded 2-(pyridin-4-ylmethoxy)benzonitrile 3. The cyclization reaction of compound 3 in the presence of t-BuOK in DMF at 80°C afforded 4-(3-aminobenzofuran-2-yl) pyridine 4 (Chen et al., 2013; Loidreau et al., 2013). Accordingly, the final compounds 5a-p were prepared by the reaction of compound 4 with different benzyl chloride derivatives in dry acetonitrile under reflux conditions (1–6 h). After the completion of the reaction, the final products were collected by filtration and washed with n-hexane to afford target compounds in good yields ranging from 56% to 74%.

Synthesis of N-benzyl-4-(3-aminobenzofuran-2-yl)pyridinium chloride compounds 5a-p.

 2.2 Biological screenings 2.2.1 Cholinesterase inhibition

The in-vitro cholinesterase inhibitory activity of synthesized 3-aminobenzofuran-based compounds 5a-p was evaluated by using the Ellman’s method (Ellman et al., 1961). This method is based on the reaction of acetylthiocholine with 5,5′´-dithio-bis-(2-nitrobenzoic) acid (DTNB) to yield the colored product. The obtained IC50 values are summarized in Table 1 and compared with donepezil as the standard drug. Accordingly, almost all 3-aminobenzofuran derivatives exhibited moderate to good inhibitory activity with IC50s ranging from 0.64 to 81.06 μM. Among the tested compounds, analog 5f was the most effective inhibitor against AChE and BuChE, while compound 5e containing 3-methoxybenzyl moiety showed the least inhibitory activity on both. The nonpolar group (OCH3) has decreased the AChE inhibitory potency due to increased lipophilic characteristics.

Inhibitory activity of the target compounds 5a-p against AChE and BuChE.

Compounds R IC50 (μM) a AChE IC50 (μM) BuChE
5a H 0.81 ± 0.02 0.82 ± 0.07
5b 2-Me 3.29 ± 0.01 17.35 ± 2.45
5c 3-Me 3.32 ± 0.04 12.89 ± 3.56
5d 4-Me 29.31 ± 0.82 25.33 ± 1.91
5e 3-OCH3 81.06 ± 1.61 >100
5f 2-F 0.64 ± 0.04 0.55 ± 0.07
5g 3-F 1.68 ± 0.02 2.89 ± 0.42
5h 4-F 0.88 ± 0.04 5.05 ± 0.73
5i 2-Cl 0.70 ± 0.01 0.99 ± 0.05
5j 3-Cl 2.99 ± 0.03 18.77 ± 1.11
5k 4-Cl 16.60 ± 0.52 31.18 ± 2.56
5l 2-Br 1.34 ± 0.01 10.54 ± 0.19
5m 3-Br 4.47 ± 0.02 13.95 ± 1.20
5n 4-Br 15.84 ± 0.91 22.55 ± 3.33
5o 2-NO2 7.84 ± 0.05 28.63 ± 0.13
5p 4-NO2 20.55 ± 0.8 28.26 ± 0.48
Donepezil — 0.016 ± 0.001 3.99 ± 0.27

The concentration (mean ± SEM of three experiments) required for 50% inhibition. The bold value was the most active compound.

Based on the structure-activity relationship (SAR) study, the potency of compounds was influenced by the type and the position of the substitutions. The unsubstituted derivative 5a showed potent activity against the AChE enzyme with IC50 = 0.81 μM, however, the attachment of electron-donating groups such as methyl and methoxy significantly reduced the inhibitory activities of compounds. Those compounds containing electron-withdrawing groups (fluoro, chloro, and bromo) showed better inhibitory potencies than the compounds containing electron-donating groups 5b-5e.

The SAR analysis indicated that fluorobenzyl-containing compounds 5f-5h had promising enzymatic inhibitory activity (IC50s ranging from 0.64 to 1.68 μM) and the presence of fluoro substituent at ortho and para positions of the benzyl moiety led to better anti-AChE activity than meta substituted one 5g. In the chloro and bromo substituted derivatives, compounds containing ortho and metha substitutions (5i, 5j, 5l, and 5m) showed moderate inhibitory activities, however, the attachment of these substitutions to para position dramatically decreased inhibitory activity of compounds (5k and 5n). Among the electron-withdrawing-containing compounds, nitro-containing derivatives showed weak inhibitory potencies, and the compound with 2-nitrobenzyl group 5o showed better activity than that of 4-nitrobenzyl derivative 5p.

The obtained results showed that compounds bearing fluorobenzyl moiety were more effective than other benzyl derivatives. In addition, ortho position was more favorable than meta- or para- substituted analogs. All compounds except 5e showed BuChE inhibition. By comparing the IC50 values against AChE and BuChE, it could be concluded that nearly the same trend was observed. The potent inhibitory activity toward BuChE was observed in 5f. This compound showed good inhibition with an IC50 value of 0.55 μΜ. The movement of substituents involving fluorine, chlorine, bromine, and methyl from ortho to para resulted in decreased inhibitory activity.

 2.2.2 Kinetics studies

The inhibition model of acetylcholinesterase can be categorized into irreversible-type inhibition and reversible-type inhibition. Therefore, to achieve further insight into the mode of interaction of designed compounds on AChE, the rate of enzyme activity was measured at different concentrations of the most potent compound 5f 0.32, 0.64, 1.27 μM and in the presence of substrate (ATCh). The type of inhibition can be concluded with a graphical analysis of the Lineweaver-Burk reciprocal plots (Baharloo et al., 2015). The higher concentration of inhibitor showed increasing slopes and intercepts. This proves a mixed-type inhibitory pattern on AChE (Figure 2).

The Lineweavere-Burk plot for the inhibition of AChE by compound 5f with increasing substrate concentration.

 2.2.3 Inhibition of β-amyloid aggregation of selected compounds

The aggregation of the β-amyloid peptide is a negative event in the pathogenesis of Alzheimer’s disease, so, anti-amyloid therapy is an important factor in the treatment of Alzheimer’s. To evaluate the anti-aggregating activity of designed compounds, the five most potent derivatives, namely 5a, 5f, 5h, 5i, and 5l were selected and evaluated against self-induced and AChE-induced Aβ aggregation. For this purpose, we used the thioflavin T (ThT) assay. Donepezil was used as a reference compound. The obtained results showed that the tested 3-aminobenzofuran compounds (5a, 5f, 5h, 5i, and 5l) at 10 μM concentration exhibited good inhibitory activity of self-induced Aβ1–42 aggregation (17.6%, 29.8%, 38.8%, 24.8%, and 25.7% inhibition, respectively) compared to donepezil as the reference drug (14.9%). Compounds 5f and 5h were about 2-folds more effective than donepezil in the inhibition of Aβ aggregation (Table 2). At 100 µM concentration, compounds 5a, 5f, 5h, 5i, and 5l showed moderate to good activity to inhibit AChE-induced Aβ aggregation. Notably, compounds 5f and 5h were more potent (30.1% and 35.6, respectively) than the reference drug (25.7%). The ThT assay indicated that target compounds could inhibit the self-induced Aβ1–42 aggregation and AChE-induced Aβ aggregation.

Inhibition of self-induced and AChE-induced Aβ1–42 aggregation by selected compounds.

Compounds Inhibition of Aβ aggregation (%)
Self-induced a AChE-induced b
5a 17.6 ± 3.8 22.4 ± 1.6
5f 29.8 ± 1.8 30.1 ± 1.9
5h 38.8 ± 2.8 35.6 ± 1.5
5i 24.8 ± 1.5 26.5 ± 3.8
5l 25.7 ± 2.7 22.4 ± 2.3
Donepezil 14.9 ± 2.5 25.7 ± 1.9

Inhibition of Aβ1–42 aggregation was produced by the tested compound at 10 μM concentration. Values are expressed as means ± SEM of three experiments.

Co-aggregation inhibition of Aβ1–42 and AChE (0.01 u/ml) by the tested compounds at 100 μM concentration was detected by the ThT assay. Values are expressed as means ± SEM of three experiments.

 2.2.4 Neuronal cell treatment and viability measurements

Safety is an important factor for CNS agents. In order to evaluate the cytotoxic effect of selected compounds 5a, 5f, 5h, 5i, and 5l, the in-vitro cell viability assay was investigated on the PC12 cell line using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. The PC12 cells were incubated with varying concentrations (0.01–100 μM) of the test compounds for 24 h. The obtained results revealed that all tested compounds were nontoxic to PC12 cells (Table 3). The results are expressed as the percentage of viable cells.

Effects of compounds 5a, 5f, 5h, 5i, and 5l on cell viability in PC12 cells.

Compounds Viability (%) of PC12 cells a , b
5a 85.9 ± 1.5
5f 86.4 ± 2.6
5h 88.2 ± 2.4
5i 90.2 ± 4.1
5l 87.1 ± 2.9

Cell viability is expressed as the mean percentage of viable cells.

Mean percentage of viable cells compared with the untreated cells was determined to be 56.2 ± 1.96%.

 2.2.5 Molecular docking studies

To get a better insight into the binding patterns between AChE and our new 3-aminobenzofuran derivatives, docking simulation were performed for the most active compound 5f in the active site of AChE (PDB code: 1EVE) by using AutoDock software. The two- and three-dimensional modes of interactions were prepared and illustrated in Figure 3. Compound 5f was anchored in the mid-gorge by some attractive charge among the Trp84, Phe330, and Glu199. Moreover, the pyridine ring was stacked against Trp84. The pendant 2-fluouropheny ring was sandwiched in between Trp84 and Phe330. The amino benzofuran ring made a T-shape stacking with Tyr121. A hydrogen bond between amino function and Tyr121 could stabilize such interaction.

(A) 3D mode of interactions of compound 5f with AChE. (B) 2D docking models of compound 5f with AChE.

 3 Experimental 3.1 Chemistry

All reagents and solvents were obtained from commercial suppliers and used without purification. 1H NMR and 13C NMR spectra were acquired on a Bruker 500, 300 MHz NMR spectrometer and referenced to TMS. IR (KBr-disc) spectra were obtained by using a Bruker spectrometer. Melting points were determined by using a Kofler hot stage apparatus. All Reactions were monitored with thin layer TLC, using silica gel (60 Å) purchased from Merck. Mass analysis was carried out using an Agilent mass spectrometer. The elemental analysis for C, H, and N was carried out with an ElementarAnalysen system GmbH VarioEL.

3.1.1 General procedure for the preparation of 2-((pyridine-4-yl) methoxy) benzonitrile 3

4-(Bromomethyl) pyridine 2 (10 mmol) was added to a mixture of 2-hydroxybenzonitrile 1 (10 mmol) and K2CO3 (20 mmol) in DMF (10 ml) and stirred at 80°C for 8 h. After completion of the reaction, the reaction mixture was slowly cooled down to room temperature and poured into ice and water. The precipitated solid was filtered, washed, and recrystallized from EtOH to afford 2-((pyridine-4-yl) methoxy) benzonitrile intermediate 3.

White solid, yield: (83%). IR (KBr) (ν max /cm−1): 3388, 2220, 1591, 1484, 1444, 1384, 1285, 1156, 876, 754. 1H NMR (500 MHz, DMSO-d 6): δ = 5.22 (s, 2H, CH2), 6.95 (d, J = 8.5 Hz, 2H, Ar-H), 7.06 (t, J = 7.5 Hz, 2H, Ar-H), 7.40 (d, J = 6.0 Hz, 2H, Ar-H), 7.50–7.54 (m, 1H, Ar-H), 7.62 (dd, J = 7.5, 1.5 Hz, 1H, Ar-H).

 3.1.2 General procedure for the preparation of 2-(pyridine-4-yl) 3-aminobenzofuran derivative 4

A mixture of intermediate 3 (3 mmol) and potassium tert-butoxide (5 mmol) in DMF (5 ml) was stirred at 80°C for 5 h. After the completion of the reaction, the reaction mixture was cooled down to room temperature and was poured into ice and water. The precipitated solid was filtered, washed, and recrystallized from EtOH to afford 2-(pyridine-4-yl) 3-aminobenzofuran 4.

Yellow solid, yield: (73%). IR (KBr) (ν max /cm−1): 3360, 3311, 3191, 1596, 1409, 1355, 1274, 1212, 1166, 1143, 993, 822, 734, 682, 600, 527. 1H NMR (500 MHz, DMSO-d 6): δ = 5.83 (s, 2H, CH2), 7.24 (t, J = 10.0 Hz, 1H, Ar-H), 7.38 (t, J = 10.0 Hz, 1H, Ar-H), 7.48 (d, J = 10.0 Hz, 1H, Ar-H), 7.65 (d, J = 5.0 Hz, 2H, Ar-H), 7.91 (d, J = 10.0 Hz, 1H, Ar-H), 8.53 (d, J = 5.0 Hz, 2H, Ar-H).

 3.1.3 General procedure for the preparation of <italic>N</italic>-benzyl-4-(3-aminobenzofuran-2-yl) pyridinium bromides (<bold>5a-p</bold>)

A mixture of 2-(pyridine-4-yl)-3-aminobenzofuran 4 (1 mmol) and the appropriate benzyl chloride derivatives (1.2 mmol) in dry acetonitrile (7 ml) was heated under reflux for 1–6 h. The precipitated solid was collected by filtration and washed with n-hexane (5 ml) to give 5a-p in 56%–74% yields.

3.1.3.1 4-(3-Aminobenzofuran-2-yl)-1-benzylpyridin-1-ium chloride (<bold>5a</bold>)

White solid, yield: (72%); mp 160–162°C. IR (KBr) (ν max /cm−1): 3293, 3158, 3033, 1631, 1592, 1542, 1312, 1215, 1160, 1100, 1030, 875, 834, 753, 690. 1H NMR (500 MHz, DMSO-d 6): δ = 5.66 (s, 2H, CH2), 7.29 (t, J = 6.5 Hz, 1H, Ar-H), 7.43–7.46 (m, 5H, Ar-H), 7.51 (s, 4H, Ar-H), 7.97 (s, 2H, NH2), 8.10 (d, J = 7.5 Hz, 1H, Ar-H), 8.79 (d, J = 6.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 60.7, 111.5, 116.7, 122.9, 128.2, 128.3, 128.6, 129.0, 130.4, 135.1, 140.1, 140.3, 142.1, 142.6, 142.7, 154.6. Anal. Calcd. for C20H17ClN2O, C, 71.32; H, 5.09; N, 8.32; Found C, 71.60; H, 4.79; N, 8.10.

 3.1.3.2 4-(3-Aminobenzofuran-2-yl)-1-(2-methylbenzyl) pyridin-1-ium chloride (<bold>5b</bold>)

White solid, yield: (67%); mp 182–184°C. IR (KBr) (ν max /cm−1): 3326, 3145, 1722, 1633, 1592, 1541, 1452, 1315, 1197, 1149, 1102, 1031, 968, 837, 746, 655. 1H NMR (500 MHz, DMSO-d 6): δ = 2.31 (s, 3H, CH3), 5.70 (s, 2H, CH2), 7.11 (d, J = 6.5 Hz, 1H, Ar-H), 7.25–7.30 (m, 4H, Ar-H), 7.43 (s, 2H, Ar-H), 7.54 (d, J = 12.0 Hz, 2H, Ar-H), 8.00 (s, 2H, NH2), 8.11 (d, J = 7.0 Hz, 1H, Ar-H), 8.62 (d, J = 4.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 18.7, 61.3, 111.7, 116.6, 116.8, 121.9, 122.1, 122.7, 126.5, 128.2, 128.8, 130.7, 133.2, 136.5, 140.2, 140.4, 142.2, 142.9, 154.6. Anal. Calcd. for C21H19ClN2O, C, 71.89; H, 5.46; N, 7.98; Found C, 72.06; H, 5.22; N, 8.15.

 3.1.3.3 4-(3-Aminobenzofuran-2-yl)-1-(3-methylbenzyl) pyridin-1-ium chloride (<bold>5c</bold>)

White solid, yield: (56%); mp 190–192°C. IR (KBr) (ν max /cm−1): 3122, 1974, 1639, 1542, 1226, 1162, 1048, 844, 762, 653. 1H NMR (500 MHz, DMSO-d 6): δ = 2.41 (s, 3H, CH3), 5.59 (s, 2H, CH2), 7.40 (d, J = 7.0 Hz, 2H, Ar-H), 7.47 (d, J = 7.0 Hz, 2H, Ar-H), 7.50 (d, J = 10.5 Hz, 2H, Ar-H), 7.70 (t, J = 8.0 Hz, 1H, Ar-H), 7.74 (d, J = 8.0 Hz, 1H, Ar-H), 7.80 (d, J = 4.5 Hz, 1H, Ar-H), 8.22 (s, 2H, NH2), 8.35 (d, J = 8.0 Hz, 1H, Ar-H), 8.96 (d, J = 7.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 20.9, 60.7, 116.6, 116.8, 122.1, 122.7, 125.4, 128.1, 128.7, 128.8, 129.5, 130.4, 135.1, 138.4, 140.3, 140.4, 141.7, 142.1, 154.6. Anal. Calcd. for C21H19ClN2O, C, 71.89; H, 5.46; N, 7.98; Found C, 72.02; H, 5.83; N, 7.77.

 3.1.3.4 4-(3-Aminobenzofuran-2-yl)-1-(4-methylbenzyl) pyridin-1-ium chloride (<bold>5d</bold>)

White solid, yield: (57%); mp 220–222°C. IR (KBr) (ν max /cm−1): 3313, 3136, 3038, 1643, 1537, 1350, 1154, 1028, 829, 752, 666. 1H NMR (500 MHz, DMSO-d 6): δ = 2.29 (s, 3H, CH3), 5.58 (s, 2H, CH2), 7.23 (d, J = 7.5 Hz, 2H, Ar-H), 7.28 (t, J = 7.0 Hz, 2H, Ar-H), 7.41 (d, J = 7.5 Hz, 2H, Ar-H), 7.50 (t, J = 8.0 Hz, 1H, Ar-H), 7.54 (d, J = 8.0 Hz, 1H, Ar-H), 7.59 (s, 1H, Ar-H), 8.01 (s, 2H, NH2), 8.15 (d, J = 8.0 Hz, 1H, Ar-H), 8.76 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 20.6, 60.6, 116.6, 122.3, 122.4, 122.7, 128.1, 128.3, 129.5, 130.4, 132.2, 138.4, 140.2, 142.0, 142.4, 142.5, 154.5. Anal. Calcd. for C21H19ClN2O, C, 71.89; H, 5.46; N, 7.98; Found C, 71.57; H, 5.80; N, 7.61.

 3.1.3.5 4-(3-Aminobenzofuran-2-yl)-1-(3-methoxybenzyl) pyridin-1-ium chloride (<bold>5e</bold>)

White solid, yield: (61%); mp 210–212°C. IR (KBr) (ν max /cm−1): 3134, 1638, 1594, 1541, 1310, 1265, 1223, 1160, 1103, 1042, 840, 754, 694. 1H NMR (500 MHz, DMSO-d 6): δ = 3.74 (s, 3H, OCH3), 5.61 (s, 2H, CH2), 6.93 (d, J = 8.5 Hz, 1H, Ar-H), 7.08 (d, J = 7.0 Hz, 1H, Ar-H), 7.18 (s, 1H, Ar-H), 7.24 (t, J = 7.5 Hz, 1H, Ar-H), 7.32 (t, J = 7.5 Hz, 1H, Ar-H), 7.45 (d, J = 8.0 Hz, 1H, Ar-H), 7.49 (d, J = 8.0 Hz, 1H, Ar-H), 7.69 (s, 2H, Ar-H), 8.00 (s, 2H, NH2), 8.19 (d, J = 7.5 Hz, 1H, Ar-H), 8.82 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 55.2, 60.5, 111.5, 114.2, 116.6, 120.4, 122.3, 122.4, 122.7, 128.1, 130.3, 136.6, 140.3, 140.5, 141.9, 142.5, 142.6, 154.6, 159.5. Anal. Calcd. for C21H19ClN2O2, C, 68.76; H, 5.22; N, 7.64; Found C, 69.05; H, 5.51; N, 7.30.

 3.1.3.6 4-(3-Aminobenzofuran-2-yl)-1-(2-fluorobenzyl) pyridin-1-ium chloride (<bold>5f</bold>)

White solid, yield: (73%); mp 253–255°C. IR (KBr) (ν max /cm−1): 3175, 2982, 1635, 1541, 1314, 1225, 1159, 1107, 1040, 833, 757, 648. 1H NMR (500 MHz, DMSO-d 6): δ = 5.74 (s, 2H, CH2), 7.26–7.32 (m, 3H, Ar-H), 7.46–7.55 (m, 3H, Ar-H), 7.58 (d, J = 7.5 Hz, 1H, Ar-H), 7.69 (s, 2H, Ar-H), 8.02 (s, 2H, NH2), 8.17 (d, J = 8.0 Hz, 1H, Ar-H), 8.68 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 55.3, 115.8, 116.6, 122.1, 122.5, 125.1, 128.1, 130.5, 130.9, 131.5, 140.7, 141.8, 142.1, 142.7, 143.6, 154.7, 159.3, 161.3 (d, J = 240 Hz). Anal. Calcd. for C20H16ClFN2O, C, 67.70; H, 4.55; N, 7.90; Found C, 67.44; H, 4.24; N, 7.55.

 3.1.3.7 4-(3-Aminobenzofuran-2-yl)-1-(3-fluorobenzyl) pyridin-1-ium chloride (<bold>5g</bold>)

White solid, yield: (65%); mp 267–269°C. IR (KBr) (ν max /cm−1): 3298, 3167, 2981, 1630, 1543, 1455, 1313, 1253, 1158, 1098, 1036, 879, 835, 750, 692. 1H NMR (500 MHz, DMSO-d 6): δ = 5.66 (s, 2H, CH2), 7.24 (t, J = 8.0 Hz, 1H, Ar-H), 7.29 (t, J = 7.0 Hz, 1H, Ar-H), 7.36 (d, J = 7.0 Hz, 1H, Ar-H), 7.43–7.47 (m, 3H, Ar-H), 7.48–7.54 (m, 3H, Ar-H), 7.97 (s, 2H, NH2), 8.10 (d, J = 8.0 Hz, 1H, Ar-H), 8.80 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 60.0, 115.3, 115.5, 115.7, 116.7, 122.0, 122.6, 124.4, 128.2, 130.5, 131.2, 137.3, 140.3, 140.4, 142.2, 142.6, 142.7, 159.6 (d, J = 237 Hz). Anal. Calcd. for C20H16ClFN2O, C, 67.70; H, 4.55; N, 7.90; Found C, 67.48; H, 4.24; N, 7.66.

 3.1.3.8 4-(3-Aminobenzofuran-2-yl)-1-(4-fluorobenzyl) pyridin-1-ium chloride (<bold>5h</bold>)

White solid, yield: (71%); mp 258–260°C. IR (KBr) (ν max /cm−1): 3296, 3159, 2977, 1631, 1543, 1313, 1226, 1099, 1032, 876, 826, 753, 658. 1H NMR (500 MHz, DMSO-d 6): δ = 5.63 (s, 2H, CH2), 7.29 (t, J = 9.0 Hz, 3H, Ar-H), 7.40 (d, J = 6.0 Hz, 2H, Ar-H), 7.50 (d, J = 8.0 Hz, 1H, Ar-H), 7.54 (d, J = 7.5 Hz, 1H, Ar-H), 7.62 (t, J = 6.5 Hz, 2H, Ar-H), 7.96 (s, 2H, NH2), 8.09 (d, J = 7.5 Hz, 1H, Ar-H), 8.79 (d, J = 7.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 59.9, 115.8, 116.0, 116.8, 122.6, 128.1, 130.4, 130.8, 131.3, 140.2, 140.3, 142.1, 142.5, 142.6, 154.6, 161.3 (d, J = 237 Hz). Anal. Calcd. for C20H16ClFN2O, C, 67.70; H, 4.55; N, 7.90; Found C, 67.45; H, 4.89; N, 8.12.

 3.1.3.9 4-(3-Aminobenzofuran-2-yl)-1-(2-chlorobenzyl) pyridin-1-ium chloride (<bold>5i</bold>)

White solid, yield: (64%); mp 135–137°C. IR (KBr) (ν max /cm−1): 3347, 3290, 3171, 3081, 1637, 1592, 1545, 1467, 1314, 1216, 1158, 1101, 1042, 871, 827, 751, 671. 1H NMR (500 MHz, DMSO-d 6): δ = 5.76 (s, 2H, CH2), 7.30 (t, J = 7.0 Hz, 1H, Ar-H), 7.41 (d, J = 7.0 Hz, 2H, Ar-H), 7.45 (d, J = 8.0 Hz, 2H, Ar-H), 7.52 (t, J = 8.0 Hz, 2H, Ar-H), 7.57 (t, J = 8.0 Hz, 2H, Ar-H), 7.99 (s, 2H, NH2), 8.11 (d, J = 7.5 Hz, 1H, Ar-H), 8.65 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 58.7, 115.7, 116.4, 122.2, 122.6, 128.0, 128.2, 130.0, 130.6, 130.7, 132.4, 132.8, 140.6, 140.7, 142.2, 142.9, 143.0, 154.7. Anal. Calcd. for C20H16Cl2N2O, C, 64.70; H, 4.34; N, 7.55; Found C, 64.56; H, 4.02; N, 7.34.

 3.1.3.10 4-(3-Aminobenzofuran-2-yl)-1-(3-chlorobenzyl) pyridin-1-ium chloride (<bold>5j</bold>)

White solid, yield: (59%); mp 180–182°C. IR (KBr) (ν max /cm−1): 3291, 3139, 1635, 1540, 1313, 1208, 1160, 1097, 1032, 875, 833, 759, 688. 1H NMR (500 MHz, DMSO-d 6): δ = 5.64 (s, 2H, CH2), 7.29 (t, J = 7.5 Hz, 1H, Ar-H), 7.43 (d, J = 5.5 Hz, 2H, Ar-H), 7.45–7.54 (m, 5H, Ar-H), 7.68 (s, 1H, Ar-H), 7.97 (d, J = 5.5 Hz, 2H, Ar-H), 8.09 (d, J = 7.5 Hz, 1H, Ar-H), 8.80 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 59.9, 116.8, 121.9, 122.1, 122.6, 127.1, 128.2, 128.8, 130.5, 130.9, 133.5, 137.4, 140.3, 140.4, 142.2, 142.6, 142.7, 154.6. Anal. Calcd. for C20H16Cl2N2O, C, 64.70; H, 4.34; N, 7.55; Found C, 65.00; H, 4.63; N, 7.24.

 3.1.3.11 4-(3-Aminobenzofuran-2-yl)-1-(4-chlorobenzyl) pyridin-1-ium chloride (<bold>5k</bold>)

Yellow solid, yield: (69%); mp 192–194°C. IR (KBr) (ν max /cm−1): 3145, 1640, 1593, 1541, 1317, 1217, 1164, 1098, 1027, 825, 761. 1H NMR (500 MHz, DMSO-d 6): δ = 5.64 (s, 2H, CH2), 7.28 (t, J = 7.5 Hz, 1H, Ar-H), 7.50 (d, J = 7.6 Hz, 2H, Ar-H), 7.53 (d, J = 7.6 Hz, 2H, Ar-H), 7.56–7.60 (m, 3H, Ar-H), 7.62 (d, J = 4.0 Hz, 1H, Ar-H), 8.02 (s, 2H, NH2), 8.15 (d, J = 8.0 Hz, 1H, Ar-H), 8.79 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 59.8, 116.8, 122.1, 122.3, 122.5, 128.1, 129.0, 130.3, 133.7, 134.1, 140.5, 140.6, 142.1, 142.6, 142.7, 154.7. Anal. Calcd. for C20H16Cl2N2O, C, 64.70; H, 4.34; N, 7.55; Found C, 64.45; H, 4.09; N, 7.78.

 3.1.3.12 4-(3-Aminobenzofuran-2-yl)-1-(2-bromobenzyl) pyridin-1-ium chloride (<bold>5l</bold>)

White solid, yield: (61%); mp 191–193°C. IR (KBr) (ν max /cm−1): 3293, 3171, 3076, 1636, 1544, 1463, 1314, 1214, 1155, 1101, 1032, 870, 826, 750, 652. 1H NMR (500 MHz, DMSO-d 6): δ = 5.73 (s, 2H, CH2), 7.31 (t, J = 8.0 Hz, 2H, Ar-H), 7.39 (t, J = 7.5 Hz, 2H, Ar-H), 7.47 (d, J = 6.5 Hz, 2H, Ar-H), 7.51 (d, J = 10.0 Hz, 1H, Ar-H), 7.54 (d, J = 8.5 Hz, 1H, Ar-H), 7.57 (d, J = 8.0 Hz, 1H, Ar-H), 7.99 (s, 2H, NH2), 8.11 (d, J = 8.0 Hz, 1H, Ar-H), 8.64 (d, J = 7.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 60.9, 116.6, 122.0, 122.1, 122.6, 122.9, 128.2, 128.6, 130.3, 130.9, 133.2, 134.0, 140.6, 140.7, 142.3, 143.1, 143.9, 154.7. Anal. Calcd. for C20H16BrClN2O, C, 57.78; H, 3.88; N, 6.74; Found C, 57.45; H, 3.57; N, 6.47.

 3.1.3.13 4-(3-Aminobenzofuran-2-yl)-1-(3-bromobenzyl) pyridin-1-ium chloride (<bold>5m</bold>)

White solid, yield: (74%); mp 270–272°C. IR (KBr) (ν max /cm−1): 3292, 3159, 1634, 1539, 1313, 1160, 1098, 1032, 834, 757, 671. 1H NMR (500 MHz, DMSO-d 6): δ = 5.63 (s, 2H, CH2), 7.30 (t, J = 7.0 Hz, 1H, Ar-H), 7.41 (d, J = 6.5 Hz, 2H, Ar-H), 7.51–7.57 (m, 3H, Ar-H), 7.61 (d, J = 7.5 Hz, 1H, Ar-H), 7.81 (s, 1H, Ar-H), 7.97 (s, 2H, NH2), 8.09 (d, J = 7.5 Hz, 2H, Ar-H), 8.79 (d, J = 6.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 59.9, 115.6, 116.8, 121.9, 122.1, 122.6, 127.3, 128.2, 130.6, 131.2, 131.8, 137.6, 138.1, 140.3, 142.2, 142.6, 142.7, 154.6. Anal. Calcd. for C20H16BrClN2O, C, 57.78; H, 3.88; N, 6.74; Found C, 58.03; H, 3.61; N, 6.38.

 3.1.3.14 4-(3-Aminobenzofuran-2-yl)-1-(4-bromobenzyl) pyridin-1-ium chloride (<bold>5n</bold>)

White solid, yield: (68%); mp 254–257°C. IR (KBr) (ν max /cm−1): 3171, 1636, 1592, 1540, 1314, 1214, 1162, 1100, 1015, 823, 759. 1H NMR (500 MHz, DMSO-d 6): δ = 5.63 (s, 2H, CH2), 7.29 (d, J = 7.5 Hz, 1H, Ar-H), 7.43 (d, J = 5.5 Hz, 2H, Ar-H), 7.49 (t, J = 8.0 Hz, 2H, Ar-H), 7.53 (d, J = 7.5 Hz, 2H, Ar-H), 7.64 (d, J = 7.5 Hz, 2H, Ar-H), 7.96 (s, 2H, NH2), 8.10 (d, J = 8.0 Hz, 1H, Ar-H), 8.77 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6): δ = 59.9, 116.6, 116.8, 121.9, 122.1, 122.3, 122.6, 128.1, 130.5, 132.0, 134.5, 140.3, 140.4, 142.1, 142.7, 154.6. Anal. Calcd. for C20H16BrClN2O, C, 57.78; H, 3.88; N, 6.74; Found C, 57.59; H, 4.02; N, 6.52.

 3.1.3.15 4-(3-Aminobenzofuran-2-yl)-1-(2-nitrobenzyl) pyridin-1-ium chloride (<bold>5o</bold>)

Yellow solid, yield: (67%); mp 148–150°C. IR (KBr) (ν max /cm−1): 3167, 2986, 1707, 1639, 1525, 1337, 1170, 1107, 1045, 854, 789, 736. 1H NMR (500 MHz, DMSO-d 6): δ = 6.02 (s, 2H, CH2), 7.13 (d, J = 7.5 Hz, 1H, Ar-H), 7.32 (t, J = 8.0 Hz, 2H, Ar-H), 7.53 (d, J = 8.0 Hz, 2H, Ar-H), 7.57 (t, J = 7.0 Hz, 1H, Ar-H), 7.71 (d, J = 7.5 Hz, 1H, Ar-H), 7.80 (d, J = 7.5 Hz, 1H, Ar-H), 8.04 (s, 2H, NH2), 8.12 (d, J = 8.0 Hz, 1H, Ar-H), 8.24 (d, J = 7.5 Hz, 1H, Ar-H), 8.66 (d, J = 6.5 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 58.2, 116.7, 122.0, 122.2, 122.6, 125.5, 128.2, 129.1, 129.9, 130.3, 130.6, 134.8, 140.7, 142.4, 143.3, 144.0, 147.3, 154.7. Anal. Calcd. for C20H16ClN3O3, C, 62.91; H, 4.22; N, 11.01; Found C, 63.11; H, 3.95; N, 11.35.

 3.1.3.16 4-(3-Aminobenzofuran-2-yl)-1-(4-nitrobenzyl) pyridin-1-ium chloride (<bold>5p</bold>)

Yellow solid, yield: (73%); mp 173–175°C. IR (KBr) (ν max /cm−1): 3302, 3178, 3104, 1637, 1533, 1340, 1213, 1165, 1103, 1031, 827, 753, 689. 1H NMR (500 MHz, DMSO-d 6): δ = 5.81 (s, 2H, CH2), 7.31 (t, J = 7.0 Hz, 1H, Ar-H), 7.49–7.57 (m, 3H, Ar-H), 7.74 (d, J = 8.0 Hz, 2H, Ar-H), 7.99 (s, 2H, NH2), 8.10 (d, J = 7.5 Hz, 2H, Ar-H), 8.28 (d, J = 7.5 Hz, 2H, Ar-H), 8.79 (d, J = 6.0 Hz, 2H, Ar-H). 13C NMR (125 MHz, DMSO-d 6 ): δ = 59.7, 116.8, 122.0, 122.2, 122.5, 123.9, 124.1, 128.2, 129.4, 130.6, 140.7, 142.2, 142.3, 142.8, 147.6, 154.7. Anal. Calcd. for C20H16ClN3O3, C, 62.91; H, 4.22; N, 11.01; Found C, 62.68; H, 4.51; N, 10.83.

 3.2 <italic>In vitro</italic> biological evaluations 3.2.1 Cholinesterase inhibition assay

The method described by Ellman was used to evaluate the inhibitory activity of compounds 5a-p against AChE, according to procedures previously reported. AChE from E. electricus, and horse serum BuChE (eqBuChE, Sigma-Aldrich) 5,5-Dithiobis-(2-nitrobenzoic acid) (DTNB), and acetylthiocholine iodide (ATC) were purchased from Sigma Aldrich. Donepezil was used as a standard drug and all experiments were assayed in triplicate. In this procedure, five different concentrations of each compound were used at 25°C. To determine the IC50, 100 μl of DTNB, 3 ml phosphate buffer (0.1 M, pH = 8.0), 50 μl of the enzyme, and 50 μl of each compound were incubated in 24 well plates for 5 min followed by the addition of 20 μl of the substrate (acetylthiocholine iodide) and absorbance was detected at 415 nm for 6 min, and then the percent inhibition was plotted from inhibition curves. For the in-vitro BuChE assay similar method has been used.

 3.2.2 Kinetics study

To understand further insight into the inhibition model of compounds, the kinetic study was performed for the most active compound 5f according to procedures previously reported (Baharloo et al., 2015). The experiment was assayed in triplicate.

 3.2.3 <italic>In vitro</italic> inhibition of self-induced and AChE-induced Aβ<sub>1–42</sub> aggregation

To assess the inhibitory effect of compounds 5a, 5f, 5h, 5i, and 5l on the β-Amyloid aggregation, we used a thioflavin T (ThT)-based fluorescence assay to determine the self-induced and AChE-induced Aβ1–42 aggregation (Levine, 1993). Aβ1–42 (Sigma A9810) 50 μM was dissolved in ammonium hydroxide (1% v/v) for pre-fibrillation and incubated for 72 h at 37°C. Aβ1–42 (10 µl) in the absence and presence of human recombinant AChE (0.01 u/mL, Sigma C1682) were added to phosphate buffer (0.05 M, pH = 7.4) and incubated at 37°C for 48 h with or without target compounds 5a, 5f, 5h, 5i, and 5l (100 μM). Next, 50 μl of thioflavin T (ThT, 200 μM) containing 50 mM glycine-NaOH buffer (pH 8.5) was added. Fluorescences were recorded (λexc = 446 nm; λem = 490 nm) by Microplate Reader (Spectra Max). Donepezil (100 μM, Sigma D-6821) was used as a reference drug. The aggregation inhibition of the tested compounds was calculated on AChE or self-induced Aβ-aggregation according to the equation (1−IFi/IFc) × 100, where IFi and IFc are the fluorescence intensities in the presence of inhibitors and in the absence of inhibitors, respectively.

 3.2.4 Cell viability assay

In order to evaluate cell viability of 5a, 5f, 5h, 5i, and 5l, the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay was performed using PC12 cell line. Cells were seeded in 96-well plates at a density of 5,000 cells/well for 24 h, and then cells were treated with tested compounds and glutamate (5 mM) and incubated at 37°C for 24 h. After that, the medium was removed and 20 μl of the MTT reagent (5 mg/ml) was added and incubated at 37 °C for 4 h. Then, the medium was replaced with 150 μl DMSO to solve formazan crystals. The absorbance was recorded by microplate reader apparatus (Biotek, Winooski, VT, United States) at 570 nm. The assay was performed in three independent experiments and triplicate.

 3.2.5 Docking simulations

The molecular docking studies were performed using the program Autodock Vina (Trott and Olson 2010). The crystal structure of acetyl cholinesterase (1EVE) was derived from the Protein Data Bank (http://www.rcsb.org/). The co-crystallized ligand and water molecules were deleted from the protein structure. The top 3-aminocoumarin derivative 5f was selected for the docking study. The selected ligand was constructed using Marvin Sketch, 2012, Chem Axon (http://www.chemaxon.com). The center of the grid box were set as follow; x = 2.071, y = 63.616, z = 67.737, and the active site box were set at 15 Å × 15 Å × 15 Å. Molecular visualizations were carried out by Discovery Studio 4.5 client software (Accelrys, Inc., San Diego, CA, United States).

 4 Conclusion

In the present study, a novel series of 3-aminobenzofuran derivatives with N-benzylpyridinium moiety were designed, synthesized, and evaluated as novel agents for the treatment of AD. The in-vitro assays revealed that most target compounds had moderate to good anti-AChE and -BuChE activity with no toxicity against PC12 cells. The best result was obtained from 2-fluorobenzyl derivative 5f which exhibited potent AChE and BuChE inhibitory activity with IC50 = 0.64 and 0.55 μM, respectively. Moreover, compounds 5f and 5h have remarkable anti-aggregation activity compared to donepezil as the reference drug. Docking’s study demonstrated that 3-aminobenzofuran (hydrophobic aromatic fragment) can be positioned in the peripheral anionic site and the N-benzylpyridinium fragment bound to the catalytic anionic site of AChE. These results showed that compound 5f could be considered a promising multifunctional derivative for further studies in the field of new anti-Alzheimer agents.

 Data availability statement

The original contributions presented in the study are included in the article/Supplementary Materials; further inquiries can be directed to the corresponding author.

 Author contributions

ZH and RM performed synthesis and characterization of the target compounds. SNAB evaluated anti-Aβ aggregation. HN and TA performed AChE, BuChE, and kinetics studies. RF participated in the ChEs inhibition assay. SM and AA wrote the first draft of the manuscript and performed docking studies. AF controlled the synthetic results and reviewed the manuscript for proofreading. All authors reviewed and agreed to the content of the manuscript.

 Funding

This work was supported and funded by Tehran University of Medical Sciences, Grant No. 99-3-104-51406.

 Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

 Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2022.882191/full#supplementary-material

References Al-Qirim T. Shattat G. Sweidan K. El-Huneidi W. Sheikha G. A. Khalaf R. A. (2012). In vivo antihyperlipidemic activity of a new series of N-(Benzoylphenyl) and N-(Acetylphenyl)-1-benzofuran-2-carboxamides in rats. Arch. Pharm. Weinh. 345, 401–406. 10.1002/ardp.201100225 Alper-Hayta S. Arisoy M. Temiz-Arpaci Ö. Yildiz I. Aki E. Özkan S. (2008). Synthesis, antimicrobial activity, pharmacophore analysis of some new 2-(substitutedphenyl/benzyl)-5-[(2-benzofuryl)carboxamido]benzoxazoles. Eur. J. Med. Chem. 43, 2568–2578. 10.1016/j.ejmech.2007.12.019 Baharloo F. Moslemin M. H. Nadri H. Asadipour A. Mahdavi M. Emami S. (2015). Benzofuran-derived benzylpyridinium bromides as potent acetylcholinesterase inhibitors. Eur. J. Med. Chem. 93, 196–201. 10.1016/j.ejmech.2015.02.009 Byun J. H. Kim H. Kim Y. Mook-Jung I. Kim D. J. Lee W. K. (2008). Aminostyrylbenzofuran derivatives as potent inhibitors for Aβ fibril formation. Bioorg. Med. Chem. Lett. 18, 5591–5593. 10.1016/j.bmcl.2008.08.111 Camps P. Formosa X. Galdeano C. Gómez T. Muñoz-Torrero D. Scarpellini M. (2008). Novel donepezil-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation. J. Med. Chem. 51, 3588–3598. 10.1021/jm8001313 Castro A. Martinez A. (2001). Peripheral and dual binding site acetylcholinesterase inhibitors: Implications in treatment of alzheimer’s disease. Mini Rev. Med. Chem. 1, 267–272. 10.2174/1389557013406864 Cavalli A. Bolognesi M. L. Minarini A. Rosini M. Tumiatti V. Recanatini M. (2008). Multi-target-Directed ligands to combat neurodegenerative diseases. J. Med. Chem. 51, 347–372. 10.1021/jm7009364 Chen W. Deng X.-Y. Li Y. Yang L.-J. Wan W.-C. Wang X.-Q. (2013). Synthesis and cytotoxic activities of novel hybrid 2-phenyl-3-alkylbenzofuran and imidazole/triazole compounds. Bioorg. Med. Chem. Lett. 23, 4297–4302. 10.1016/j.bmcl.2013.06.001 Choi H. D. Seo P. J. Son B. W. Kang B. W. (2004). Synthesis of 2-(4-hydroxyphenyl)benzofurans and their application to -amyloid aggregation inhibitor. Arch. Pharm. Res. 27, 19. 10.1007/BF02980039 Choi M.-J. Jung K. H. Kim D. Lee H. Zheng H.-M. Park B. H. (2011). Anti-cancer effects of a novel compound HS-113 on cell growth, apoptosis, and angiogenesis in human hepatocellular carcinoma cells. Cancer Lett. 306, 190–196. 10.1016/j.canlet.2011.03.005 Cummings J. L. Morstorf T. Zhong K. (2014). Alzheimer’s disease drug-development pipeline: Few candidates, frequent failures. Alzheimer's Res. Ther. 6, 37–43. 10.1186/alzrt269 Ellman G. L. Courtney K. D. Andres V. Featherstone R. M. (1961). A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7, 88–95. 10.1016/0006-2952(61)90145-9 Forette F. R. Anand G. Gharabawi A. (1999). A phase II study in patients with Alzheimer's disease to assess the preliminary efficacy and maximum tolerated dose of rivastigmine (ExelonR). Eur. J. Neurol. 6, 423–429. 10.1046/j.1468-1331.1999.640423.x Gauthier S. Reisberg B. Zaudig M. Petersen R. C. Ritchie K. Broich K. (2006). Mild cognitive impairment. Lancet 367, 1262–1270. 10.1016/S0140-6736(06)68542-5 Goyal D. Kaur A. Goyal B. (2018). Benzofuran and indole: Promising scaffolds for drug development in Alzheimer's disease. ChemMedChem 13, 1275–1299. 10.1002/cmdc.201800156 Greenough M. A. Camakaris J. Bush A. I. (2013). Metal dyshomeostasis and oxidative stress in Alzheimer’s disease. Neurochem. Int. 62, 540–555. 10.1016/j.neuint.2012.08.014 Howlett D. R. Perry A. E. Godfrey F. Swatton J. E. Jennings K. H. C. Wood S. J. (1999). Inhibition of fibril formation in β-amyloid peptide by a novel series of benzofurans. Biochem. J. 340, 283–289. 10.1042/bj3400283 Inestrosa N. C. Alvarez A. Pérez C. A. Moreno R. D. Vicente M. Linker C. (1996). Acetylcholinesterase accelerates assembly of amyloid-beta-peptides into Alzheimer’s fibrils: Possible role of the peripheral site of the enzyme. Neuron 16, 881–891. 10.1016/s0896-6273(00)80108-7 Kapková P. Alptüzün V. Frey P. Erciyas E. Holzgrabe U. (2006). Search for dual function inhibitors for Alzheimer’s disease: Synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Aβ fibril formation inhibition capacity. Bioorg. Med. Chem. 14, 472–478. 10.1016/j.bmc.2005.08.034 Koellner G. Kryger G. Millard C. B. Silman I. Sussman J. L. Steiner T. (2000). Active-site gorge and buried water molecules in crystal structures of acetylcholinesterase from Torpedo californica . J. Mol. Biol. 296, 713–735. 10.1006/jmbi.1999.3468 Lai R. Albala B. Kaplow J. M. Aluri J. YenSatlin M. A. Satlin A. (2012). First-in-human study of E2609, a novel BACE1 inhibitor, demonstrates prolonged reductions in plasma beta-amyloid levels after single dosing. Alzheimers Dement. 8, P96. 10.1016/j.jalz.2012.05.237 Lane R. M. Kivipelto M. Greig N. H. (2004). Acetylcholinesterase and its inhibition in Alzheimer disease. Clin. Neuropharmacol. 27, 141–149. 10.1097/00002826-200405000-00011 León R. Garcia A. G. Marco-Contelles J. (2013). Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimer’s disease. Med. Res. Rev. 33, 139–189. 10.1002/med.20248 Levine H. (1993). Thioflavine T interaction with synthetic Alzheimer’s disease β-amyloid peptides: Detection of amyloid aggregation in solution. Protein Sci. 2, 404–410. 10.1002/pro.5560020312 Li F. Wu J.-J. Wang J. Yang X.-L. Cai P. Liu Q.-H. (2017). Synthesis and pharmacological evaluation of novel chromone derivatives as balanced multifunctional agents against Alzheimer’s disease. Bioorg. Med. Chem. 25, 3815–3826. 10.1016/j.bmc.2017.05.027 Loidreau Y. Dubouilh-Benard C. Marchand P. Nourrisson M.-R. Duflos M. Buquet C. (2013). Efficient new synthesis of N-Arylbenzo[b]furo[3, 2-d]pyrimidin-4-amines and their benzo[b]thieno[3, 2-d]pyrimidin-4-amine analogues via a microwave-assisted dimroth rearrangement. J. Heterocycl. Chem. 50, 1187–1197. 10.1002/jhet.1716 Longo F. M. Massa S. M. (2004). Neuroprotective strategies in Alzheimer’s disease. NeuroRX 1, 117–127. 10.1602/neurorx.1.1.117 Marco-Contelles J. León R. de los Ríos C. Guglietta A. Terencio J. López M. G. (2006). Novel multipotent Tacrine−Dihydropyridine hybrids with improved acetylcholinesterase inhibitory and neuroprotective activities as potential drugs for the treatment of alzheimer’s disease. J. Med. Chem. 49, 7607–7610. 10.1021/jm061047j McKhann G. M. Knopman D. S. Chertkow H. Hyman B. T. Jack C. R. Kawas C. H. (2011). The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimer's. &amp. Dement. 7, 263–269. 10.1016/j.jalz.2011.03.005 Mehrabi M. Pourshojaei Y. Moradi A. Sharifzadeh M. Khosravani L. Sabourian R. (2017). Design, synthesis, molecular modeling and anticholinesterase activity of benzylidene-benzofuran-3-ones containing cyclic amine side chain. Future Med. Chem. 9, 659–671. 10.4155/fmc-2016-0237 Mesulam M. M. Asunction M. M. (1987). Cholinesterases within neurofibrillary tangles related to age and Alzheimer's disease. Ann. Neurol. 22, 223–228. 10.1002/ana.410220206 Muñoz-Ruiz P. Rubio L. García-Palomero E. Dorronsoro I. del Monte-Millán M. Valenzuela R. (2005). Design, synthesis, and biological evaluation of dual binding site acetylcholinesterase inhibitors: New disease-modifying agents for alzheimer’s disease. J. Med. Chem. 48, 7223–7233. 10.1021/jm0503289 Nadri H. Pirali-Hamedani M. Shekarchi M. Abdollahi M. Sheibani V. Amanlou M. (2010). Design, synthesis and anticholinesterase activity of a novel series of 1-benzyl-4-((6-alkoxy-3-oxobenzofuran-2(3H)-ylidene) methyl) pyridinium derivatives. Bioorg. Med. Chem. 18, 6360–6366. 10.1016/j.bmc.2010.07.012 Nevagi R. J. Dighe S. N. Dighe S. N. (2015). Biological and medicinal significance of benzofuran. Eur. J. Med. Chem. 97, 561–581. 10.1016/j.ejmech.2014.10.085 Poprac P. Jomova K. Simunkova M. Kollar V. Rhodes C. J. Valko M. (2017). Targeting free radicals in oxidative stress-related human diseases. Trends Pharmacol. Sci. 38, 592–607. 10.1016/j.tips.2017.04.005 Pouramiri B. Mahdavi M. Moghimi S. Firoozpour L. Nadri H. Moradi A. (2016). Synthesis and antiacetylcholinesterase activity evaluation of new 2-aryl benzofuran derivatives. Lett. Drug Des. Discov. 13, 897–902. 10.2174/1570180813666160610124637 Rizzo S. Tarozzi A. Bartolini M. Da Costa G. Bisi A. Gobbi S. (2012). 2-Arylbenzofuran-based molecules as multipotent Alzheimer’s disease modifying agents. Eur. J. Med. Chem. 58, 519–532. 10.1016/j.ejmech.2012.10.045 Rosini M. Simoni E. Minarini A. Melchiorre C. (2014). Multi-target design strategies in the context of alzheimer’s disease: Acetylcholinesterase inhibition and NMDA receptor antagonism as the driving forces. Neurochem. Res. 39, 1914–1923. 10.1007/s11064-014-1250-1 Saxena A. Fedorko J. M. Vinayaka C. R. Medhekar R. Radic Z. Taylor P. (2003). Aromatic amino-acid residues at the active and peripheral anionic sites control the binding of E2020 (AriceptR) to cholinesterases. Eur. J. Biochem. 270, 4447–4458. 10.1046/j.1432-1033.2003.03837.x Scarpini E. Scheltens P. Feldman H. (2003). Treatment of alzheimer’s disease: Current status and new perspectives. Lancet Neurol. 2, 539–547. 10.1016/s1474-4422(03)00502-7 Schneider L. S. (2000). A critical review of cholinesterase inhibitors as a treatment modality in Alzheimer’s disease. Dialogues Clin. Neurosci. 2, 111–128. 10.31887/DCNS.2000.2.2/lschneider Smith C. P. Bores G. M. Petko W. Li M. Selk D. E. Rush D. K. (1997). Pharmacological activity and safety profile of P10358, a novel, orally active acetylcholinesterase inhibitor for Alzheimer’s disease. J. Pharmacol. Exp. Ther. 280, 710–720. Talesa V. N. (2021). Acetylcholinesterase in Alzheimer’s disease. Mech. Ageing Dev. 122, 1961–1969. 10.1016/s0047-6374(01)00309-8 Trott O. Olson A. J. (2010). AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem. 31, 455–461. 10.1002/jcc.21334 Weinstock M. (1999). Selectivity of cholinesterase inhibition: Clinical implications for the treatment of Alzheimer's disease. CNS Drugs 12, 307–323. 10.2165/00023210-199912040-00005