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Article

Impact of N-Alkylamino Substituents on Serotonin Receptor (5-HTR) Affinity and Phosphodiesterase 10A (PDE10A) Inhibition of Isoindole-1,3-dione Derivatives

by
Anna Czopek
1,*,
Anna Partyka
2,
Adam Bucki
1,
Maciej Pawłowski
1,
Marcin Kołaczkowski
1,
Agata Siwek
3,
Monika Głuch-Lutwin
3,
Paulina Koczurkiewicz
4,
Elżbieta Pękala
4,
Anna Jaromin
5,
Bożena Tyliszczak
6,
Anna Wesołowska
2 and
Agnieszka Zagórska
1
1
Department of Medicinal Chemistry, Jagiellonian University Medical College, 9 Medyczna Street, 30-688 Krakow, Poland
2
Department of Clinical Pharmacy, Jagiellonian University Medical College, 9 Medyczna Street, 30-688 Krakow, Poland
3
Department of Pharmacobiology, Jagiellonian University Collegium Medicum, 9 Medyczna Street, 30-688 Krakow, Poland
4
Department of Pharmaceutical Biochemistry, Jagiellonian University Collegium Medicum, 9 Medyczna Street, 30-688 Krakow, Poland
5
Department of Lipids and Liposomes, Faculty of Biotechnology, University of Wroclaw, 14a Joliot-Curie, 50-383 Wroclaw, Poland
6
Faculty of Materials Engineering and Physics, Cracow University of Technology, Institute of Materials Science, 24 Warszawska Street, 31-155 Krakow, Poland
*
Author to whom correspondence should be addressed.
Molecules 2020, 25(17), 3868; https://doi.org/10.3390/molecules25173868
Submission received: 4 August 2020 / Revised: 22 August 2020 / Accepted: 23 August 2020 / Published: 25 August 2020
(This article belongs to the Special Issue Medicinal Chemistry in Europe II)
Browse Figures
Versions Notes

Abstract

:
In this study, a series of compounds derived from 4-methoxy-1H-isoindole-1,3(2H)-dione, potential ligands of phosphodiesterase 10A and serotonin receptors, were investigated as potential antipsychotics. A library of 4-methoxy-1H-isoindole-1,3(2H)-dione derivatives with various amine moieties was synthesized and examined for their phosphodiesterase 10A (PDE10A)-inhibiting properties and their 5-HT1A and 5-HT7 receptor affinities. Based on in vitro studies, the most potent compound, 18 (2-[4-(1H-benzimidazol-2-yl)butyl]-4-methoxy-1H-isoindole-1,3(2H)-dione), was selected and its safety in vitro was evaluated. In order to explain the binding mode of compound 18 in the active site of the PDE10A enzyme and describe the molecular interactions responsible for its inhibition, computer-aided docking studies were performed. The potential antipsychotic properties of compound 18 in a behavioral model of schizophrenia were also investigated.

Graphical Abstract

1. Introduction

Isoindole-1,3-diones (phthalimides) and their N-substituted analogs have been a very interesting and topical research area due to their wide structural diversity and broad-spectrum biological activities. The sulphonamide and amide derivatives of N-phenyl-phthalimide (compounds 3a–e and 4a–e, Figure 1) displayed potent inhibitory activity on neutrophil recruitment, which correlated with their inhibitory effect on tumor necrosis factor α (TNF-α) level [1]. N-1-Adamantyl-4-aminophthalimide (compound 2′, Figure 1) exhibits anti-HIV-1 and anti-HIV-2 activity in CEM cell cultures [2]. The N-pyridinyl and N-quinolinyl substituted derivatives of phthalimides (compounds 8′ and 12′, Figure 1) demonstrated cytotoxicity against the growth of a number of cultured cell-lines [3]. 1,3-Dioxoisoindoline-5-carboxamides (compound 4d′, Figure 1) are potent T-type calcium channel blockers [4], whereas 1,3-dioxoisoindoline-5-carboxylic acid derivatives (compounds 2c′ and 3c′, Figure 1) are potent xanthine oxidase inhibitors [5]. Moreover, (ZE)-2-[4-(1-hydrazono-ethyl)phenyl]isoindoline-1,3-dione (compound 12′, Figure 1) has shown remarkable anti-microbial activity [6]. In the central nervous system (CNS), N-phenylphthalimide derivatives (ADD213063 and ADD219048, Figure 1) have exhibited original anticonvulsant properties [7]. Pazinaclone (DN-2327, Figure 1) produces sedative and anxiolytic effects by acting as a partial agonist of GABAA benzodiazepine receptors [8]. Potent acetylcholinesterase inhibitors (AChEIs) were identified in a group of 2-fluorinated-benzylamino-alkyl-isoindoline-1,3-diones [9], 2-(benzylamino-2-hydroxyalkyl)isoindoline-1,3-diones [10] (compounds 6′ and 12′, Figure 1) and 2-(2-(4-benzoylpiperazin-1-yl)ethyl)isoindoline-1,3-dione (compound 4e′, Figure 1) derivatives [11]. NAN-190 (2-methoxyphenyl)-4-(4-phthalimidobutyl)piperazine, Figure 2) is a selective antagonist of serotonin 1A subtype receptors (5-HT1ARs) that potently blocks the alfa 2 adrenergic receptor (α2ARs) [12].
Schizophrenia is a multifactorial mental illness that affects 1% of the population. Both genetic and environmental contributions play an important role in the manifestation of a wide range of behavioral, emotional, and cognitive abnormalities in schizophrenia. Since the introduction of chlorpromazine, clinical practice has relied upon antipsychotic drugs (APDs) over the past half century, with numerous first-, second-, and third-generation antipsychotics discovered during this time. Typical, or first-generation, APDs (chlorpromazine and haloperidol) exhibited high-affinity dopamine D2 receptor antagonism, which causes both antipsychotic actions and many side effects e.g., extrapyramidal and endocrine. Atypical, or second generation, antipsychotics (SGAs) were then developed to avoid the extrapyramidal side effects. SGAs include compounds such as clozapine, olanzapine, and quetiapine that exhibit relatively moderate affinity for D2 and 5-HT2A receptors or drugs like risperidone that effectively block both serotonin 5-HT2A and dopamine D2 receptors [13,14]. The first representative of the third generation of APDs was aripiprazole, whose mechanism of action was ascribed to partial agonism of D2. Although aripiprazole has effects on several other receptors, this drug is the first “dopamine stabilizer” based on D2 partial agonist properties. However, the data available on the mechanism of action of aripiprazole are inconsistent with a mode of action related to the partial agonism of D2. Therefore, a recent hypothesis regarding the functional selectivity of aripiprazole for D2 has emerged that seems to describe its mechanism of action more accurately [15,16]. Although all approved antipsychotic drugs show affinity for dopamine D2 receptors, there is evidence that modulation of the serotonergic system leads to enhanced antipsychotic therapy [17,18]. Partial agonism of 5-HT1A, and antagonism of 5-HT2A, 5-HT6, and 5-HT7 receptors, contributes to a reduced risk of extrapyramidal side effects and improved specific cognition domains of atypical antipsychotic drugs [14].
The phosphodiesterase 10A (PDE10A) enzyme is highly expressed in the striatal medium spiny neurons (MSNs), where it modulates both dopamine D2- and D1-dependent signaling. Striatal MSNs pathways are divided into direct dopamine D1 receptor-mediated and indirect dopamine D2 receptor-mediated striatal output pathways [19]. Dopamine D1 receptors in direct pathway MSNs are coupled with Gs proteins, which activate adenylate cyclase to increase cyclic adenosine monophosphate (cAMP) concentration, whereas the stimulation of D2 receptors inhibits the activity of adenylyl cyclase, resulting in a decrease in the level of cAMP. On the other hand, inhibition of PDE10A in the dendritic membranes of MSNs results in suppression of D2-mediated signaling, which is similar to the effects of D2 antagonists. Upregulation of cyclic nucleotide levels in indirect pathway MSNs could be an alternative approach for novel antipsychotics [20,21], whereas activation of direct pathway MSNs could be associated with improvement of cognitive functions. Thus, in contrast to the marketed antipsychotics, phosphodiesterase inhibitors (PDEIs) influence both the indirect and direct pathways, and the additional action of these compounds on the direct pathway could help distinguish them clinically from D2 antagonists [22]. Moreover, PDEIs may have potential therapeutic utility in the treatment of cognitive impairment associated with schizophrenia or may be useful as an adjunctive treatment for negative symptoms in patients with schizophrenia [19].
In complex diseases such as schizophrenia, single-target drugs have turned out as failures, whereas multi-target drugs have been found to be much more efficacious. In clinical practice, many combinations of psychotropics have been tried for schizophrenia, based on a trial-and-error paradigm guided by clinical experience and patient response. An overall superior and safer solution seems to be the modern concept of designer multiple-targeting ligands (DMLs). The DMLs are also described as “polypharmacology by design”, which claims parallel modulation of defined multiple biological targets by designer small molecule drugs [23]. An exemplification of this idea is atypical antipsychotics, which target a number of G protein-coupled receptors (GPCRs) simultaneously. Currently, novel strategies in designing drugs effective in treatment of schizophrenia focus on targets beyond the dopaminergic hypothesis of the disease [24].
In order to search for novel potential antipsychotic agents, we rationally synthesized a series of N-substituted isoindole-1,3-dione derivatives, which were designed to interact with the serotonin 5-HT1A/5-HT7 receptor and/or inhibit PDE10A. The core 1H-isoindole-1,3(2H)-dione moiety was selected from the structure of the 5-HTlA antagonist, NAN-190 (Figure 2). Next, a methoxy moiety was introduced at position 4 of the isoindole-1,3-dione so as to be able to obtain structural analogs of PDE10AIs (compound B-3, Figure 2) [25]. The isoindole-1,3-dione core was connected by one to five methylene linkers with amines. For determining the impact of N-alkylamine substitution of isoindole-1,3-dione on 5-HTR affinity and PDE10A inhibitory activity, different heterocyclic amine substituents were investigated. Modifications of amine substituents comprised changes in the size of the heterocyclic amine ring from 1H-imidazole and pyridine, to benzimidazole, 6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline, 1,2,3,4-tetrahydroisoquinoline, and the decahydroisoquinoline moiety. Previously, these amines were used in the design of potent 5-HT1A and 5-HT7 ligands (compound 18 and PZ-376, Figure 2) [26,27,28], and they are partially saturated analogs of isoquinoline, which is present in the structure of papaverine, a potent PDE10A inhibitor. Moreover, the benzimidazole moiety can be found in the structure of numerous PDE inhibitors and serotonin ligands (compound 10, Figure 2) [29,30]. Finally, a phenyl ring was chosen instead of a heterocyclic amine group in order to examine the effect of amine substitution on selected 5-HTRs affinity and PDE10A inhibitory activity.
The series of designed ligands were synthesized and evaluated in adequate biological assays, a luminescence PDE inhibition assay, as well as a radioligand binding assay for 5-HT1A and 5-HT7 receptors. Computer-aided studies were undertaken to identify the structural elements responsible for in vitro activity. Finally, for the most active compound, Compound 18, in vitro safety studies were performed and preliminary in vivo activity was tested in an animal model of schizophrenia.

2. Results and Discussion

2.1. Chemistry

The series of rationally designed 4-methoxy-1H-isoindole-1,3(2H)-dione derivatives (3–23) were synthesized in average to good yields (30–75%), as shown in Scheme 1. The starting 2,3-dimethylphenyl methyl ether (1) was synthesized by a procedure published elsewhere [31]. The intermediate compound, 4-methoxy-2-benzofuran-1,3-dione (2), was obtained from 1, according to a previously described procedure [32] with slight modifications. The aminoalkylamine moieties derived from 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline, 1,2,3,4-tetrahydroisoquinoline, decahydroisoquinoline, and 1H-1,3-benzodiazole were obtained in line with the earlier reported methods (Scheme 2) [33,34], while those containing 1H-imidazole, pyridine, and phenyl rings were commercially available.

2.2. In Vitro Activity of Compounds 3–23

2.2.1. PDE10A Inhibitory Activity

The novel series of compounds was derived from a 4-methoxy-2,3-dihydro-1H-isoindole-1,3-dione (4-methoxyphthalimide, Figure 1) fragment, which was connected via different lengths of a carbon-chain linker (C1–C5) to various amine fragments (e.g., 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline; 1H-imidazole; 1,2,3,4-tetrahydroisoquinoline; 1H-benzimidazole; and decahydroisoquinoline) or to a phenyl ring (3–17). In this series, seven compounds (7, 8, 11, 12, 15–17) displayed PDE10A inhibitory activity in the luminescence PDE inhibition assay at a concentration of 10 µM (7–92%, Table 1). Furthermore, four analogs of the most promising 4-methoxyphthalimide derivatives (15, 17–19), containing the phthalimide moiety, were synthesized (20–23). Among them, three of the four phthalimide derivatives (21–23) showed moderate activity toward PDE10A (45–73%, Table 1).
Initially, among compounds with a linker length of one to three methylene units (3–17), the highest percentage of PDE10A inhibition (70–86%) was exhibited by compounds containing the 1H-benzimidazole moiety (15, 17). Therefore, the influence of the length of the linker on inhibition of PDE10A was investigated in this group of compounds. In the case of the 1H-benzimidazole containing compounds, 11, 15, and 17–19, the elongation of the linker from one to five methylene groups resulted in an increase and then a decrease in the inhibition of PDE10A. The most active compound among them, compound 18 (92% inhibition), has a linker of four methylene units that connects the 4-methoxyphthalimide fragment with the 1H-benzimidazole moiety. The modifications of the 1H-benzimidazole moiety, such as replacement with 1,2,3,4-tetrahydroisoquinoline fragment (4, 7), or its saturation (8 vs. 7), as well as removal of one aromatic ring in this part (10, 13, 14) decreased the observed affinity to PDE10A. Interestingly, compounds 12 and 16, containing a phenyl moiety at the terminal location, despite the lack of a functional amine group, showed very low activity toward PDE10A.
In addition, the relevance of the introduction of a 4-methoxyl group to the 4-methoxy-2,3-dihydro-1H-isoindole-1,3-dione fragment was also verified. For this purpose, a small phthalimide series without a 4-methoxy group at position 4 (Table 1) connected via an alkylene linker to the 1H-benzimidazole moiety (20–23) was synthesized. The activity of compounds 20–23 was significantly lower than that of their 4-methoxy analogs (15, 17–19). Moreover, similar to the 4-methoxy series, the inhibitory activity of compounds 20–23 increased with the length of the linker up to four methylene units and then slightly decreased.
In the next step, the five most active compounds chosen (15, 17–19, 22) were quantitatively tested in the luminescence PDE inhibition assay, alongside papaverine as the reference drug. The effectiveness of inhibition was expressed as the half maximal inhibitory concentration (IC50) values. The chosen compounds displayed a percentage of inhibition above 70% at the concentration of 10 µM. All investigated compounds (15, 17–19, 22) displayed satisfactory IC50 values (886 nM–6.71 µM, Table 1 and Figure 3) in comparison with papaverine (5.755 µM). It is noteworthy that the most potent PDE10A inhibitor, compound 18 (IC50 = 886 nM), was in-line with the predictions stipulated by Lipinski’s Rule of Five, which describes “drug-like” parameters of small molecules in terms of lipophilicity, size, polarity, solubility, flexibility, and saturation [35] (see graph, Figure S1, in Supporting Materials).

2.2.2. Serotonin Receptor Affinity

In the next phase of the current study, the binding affinities of novel 4-methoxy-2,3-dihydro-1H-isoindole-1,3-dione derivatives for 5-HT1A and 5-HT7 receptors were determined in a radioligand binding assay (Table 1). The results revealed that the majority of the tested compounds displayed very low-to-moderate affinity for the 5-HT1A receptor (6–59%) at a concentration of 1 µM, but only a few showed any affinity for the 5-HT7 receptor (7, 16–23). The highest 5-HT1A or 5-HT7 receptor affinity was observed for compounds 13 (59% for 5-HT1A) and 7 (51% for 5-HT7), respectively. Among the investigated series, three compounds (7, 20, and 23) showed a low but significant (above 20%) percentage of binding for both 5-HT1A and 5-HT7 receptors (33%, 26%, 48% and 51%, 36%, 34%, respectively).
In summary, the present study determined that the majority of the 2,3-dihydro-1H-isoindole-1,3-dione derivatives (3–23) showed affinity toward the 5-HT1A receptor, whereas only few bind at the 5-HT7 receptor site. In the case of 1H-benzimidazole derivatives (compounds 15, 17–19), which significantly inhibited PDE10A (IC50 = 886 nM–6.71 µM), low affinity for 5-HT1A receptors (16–44%), and even lower for 5-HT7 receptors (0–10%) was observed.
Furthermore, because compound 18 contains structural moieties such as benzimidazole and phthalimide, which are also present in serotonin 5-HT2A and dopamine D2 receptor antagonists [14], it was decided to test the affinity of Compound 18 to these receptors. The obtained results (appendix below Table 1) revealed that at a concentration of 1 µM compound 18 displayed negligible percentage of binding for 5-HT2A and none for D2 receptors (8.8% and 0%, respectively).

2.3. Molecular Modeling Studies

In line with in vitro results, the most active 4-methoxy-2,3-dihydro-1H-isoindole-1,3-dione derivative with a bezimidazol-2-yl butyl moiety (18) was selected to clarify and draw useful information regarding the nature of the interactions of PDE10A with its ligands, and insights into structure-activity relationships were investigated. We elucidated putative binding modes of several derivatives throughout the process of docking to the protein target, which was represented by the optimized crystal structure of the studied enzyme. As a representative example, binding interactions were presented for compound 18 (2-[4-(1H-1,3-benzodiazol-2-yl)butyl]-4-methoxy-2,3-dihydro-1H-isoindole-1,3-dione) (Figure 4).
The 2,3-dihydro-1H-isoindole-1,3-dione moiety, bound in the catalytic active site, interacted with Gln716 (H-bond) and with Phe719 (π-π stacking). In the case of the most active compound (18), the 4-methoxy group acted as the H-bond acceptor, whereas unsubstituted analogs interacted through the carbonyl group of the imide moiety. The oxygen atom of the phthalimide was less electronegative than the one of the methoxy group, thus making the H-bond accepting properties weaker and disadvantageous in comparison with that of the 4-methoxy-substituted analogs. Moreover, the H-bond formed by the latter group attracted the heteroaryl ring of the ligand closer to Phe719/686, thereby facilitating the π-π interaction in the hydrophobic clamp. The 1H-1,3-benzodiazole fragment accepted the H-bond from Tyr683 in the selectivity pocket. The interaction was secured by the optimal length of the linker—4 carbon atoms and resulted in favorable scoring function value −8.885 (glide gscore) (Figure 4). Both longer and shorter aliphatic chains decreased the inhibitory potential (see Table 1), enforcing suboptimal arrangement of the terminal moieties in the active site, which resulted in the loss of one of the aforementioned key interactions (e.g., in the case of compound 19) or decrease in scoring function value (−8.254 for compound 15).

2.4. Cytotoxicity

In the subsequent stage of the study, the safety profile of the most active compound, 18, was analyzed. Such analysis requires the exclusion of adverse effects of organ toxicity before proceeding to further in vivo studies. According to the guidelines for the study of biologically active molecules, cell lines are a good alternative to animal models at the initial stage of the drug cytotoxicity evaluation process. The two cell lines used in this study, namely, the SHSY-5Y and HepG2 cell lines are approved in vitro models, which can be used to obtain preliminary results regarding possible neuro- and hepato-toxicity [36].
The MTT assay, which measures the metabolic status of cells, was used to determine cytotoxicity. The results of the experiments clearly indicate that compound 18 is safe. Decreasing cell viability (HepG2/SHSY-5Y) is observed only at higher concentrations of compound 18, while the reference standard, doxorubicin (DOX), a well-described cytotoxic agent, demonstrated significantly decreased cell viability already at much lower concentrations (Figure 5).

2.5. Behavioral Evaluation

For further behavioral characterization, compound 18, with the highest PDE10A inhibitory activity and satisfactory cytotoxicity profile, was selected. Thus, the potential antipsychotic properties of compound 18 as an inhibitory effect on PDE10A in a behavioral animal model was determined. The obtained results revealed that treatment of mice with d-amphetamine (AMPH) significantly increased horizontal locomotor activity throughout the duration of the test. Papaverine dose-dependently antagonized this response at both tested doses of 40 and 60 mg/kg for 60 min. Compound 18 administered at a dose of 60 mg/kg decreased AMPH-induced hyperactivity, but only for the first 10 min after injection (Figure 6). The lower doses of compound 18, as well as papaverine, did not change the stimulating effect of AMPH (data not shown). To assess if a nonspecific suppression of locomotion contributes to the ability of the tested compounds to oppose AMPH-induced hyperactivity, the influence of these compounds on spontaneous locomotor activity was measured. The locomotor-suppressing effects were observed after the administration of papaverine (40 and 60 mg/kg) as well as 18 (60 mg/kg) (see Table S1 in Supporting Materials).
In summary, the suppression of AMPH-induced hyperlocomotion suggests antipsychotic-like properties of compound 18, as well as of papaverine. However, these effects are transient and may only reflect the decrease in spontaneous locomotor activity. Our findings are consistent with previous studies conducted with papaverine in rats [19,37], showing that the period of papaverine-induced suppression of spontaneous locomotor activity fully included time of reversal of hyperlocomotion produced by AMPH injection. Similar findings are reported by Schmidt et al. [38] for compound TP-10, which is a PDE-10 inhibitor with improved potency and selectivity. The aforementioned results suggest that antipsychotic-like properties of PDE10A inhibitors detected with locomotor-based paradigms need to be treated with caution, due to concurrent inhibition of spontaneous locomotor activity. Moreover, at this stage of our preliminary study, we can only speculate that the cause of compound 18′s transient effect on AMPH-induced hyperlocomotor activity may be a result of either rapid redistribution to the other brain structures or rapid metabolism. In order to overcome possible pharmacokinetic and metabolic stability problems, we plan to further optimize the leading structure of compound 18 and conduct extended in vitro and in vivo investigations.

3. Materials and Methods

3.1. Chemistry

All chemicals and solvents were purchased from commercial suppliers (Aldrich, Poznań, Poland and Chempur, Piekary Śląskie, Poland) and were used without further purification. Melting points were measured in open capillaries on an Electrothermal 9300 apparatus. Thin-layer chromatography (TLC) was run on Merck silica gel 60 F254 aluminium sheets (Merck; Darmstadt, Germany), using the following mixtures of solvents: (S1) dichloromethane (9)/methanol (0.3), (S2) dichloromethane (9)/methanol (0.7), (S3) dichloromethane (9)/methanol (1). Analytical HPLC was conducted on a Waters HPLC instrument with a Waters 485 Tunable Absorbance Detector UV, equipped with a Symetry column (C18, 3.5 µm, 4.6 × 30 mm) using a water/acetonitrile gradient with 0.1% trifluoroacetic acid (TFA) as the mobile phase at a flow rate of 5 mL/min.
Additionally, the liquid chromatography/mass spectrometry (LC/MS) analysis was performed on a Waters Acquity TQD system, with a Waters TQD quadrupole mass spectrometer with detection by UV (DAD) using an Acquity UPLC BEH C18 column (1.7 μm, 2.1 mm × 100 mm). A water/acetonitrile gradient with 0.1% TFA was used as a mobile phase at a flow rate of 0.3 mL/min. The UPLC/MS purity of the investigated compounds (3–23) proved to be over 98%. NMR spectra were recorded on a Varian Mercury 300 MHz spectrometer (Varian Inc., Palo Alto, CA, USA) using the solvent (CDCl3 or DMSO-d6) signal as an internal standard; chemical shifts are expressed in parts per million (ppm). Signal multiplets are represented by the following abbreviations: s (singlet), brs (broad singlet), d (doublet), t (triplet), m (multiplet).

3.1.1. General Procedure for Synthesis of 4-Methoxy-2-benzofuran-1,3-dione (2)

The 4-methoxy-2-benzofuran-1,3-dione was obtained from 1, according to a previously published procedure [32], with slight modifications. Briefly, 2,3-dimethylphenyl methyl ether (3.4 g, 25 mmol) was dissolved in water (98 mL) and tert-butanol (42 mL). After potassium permanganate (25 g, 160 mmol) was added, the reaction mixture was refluxed for 12 h. The resulting suspension was filtered over Celite, concentrated to 50 mL, acidified with 37% hydrochloric acid, and left standing overnight at room temperature. The 3-methoxybenzene-1,2-dicarboxylic acid crystallized as a white solid (4.34 g) and was refluxed for 4 h in anhydrous tetrahydrofuran (24 mL) with the addition of acetic anhydride (7 mL). Upon cooling to room temperature, the reaction mixture was concentrated in vacuo and the white solid was dried at 50 °C for 48 h, to afford 4-methoxy-2-benzofuran-1,3-dione (3.82, 97%). HPLC: Rt = 0.931, MS calcd for [M + H]+: C9H6O4 m/z: 178.14, found: 178.97; 1H-NMR (300 MHz, DMSO-d6) δ ppm 3.99 (s, 3 H) 7.59 (dd, J = 9.67, 7.91 Hz, 2 H) 7.90–7.97 (m, 1 H).

3.1.2. General Procedure for Synthesis of the Final Series of Compounds (3–23)

The final compounds (3–23) were obtained within two different pathways, described in procedures A and B. Procedure A (3–5, 9, 12, 16): a stoichiometric amount of 4-methoxy-2-benzofuran-1,3-dione (0.196 g, 1.1 mmol) and appropriate amine (1.1 mmol) in glacial acetic acid (2 mL) was refluxed for 48 h, with stirring. Upon cooling to room temperature, the reaction mixture was extracted with diethyl ether and concentrated in vacuum [39]. Procedure B (6–8, 10, 11, 13–15, 17–23): an amount of 4-methoxy-2-benzofuran-1,3-dione (0.178 g, 1.0 mmol), along with specific amounts of an appropriate amine (1.2 mmol), trimethylamine (0.28 mL, 2 mmol), and 4 Å molecular sieves were added in anhydrous toluene (4 mL) and the mixture was refluxed and stirred overnight. The reaction mixture was then filtered and the solvent was evaporated in vacuum [40]. All the final compounds (3–23) were purified by column chromatography using dichloromethane (9)/methanol (0.7) as eluent.

2-[2-(6,7-Dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (3)

Yellow powdery crystals. Yield: 42%; mp 108–109 °C; TLC: Rf = 0.44 (S1); HPLC: tR = 0.979; MS calcd for [M + H]+: C22H24N2O5 m/z: 396.17, found: 397.16; 1H-NMR (300 MHz, CDCl3-d) δ ppm 2.72–2.82 (m, 6 H) 3.62 (s, 2 H) 3.78–3.82 (s, 6 H) 3.84–3.90 (m, 2 H) 3.99 (s, 3 H) 6.52 (d, J = 16.16 Hz, 2 H) 7.12–7.20 (m, 1 H) 7.34–7.43 (m, 1 H) 7.61 (dd, J = 8.46, 7.44 Hz, 1 H).

2-[2-(3,4-Dihydroisoquinolin-2(1H)-yl)ethyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (4)

White powdery crystals. Yield: 75%; mp 157–158 °C; TLC: Rf = 0.27 (S1); HPLC: tR = 0.906; MS calcd for [M + H]+: C20H20N2O3 m/z: 336.38, found: 337.14; 1H-NMR (300 MHz, CDCl3-d) δ ppm 2.76–2.87 (m, 6 H) 3.70 (s, 2 H) 3.88 (t, J = 6.54 Hz, 2 H) 3.99 (s, 3 H) 6.96–7.02 (m, 1 H) 7.04–7.11 (m, 3 H) 7.15 (d, J = 8.46 Hz, 1 H) 7.39 (d, J = 7.44 Hz, 1 H) 7.61 (dd, J = 8.46, 7.18 Hz, 1 H).

2-[2-(Octahydroisoquinolin-2(1H)-yl)ethyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (5)

Creamy powdery crystals. Yield: 35%; mp 145–146 °C; TLC: Rf = 0.55 (S2); HPLC: tR = 1.124; MS calcd for [M + H]+: C20H26N2O3 m/z: 342.43, found: 343.19; 1H-NMR (300 MHz, CDCl3-d) δ ppm 0.79–1.00 (m, 3 H) 1.08–1.30 (m, 4 H) 1.45–1.71 (m, 6 H) 1.94–2.05 (m, 1 H) 2.57 (t, J = 7.05 Hz, 2 H) 2.79–2.86 (m, 1 H) 2.99 (d, J = 10.77 Hz, 1 H) 3.78 (t, J = 7.05 Hz, 2 H) 4.01 (s, 3 H) 7.18 (d, J = 8.21 Hz, 1 H) 7.42 (dd, J = 7.31, 0.64 Hz, 1 H) 7.64 (dd, J = 8.34, 7.31 Hz, 1 H).

2-[3-(6,7-Dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)propyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (6)

Creamy powdery crystals. Yield: 39%; mp 107–109 °C; TLC: Rf = 0.38 (S2); HPLC: tR = 1.018; MS calcd for [M + H]+: C23H26N2O5 m/z: 410.18, found: 411.18; 1H-NMR (300 MHz, CDCl3-d) δ ppm 1.92 (quin, J = 6.86 Hz, 2 H) 2.53–2.71 (m, 6 H) 3.45 (s, 2 H) 3.72–3.84 (m, 8 H) 3.96 (s, 3 H) 6.45 (d, J = 5.90 Hz, 2 H) 7.08 (d, J = 8.46 Hz, 1 H) 7.35 (d, J = 7.18 Hz, 1 H) 7.56 (dd, J = 8.34, 7.31 Hz, 1 H).

2-[3-(3,4-Dihydroisoquinolin-2(1H)-yl)propyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (7)

Yellow powdery crystals. Yield: 48%; mp 92–93 °C; TLC: Rf = 0.32 (S2); HPLC: tR = 1.006; MS calcd for [M + H]+: C21H22N2O3 m/z: 350.41, found: 351.36; 1H-NMR (300 MHz, CDCl3-d) δ ppm 1.94 (quin, J = 6.92 Hz, 2 H) 2.58 (t, J = 7.05 Hz, 2 H) 2.63–2.69 (m, 2 H) 2.74–2.81 (m, 2 H) 3.55 (s, 2 H) 3.77 (t, J = 6.92 Hz, 2 H) 3.96 (s, 7 H) 3.93–3.99 (m, 3 H) 6.92–7.12 (m, 5 H) 7.36 (dd, J = 7.18, 0.51 Hz, 1 H) 7.56 (dd, J = 8.46, 7.18 Hz, 1 H).

2-[3-(Octahydroisoquinolin-2(1H)-yl)propyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (8)

Creamy powdery crystals. Yield: 46%; mp 103–104 °C; TLC: Rf = 0.47 (S3); HPLC: tR = 1.161; MS calcd for [M + H]+: C21H28N2O3 m/z: 356.21, found: 357.21; 1H-NMR (300 MHz, CDCl3-d) δ ppm 0.78–0.93 (m, 3 H) 1.12–1.28 (m, 4 H) 1.43–1.71 (m, 6 H) 1.86–1.99 (m, 3 H) 2.48 (t, J = 7.44 Hz, 2 H) 2.82 (d, J = 9.23 Hz, 1 H) 3.00 (d, J = 11.03 Hz, 1 H) 3.69 (t, J = 6.80 Hz, 2 H) 4.00 (s, 3 H) 7.17 (d, J = 8.21 Hz, 1 H) 7.40 (dd, J = 7.31, 0.64 Hz, 1 H) 7.63 (dd, J = 8.46, 7.18 Hz, 1 H).

2-Benzyl-4-methoxy-1H-isoindole-1,3(2H)-dione (9)

White powdery crystals. Yield: 75%; mp 167–168 °C; TLC: Rf = 0.70 (S1); HPLC: tR = 1.435; MS calcd for [M + H]+: C16H13NO3 m/z: 267.09, found: 268.09; 1H-NMR (300 MHz, CDCl3-d) δ ppm 4.00 (s, 3 H) 4.81 (s, 2 H) 7.17 (d, J = 7.95 Hz, 1 H) 7.21–7.33 (m, 3 H) 7.40–7.46 (m, 3 H) 7.64 (dd, J = 8.46, 7.44 Hz, 1 H).

4-Methoxy-2-(pyridin-2-ylmethyl)-1H-isoindole-1,3(2H)-dione (10)

Creamy powdery crystals. Yield: 53%; mp 144–145 °C; TLC: Rf = 0.56 (S2); HPLC: tR = 0.755; MS calcd for [M + H]+: C15H12N2O3 m/z: 268.08, found: 269.09; 1H-NMR (300 MHz, CDCl3-d) δ ppm 4.00 (s, 3 H) 4.97 (s, 2 H) 7.10–7.17 (m, 1 H) 7.18–7.28 (m, 2 H) 7.46 (d, J = 7.95 Hz, 1 H) 7.56–7.69 (m, 2 H) 8.50 (dd, J = 4.87, 2.56 Hz, 1 H).

2-(1H-Benzimidazol-2-ylmethyl)-4-methoxy-1H-isoindole-1,3(2H)-dione (11)

Creamy powdery crystals. Yield: 30%; mp 239–240 °C; TLC: Rf = 0.34 (S3); HPLC: tR = 0.851; MS calcd for [M + H]+: C17H13N3O3 m/z: 307.30, found: 308.29; 1H-NMR (300 MHz, CDCl3-d) δ ppm 3.96 (s, 3 H) 5.14 (s, 2 H) 7.15 (d, J = 8.46 Hz, 1 H) 7.18–7.28 (m, 3 H) 7.41 (dd, J = 7.18, 0.51 Hz, 1 H) 7.63 (dd, J = 8.46, 7.44 Hz, 2 H).

4-Methoxy-2-(2-phenylethyl)-1H-isoindole-1,3(2H)-dione (12)

White powdery crystals. Yield: 43%; mp 123–124 °C; TLC: Rf = 0.73 (S1); HPLC: tR = 1.533; MS calcd for [M + H]+: C17H15NO3 m/z: 281.31, found: 282.05; 1H-NMR (300 MHz, CDCl3-d) δ ppm 2.93–3.00 (m, 2 H) 3.85–3.92 (m, 2 H) 4.01 (s, 3 H) 7.15–7.32 (m, 6 H) 7.38–7.42 (m, 1 H) 7.63 (dd, J = 8.46, 7.44 Hz, 1 H).

4-Methoxy-2-[2-(pyridin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione (13)

Creamy powdery crystals. Yield: 71%; mp 155–157 °C; TLC: Rf = 0.24 (S1); HPLC: tR = 0.797; MS calcd for [M + H]+: C16H14N2O3 m/z: 282.10, found: 283.11; 1H-NMR (300 MHz, CDCl3-d) δ ppm 3.12–3.19 (m, 2 H) 4.00 (s, 3 H) 4.06 (dd, J = 7.95, 6.67 Hz, 2 H) 7.08–7.20 (m, 3 H) 7.39 (dd, J = 7.31, 0.64 Hz, 1 H) 7.52–7.67 (m, 2 H) 8.49–8.53 (m, 1 H).

2-[2-(1H-Imidazol-4-yl)ethyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (14)

White powdery crystals. Yield: 30%; mp 227–228 °C; TLC: Rf = 0.14 (S2); HPLC: tR = 0.774; MS calcd for [M + H]+: C14H13N3O3 m/z: 271.27, found: 272.14; 1H-NMR (300 MHz, DMSO-d6) δ ppm 2.81–2.88 (m, 2 H) 3.74 (t, J = 6.80 Hz, 2 H) 3.92 (s, 3 H) 7.11 (s, 1 H) 7.33–7.47 (m, 2 H) 7.75 (dd, J = 8.46, 7.44 Hz, 1 H) 8.24 (d, J = 1.03 Hz, 1 H).

2-[2-(1H-Benzimidazol-2-yl)ethyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (15)

Creamy powdery crystals. Yield: 40%; mp 197–198 °C; TLC: Rf = 0.37 (S3); HPLC: tR = 0.871; MS calcd for [M + H]+: C18H15N3O3 m/z: 321.11, found: 322.31; 1H-NMR (300 MHz, DMSO-d6) δ ppm 3.10 (t, J = 7.33 Hz, 2 H) 3.89–3.98 (m, 5 H) 7.05–7.12 (m, 2 H) 7.37 (d, J = 7.62 Hz, 1 H) 7.39–7.47 (m, 3 H) 7.72–7.79 (m, 1 H).

4-Methoxy-2-(3-phenylpropyl)-1H-isoindole-1,3(2H)-dione (16)

White powdery crystals. Yield: 73%; mp 94–95 °C; TLC: Rf = 0.80 (S1); HPLC: tR = 1.572; MS calcd for [M + H]+: C18H17NO3 m/z: 295.21, found: 296.32; 1H-NMR (300 MHz, CDCl3-d) δ ppm 2.01 (dt, J = 14.68, 7.66 Hz, 2 H) 2.62–2.71 (m, 2 H) 3.71 (t, J = 7.18 Hz, 2 H) 4.01 (s, 3 H) 7.10–7.28 (m, 6 H) 7.41 (dd, J = 7.18, 0.51 Hz, 1 H) 7.64 (dd, J = 8.34, 7.31 Hz, 1 H).

2-[3-(1H-Benzimidazol-2-yl)propyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (17)

Creamy powdery crystals. Yield: 45%; mp 217–218 °C; TLC: Rf = 0.37 (S2); HPLC: tR = 0.910; MS calcd for [M + H]+: C19H17N3O3 m/z: 335.13, found: 336.34; 1H-NMR (300 MHz, CDCl3-d) δ ppm 2.12–2.22 (m, 2 H) 2.88–2.96 (m, 2 H) 3.71–3.80 (m, 2 H) 4.06 (s, 3 H) 7.18–7.28 (m, 4 H) 7.47 (dd, J = 7.31, 0.64 Hz, 1 H) 7.59 (dd, J = 5.51, 2.95 Hz, 1 H) 7.70 (dd, J = 8.46, 7.44 Hz, 1 H).

2-[4-(1H-Benzimidazol-2-yl)butyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (18)

Creamy powdery crystals. Yield: 45%; mp 69–70 °C; TLC: Rf = 0.28 (S2); HPLC: tR = 1.002; C20H19N3O3 m/z: 349.14, found: 350.17; 1H-NMR (300 MHz, CDCl3-d) δ ppm 1.67–1.92 (m, 4 H) 2.97 (t, J = 7.33 Hz, 2 H) 3.67 (t, J = 6.74 Hz, 2 H) 3.95 (s, 3 H) 7.12–7.20 (m, 3 H) 7.37 (d, J = 7.03 Hz, 1 H) 7. –7.55 (m, 2 H) 7.61 (t, J = 7.91 Hz, 1 H); 13C-NMR (75 MHz, CDCl3-d) δ ppm 25.26, 27.83, 28.27, 36.80, 56.28, 115.46, 117.15, 117.52, 122.08, 134.09, 136.21, 154.51, 156.59, 167.36, 168.25.

2-[5-(1H-Benzimidazol-2-yl)pentyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (19)

Creamy powdery crystals. Yield: 50%; mp 108–109 °C; TLC: Rf = 0.38 (S2); HPLC: tR = 1.072; MS calcd for [M + H]+: C21H21N3O3 m/z: 363.41, found: 364.12; 1H-NMR (300 MHz, CDCl3-d) δ ppm 1.32–1.46 (m, 2 H) 1.69 (quin, J = 7.18 Hz, 2 H) 1.90 (dt, J = 15.68, 7.69 Hz, 2 H) 2.91 (t, J = 7.33 Hz, 2 H) 3.64 (t, J = 7.03 Hz, 2 H) 4.00 (s, 3 H) 7.14–7.21 (m, 3 H) 7.41 (d, J = 7.03 Hz, 1 H) 7.53 (dd, J = 5.86, 2.93 Hz, 2 H) 7.64 (dd, J = 8.50, 7.33 Hz, 1 H); 13C-NMR (75 MHz, CDCl3-d) δ ppm 26.07, 27.13, 28.03, 29.00, 37.21, 56.28, 115.43, 117.24, 117.47, 122.02, 134.17, 136.15, 154.73, 156.57, 167.35, 168.23.

2-[2-(1H-Benzimidazol-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione (20)

White powdery crystals. Yield: 55%; mp 202–203 °C; TLC: Rf = 0.35 (S3); HPLC: tR = 0.827; MS calcd for [M + H]+: C17H13N3O2 m/z: 291.30, found: 292.06; 1H-NMR (300 MHz, DMSO-d6) δ ppm 3.14 (t, J = 7.33 Hz, 2 H) 4.00 (t, J = 7.33 Hz, 2 H) 7.06–7.12 (m, 2 H) 7.38–7.46 (m, 2 H) 7.78–7.87 (m, 4 H).

2-[3-(1H-Benzimidazol-2-yl)propyl]-1H-isoindole-1,3(2H)-dione (21)

White powdery crystals. Yield: 66%; mp 190–191 °C; TLC: Rf = 0.37 (S3); HPLC: tR = 0.869; MS calcd for [M + H]+: C18H15N3O2 m/z: 305.12, found: 306.10; 1H-NMR (300 MHz, CDCl3-d) δ ppm 2.15–2.27 (m, 2 H) 2.89–2.98 (m, 2 H) 3.74–3.83 (m, 2 H) 7.17–7.25 (m, 2 H) 7.53–7.61 (m, 2 H) 7.71–7.78 (m, 2 H) 7.82–7.89 (m, 2 H).

2-[4-(1H-Benzimidazol-2-yl)butyl]-1H-isoindole-1,3(2H)-dione (22)

Creamy powdery crystals. Yield: 43%; mp 179–180 °C; TLC: Rf = 0.28 (S2); HPLC: tR = 1.001; MS calcd for [M + H]+: C19H17N3O2 m/z: 319.13, found: 320.10; 1H-NMR (300 MHz, CDCl3-d) δ ppm 1.73–1.94 (m, 4 H) 3.00 (t, J = 7.33 Hz, 2 H) 3.75 (t, J = 6.74 Hz, 2 H) 7.16–7.23 (m, 2 H) 7.49–7.58 (m, 2 H) 7. –7.74 (m, 2 H) 7.79–7.86 (m, 2 H).

2-[5-(1H-Benzimidazol-2-yl)pentyl]-1H-isoindole-1,3(2H)-dione (23)

White powdery crystals. Yield: 59%; mp 168–169 °C; TLC: Rf = 0.30 (S2); HPLC: tR = 1.080; MS calcd for [M + H]+: C20H19N3O2 m/z: 333.15, found: 334.15; 1H-NMR (300 MHz, CDCl3-d) δ ppm 1.37–1.50 (m, 2 H) 1.74 (quin, J = 7.18 Hz, 2 H) 1.94 (dt, J = 15.39, 7.84 Hz, 2 H) 2.93 (t, J = 7.33 Hz, 2 H) 3.70 (t, J = 7.03 Hz, 2 H) 7.16–7.23 (m, 2 H) 7.54 (dd, J = 5.86, 2.93 Hz, 2 H) 7.67–7.74 (m, 2 H) 7.79–7.86 (m, 2 H).

3.2. Pharmacology

3.2.1. Protocols for Measuring PDE10A Inhibition In Vitro

Test and reference compounds were dissolved in dimethyl sulfoxide (DMSO) at a concentration of 1 mM and further diluted in assay buffer in order to obtain the final concentration of compounds: 10 µM and 3 µM, respectively. All reactions were carried out at 37 °C in white, half-area 96-well plates (Perkin Elmer, Waltham, MA, USA). The inhibition of PDE 10A enzyme was measured using the PDElight HTS cAMP phosphodiesterase assay kit (Lonza) according to the manufacturer’s recommendations. 2.5 U of PDE 10A enzyme was preincubated either with DMSO (vehicle control) or compound for 20 min before incubation with the substrate, cAMP (final concentration 1.25 µM), for 1 h. Then, PDELight AMP Detection Reagent was added. After 10 min incubation, the luminescence was measured in a multifunction plate reader (POLARstar Omega, BMG Labtech, Ortenberg, Germany). The results were expressed as percent of inhibition or, for the most active compounds selected, as the half maximal inhibitory concentration values.

3.2.2. Radioligand Binding Studies

Radioligand binding studies with serotonin 5-HT1A and 5-HT7 receptors were conducted according to methods previously described [41,42], whereas percent of inhibition of the control binding for 5-HT2A and D2 were performed according to protocols described online (www.cerep.fr). Briefly: binding experiments were conducted in 96-well microplates in a total final volume of 250 μL of appropriate buffers. Reaction mix included 50 μL solution of test compound, 50 μL of radioligand ([3H]8-OH-DPAT for 5-HT1A, and [3H]-LSD for 5-HT7, respectively) and 150 μL of diluted membranes (see description and Table S2 in Supporting Materials). Specific assay conditions for each receptor are described elsewhere [41]. The radioactivity was measured in a MicroBeta2 scintillation counter (PerkinElmer, USA). Each compound was tested in the assay as duplicate samples at 1 µM final concentrations. Results were expressed as percent inhibition of specific binding.

3.3. Molecular Modeling

The phosphodiesterase 10A model was developed on the basis of the experimental structure of the enzyme (PDB ID: 3SNI) [43]. The structure was refined using default settings in the Protein Preparation Wizard. Water molecules (except for the buried water molecules) and hetero groups, other than the ligand, were deleted and the whole system was minimized (OPLS3 force field). The model was tested extensively with docking studies involving PDE 10A inhibitors. The resulting consistent binding modes of the reference compounds of experimentally proven affinity were used as the basis for verifying the accuracy of the model that served as molecular target in docking studies. Ligand structures were optimized using the LigPrep tool. The Glide SP flexible docking procedure was carried out using default parameters. H-bond constraint, as well as centroid of a grid box, were located on Gln716.
Glide, LigPrep, and Protein Preparation Wizard were implemented in the Small-Molecule Drug Discovery Suite (Schrödinger, Inc., NY, USA), which was licensed to the Jagiellonian University Medical College.

3.4. Cytotoxicity

3.4.1. Cells Culture

The HePG2 human liver cancer cell-line, (ATCC® 59195™) and the SH-SY5Y human neuroblastoma cell-line (ATCC® CRL-2266™) were used in the study. The cells were cultured in standard conditions (37 °C, 5% CO2), in EMEM (HepG2 and SH-SY5Y), supplemented with 10% fetal bovine serum (FBS) (Gibco, Thermo Fisher Scientific, Waltham, MA. USA) and antibiotics (Lonza, Köln, Germany).

3.4.2. Cytotoxicity Analysis—MTT

The MTT assay was used to determine the cytotoxic effects of the analyzed compounds. Cells were seeded at a density of 2 × 104 in 96-well plates. Following overnight culture, cells were then treated with increasing concentrations of compound 18 (0.1–100 µM) and incubated for 24 h. Following cell exposure for 24 h, 10 µL MTT reagent (Sigma Aldrich) was added to each well and, after 3 h of incubation (37 °C, 5% CO2), the medium was aspirated and the formazan produced in the cells appeared as dark crystals in the bottom of the wells. Next, Crystal DMSO was added to each well. Then, the optical density (OD) of each well was determined at 570 nm on a plate-reader (Spectra iD3, Molecular Devices, San Jose, CA, USA). The number of metabolically active and living cells is directly proportional to the absorbance of the samples. The results are presented in Figure 5 as the percentage of control ± SEM. Doxorubicin was used as reference standard (cytotoxic agent).

3.5. In Vivo Studies

The experiments were performed on male CD-1 mice (in the accredited animal facility at the Jagiellonian University Medical College, Krakow, Poland), and mice were kept in groups of ten in Makrolon type 3 cages (dimensions 26.5 × 15 × 42 cm). The animals were kept in an environmentally controlled room (ambient temperature 22 ± 2 °C; relative humidity 50–60%; 12:12 light:dark cycle, lights on at 8:00). They were allowed to acclimatize with the environment for one week before commencement of the experiments. Standard laboratory food (Ssniff M-Z) and filtered water were freely available. All the experimental procedures were approved by the I Local Ethics Commission at the Jagiellonian University in Krakow (Approval Nos.: 125/2017, 123/2015, and 158/2017).
All the experiments were conducted in the light phase between 09.00 and 14.00 h. Each experimental group consisted of 7–10 animals per treatment dose. The animals were used only once.

3.5.1. d-Amphetamine-Induced Hyperlocomotor Activity in CD-1 Mice

Locomotor activity was recorded with an Opto M3 multi-channel activity monitor (MultiDevice Software v.1.3, Columbus Instruments, Columbus, OH, USA). The CD-1 mice were individually placed in plastic cages (22 × 12 × 13 cm) immediately after drug administration, and then ambulation was counted during 1 h with data recording every 10 min. The cages were cleaned up with 70% ethanol after each mouse.

3.5.2. Spontaneous Locomotor Activity in CD-1 Mice

Locomotor activity was recorded according to the method described above.

3.5.3. Drugs

The following drugs were used: d-amphetamine (sulfate, Sigma-Aldrich, Poznań, Poland), papaverine (hydrochloride, Sigma-Aldrich, Poznań, Poland), and tested compound 18. D-amphetamine and papaverine were dissolved in distilled water; the tested compound (18) was suspended in a 1% aqueous solution of Tween 80 immediately before administration. Papaverine and 18 were administered intraperitoneally (ip) and d-amphetamine subcutaneously (sc) just prior to the test starting. All compounds were injected at a volume of 10 mL/kg. Control animals received a vehicle injection according to the same schedule. Figure 6 shows only the doses at which the antipsychotic-like activity of AMPH, papaverine, and compound 18 were observed.

3.5.4. Statistics

All the data are presented as the mean ± SEM. The statistical significance of the results was evaluated by a one-way ANOVA, followed by a Bonferroni’s Comparison Test.

4. Conclusions

In this study, we describe the synthesis of a library of novel 4-methoxy-2,3-dihydro-1H-isoindole-1,3-dione derivatives with various aminoalkyl moieties, as potential inhibitors of PDE10A and serotonin receptor ligands. Among the synthesized and tested compounds, 1H-benzimidazole derivatives were identified as potent PDE10A inhibitors. Compound 18, the most potent PDE10 inhibitor (IC50 = 886 ± 0.017 nM) of the group, with drug-like properties as defined by Lipinski’s Rule of five, was selected for further pharmacological evaluation. In order to explain its inhibitory activity towards PDE10A, the binding mode of compound 18 was determined. Molecular modeling studies showed that H-bonds formed by the 4-methoxy group in the phthalimide moiety as well as the optimal length of the carbon linker are crucial for interactions with PDE10A. Preliminary in vitro neurotoxicity and hepatotoxicity studies revealed that the compound is safe and did not exhibit noteworthy cytotoxicity. Furthermore, significant antipsychotic properties of 2-[4-(1H-benzimidazol-2-yl)butyl]-4-methoxy-1H-isoindole-1,3(2H)-dione (compound 18) was identified in the d-AMPH-induced hyperlocomotor activity test in mice, but further pharmacological studies are needed to explain the mechanism underlying its antipsychotic activity. This study successfully identified a number of compounds with significant PDE10A inhibitory activity and provided further information into the molecular basis of their interaction with PDE10A.

Supplementary Materials

The following are available online, Figure S1: The spider graph of drug-like parameters of compound 18, Figure S2. Effects of papaverine and compound 18 on d-amphetamine-induced hyperlocomotor activity in CD-1 mice, Table S1: Effects of papaverine and compound 18 on spontaneous locomotor activity in CD-1 mice, Table S2. Detailed conditions of the in vitro binding assays for the 5-HT1A and 5-HT7 receptors and examples of NMR spectra.

Author Contributions

Conceptualization, A.C. and A.Z.; methodology, A.C., A.S., M.G.-L., and A.B.; software, A.B. and M.K.; validation, P.K., M.G.-L., and A.P.; formal analysis, B.T. and A.J.; investigation, A.C., A.B., A.P., and P.K.; data curation, A.C.; writing—original draft preparation, A.C., A.Z., A.B., P.K., and A.P.; writing—review and editing, A.C. and A.Z.; visualization, A.B., A.P., and M.G.-L.; supervision, M.K., M.P., E.P., and A.W.; project administration, A.C. and A.Z.; funding acquisition, M.P., A.C., and A.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This study was co-founded by National Science Centre (NSC) Poland grants (No. DEC-2012/07/B/NZ7/01173 and 2016/21/D/NZ7/01573) and Funds for Statutory Activity of Jagiellonian University Medical College (N42/DBS/000104, N42/DBS/0001784, N42/DBS/000020).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lima, L.M.; Castro, P.; Machado, A.L.; Fraga, C.A.M.; Lugnier, C.; De Moraes, V.L.G.; Barreiro, E.J. Synthesis and anti-inflammatory activity of phthalimide derivatives, designed as new thalidomide analogues. Bioorg. Med. Chem. 2002, 10, 3067–3073. [Google Scholar] [CrossRef]
  2. Van Derpoorten, K.; Balzarini, J.; De Clercq, E.; Poupaert, J.H. Anti-HIV activity of N-1-adamantyl-4-aminophthalimide. Biomed. Pharmacother. 1997, 51, 464–468. [Google Scholar] [CrossRef]
  3. Hall, I.H.; Wong, O.T.; Scovill, J.P. The cytotoxicity of N-pyridinyl and N-quinolinyl substituted derivatives of phthalimide and succinimide. Biomed. Pharmacother. 1995, 49, 251–258. [Google Scholar] [CrossRef]
  4. Kim, H.S.; Kim, Y.; Doddareddy, M.R.; Seo, S.H.; Rhim, H.; Tae, J.; Pae, A.N.; Choo, H.; Cho, Y.S. Design, synthesis, and biological evaluation of 1,3-dioxoisoindoline-5-carboxamide derivatives as T-type calcium channel blockers. Biorg. Med. Chem. Lett. 2007, 17, 476–481. [Google Scholar] [CrossRef] [PubMed]
  5. Gunduğdu, Ö.; Noma, S.A.A.; Taskin-Tok, T.; Ateş, B.; Kishali, N. Evaluation of xanthine oxidase inhibitor properties on isoindoline-1,3-dion derivatives and calculation of interaction mechanism. J. Mol. Struct. 2020, 1204, 127523. [Google Scholar] [CrossRef]
  6. Lamie, P.F.; Philoppes, J.N.; El-Gendy, A.O.; Rarova, L.; Gruz, J. Design, synthesis and evaluation of novel phthalimide derivatives as in vitro anti-microbial, anti-oxidant and anti-inflammatory agents. Molecules 2015, 20, 16620–16642. [Google Scholar] [CrossRef] [Green Version]
  7. Bailleux, V.; Vallée, L.; Nuyts, J.P.; Vamecq, J. Original anticonvulsant properties of two N-phenylphthalimide derivatives. Biomed. Pharmacother. 1993, 47, 463–464. [Google Scholar] [CrossRef]
  8. Atack, J.R. The benzodiazepine binding site of GABAA receptors as a target for the development of novel anxiolytics. Expert Opin. Investig. Drugs 2005, 14, 601–618. [Google Scholar] [CrossRef]
  9. Bajda, M.; Więckowska, A.; Hebda, M.; Guzior, N.; Sotriffer, C.; Malawska, B. Structure-Based Search for New Inhibitors of Cholinesterases. Int. J. Mol. Sci. 2013, 14, 5608–5632. [Google Scholar] [CrossRef] [Green Version]
  10. Panek, D.; Wiȩckowska, A.; Pasieka, A.; Godyń, J.; Jończyk, J.; Bajda, M.; Knez, D.; Gobec, S.; Malawska, B. Design, synthesis, and biological evaluation of 2-(benzylamino-2-hydroxyalkyl)isoindoline-1,3-diones derivatives as potential disease-modifying multifunctional anti-Alzheimer agents. Molecules 2018, 23, 347. [Google Scholar] [CrossRef] [Green Version]
  11. Mohammadi-Farani, A.; Abdi, N.; Moradi, A.; Aliabadi, A. 2-(2-(4-Benzoylpiperazin-1-yl)ethyl)isoindoline-1,3-dione derivatives: Synthesis, docking and acetylcholinesterase inhibitory evaluation as anti-alzheimer agents. Iran. J. Basic Med. Sci. 2017, 20, 59–64. [Google Scholar] [CrossRef] [PubMed]
  12. Foong, J.P.P.; Bornstein, J.C. 5-HT antagonists NAN-190 and SB 269970 block α2-adrenoceptors in the guinea pig. Neuroreport 2009, 20, 325–330. [Google Scholar] [CrossRef] [PubMed]
  13. Huttunen, M. The evolution of the serotonin-dopamine antagonist concept. J. Clin. Psychopharmacol. 1995, 15, 4S–10S. [Google Scholar] [CrossRef] [PubMed]
  14. Meltzer, H.Y.; Massey, B.W. The role of serotonin receptors in the action of atypical antipsychotic drugs. Curr. Opin. Pharmacol. 2011, 11, 59–67. [Google Scholar] [CrossRef]
  15. Stahl, S.M. Dopamine system stabilizers, aripiprazole, and the next generation of antipsychotics, part 1: “Goldilocks” actions at dopamine receptors. J. Clin. Psychiatry 2001, 62, 841–842. [Google Scholar] [CrossRef]
  16. Mailman, R.; Murthy, V. Third Generation Antipsychotic Drugs: Partial Agonism or Receptor Functional Selectivity? Curr. Pharm. Des. 2010, 16, 488–501. [Google Scholar] [CrossRef] [Green Version]
  17. McCreary, A.; Newman-Tancredi, A. Serotonin 5-HT1A Receptors and Antipsychotics - An Update in Light of New Concepts and Drugs. Curr. Pharm. Des. 2015, 21, 3725–3731. [Google Scholar] [CrossRef]
  18. Kusumi, I.; Boku, S.; Takahashi, Y. Psychopharmacology of atypical antipsychotic drugs: From the receptor binding profile to neuroprotection and neurogenesis. Psychiatry Clin. Neurosci. 2015, 69, 243–258. [Google Scholar] [CrossRef]
  19. Siuciak, J.A.; Strick, C.A. Treating neuropsychiatric disorders with PDE10A inhibitors. Drug Discov. Today Ther. Strateg. 2006, 3, 527–532. [Google Scholar] [CrossRef]
  20. Chappie, T.A.; Helal, C.J.; Hou, X. Current landscape of phosphodiesterase 10A (PDE10A) inhibition. J. Med. Chem. 2012, 55, 7299–7331. [Google Scholar] [CrossRef]
  21. Zagorska, A.; Partyka, A.; Bucki, A.; Gawalskax, A.; Czopek, A.; Pawlowski, M. Phosphodiesterase 10 Inhibitors—Novel Perspectives for Psychiatric and Neurodegenerative Drug Discovery. Curr. Med. Chem. 2018, 25, 3455–3481. [Google Scholar] [CrossRef] [PubMed]
  22. Suzuki, K.; Harada, A.; Suzuki, H.; Capuani, C.; Ugolini, A.; Corsi, M.; Kimura, H. Combined treatment with a selective PDE10A inhibitor TAK-063 and either haloperidol or olanzapine at subeffective doses produces potent antipsychotic-like effects without affecting plasma prolactin levels and cataleptic responses in rodents. Pharmacol. Res. Perspect. 2018, 6. [Google Scholar] [CrossRef] [PubMed]
  23. Proschak, E.; Stark, H.; Merk, D. Polypharmacology by Design: A Medicinal Chemist’s Perspective on Multitargeting Compounds. J. Med. Chem. 2019, 62, 420–444. [Google Scholar] [CrossRef] [PubMed]
  24. Kondej, M.; Stępnicki, P.; Kaczor, A.A. Multi-target approach for drug discovery against schizophrenia. Int. J. Mol. Sci. 2018, 19, 3105. [Google Scholar] [CrossRef] [Green Version]
  25. Christopher, D.C.; BUNDA, J.L.; Broc, A.F.; SHIPE, W. Pyrimidinones as AS PDE10 Inhibitors. U.S. Patent WO2010138585, 12 February 2010. [Google Scholar]
  26. Medina, R.A.; Sallander, J.; Benhamú, B.; Porras, E.; Campillo, M.; Pardo, L.; López-Rodríguez, M.L. Synthesis of new serotonin 5-HT7 receptor ligands. Determinants of 5-ht7/5-ht1a receptor selectivity. J. Med. Chem. 2009, 52, 2384–2392. [Google Scholar] [CrossRef]
  27. Zagórska, A.; Bucki, A.; Kołaczkowski, M.; Siwek, A.; Głuch-Lutwin, M.; Starowicz, G.; Kazek, G.; Partyka, A.; Wesołowska, A.; Słoczyńska, K.; et al. Synthesis and biological evaluation of 2-fluoro and 3-trifluoromethyl-phenyl-piperazinylalkyl derivatives of 1H-imidazo [2,1-f]purine-2,4(3H,8H)-dione as potential antidepressant agents. J. Enzyme Inhib. Med. Chem. 2016, 31, 10–24. [Google Scholar] [CrossRef] [Green Version]
  28. Zajdel, P.; Marciniec, K.; Maślankiewicz, A.; Satała, G.; Duszyńska, B.; Bojarski, A.J.; Partyka, A.; Jastrzbska-Wisek, M.; Wróbel, D.; Wesołowska, A.; et al. Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT 1A/5-HT 2A/5-HT 7 and D 2/D 3/D 4-Agents: The synthesis and pharmacological evaluation. Bioorg. Med. Chem. 2012, 20, 1545–1556. [Google Scholar] [CrossRef]
  29. Kehler, J.; Ritzen, A.; Langgård, M.; Petersen, S.L.; Farah, M.M.; Bundgaard, C.; Christoffersen, C.T.; Nielsen, J.; Kilburn, J.P. Triazoloquinazolines as a novel class of phosphodiesterase 10A (PDE10A) inhibitors. Bioorg. Med. Chem. Lett. 2011, 21, 3738–3742. [Google Scholar] [CrossRef]
  30. Chino, A.; Masuda, N.; Amano, Y.; Honbou, K.; Mihara, T.; Yamazaki, M.; Tomishima, M. Novel benzimidazole derivatives as phosphodiesterase 10A (PDE10A) inhibitors with improved metabolic stability. Bioorg. Med. Chem. 2014, 22, 3515–3526. [Google Scholar] [CrossRef]
  31. Bieszczad, B.; Barbasiewicz, M. The Key Role of the Nonchelating Conformation of the Benzylidene Ligand on the Formation and Initiation of Hoveyda-Grubbs Metathesis Catalysts. Chem. A Eur. J. 2015, 21, 10322–10325. [Google Scholar] [CrossRef] [PubMed]
  32. Gallagher, N.J.; Lyons, J.F.; Thompson, N.T.; Yyle, S.M.; Stephen, M.M.; Christopher, W. Pharmaceutical Combinations. U.S. Patent WO2008044041, 17 April 2008. [Google Scholar]
  33. Vooturi, S.K.; Firestine, S.M. Solution-phase parallel synthesis of novel membrane-targeted antibiotics. J. Comb. Chem. 2010, 12, 151–160. [Google Scholar] [CrossRef]
  34. Elshihawy, H.; Helal, M.A.; Said, M.; Hammad, M.A. Design, synthesis, and enzyme kinetics of novel benzimidazole and quinoxaline derivatives as methionine synthase inhibitors. Bioorg. Med. Chem. 2014, 22, 550–558. [Google Scholar] [CrossRef] [PubMed]
  35. Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 1997, 23, 3–25. [Google Scholar] [CrossRef]
  36. Venkataramana, M.; Chandra Nayaka, S.; Anand, T.; Rajesh, R.; Aiyaz, M.; Divakara, S.T.; Murali, H.S.; Prakash, H.S.; Lakshmana Rao, P.V. Zearalenone induced toxicity in SHSY-5Y cells: The role of oxidative stress evidenced by N-acetyl cysteine. Food Chem. Toxicol. 2014, 65, 335–342. [Google Scholar] [CrossRef] [PubMed]
  37. Weber, M.; Breier, M.; Ko, D.; Thangaraj, N.; Marzan, D.E.; Swerdlow, N.R. Evaluating the antipsychotic profile of the preferential PDE10A inhibitor, papaverine. Psychopharmacology 2009, 203, 723–735. [Google Scholar] [CrossRef] [Green Version]
  38. Schmidt, C.J.; Chapin, D.S.; Cianfrogna, J.; Corman, M.L.; Hajos, M.; Harms, J.F.; Hoffman, W.E.; Lebel, L.A.; McCarthy, S.A.; Nelson, F.R.; et al. Preclinical characterization of selective phosphodiesterase 10A inhibitors: A new therapeutic approach to the treatment of schizophrenia. J. Pharmacol. Exp. Ther. 2008, 325, 681–690. [Google Scholar] [CrossRef] [Green Version]
  39. Kurys, B.E.; Fink, D.M.; Fink, D.M.; Freed, B.S.; Merriman, G.H. N-(pyridinylamino)isoindolines and Related Compounds. U.S. Patent No 6,004,977, 29 October 1997. [Google Scholar]
  40. Dhanya, R.P.; Sidique, S.; Sheffler, D.J.; Nickols, H.H.; Herath, A.; Yang, L.; Dahl, R.; Ardecky, R.; Semenova, S.; Markou, A.; et al. Design and synthesis of an orally active metabotropic glutamate receptor subtype-2 (mGluR2) positive allosteric modulator (PAM) that decreases cocaine self-administration in rats. J. Med. Chem. 2011, 54, 342–353. [Google Scholar] [CrossRef] [Green Version]
  41. Czopek, A.; Zagorska, A.; Kolaczkowski, M.; Bucki, A.; Gryzlo, B.; Rychtyk, J.; Pawlowsk, M.; Siwek, A.; Satala, G.; Bojarski, A.; et al. New Spirohydanoin Derivatives-Synthesis, Pharmacological Evaluation, and Molecular Modeling Study. Acta Pol. Pharm. 2016, 73, 1545–1554. [Google Scholar]
  42. Intagliata, S.; Modica, M.N.; Pittalà, V.; Salerno, L.; Siracusa, M.A.; Cagnotto, A.; Salmona, M.; Kurczab, R.; Romeo, G. New N- and O-arylpiperazinylalkyl pyrimidines and 2-methylquinazolines derivatives as 5-HT7and 5-HT1Areceptor ligands: Synthesis, structure-activity relationships, and molecular modeling studies. Bioorg. Med. Chem. 2017, 25, 1250–1259. [Google Scholar] [CrossRef] [PubMed]
  43. Malamas, M.S.; Stange, H.; Schindler, R.; Lankau, H.J.; Grunwald, C.; Langen, B.; Egerland, U.; Hage, T.; Ni, Y.; Erdei, J.; et al. Novel triazines as potent and selective phosphodiesterase 10A inhibitors. Bioorg. Med. Chem. Lett. 2012, 22, 5876–5884. [Google Scholar] [CrossRef] [PubMed]
Sample Availability: Samples of the compounds 3–23 are available from the authors.
Molecules 25 03868 g001 550
Figure 1. Examples of phthalimide derivatives with various biological activity [1,2,3,4,5,6,7,8,9,10,11,12].
Figure 1. Examples of phthalimide derivatives with various biological activity [1,2,3,4,5,6,7,8,9,10,11,12].
Molecules 25 03868 g001
Molecules 25 03868 g002 550
Figure 2. General structure of novel compounds 3–23, designed based on potent phosphodiesterase 10A (PDE10) inhibitors and active serotonin receptor ligands [20,25,26,28,29,30]. The phthalimide cores and amine groups are highlighted in blue and green, respectively.
Figure 2. General structure of novel compounds 3–23, designed based on potent phosphodiesterase 10A (PDE10) inhibitors and active serotonin receptor ligands [20,25,26,28,29,30]. The phthalimide cores and amine groups are highlighted in blue and green, respectively.
Molecules 25 03868 g002
Molecules 25 03868 sch001 550
Scheme 1. Reagents and conditions of the chemical synthesis route: (a) CH3I, K2CO3, DMF, 75 °C, 12 h; (b) KMnO4, H2O/tBuOH, reflux, 12 h; AcOH, THF, reflux, 4 h; (c1) appropriate amine, AcOH, reflux, 48 h; (c2) appropriate amine, TEA, 4Å molecular sieves, toluene, reflux, 16 h. 2,3-Dimethylphenol and phthalic anhydride were commercially available.
Scheme 1. Reagents and conditions of the chemical synthesis route: (a) CH3I, K2CO3, DMF, 75 °C, 12 h; (b) KMnO4, H2O/tBuOH, reflux, 12 h; AcOH, THF, reflux, 4 h; (c1) appropriate amine, AcOH, reflux, 48 h; (c2) appropriate amine, TEA, 4Å molecular sieves, toluene, reflux, 16 h. 2,3-Dimethylphenol and phthalic anhydride were commercially available.
Molecules 25 03868 sch001
Molecules 25 03868 sch002 550
Scheme 2. Reagents and conditions of the chemical substitution routes: (a) appropriate amine, N-bromoalkylphthalimide, K2CO3, MeCN, reflux, 12 h; 40% CH3NH2, 20% NaOH, room temperature, 2 h; (b) appropriate amino acid, 1,2-phenylendiamine, 4N HCl, microwave heating, 100 °C, 40 min [33,34].
Scheme 2. Reagents and conditions of the chemical substitution routes: (a) appropriate amine, N-bromoalkylphthalimide, K2CO3, MeCN, reflux, 12 h; 40% CH3NH2, 20% NaOH, room temperature, 2 h; (b) appropriate amino acid, 1,2-phenylendiamine, 4N HCl, microwave heating, 100 °C, 40 min [33,34].
Molecules 25 03868 sch002
Molecules 25 03868 g003 550
Figure 3. Dose-response curve of the most active compounds 15, 17, 18, 19, 22 and reference drug-papaverine on PDE 10A activity measured by the luminescence method.
Figure 3. Dose-response curve of the most active compounds 15, 17, 18, 19, 22 and reference drug-papaverine on PDE 10A activity measured by the luminescence method.
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Molecules 25 03868 g004 550
Figure 4. The predicted binding mode of compound 18 in the active site of phosphodiesterase 10A (PDB ID: 3SNI). Crucial interactions of the compound in the catalytic site with Gln716 and Phe719, as well as its positioning in the selectivity pocket (Tyr683) predict inhibitory activity of the series of rationally-designed derivatives synthesized in this study. Amino acid residues engaged in ligand binding (within 4 Å from the ligand atoms) are displayed as sticks, whereas crucial residues, e.g., forming H-bonds (dotted yellow lines) or π-π stacking (dotted cyan lines), are represented as thick sticks.
Figure 4. The predicted binding mode of compound 18 in the active site of phosphodiesterase 10A (PDB ID: 3SNI). Crucial interactions of the compound in the catalytic site with Gln716 and Phe719, as well as its positioning in the selectivity pocket (Tyr683) predict inhibitory activity of the series of rationally-designed derivatives synthesized in this study. Amino acid residues engaged in ligand binding (within 4 Å from the ligand atoms) are displayed as sticks, whereas crucial residues, e.g., forming H-bonds (dotted yellow lines) or π-π stacking (dotted cyan lines), are represented as thick sticks.
Molecules 25 03868 g004
Molecules 25 03868 g005 550
Figure 5. Viability of SHSY-5Y and HepG2 cells treated with compound 18 in the MTT test; doxorubicin (DOX) was used as reference control. (A): compound 18 (SHSY-5Y), (B): DOX (SHSY-5Y), (C): compound 18 (HepG2), (D): DOX (HepG2). Graphs represent the viability of cells as a % of control (non-treated cells). Values represent means ± SEM of three independent experiments. Statistical significance (*) vs. control was determined using the Mann-Whitney test, p < 0.05.
Figure 5. Viability of SHSY-5Y and HepG2 cells treated with compound 18 in the MTT test; doxorubicin (DOX) was used as reference control. (A): compound 18 (SHSY-5Y), (B): DOX (SHSY-5Y), (C): compound 18 (HepG2), (D): DOX (HepG2). Graphs represent the viability of cells as a % of control (non-treated cells). Values represent means ± SEM of three independent experiments. Statistical significance (*) vs. control was determined using the Mann-Whitney test, p < 0.05.
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Molecules 25 03868 g006 550
Figure 6. Effects of papaverine and compound 18 on d-amphetamine-induced hyperlocomotor activity in CD-1 mice. Data are expressed as the mean of the number of movements recorded after 10, 20, 30, and 60 min of the papaverine-treated groups (at doses of 40 and 60 mg, respectively) and the compound 18-treated group (at a dose of 60 mg) ± S.E.M. * p < 0.05, ** p < 0.01, **** p < 0.0001, versus the respective vehicle-treated group, ^^ p < 0.01, ^^^ p < 0.001, ^^^^ p < 0.0001, and versus the respective AMPH-treated group (one way ANOVA followed by Bonferroni’s post-hoc test). AMPH-d-amphetamine.
Figure 6. Effects of papaverine and compound 18 on d-amphetamine-induced hyperlocomotor activity in CD-1 mice. Data are expressed as the mean of the number of movements recorded after 10, 20, 30, and 60 min of the papaverine-treated groups (at doses of 40 and 60 mg, respectively) and the compound 18-treated group (at a dose of 60 mg) ± S.E.M. * p < 0.05, ** p < 0.01, **** p < 0.0001, versus the respective vehicle-treated group, ^^ p < 0.01, ^^^ p < 0.001, ^^^^ p < 0.0001, and versus the respective AMPH-treated group (one way ANOVA followed by Bonferroni’s post-hoc test). AMPH-d-amphetamine.
Molecules 25 03868 g006
Table
Table 1. Screening data from a luminescence PDE inhibition assay and a radioligand binding assay for 5-HT1A and 5-HT7 (%) of 4-methoxy-1H-isoindole-1,3(2H)-dione and 1H-isoindole-1,3(2H)-dione derivatives displaying phosphodiesterase 10A inhibitory activity and binding affinity for serotonin 5-HT1A and 5-HT7 receptors as well as selected IC50 values of the most active compounds for PDE10A.
Table 1. Screening data from a luminescence PDE inhibition assay and a radioligand binding assay for 5-HT1A and 5-HT7 (%) of 4-methoxy-1H-isoindole-1,3(2H)-dione and 1H-isoindole-1,3(2H)-dione derivatives displaying phosphodiesterase 10A inhibitory activity and binding affinity for serotonin 5-HT1A and 5-HT7 receptors as well as selected IC50 values of the most active compounds for PDE10A.
CompdRnPDE10A [%] 1IC50 PDE10A [µM] ± SEM 35-HT1A5-HT7
10µM3µM1 µM 2 ± SEM 3
Molecules 25 03868 i0013A200-27 ± 30 ± 0
4B200-12 ± 40 ± 0
5C200-25 ± 30 ± 0
6A300-32 ± 40 ± 0
7B31918-33 ± 251 ± 2
8C377-28 ± 30 ± 0
9D100-6 ± 20 ± 0
10E100-10 ± 10 ± 2
11F1157-39 ± 30 ± 1
12D2105-13 ± 20 ± 0
13E200-59 ± 40 ± 2
14G200-21 ± 10 ± 0
15F270406.710 ± 0.19544 ± 50 ± 3
16D31311-32 ± 314 ± 0
17F386731.001 ± 0.00916 ± 510 ± 3
18 4F492790.886 ± 0.01728 ± 33 ± 1
19F575524.305 ± 0.36528 ± 26 ± 0
Molecules 25 03868 i00220F210-26 ± 236 ± 0
21F34516-27 ± 214 ± 2
22F473475.645 ± 0.49520 ± 315 ± 2
23F55826-48 ± 334 ± 2
Papaverine75 545.755 ± 0.055--
Methiothiepin---100 ± 099 ± 1
DMSO00---
1 The percentage of inhibition was calculated respective to vehicle control (DMSO); A: 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline, B: 1,2,3,4-tetrahydroisoquinoline, C: decahydroisoquinoline, D: phenyl, E: 2-pyridine, F: 2-benzimidazole, G: 1H-imidazole; 2 % of control specific binding; 3 SEM of three independent experiments performed in duplicate; 4 Additionally, the percent of inhibition of the control binding for 5-HT2A and D2 for compound 18 were evaluated. The screening results were 8.8% and 0%, for 5-HT2A and for D2 receptors, respectively, at a concentration of 1 µM. The screening tests for 5-HT2A and D2 receptors were performed in the CEREP Laboratories, France—Eurofins Scientific (www.cerep.fr).

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Czopek, A.; Partyka, A.; Bucki, A.; Pawłowski, M.; Kołaczkowski, M.; Siwek, A.; Głuch-Lutwin, M.; Koczurkiewicz, P.; Pękala, E.; Jaromin, A.; et al. Impact of N-Alkylamino Substituents on Serotonin Receptor (5-HTR) Affinity and Phosphodiesterase 10A (PDE10A) Inhibition of Isoindole-1,3-dione Derivatives. Molecules 2020, 25, 3868. https://doi.org/10.3390/molecules25173868

AMA Style

Czopek A, Partyka A, Bucki A, Pawłowski M, Kołaczkowski M, Siwek A, Głuch-Lutwin M, Koczurkiewicz P, Pękala E, Jaromin A, et al. Impact of N-Alkylamino Substituents on Serotonin Receptor (5-HTR) Affinity and Phosphodiesterase 10A (PDE10A) Inhibition of Isoindole-1,3-dione Derivatives. Molecules. 2020; 25(17):3868. https://doi.org/10.3390/molecules25173868

Chicago/Turabian Style

Czopek, Anna, Anna Partyka, Adam Bucki, Maciej Pawłowski, Marcin Kołaczkowski, Agata Siwek, Monika Głuch-Lutwin, Paulina Koczurkiewicz, Elżbieta Pękala, Anna Jaromin, and et al. 2020. "Impact of N-Alkylamino Substituents on Serotonin Receptor (5-HTR) Affinity and Phosphodiesterase 10A (PDE10A) Inhibition of Isoindole-1,3-dione Derivatives" Molecules 25, no. 17: 3868. https://doi.org/10.3390/molecules25173868

APA Style

Czopek, A., Partyka, A., Bucki, A., Pawłowski, M., Kołaczkowski, M., Siwek, A., Głuch-Lutwin, M., Koczurkiewicz, P., Pękala, E., Jaromin, A., Tyliszczak, B., Wesołowska, A., & Zagórska, A. (2020). Impact of N-Alkylamino Substituents on Serotonin Receptor (5-HTR) Affinity and Phosphodiesterase 10A (PDE10A) Inhibition of Isoindole-1,3-dione Derivatives. Molecules, 25(17), 3868. https://doi.org/10.3390/molecules25173868

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