Design and Synthesis of New Benzothiazole Compounds as Selective hMAO-B Inhibitors

In the current work a new class of novel benzothiazole-hydrazone derivatives was designed and synthesized as hMAO-B inhibitors. Structures of the obtained compounds (3a–3j) were characterized by IR, 1H-NMR, 13C-NMR, and HRMS spectroscopic methods. The inhibitory activity of compounds (3a–3j) against hMAO-A and hMAO-B enzymes was evaluated by using an in vitro fluorometric method. According to activity results, some of the synthesized compounds displayed selective and significant hMAO-B enzyme inhibitor activity. Compound 3e was the most active derivative in the series with an IC50 value of 0.060 µM. Furthermore, cytotoxicity of compound 3e was investigated and found to be non-cytotoxic. Absorption, distribution, metabolism, and excretion (ADME) and blood-brain barrier (BBB) permeability predictions were performed for all compounds. It was determined that these compounds may have a good pharmacokinetic profiles. Bınding modes between the most active compound 3e and the hMAO-B enzyme were analyzed by docking studies. It was observed that there is a strong interaction between compound 3e and enzyme active site.


Introduction
Monoamine oxidase (MAO) is an important flavoenzyme existing in the outer mitochondrial membrane of neuronal, glial, and many other cells, and is responsible for the oxidative deamination of amines in the brain, as well as peripheral tissues to regulate their level. MAO exists in two isoforms: namely, MAO-A and MAO-B, which have been identified based on their amino acid sequences, three-dimensional structure, substrate preference, and inhibitor selectivity [1,2]. Monoamine oxidase enzyme inhibitors (MAOIs), in general, have inhibitory activity against both of MAO-A and MAO-B [3]. However, researchers have focused to develop a selective MAOI to avoid food-drug and drug-drug interactions of non-selective MAOIs, as well as their side effects [4,5]. Selective inhibition of MAO-A, which specifically metabolizes serotonin, norepinephrine, and tyramine is effective in the depression treatment, while selective inhibition of MAO-B, which specifically degrades dopamine, is effective in the treatment of Parkinson's disease (PD) [5,6]. It is known that PD is a neurodegenerative disorder characterized by progressive loss of dopaminergic neurons in the substantia nigra pars compacta [7,8]. Therefore, in the treatment of PD, it has been targeted to increase dopaminergic activity through dopamine supplementation, decrease dopamine breakdown, or activate dopaminergic receptors [9,10]. MAO-B inhibitors are useful in the treatment of the early stages of PD and, later, as an adjunct to activity through dopamine supplementation, decrease dopamine breakdown, or activate dopaminergic receptors [9,10]. MAO-B inhibitors are useful in the treatment of the early stages of PD and, later, as an adjunct to other drug therapies [11,12]. MAO-B inhibitors have a good safety profile. They also possess an effect in the improvement of motor symptoms and, thus, delay the need for levodopa in the treatment of PD. Furthermore, studies have indicated that MAO-B inhibitors have a neuroprotective effect against neurodegeneration [13]. Therefore, the development of novel, selective, and reversible MAO-B inhibitors with fewer side effects is still necessary.
In terms of crystal structure, the hMAO-B enzyme possesses two cavities connected by the amino acid ILE199. The entrance cavity has a volume of 290 Å 3 and, possesses a hydrophobic character. The second cavity, with a volume of 390 Å 3 , contains the substrate binding site in which coenzyme FAD is located. Crystallographic data of the substrate cavity has displayed that the amino acid side chains, coating the cavity, are very hydrophobic and favorable to interact with an amine moiety. The FAD and two closely-parallel tyrosyl residues (398 and 435) constitute an 'aromatic cage' [14,15].
The previous studies have shown that benzothiazole derivatives have potent and selective inhibitory activity against the MAO-B enzyme [16][17][18][19]. In these studies, a similar design strategy of target compounds has been followed. Synthesized compounds have been designed to possess three essential parts: (i) a 2-mercapto-or amino-substituted benzothiazole core; (ii) an aromatic or heteroaromatic ring sytem; and (iii) a linker, bearing H-acceptor and/or H-donor nitrogens, between the benzothiazole core and (hetero)aromatic ring system ( Figure 1). Docking analyses have revealed that the benzothiazole core binds within the substrate cavity space, the heteroaryl residue of the molecules is located in the entrance cavity space of MAO-B enzyme, and nitrogen atoms of the linker are stabilized by hydrogen bond interactions with amino acid residues of the enzyme active site [16,18]. In addition to benzothiazole derivatives, hydrazine-based compounds, which bear an azomethine -NHN=CH-functional group, have displayed a selective inhibitory activity against 20,21]. The C=N double bond of hydrazone and the terminal nitrogen atom significantly influence the physical and chemical properties. The C-atom in hydrazone has both electrophilic and nucleophilic properties [22]. Due to MAO-B inhibitory potency and the physicochemical character of the hydrazone moiety, it has been preferred as a linker between the benzothiazole core and the (hetero)aromatic ring system in the design of target compounds as outlined in Figure 1.
In light of the above information, new benzothiazole derivatives consisting of a hydrazone moiety were synthesized as novel, selective, and potent MAO-B inhibitory agents. Additionally, we aimed to determine the in vitro cytotoxic effect of compounds in case they had significant enzyme inhibitory activity.

Chemistry
The compounds 3a-3j were synthesized as summarized in Scheme 1. Initially, O-ethyl S-(5-methoxybenzothiazol-2-yl) (1) carbonothioate was prepared by a reaction of 2-mercapto-5-methoxybenzothiazole and ethyl 2-chloroacetate in the presence of potassium carbonate. Then, the reaction of compound 1 and excess of hydrazine hydrate gave S-(5-methoxybenzothiazol-2-yl) hydrazinecarbothioate (2). In the last step, compounds 3a-3j were prepared via the reaction of compound 2 and an appropriate heterocyclic aldehyde. The structure of the synthesized compounds were elucidated by IR, 1 H-NMR, 13 C-NMR, and HRMS analysis. In the IR spectra, the N-H bond of hydrazide was observed over 3061 cm −1 . Carbonyl and imine groups had bands at 1654-1699 cm −1 and 1307-1392 cm −1 , respectively. In the 1 H-NMR spectra, protons of methoxy and methylene, neighboring to carbonyl, gave singlet peaks at 3.81-3.82 ppm and 4.55-4.70 ppm, respectively. The benzimidazole H 5 proton gave a doublet peak at 6.99 ppm with coupling constant values of 8.8 Hz and 2.5 Hz. Benzimidazole H 4 and H 6 protons were observed at 7.37-7.42 ppm and 7.86-7.87 ppm. A proton of methine (CH) in the hydrazide moiety was recorded as a singlet peak at 7.87-8.29 ppm. A proton of nitrogen in the same group had a singlet peak at about 11.40 ppm. Other aromatic peaks were observed between 6.09 ppm and 8.88 ppm. In the 13 C-NMR spectra, aliphatic carbons were observed between 14.01 ppm and 56.01 ppm, while aromatic ones were recorded between 104.96 ppm and 169.23 ppm. In the HRMS spectra, all masses were matched well with the expected M + H values.

Chemistry
The compounds 3a-3j were synthesized as summarized in Scheme 1. Initially, O-ethyl S-(5methoxybenzothiazol-2-yl) (1) carbonothioate was prepared by a reaction of 2-mercapto-5methoxybenzothiazole and ethyl 2-chloroacetate in the presence of potassium carbonate. Then, the reaction of compound 1 and excess of hydrazine hydrate gave S-(5-methoxybenzothiazol-2-yl) hydrazinecarbothioate (2). In the last step, compounds 3a-3j were prepared via the reaction of compound 2 and an appropriate heterocyclic aldehyde. The structure of the synthesized compounds were elucidated by IR, 1 H-NMR, 13 C-NMR, and HRMS analysis. In the IR spectra, the N-H bond of hydrazide was observed over 3061 cm −1 . Carbonyl and imine groups had bands at 1654-1699 cm −1 and 1307-1392 cm −1 , respectively. In the 1 H-NMR spectra, protons of methoxy and methylene, neighboring to carbonyl, gave singlet peaks at 3.81-3.82 ppm and 4.55-4.70 ppm, respectively. The benzimidazole H5 proton gave a doublet peak at 6.99 ppm with coupling constant values of 8.8 Hz and 2.5 Hz. Benzimidazole H4 and H6 protons were observed at 7.37-7.42 ppm and 7.86-7.87 ppm. A proton of methine (CH) in the hydrazide moiety was recorded as a singlet peak at 7.87-8.29 ppm. A proton of nitrogen in the same group had a singlet peak at about 11.40 ppm. Other aromatic peaks were observed between 6.09 ppm and 8.88 ppm. In the 13 C-NMR spectra, aliphatic carbons were observed between 14.01 ppm and 56.01 ppm, while aromatic ones were recorded between 104.96 ppm and 169.23 ppm. In the HRMS spectra, all masses were matched well with the expected M + H values.

MAO-A and MAO-B Inhibition Assay
The in vitro fluorometric enzymatic assay, allowing to sensitively detect monoamine oxidase activity, was applied to investigate hMAO-A and hMAO-B inhibitory potential of compounds 3a-3j. The method was performed in two steps, as previously described [21]. In the first step, compounds 3a-3j were screened at 10 −3 and 10 −4 M concentrations to determine the compounds that have more

MAO-A and MAO-B Inhibition Assay
The in vitro fluorometric enzymatic assay, allowing to sensitively detect monoamine oxidase activity, was applied to investigate hMAO-A and hMAO-B inhibitory potential of compounds 3a-3j. The method was performed in two steps, as previously described [21]. In the first step, compounds 3a-3j were screened at 10 −3 and 10 −4 M concentrations to determine the compounds that have more than 50% inhibition potency. Table 1 presents the hMAO-A and hMAO-B inhibitory activity of compounds 3a-3j. In the second step, selected compounds were used at concentrations of 10 −5 -10 −9 M to calculate their IC 50 values ( Table 2).
As seen in the Table 1, all compounds showed low inhibitory potency against hMAO-A, whereas compounds 3a, 3e, 3f, and 3h showed more than 50% inhibition against hMAO-B and, thus, they were selected for the second step, in which IC 50 values of 15.450, 0.060, 0.963, and 0.075 µM were recorded, respectively. Selegiline, a standard drug against hMAO-B, displayed an IC 50 of 0.044 µM ( Table 2). Enzymatic assay revealed that, synthesized compounds had a selectivity towards hMAO-B, as expected. It can be concluded that compound 3e is the most active compound with a significant IC 50 of 0.060 µM against hMAO-B and, thus, it has been subjected to enzyme kinetic and cytotoxicity assays.

Enzyme Kinetic Studies
The mechanism of hMAO-B inhibition was investigated by enzyme kinetic studies. Lineweaver-Burk graphs were used to estimate the type of inhibition. Data were analyzed by recording substrate-velocity curves in the various concentrations (IC 50 /2, IC 50 and 2 × IC 50 ) of the most active compound, 3e. The velocity measurements were performed by using different substrate concentrations (20 µM-0.625 µM). The K i (intercept on the x-axis) value of compound 3e was determined from the secondary plot of the 1/V versus varying concentrations.
The graphical analysis of inhibition type for compound 3e is displayed in Figure 2. The Lineweaver-Burk graphics present the inhibition type as a mixed-type, competitive, uncompetitive, or non-competitive. In the mix-typed inhibition, the control and inhibitor lines cross neither x-nor y-axis at the same point. Competitive inhibitors possess the same intercept on y-axis, but there are diverse slopes and intercepts on x-axis between the two data sets. There is no crosses between the lines in uncompetitive-type inhibition. Non-competitive inhibition has plots with the same intercept on the x-axis, but there are different slopes and intercepts on the y-axis, as seen in the Figure 2. Thus, it can be declared that the mechanism of hMAO-B inhibition of 3e is non-competitive, clarifying that the inhibitor can bind to either free enzyme or enzyme-substrate complex. The K i value for compound 3e was calculated as 0.061 µM for the inhibition of hMAO-B.

Cytotoxicity Test
The healthy NIH/3T3 mouse embryonic fibroblast cell line (ATCC CRL1658), proposed by ISO (10993-5, 2009) for preliminary cytotoxicity screening of drug candidates, was used to evaluate the cytotoxicity of compound 3e [23]. The IC50 value of the compound 3e is represented in Table 3. It was determined that IC50 (19.002 µM) of compound 3e against NIH/3T3 is ca. 300-fold higher than its IC50 (0.06 µ M) against hMAO-B enzyme. This finding indicates that compound 3e is not cytotoxic at its effective concentration. Table 3. Cytotoxic activity of the compound 3e against NIH/3T3 cell line.

Cytotoxicity Test
The healthy NIH/3T3 mouse embryonic fibroblast cell line (ATCC CRL1658), proposed by ISO (10993-5, 2009) for preliminary cytotoxicity screening of drug candidates, was used to evaluate the cytotoxicity of compound 3e [23]. The IC 50 value of the compound 3e is represented in Table 3. It was determined that IC 50 (19.002 µM) of compound 3e against NIH/3T3 is ca. 300-fold higher than its IC 50 (0.06 µM) against hMAO-B enzyme. This finding indicates that compound 3e is not cytotoxic at its effective concentration.

Prediction of ADME Parameters and BBB Permeability
As an important drug discovery approach it will be beneficial to evaluate the pharmacokinetic profiles of drug candidates during the early development phases. In recent years, by the help of combinatorial chemistry number of drug candidates, for which early data on absorption, distribution, metabolism, and excretion (ADME) are needed, has significantly increased [24]. Thus, predictions of ADME properties of the obtained compounds (3a-3j) were calculated using online Molinspiration chemical property software [25]. This program is based on to evaluate Lipinski's rule of five, which predicts the ADME properties of drug like compounds, and is very important to optimize a biologically-active compound. According to Lipinski's rule, an orally-active drug should not possess more than one violation. The theoretical calculations of ADME parameters (topological polar surface area (TPSA), molecular volume (MV), number of hydrogen acceptors (nOHNH), number of hydrogen donors (nON), partition coefficient (log P), and molecular weight (MW)) are accessible in Table 4 along with the violations of Lipinski's rule. In regard to these data, the obtained compounds (3a-3j) suited Lipinski's rule by displaying no violation. As a result, it can be suggested that the synthesized compounds may have good pharmacokinetic profiles, increasing their pharmacological significance.
It is known that drugs that specifically target the central nervous system (CNS) have to pass the blood-brain barrier (BBB). Thus, penetration of the BBB is very important for CNS drug candidates, and should be clarified early in drug discovery studies [26]. Therefore, BBB permeability of the synthesized compounds (3a-3j) was calculated by a CBLigand-BBB prediction server [27]. This online predictor applies two different algorithms, AdaBoost and Support Vector Machine (SVM), combining with four different fingerprints, employed to predict if a compound can pass (+) or cannot pass (−) the BBB. Predictor scores are higher than 0 if a compound can pass the BBB. Calculations for all compounds shwing BBB (+) are shown in Table 4, which are essential for MAO inhibitors to display their biological activity.

Molecular Docking Studies
According to enzyme activity assay, it was found that compound 3e was the most active and selective derivative in the series on hMAO-B enzyme. Its binding modes were obtained with the help of docking studies. The X-ray crystal structure of hMAO-B (PDB ID: 2V5Z) [1] was obtained from Protein Data Bank server [28]. The docking pose of compound 3e on hMAO-B is presented in Figure 3.
In Figure 3, it is seen that the benzothiazole substructure is very near the FAD cofactor, whereas the 5-nitrothiophen substructure has a position in the entrance of the cavity. The benzothiazole moiety creates a π-π interaction with the phenyl of Tyr435. The carbonyl of hydrazone is in an interaction with hydroxyl of Tyr435 by forming a hydrogen bond. The imine nitrogen of hydrazone moiety establishes a hydrogen bond with amino of Ile199. The last interaction is observed between the nitro group and Tyr326. The hydroxyl of this amino acid residue forms a hydrogen bond with the oxygen of the nitro group at the fifth position of thiophene. It is thought that this additional interaction is important for compound 3e in terms of explaining its inhibitory activity. It may be declared that the presence of an electron withdrawing group such as nitro at this position has a positive contribution to the activity. This suggestion is also supported by compound 3h, which has a nitro group at the same position of furan ring, and which is the second most active derivative. Prompted from the results of enzyme inhibition and docking studies, it can be suggested that he presence of an electron-withdrawing group, such as the nitro at the fifth position of thiophene or the furan ring, is very important for enzyme inhibitory activity. moiety creates a π-π interaction with the phenyl of Tyr435. The carbonyl of hydrazone is in an interaction with hydroxyl of Tyr435 by forming a hydrogen bond. The imine nitrogen of hydrazone moiety establishes a hydrogen bond with amino of Ile199. The last interaction is observed between the nitro group and Tyr326. The hydroxyl of this amino acid residue forms a hydrogen bond with the oxygen of the nitro group at the fifth position of thiophene. It is thought that this additional interaction is important for compound 3e in terms of explaining its inhibitory activity. It may be declared that the presence of an electron withdrawing group such as nitro at this position has a positive contribution to the activity. This suggestion is also supported by compound 3h, which has a nitro group at the same position of furan ring, and which is the second most active derivative. Prompted from the results of enzyme inhibition and docking studies, it can be suggested that he presence of an electron-withdrawing group, such as the nitro at the fifth position of thiophene or the furan ring, is very important for enzyme inhibitory activity.

Chemistry
All chemicals were obtained either from Sigma-Aldrich (Sigma-Aldrich Corp., St. Louis, MO, USA) or Merck (Merck KGaA, Darmstadt, Germany), and used without further chemical purification. Melting points of the compounds were measured by using an automatic melting point determination instrument (MP90, Mettler-Toledo, OH, USA) and were presented as uncorrected. 1 H and 13 C-NMR spectra were recorded in DMSO-d6 by a Bruker digital FT-NMR spectrometer (Bruker Bioscience, MA, USA) at 300 MHz and 75 MHz, respectively. The IR spectra of the compounds were recorded using an IRAffinity-1S Fourier transform IR (FTIR) spectrometer (Shimadzu, Tokyo, Japan). The HRMS studies were performed on an LCMS-IT-TOF system (Shimadzu, Tokyo, Japan). Chemical purities of the compounds were checked by classical TLC applications, which was performed on a

Chemistry
All chemicals were obtained either from Sigma-Aldrich (Sigma-Aldrich Corp., St. Louis, MO, USA) or Merck (Merck KGaA, Darmstadt, Germany), and used without further chemical purification. Melting points of the compounds were measured by using an automatic melting point determination instrument (MP90, Mettler-Toledo, OH, USA) and were presented as uncorrected. 1 H and 13 C-NMR spectra were recorded in DMSO-d 6 by a Bruker digital FT-NMR spectrometer (Bruker Bioscience, MA, USA) at 300 MHz and 75 MHz, respectively. The IR spectra of the compounds were recorded using an IRAffinity-1S Fourier transform IR (FTIR) spectrometer (Shimadzu, Tokyo, Japan). The HRMS studies were performed on an LCMS-IT-TOF system (Shimadzu, Tokyo, Japan). Chemical purities of the compounds were checked by classical TLC applications, which was performed on a silica gel 60 F254 (Merck KGaA, Darmstadt, Germany). (1) A mixture of 5-methoxybenzothiazole-2-thiol (30 mmol, 5.74 g), ethyl 2-chloroacetate (30 mmol, 3.21 mL), and potassium carbonate (30 mmol, 4.14 g) was refluxed in acetone for 10 h. After completion of the reaction, the acetone was evaporated, and the precipitated product was washed with deionised water, dried, and recrystallized from EtOH.

MAO-A and MAO-B Inhibition Assay
An enzyme inhibition assay was performed according to our recent study [21]. The inhibitor (20 µL/well) and hMAO-A (100 µL/well) or hMAO-B solution (100 µL/well) was added to the fine black-bottom 96-well microtiter plate and the mixture was incubated at 37 • C for 30 min. After the incubation period, the reaction was started by adding a working solution (100 µL/well) (200 mM Amplex Red reagent, 1 U/mL horseradish peroxidase and 1 mM p-tyramine) and all pipetting processes were performed using a Biotek Precision XS robotic system (BioTek Instruments, Winooski, VT, USA).
The production of H 2 O 2 and, subsequently, of resorufin was quantified at 37 • C in a BioTek-Synergy H1 microplate reader based on the fluorescence generated (excitation, 535 nm, emission, 587 nm) over a 15 min period, in which the fluorescence increased linearly. Control experiments were carried out simultaneously by replacing the inhibitor solution with 2% DMSO (20 µL). In order to check the probable inhibitory effect of inhibitors on horseradish peroxidase, a parallel reading was achieved by replacing enzyme solutions with 3% H 2 O 2 solution (20 mM 100 µL/well). In addition, the probable capacity of the inhibitors to modify the fluorescence generated in the reaction mixture due to non-enzymatic inhibition was determined by mixing inhibitor and working solutions.
The specific fluorescence emission (used to obtain the final results) was calculated after subtraction of the background activity, which was determined from vials containing all components except the hMAO isoforms, which were replaced by phosphate buffer (100 µL/well). Blank, control and all concentrations of inhibitors were analyzed in quadruplicate and inhibition percent was calculated by using following equation: where FC t2 is the fluorescence of a control well measured at t 2 time; FC t1 is the fluorescence of a control well measured at t 1 time; FI t2 is the fluorescence of an inhibitor well measured at t 2 time; and FI t1 is the fluorescence of an inhibitor well measured at t 1 time. The IC 50 values were calculated from a dose-response curve obtained by plotting the percentage inhibition versus the log concentration with the use of GraphPad PRISM software (version 5.0, GraphPad Software Inc., La Jolla, CA, USA). The results are displayed as the mean ± standard deviation (SD).

Enzyme Kinetic Studies
The same materials were used in the MAO inhibition assay. The most active compound, 3e, was studied at three different concentrations (IC 50 /2, IC 50 , and 2 × IC 50 ). The solutions of inhibitor (20 µL/well) and enzyme added to the fine black-bottom 96-well microtiter plate and then the mixture was incubated at 37 • C for 30 min. After incubation period, the working solution, including various concentrations (20, 10, 5, 2.5, 1.25, and 0.625 µM) of tyramine (100 µL/well), was added. The increase of the fluorescence (Ex/Em = 535/587 nm) was recorded for 30 min. A parallel experiment was performed without using an inhibitor. All processes were assayed in quadruplicate. Lineweaver-Burk plots were obtained by using Microsoft Office Excel 2013 to analyze the inhibition type. The slopes of the Lineweaver-Burk plots were replotted versus the inhibitor concentration, and the K i values were determined from the x-axis intercept as −K i [21].

Cytotoxicity Test
NIH/3T3 mouse embryonic fibroblast cell line (ATCC ® CRL-1658™, London, UK) was used in the cytotoxicity test and, initially, NIH/3T3 cells were incubated in Dulbecco's Modified Eagle's Medium (DMEM). NIH/3T3 cells were added to 96-well culture plates (10,000 cells/well). Synthesized compounds and reference agents were added to the 96-well culture plates at various concentrations ranging from 1000 µM to 0.316 µM. MTT assay was performed as previously described [29][30][31]. Dose-response curves were plotted against compound concentrations applied to determine IC 50 values. The following formula was used to calculate the inhibition percentage for each concentration: % inhibition = 100 − (mean sample × 100/mean solvent)

Prediction of ADME Parameters and BBB Permeability
Online Molinspiration property calculation program was used to predict ADME parameters of compounds (3a-3j) [25]. The BBB permeability of the compounds was evaluated by an online BBB predictor [27].

Molecular Docking Studies
A structure based in silico procedure was applied to discover the binding modes of compound 3e to hMAO-B enzyme active sites. The crystal structure hMAO-B (PDB ID: 1S2Q) [1], which was crystallized with safinamide, were retrieved from the Protein Data Bank server (www.pdb.org).
The structures of ligands were built using the Schrödinger Maestro [32] interface and then were submitted to the Protein Preparation Wizard protocol of the Schrödinger Suite 2016 Update 2 [33]. The ligands were prepared by the LigPrep 3.8 [34] to assign the protonation states at pH 7.4 ± 1.0 and the atom types, correctly. Bond orders were assigned and hydrogen atoms were added to the structures. The grid generation was formed using Glide 7.1 [35]. The grid box with dimensions of 20 Å × 20 Å × 20 Å was centered in the vicinity of the flavin (FAD) N5 atom on the catalytic site of the protein to cover all binding sites and neighboring residues [36][37][38]. Flexible docking runs were performed with single precision docking mode (SP).

Conclusions
Synthesis of novel compounds, incorporating significant pharmacophore groups, is an important medicinal chemistry principle to develop new biologically-active agents. Depending on this approach, in this study, 10 new benzothiazole compounds carrying hydrazone and heteroaryl groups were designed and synthesized as selective hMAO-B inhibitors. Enzymatic studies confirmed the selectivity of compounds toward hMAO-B enzyme and displayed the potency of compound 3e against this enzyme. Toxicological and ADME studies enhanced the biological importance of this compound. The docking studies clearly explained the molecular interactions between the compound 3e and hMAO-B. In conclusion, this information may have an effect on medicinal chemists to synthesize more potent and safer hMAO-B inhibitors, which may be helpful for the treatment of patients with PD.