In Vitro Study of Multi-Therapeutic Properties of Thymus bovei Benth. Essential Oil and Its Main Component for Promoting Their Use in Clinical Practice

Thymus bovei Benth. (TB) is an important plant in the traditional medicine of the Mediterranean region. This study investigates the health-promoting properties of TB essential oil (TB-EO) for its possible use in clinical practice with regards to its cytotoxic, anti-herpes simplex virus type 2 (HSV-2), and antihypertensive (through inhibition of human angiotensin-converting enzyme; ACE) properties. The phytochemical profile of EO (99.9%) was analyzed by Gas Chromatography with Flame-Ionization Detection (GC-FID) and Gas Chromatography-Mass Spectrometry (GC-MS). In this study, all biological methods were performed at the level of in vitro studies. The results showed that TB-EO exerted remarked cytotoxic properties against human cervical carcinoma cells, colon cancer cells, and lung adenocarcinoma cells with the half-maximal inhibitory concentration (IC50) values of 7.22, 9.30, and 8.62 µg/mL, respectively, in comparison with that of standard anticancer drug cisplatin with IC50 values of 4.24, 5.21, and 5.43 µg/mL, respectively. Fascinatingly, TB-EO showed very weak cytotoxicity on the healthy human fetal lung fibroblast cells with an IC50 value of 118.34 µg/mL compared with that of cisplatin (IC50 = 10.08 µg/mL). TB-EO, its main component geraniol, TB-EO combined with acyclovir (ACV) along with standard ACV, have displayed pronounced inhibitory properties against the replication of HSV-2 with the half-maximal effective concentration (EC50) values of 2.13, 1.92, 0.81 and 1.94 µg/mL, respectively, with corresponding selectivity indices (SI) 98.59, 109.38, 259.26 and 108.25, respectively. TB-EO and geraniol at a concentration of 15 µg/mL showed prominent inhibitory activities against ACE with % of inhibition 95.4% and 92.2%, respectively, compared with that of standard inhibitor captopril (99.8%; 15 µg/mL). Molecular docking studies were performed to unveil the mechanism of action of geraniol as well as structural parameters necessary for anti-HSV-2 activity (through the inhibition of HSV-2 protease) and ACE inhibition. This is the first report on the chemical composition of Egyptian TB-EO along with the above-mentioned biological activities. Our results may be considered as novel findings in the course of a search for new and active anticancer, anti-HSV-2 and antihypertensive agents, and expand the medicinal value of this plant and its phytochemicals in clinical practice.


Introduction
For decades, plants have been known to be a vital source of natural preparations comprising many biologically active molecules that can be used for various applications, such as food additives and health-promoting agents in the form of functional foods and nutraceuticals. Since ancient times, aromatic plants have been widely used as flavorings, and later, they have become a subject for a search of drugs that can be used for the treatment of a wide range of diseases [1,2]. Thymus bovei Benth. (Lamiaceae), commonly known as "Thyme" is a medicinal and aromatic herb, widely distributed in the eastern Mediterranean regions [3]. This plant is considered to be one of the most important Thymus species, due to its high medicinal and curative characteristics. Traditionally, in the North African region, particularly in Egypt, this plant is being used for the treatment of skin and blood infections as well as curing a wide range of microbial infections [4]. It has been stated that this herb has anthelmintic, expectorant, antispasmodic, antiseptic properties due to its content of essential oil (EO) [5]. Moreover, medicinal properties such as curing of injuries, treatment of upper respiratory tract inflammations, and treatment of anorexia, have also been reported [6]. Plant-derived EOs are expected to possess a good bioavailability due to its lipophilic properties, and hence induce curative activities [7].
In recent years, cancer has become the most severe health issue across the globe and is the major cause of mortality worldwide [8]. In this regard, the search for new effective molecules that exhibit antitumor properties against numerous types of cancer has become one of the main topics in the field of natural product research [9]. Plants and their phytochemicals have a rich history of use, and they play a critical role in the development of sophisticated traditional medicine systems, particularly in cancer therapy [10]. EOs derived from various plant species have shown to exert excellent anticancer properties [11][12][13][14]. So far, no reports have demonstrated the anticancer activity of T. bovei.
Genital herpes is an incurable viral sexually transmitted disease, induced by herpes simplex virus type 2 (HSV-2). HSV-2 is an enveloped, double-stranded DNA virus of the Herpesviridae family [15]. This virus contaminates the genital mucosa and causes ulcers and lesions in the genital area. Following the principal infection, the virus creates a life-long latent infection within sensory dorsal root ganglia. The occurrence of recurrent infection is mainly generated by reactivation of latent infection, particularly throughout the deficiency of immunity [16,17]. It has been reported that infection with HSV-2 increases the risk of infection with human immunodeficiency virus (HIV), as well as invasive cervical carcinoma. It is known that nucleoside analogs, such as acyclovir (ACV) and its derivatives penciclovir, famciclovir, cidofovir, valacyclovir, trifluridine, and vidarabine are used to treat the HSV-2 infection [18]. However, the development of resistance to antiherpetic medications along with the undesirable side effects claims for the development of new anti-HSV-2 drugs with assorted mechanisms of action [19].
Angiotensin-converting enzyme (ACE) is a zinc-containing metallopeptidase that can elevate blood pressure by converting the inactive decapeptide angiotensin I to the effective vasoconstrictor angiotensin II, in addition, to degrading the hypotensive peptide bradykinin [20]. Due to the fundamental role of ACE in cardiovascular diseases, it has been an attractive target for drug design [21]. Up to date, no investigations have reported the ability of T. bovei-derived EO to diminish the risk of hypertension and coronary heart disease by inactivating the enzymatic properties of ACE.
The purpose of this study was to explore the cytotoxic, anti-HSV-2 and antihypertensive activities of T. bovei Benth. EO (TB-EO) and its main active compound geraniol, along with characterization of the phytochemical profile of EO as well as the quantitative analyses of total possible bioactive compounds present in hydro-ethanolic and aqueous extracts of the plant (total phenolics, total flavonoids, and total proanthocyanidins). Up to date, no previous studies were reported on the metabolic profile of Egyptian T. bovei EO along with the above-mentioned pharmacologic properties. Therefore, in this study, we present the first report on such investigations in order to expand the medicinal value of this plant and hence promote its use in clinical use.

Plant Materials
Aerial parts of T. bovei Benth. were collected from El-Hammam region (30.841852

Phytochemical Profile Analysis of EO by GC and GC-MS
Gas chromatography (GC; Agilent 6890N, Santa Clara, CA, USA) equipped with a flame ionization detector (FID) and gas chromatography-mass spectrometry (GC-MS) utilizing GC (Agilent 5975, Santa Clara, CA, USA) linked with a mass selective detector (Hewlett Packard-MSD5973, Santa Clara, CA, USA) have been used for identification of EO components. Parameters such as the instrumental setup, operational, and chromatographic settings were tracked as described earlier [23]. EO constituents were identified by matching the obtained mass spectra with Mass Finder-4 Library and Wiley GC-MS Library and by comparison with data obtained from the literature [24][25][26].

Extraction Procedure
The hydro-ethanolic extract of air-dried powder of T. bovei (HETB) was obtained by maceration for 3 days using ethanol:water (70:30 v/v) (1 g/10 mL), while the aqueous extract of air-dried powder T. bovei (AETB) (1 g/10 mL) was prepared by boiling in distilled water for 30 min and left to stand to cool down at 26 • C. The solutions were filtered by Sartorius 388 filter paper and the filtered extracts were employed for analyses.

Total Phenolic Content (TPC)
Folin-Ciocalteu method was used to determine the total phenolic contents (TPC) of HETB and AETB as described earlier [27]. TPC value was expressed as gallic acid equivalents (GAE) (mg GAE/g dry weight of plant material) (R 2 = 0.99). Experiments were conducted in triplicate.

Total Flavonoid Content (TFC)
The total flavonoid content (TFC) of HETB and AETB was assessed and expressed as rutin equivalents following the method by Hassan et al. [28]. TFC value was expressed as rutin equivalents (RE) (mg RE/g dry weight of plant material) (R 2 = 0.99). Experiments were assayed in triplicate.

Total Proanthocyanidin Content
The HCl/butan-1-ol assay was achieved to determine the total amount of proanthocyanidin in HETB and AETB and the total value was expressed as µg cyanidin chloride/g dry weight of plant material as previously described [29]. All measurements were analyzed in triplicates.  (25 mM), and 10% of heat-inactivated fetal calf serum (FCS) at pH = 7.2. Further, the human cancer cells were grown in 5% CO 2 and humidified condition at 37 • C, and subsequently sub-cultured twice for a week as previously described [30].

Cytotoxicity Assay
The potential cytotoxic effect of TB essential oil (TB-EO) on various human carcinoma cells along with normal human fetal lung fibroblast cells was screened by MTT assay (3-(4,5-dimethy lthiazol-2-yl)-2,5-diphenyltetrazolium Bromide) (Sigma-Aldrich, Berlin, Germany) as described earlier [30]. Cisplatin, a standard chemotherapy drug was selected as a reference control (Sigma-Aldrich, Prague, Czech Republic). The absorbance of the samples was detected at 570 nm using a microplate reader (Infinite M200, Tecan, Salzburg, Austria). Determination of the half-maximal inhibitory concentrations (IC 50 ) was acquired from the cell survival diagrams that necessitate suppressing 50% of cell survival. Vero cells (ATCC: CCL 81TM, UK; were gained from MUH, Prague, Czech Republic) were grown and prepared as previously described [31]. A clinical isolate of HSV-2 (obtained from HSV-2 infected patients) was kindly acquired from MUH, Prague, Czech Republic. The clinical strain was typed, identified, propagated in Vero cells, and the titers, which are expressed as 50% tissue culture infective dose (TCID 50 /mL), were assayed by cytopathic end-point method following the same procedures by Hassan et al. [31]. Viral stocks were stored at −80 • C.

Determination of Cytotoxicity
The cytotoxicity was assayed by treating Vero cell monolayers with TB-EO, geraniol (Sigma-Aldrich, Prague, Czech Republic; Figure 1), and TB-EO with ACV (Sigma-Aldrich, Prague, Czech Republic) in combination, as well as standard ACV using the neutral red dye-uptake method as previously described [31]. The 50% cytotoxic concentrations (CC 50 ) of test compounds were determined as the concentration that diminishes cell viability by 50% when compared to the untreated controls.  (25 mM), and 10% of heat-inactivated fetal calf serum (FCS) at pH = 7.2. Further, the human cancer cells were grown in 5% CO2 and humidified condition at 37 °C, and subsequently sub-cultured twice for a week as previously described [30].

Cytotoxicity Assay
The potential cytotoxic effect of TB essential oil (TB-EO) on various human carcinoma cells along with normal human fetal lung fibroblast cells was screened by MTT assay (3-(4,5-dimethylthiazol-2yl)-2,5-diphenyltetrazolium Bromide) (Sigma-Aldrich, Berlin, Germany) as described earlier [30]. Cisplatin, a standard chemotherapy drug was selected as a reference control (Sigma-Aldrich, Prague， Czech Republic). The absorbance of the samples was detected at 570 nm using a microplate reader (Infinite M200, Tecan, Salzburg, Austria). Determination of the half-maximal inhibitory concentrations (IC50) was acquired from the cell survival diagrams that necessitate suppressing 50% of cell survival.

Viral Strains, Cell Lines, Medium, and Reagents
Vero cells (ATCC: CCL 81TM, UK; were gained from MUH, Prague, Czech Republic) were grown and prepared as previously described [31]. A clinical isolate of HSV-2 (obtained from HSV-2 infected patients) was kindly acquired from MUH, Prague, Czech Republic. The clinical strain was typed, identified, propagated in Vero cells, and the titers, which are expressed as 50% tissue culture infective dose (TCID50/mL), were assayed by cytopathic end-point method following the same procedures by Hassan et al. [31]. Viral stocks were stored at −80 °C.

Determination of Cytotoxicity
The cytotoxicity was assayed by treating Vero cell monolayers with TB-EO, geraniol (Sigma-Aldrich, Prague, Czech Republic; Figure 1), and TB-EO with ACV (Sigma-Aldrich, Prague, Czech Republic) in combination, as well as standard ACV using the neutral red dye-uptake method as previously described [31]. The 50% cytotoxic concentrations (CC50) of test compounds were determined as the concentration that diminishes cell viability by 50% when compared to the untreated controls.

Antiviral Activity Against HSV-2
Antiherpetic properties of TB-EO, geraniol, and TB-EO combined with ACV against HSV-2 replication were assayed by the titer reduction method as previously described [31]. ACV was used as a reference antiherpetic drug. The 50% effective concentration (EC 50 ) was assessed as the concentration needed for 50% protection towards virus-induced cytopathic effects. Subsequently, a selectivity index (SI) was calculated as the ratio CC 50 /EC 50 .

Protein-Ligand Elaboration and Processing of Docking Analysis
The 3D-crystal structure of HSV-2 protease (PDB ID: 1AT3) and 3D-structure of geraniol (SDF file ID: 64Z) were acquired from the RCSB Protein Data Bank. PyRx docking tool within Autodock VINA software (The Scripps Research Institute, La Jolla, CA, USA) was used to evaluate the binding mode of geraniol in the active site of HSV-2 protease. All docking parameters, settings, calculations, protonation conditions, and the overall charges were tracked as previously described [32,33]. All docked complexes were presented graphically by Discovery studio visualizer version 4.0 (BIOVIA, San Diego, CA, USA) [34].

Anti-Angiotensin-Converting Enzyme (ACE) Activity
The catalytic activity of human ACE was assayed spectrophotometrically based on the formation of hippuric acid as a product following the method by Cushman and Cheung [35] with slight modification. Briefly, the activity was initiated by incubating 166 mU/mL of human ACE (Sigma-Aldrich, Prague, Czech Republic) prepared in Tris Buffer (50 mM, pH = 8.3) with TB-EO, geraniol, and captopril (standard inhibitor) at concentrations of 15 µg/mL for 80 min at 37 • C. Further, the catalytic reaction took place by adding the mixture to 110 µL of the 10 mM hippuryl-histidyl-leucine (substrate; from Sigma-Aldrich, Prague, Czech Republic). The absorbance of the hippuric acid was detected at λ 228 nm, and the % inhibition was calculated.

Protein-Ligand Preparation and Processing of Docking Analysis
The 3D-crystal structure of human angiotensin-converting enzyme (ACE) complexed with captopril (PDB ID: 1UZF) and 3D-structure of geraniol (SDF file ID: 64Z) were attained by the RCSB Protein Data Bank. Before performing the docking analysis, we authenticated the docking process by removing the co-crystallized ligand captopril from the PDB (PDB ID: 1UZF) structure and re-docked captopril using PyRx docking tool via Autodock VINA software. This software was used to evaluate the binding mode of geraniol in the active site of human ACE. All docking settings, parameters, calculations, protonation conditions, and the overall charges were followed as previously described [32]. All docked complexes were presented graphically using Discovery studio visualizer version 4.0 (BIOVIA, San Diego, CA, USA) [34].

Characterization of Total Bioactive Compounds
The quantitative analyses of total bioactive constituents (TPC, TFC, and total proanthocyanidin content) of HETB and AETB were determined spectrophotometrically. The results are shown in Table 2.
The contents of all studied phenolic constituents of HETB were observed to be higher than that of AETB. These results suggest the significance of used solvents. The polyphenols are more soluble in ethanol, therefore, HETB gave higher yields than AETB. Our findings agree with the literature, where methanol or ethanol extracts were reported to show the highest levels of total phenolics, flavonoids, and proanthocyanidins [40,41]. However, several studies describe the water as the most appropriate solvent for the acquisition of the highest phenolic contents from the plant material [42,43]. Our results indicate that T. bovei contains a lower amount of phenolic compounds extracted by ethanol with the value of TPC 85.62 mg/g DW of plant material in comparison with other ethanol extracts of Thymus species. T. vulgaris L. reached the value of TPC 158.0 µg/mg [43], T. serpyllum 113.0 mg/g [44] and T. pulegioides L. 155.38 mg/g of HEE [45]. On the other hand, TFC value of T. bovei (51.23 ± 0.43 mg/g) was found to be higher than that of different Thymus species by using an ethanol for extraction and the same procedure to determine the TFC values. Nickavar and Esbati [46] have reported the TFC value 50.39 µg/mg for T. pubescens Boiss. & Kotschy ex Celak., 37.11 µg/mg for T. kotschyanus Boiss. & Hohen., and 35.21 µg/mg for T. daenensis Celak., respectively. The TPC and TFC values may significantly vary during the season as it was observed in T. longicaulis [47]. The habitat also plays an important role in the total content of the polyphenolics. Jaouadi et al. [48] have described the variation of phenolic constituents of T. capitatus (L.) Hoffmanns. & Link harvested in six bioclimatic zones and Tohidi et al. [49] have demonstrated the variations in chemical constituents of fourteen Thymus accessions collected from different regions of Iran.

Evaluation of Cytotoxicity Properties
Over the past decade, cancer has shown the capacity to progress resistance to traditional medications, and the growing frequency of drug-resistant cancer imposes an urgent need to operate further research and treatment development. In this study, we assessed the cytotoxicity profile of TB-EO in comparison with the reference chemotherapeutic drug cisplatin towards various human cancer cell lines, along with normal human fetal lung fibroblast cells. The results exposed that TB-EO exerted remarked cytotoxic properties against human cervical carcinoma cells (HeLa-R2), colon cancer cells (LS-174-D3), and lung adenocarcinoma cells (A-549-C5) with IC 50 values of 7.22, 9.30, and 8.62 µg/mL, respectively, in comparison with that of cisplatin with IC 50 values of 4.24, 5.21, and 5.43 µg/mL, respectively (Table 3). Among the obtained results, TB-EO showed strong cytotoxicity against HeLa-R2 cells with an IC 50 value of 7.22 µg/mL. Interestingly, TB-EO showed very weak cytotoxicity on the normal human fetal lung fibroblast cells (MRC-5) with an IC 50 value of 118.34 µg/mL compared with that of cisplatin (IC 50 = 10.08 µg/mL). This indicates that TB-EO has powerful anti-tumor properties on cancer cells and no significant effect on normal cells. The cytotoxic effect of TB-EO used in this study could be attributed to the major compounds (geraniol, α-citral, β-citral, and thymol) present in TB-EO. In this study, we present the first report on the cytotoxic activities of Egyptian TB-EO. However, several studies have explored variable data of toxicology profiles of EOs on cancer cells from different Thymus species, except T. bovei [50][51][52], we cannot compare our results with them due to the variation in test methods used, as well as different cell lines sources and samples used. Finally, our results suggest that TB-EO might be used to treat cancer without affecting normal cells.

Antiviral Activities against HSV-2 Replication
Prior to carrying out the anti-HSV-2 assay, we evaluated the cytotoxicity of TB-EO, geraniol, TB-EO combined with ACV as well as standard ACV in Vero cells by the neutral red dye-uptake technique. The selectivity index is vital to control the probable toxic property of any medication on the cells that could be confused with an antiviral activity. The CC 50 values of test compounds were determined to be greater than 210 µg/mL (Table 4). Antiherpetic activity was assayed in infected Vero cells, by titer reduction assay using quantitative real-time reverse transcription PCR.  In recent years, natural products have attracted the attention of the pharmaceutical industry as an alternative or complementary therapy to the currently existing ones for the treatment of viral infections [19]. The current pharmacologic treatment of HSV infections is based on the use of ACV and related synthetic nucleoside analogs, which interact with viral DNA replication via activation by viral thymidine kinase [33]. The increasing use of antiviral drugs to treat HSV infections has resulted in drug resistance problem, which in return has switched the attention to plant-derived products in clinical practice [53]. Generally, antiviral medications are categorized into three groups: virucidals, immunomodulators, and antiviral chemotherapeutic drugs [19]. Based on the obtained results, we might classify the test compounds as antiviral chemotherapeutic agents. It has been stated that the resistance to antiviral drugs can be overcome by merging them with compounds from different classes of origin [54,55]. Thus, the results gained by combining TB-EO with ACV have led to potent anti-HSV-2 properties along with less resistance. Remarkably, TB-EO, geraniol, and TB-EO combined with ACV seem to be anti-HSV-2 drugs of future that could be used for the treatment of HSV-2 infection.

Molecular Interactions of Geraniol with HSV-2 Protease
It is known that HSV-2 encodes a serine protease that is vital for viral replication and hence represents a viable target for therapeutic intervention. Thus, a molecular docking study was carried out to unveil the binding mode of geraniol into the active site of HSV-2 protease (Figure 2). The docking score for geraniol, which is expressed as binding affinity, was recorded to be −5.4 kcal/mol. The docking results showed that geraniol bound to the active site of HSV-2 protease and hence inhibited the enzyme by establishing a hydrogen bonding contact with the hydroxyl group of geraniol and amino acid residues ASN-A220. Additional hydrophobic and other critical interactions were recognized ( Figure 3). As shown in Figure 3, all amino acid residues were previously reported in the active site of HSV-2 protease and are responsible for the stabilization of the enzyme [56]. Since geraniol bound to the active-site of the enzyme, this means that geraniol is competing with the substrate, and hence acts as a competitive inhibitor. anti-HSV-2 properties along with less resistance. Remarkably, TB-EO, geraniol, and TB-EO combined with ACV seem to be anti-HSV-2 drugs of future that could be used for the treatment of HSV-2 infection.

Molecular Interactions of Geraniol with HSV-2 Protease
It is known that HSV-2 encodes a serine protease that is vital for viral replication and hence represents a viable target for therapeutic intervention. Thus, a molecular docking study was carried out to unveil the binding mode of geraniol into the active site of HSV-2 protease (Figure 2). The docking score for geraniol, which is expressed as binding affinity, was recorded to be −5.4 kcal/mol. The docking results showed that geraniol bound to the active site of HSV-2 protease and hence inhibited the enzyme by establishing a hydrogen bonding contact with the hydroxyl group of geraniol and amino acid residues ASN-A220. Additional hydrophobic and other critical interactions were recognized ( Figure 3). As shown in Figure 3, all amino acid residues were previously reported in the active site of HSV-2 protease and are responsible for the stabilization of the enzyme [56]. Since geraniol bound to the active-site of the enzyme, this means that geraniol is competing with the substrate, and hence acts as a competitive inhibitor.  anti-HSV-2 properties along with less resistance. Remarkably, TB-EO, geraniol, and TB-EO combined with ACV seem to be anti-HSV-2 drugs of future that could be used for the treatment of HSV-2 infection.

Molecular Interactions of Geraniol with HSV-2 Protease
It is known that HSV-2 encodes a serine protease that is vital for viral replication and hence represents a viable target for therapeutic intervention. Thus, a molecular docking study was carried out to unveil the binding mode of geraniol into the active site of HSV-2 protease (Figure 2). The docking score for geraniol, which is expressed as binding affinity, was recorded to be −5.4 kcal/mol. The docking results showed that geraniol bound to the active site of HSV-2 protease and hence inhibited the enzyme by establishing a hydrogen bonding contact with the hydroxyl group of geraniol and amino acid residues ASN-A220. Additional hydrophobic and other critical interactions were recognized ( Figure 3). As shown in Figure 3, all amino acid residues were previously reported in the active site of HSV-2 protease and are responsible for the stabilization of the enzyme [56]. Since geraniol bound to the active-site of the enzyme, this means that geraniol is competing with the substrate, and hence acts as a competitive inhibitor.  Only those amino acid residues implicated in the enzyme stabilization are exposed. Hydrogen bonding and several substantial interactions with amino acid residues are displayed. Figure 3. 2D interaction diagram of geraniol in the active cavity of HSV-2 protease. Only those amino acid residues implicated in the enzyme stabilization are exposed. Hydrogen bonding and several substantial interactions with amino acid residues are displayed.

Evaluation of Anti-ACE Properties
Inhibition of ACE is one of the most imperative strategies to control hypertension and heart failure. The degree of ACE inactivation by TB-EO, geraniol, and captopril was signified by the amount of hippuric acid formed. Based on the estimated percentage of inhibition, TB-EO (15 µg/mL), and geraniol (15 µg/mL) showed prominent inhibitory activities against ACE with % inhibition 95.4 and 92.2, respectively, compared to captopril (99.8 % at a concentration of 15 µg/mL) ( Table 5). Since TB-EO inactivated potently the hydrolytic activities of ACE, we decided to test the principal active compound in TB-EO, geraniol for further evaluation against ACE. Based on the obtained results, geraniol remarkably suppressed the hydrolytic properties of ACE. Accordingly, we may suggest that the inhibitory effect of TB-EO on ACE is attributed to the presence of geraniol. In this study, we present a first report on the inhibitory activities of TB-EO and its bioactive molecule geraniol against ACE. Despite limited investigations have confirmed that plant EOs have processed in vitro anti-ACE activities, we tried to rationalize our results with such studies. For instance, Zouari et al. [57] stated that Artemisia herba-alba Asso. EO unveiled in vitro ACE inhibitory action at a concentration of 100 µg/mL (25.4%). In another study, Ajuga pseudoiva Rob. EO was pronounced to exert a dose-dependent ACE inhibitory activity of 28.3%, 53.8%, and 74.5%, at 25, 75 and 150 µg/mL of EO, respectively [58]. On the other hand, compounds derived from plant origins such as flavonoids, tannins, and peptides were described with anti-ACE activities [59][60][61]. Values are presented as the mean ± standard deviation (SD) (n = 3). TB-EO: T. bovei essential oil; Nd: Not determined.

Molecular Interactions of Geraniol with ACE
To better understand the potency of geraniol for further structure-activity relationship study, molecular docking analysis with ACE was conducted to predict the binding affinity of geraniol into the binding site of ACE (Figure 4), which contributes to rationalize the obtained biological results as well as the mechanism of action. The docking scores for geraniol and captopril, which are expressed as binding affinities, were found to be −5.2 and −6.1 kcal/mol, respectively. The docking results revealed that geraniol pound to the active cavity of ACE by forming a hydrogen bonding interaction between amino acid residue ASP-415 and the hydroxyl group of geraniol, which in turn resulted in suppressing enzymatic activity ( Figure 5). Moreover, several critical interactions were also observed. As shown in Figure 5, all amino acid residues were previously described in the active cavity of human ACE and found to be critical for the stabilization of the enzyme [62]. Although zinc is essential to the catalytic activity of ACE, geraniol did not bind to the zinc active-site and bound to the different active pocket of the enzyme. This means that geraniol is not competing with the substrate, and hence acts as a non-competitive inhibitor by preventing the formation of enzyme-product complexes.

Conclusions
Recently, plant-derived EOs have attracted the attention of healthcare providers worldwide due to the therapeutic properties against various diseases as well as the safety profiles. Our study showed that T. bovei EO exerted remarked cytotoxic properties against human cervical carcinoma cells, colon cancer cells, and lung adenocarcinoma cells without affecting normal cells compared with that of cisplatin based on the determination of IC50 concentrations that required to inhibit 50% of cell survival (see results and discussion section). Additionally, geraniol, the main component of EO, showed prominent inhibition activities against HSV-2 replication and suppressing the activity of ACE (see results and discussion section). Hereby, we present geraniol as a very promising agent in the treatment of genital herpes and hypertension. Subsequently, we confirmed the mechanism of action by using molecular docking studies. These studies have confirmed the basics of phytotherapeutical use of T. bovei in Mediterranean region and its inclusion in North African pharmacopoeias. Finally, further studies should be conducted in vivo and in clinical trials to evaluate efficacy as well as

Conclusions
Recently, plant-derived EOs have attracted the attention of healthcare providers worldwide due to the therapeutic properties against various diseases as well as the safety profiles. Our study showed that T. bovei EO exerted remarked cytotoxic properties against human cervical carcinoma cells, colon cancer cells, and lung adenocarcinoma cells without affecting normal cells compared with that of cisplatin based on the determination of IC50 concentrations that required to inhibit 50% of cell survival (see results and discussion section). Additionally, geraniol, the main component of EO, showed prominent inhibition activities against HSV-2 replication and suppressing the activity of ACE (see results and discussion section). Hereby, we present geraniol as a very promising agent in the treatment of genital herpes and hypertension. Subsequently, we confirmed the mechanism of action by using molecular docking studies. These studies have confirmed the basics of phytotherapeutical use of T. bovei in Mediterranean region and its inclusion in North African pharmacopoeias. Finally, further studies should be conducted in vivo and in clinical trials to evaluate efficacy as well as Geraniol Figure 5. 2D diagram shows the binding mode of geraniol in the active cavity of the ACE. Only those amino acid residues embroiled in ACE stabilization are viewed. Hydrogen bonding and several fundamental interactions with corresponding amino acid residues are presented.

Conclusions
Recently, plant-derived EOs have attracted the attention of healthcare providers worldwide due to the therapeutic properties against various diseases as well as the safety profiles. Our study showed that T. bovei EO exerted remarked cytotoxic properties against human cervical carcinoma cells, colon cancer cells, and lung adenocarcinoma cells without affecting normal cells compared with that of cisplatin based on the determination of IC 50 concentrations that required to inhibit 50% of cell survival (see results and discussion section). Additionally, geraniol, the main component of EO, showed prominent inhibition activities against HSV-2 replication and suppressing the activity of ACE (see results and discussion section). Hereby, we present geraniol as a very promising agent in the treatment of genital herpes and hypertension. Subsequently, we confirmed the mechanism of action by using molecular docking studies. These studies have confirmed the basics of phytotherapeutical use of T. bovei in Mediterranean region and its inclusion in North African pharmacopoeias. Finally, further studies should be conducted in vivo and in clinical trials to evaluate efficacy as well as pharmacokinetic and pharmacodynamic properties, leading to effective optimization of TB-EO and geraniol as natural cytotoxic, antiherpetic, and antihypertensive agents. Moreover, large prospective epidemiological studies should be performed.