Synthesis, Biological Assessment, and Structure Activity Relationship Studies of New Flavanones Embodying Chromene Moieties

Novel flavanones that incorporate chromene motifs are synthesized via a one-step multicomponent reaction. The structures of the new chromenes are elucidated by using IR, 1H-NMR, 13C-NMR, 1H-1H COSY, HSQC, HMBC, and elemental analysis. The new compounds are screened for their in vitro antimicrobial and cytotoxic activities. The antimicrobial properties are investigated and established against seven human pathogens, employing the agar well diffusion method and the minimum inhibitory concentrations. A majority of the assessed derivatives are found to exhibit significant antimicrobial activities against most bacterial strains, in comparison to standard reference drugs. Moreover, their cytotoxicity is appraised against four different human carcinoma cell lines: human colon carcinoma (HCT-116), human hepatocellular carcinoma (HepG-2), human breast adenocarcinoma (MCF-7), and adenocarcinoma human alveolar basal epithelial cell (A-549). All the desired compounds are subjected to in-silico studies, forecasting their drug likeness, bioactivity, and the absorption, distribution, metabolism, and excretion (ADME) properties prior to their synthetic assembly. The in-silico molecular docking evaluation of all the targeted derivatives is undertaken on gyrase B and the cyclin-dependent kinase. The in-silico predicted outcomes were endorsed by the in vitro studies.


Introduction
Computational techniques perform a crucial role in many drug discovery programs, from hit identification to the optimization of the lead and thereafter. Numerous computational tools are accessible, and these are categorized as either ligand-based or receptor-based. Screening chemical compounds allows for the elimination of searching an entire chemical space by utilizing libraries of specific, accessible molecules. This not only prevents unnecessary syntheses but also limits the number of derivatives with biologically-compelling behaviors. Sieves may be employed to make certain that the archive satisfies the criteria of biological significance or 'drug-likeness.' General sieving strategies for 'drug-likeness' [1], which are applicable for the compound databases, are based on Lipinski's rule-of-five [2], which comprises a series of guidelines centered on hydrophobicity, lipophilicity, and molecular weight and yields a straightforward profile for orally bioavailable molecules. Additional physical sieves could involve a constraint on the polar surface area or the quantity of rotatable bonds of the compounds [3].
The undesirable pharmacokinetic attributes of potential drugs impose restrictions in constructing a headway in the process of novel drug developments; hence, there is an amplified urge to develop new techniques that are intelligent enough to predict these drug traits [4][5][6]. The scrutiny of a drug's pharmacokinetic features comprises absorption, distribution, metabolism, and excretion (ADME) [7]. The ADME guidelines dictate whether drug candidates are to be proceeded with, clasped, or ceased [8].
The cyclin-dependent kinases (CDK/cyclins) constitute a taxon of heterodimeric kinases that perform vital functions in the modulation of the cell cycle progression, transcription and other crucial biological affairs, such as neuronal metabolism and differentiation [9]. The constitutive or deregulated hyperactivity of these kinases as a consequence of the overexpression, amplification, or mutation of cyclins or CDK generates the proliferation of cancer cells, and the peculiar task of the preceding kinases has been implicated in a broad assortment of human cancers [10]. Therefore, these kinases represent the biomarkers of proliferation and arrest with the pharmacological intent of the development of anticancer therapeutics [11]. The overexpression of the cyclin-dependent kinase-2 (CDK2) has been documented in various categories of human tumors [12][13][14][15][16][17]. Molecular docking evaluations have been executed to acquire an additional comprehension of the binding behavior of the generated molecules with CDK2 (Protein Data Bank (PDB) ID: 1FVV) as well as gyrase B (GyrB43) from Escherichia coli (PDB code: 4PRV), which has been reported to be a target for analyzing antibacterial activities [18].
As a continuation of our preceding work in the area of the synthesis and biological screening of the bioactive molecules [19][20][21][22] based on extensive molecular modeling and in-silico studies, we carried out the synthesis of a novel series of chromene-incorporating flavanones, endeavoring to find new and alternative drug candidates to replace those in peril of facing resistance from microorganisms.
The substantial upsurge of microorganisms' resistance to antimicrobial agents is one of the foremost concerns among scientists and clinicians worldwide. Moreover, numerous pathogenic viruses, bacteria, fungi, and protozoa have subsequently developed resistance, which renders treatment much more challenging with the existing drugs [23]. Furthermore, the abuse of synthetic antibiotics has contributed to an increased incidence of bacterial resistance to available antibacterial agents, ensuing an urgent need for natural antimicrobials [24]. To overcome the aforementioned drawbacks of the modern antimicrobial drugs and to attain more efficacious drugs, antimicrobial agents encompassing a novel mode of action should be acquired [25].
Plant-derived flavonoids are a class of naturally-occurring phenyl chromenes that are widely-distributed in edible plants and have been observed in fruits, vegetables, tea, and wine [26,27]. These natural products possess a range of biological activities, including those of the anti-inflammatory, antiallergic, antiproliferative, antibacterial, antidiabetic, antiviral, antimutagenic, antithrombotic, anticarcinogenic, estrogenic, hepatoprotective, insecticidal, and antioxidant varieties [28,29]. Figure 1 illustrates two examples of the flavanone family that are used for cancer resistance treatment (Kaempferol) and for treating inflammatory disorders (Luteolin). The antibacterial activities of flavonoids have been reported to be correlated with their chemical structures [29][30][31][32]. However, the quantitative structure-activity relationship (QSAR) for flavonoids as antibacterial agents has been capturing interest through the quantitative construction of associations between the molecular structures or properties with a variation in biological activities [18,33]. It is significant that anticancer activity, which is comprised of the most interesting pharmacological properties of flavonoids [34], proceeds via a unique mechanism, and aids in the prevention of cancer growth through the flavonoids' ability to function as anti-oxidants [35][36][37], enzyme inhibitors [38], and growth regulators [39]. Moreover, the biological performance of flavonoid molecules is reliant on their position and number of substitutions as well as their structures' condensation level, namely glucosides, homodimers, heterodimers, hydroxy groups, and isoprenyl units [40,41]. Previous studies have conveyed that a methoxy or hydroxy substituent at the C-7 position of the flavanone enhances inhibitory effects on the human colon carcinoma (HCT)-116 cell line [42]. The established results directed our attempt to explore the design of flavanone derivatives with bulkier substituents at the C-7 position and to elucidate their inhibitory effect. Even though several flavonoid derivatives, modified at the C-7 position, have been reported, Naringenin ( Figure 1), 4 ,5,7-trihydroxyflavanone derivatives, functionalized at the C-7 position, have seldom been investigated [43,44]. Naringenin functions as an essential chemical species that operates as an estrogenic substance in humans and as an endogenous regulator in plants [45]. Based on these considerations, herein, we report the synthesis of chromene-based 4 ,5,7-trihydroxyflavanone compounds ( Figure 1) and explore their antimicrobial and antiproliferative behaviors, as advocated by the theoretical predictions. The characterization of the proposed molecules was done through in-silico studies, forecasting their drug likeness, bioactivity, and ADME properties. In addition, the Naringenin derivatives Kaempferol and Luteolin exhibited distinguished biological activities. Kaempferol reduces the resistance of cancer cells to anti-cancer drugs, such as Vinblastine and Paclitaxel, while Luteolin has been employed as a Chinese traditional medicine for treating hypertension, inflammatory disorders, and cancer.
The first step of the multicomponent coupling process began with a Knoevenagel condensation between malononitrile or ethyl cyanoacetate, and the aromatic aldehydes, followed by a Michael addition of the C-8 carbon of 4 ,5,7-trihydroxyflavanone to the α,β-unsaturated malononitrile intermediate, re-aromatization, intramolecular cyclization involving the addition of the C-7 hydroxyl group of 4 ,5,7-trihydroxyflavanone onto one of the cyano groups, and subsequent tautomerization [46], as shown in Scheme 2. Although both the ortho (C6) and para (C8) positions (relative to the C-5 hydroxyl group) of 5,7-dihydroxy-2-(4-hydroxyphenyl) chroman-4-one are strongly and almost as equally activated towards the electrophilic attack, only the C-8 position reacted. The 13 C chemical shifts of the C-6 and C-8 carbons are 96.7 (C 6 ) and 95.8 (C 8 ) ppm, respectively, which indicates that they are in similar electronic environment and exhibit similar nucleophilicity. This suggests that the regiochemistry depended on steric factors to a much larger extent than electronic factors. Indeed, the C-8 position is much less hindered, especially considering the six-membered ring that may form due to hydrogen bonding between the C5-OH and the C-4 carbonyl group. Thus, a preferential attack at C-8 was observed. It is also noteworthy that the C-3 of the phenol ring did not show any reactivity under the reaction conditions since it is much less activated than C-6 and C-8. The observed downfield chemical shift of C-3 (116.0 ppm for C-3 compared to 96.7 ppm for C-6 and 95.8 ppm for C-8) clearly suggests that C-3 experiences less delocalization of electron density from the lone phenolic OH, rendering the C-3 position the least nucleophilic site compared to C-6 and C-8 positions.
The structures of the newly synthesized derivatives were confirmed by various spectroscopic and analytical techniques, such as FT-IR, 1 H-NMR, 13 C-NMR, COSY, HMBC, HSQC, and elemental analysis. The FT-IR spectra exhibited characteristic absorption bands between 2178 and 2207 for the CN group, while the NH 2 stretching were in the range of 3381-3424 cm −1 . Moreover, the C=O group displayed bands at 1634-1686 cm −1 , and the OH bands appeared as broad absorptions at 3477-3634 cm −1 . The 1 H-NMR spectra of 2a-2g, were measured in dimethyl sulfoxide (DMSO-d 6 ) where the H2 signal appeared as a doublet of doublets in the range of 5.07-5.64 ppm. The resonances of the diastereotopic H3ax and H3eq protons 3.34-3.51 and 2.72-2.83 ppm, respectively, as two doublets of doublets. The H3ax and H3eq of the chromene ring were coupled with a constant of 17.1-17.6 Hz. The value of the coupling constant between H2 and H3ax (J = 12.2-13.5 Hz) indicates a trans-diaxial coupling. Thus, the H2 was axial, and the aryl group linked to the H2 had equatorial orientation. As anticipated, the hydroxyl group attached to the C5 appeared as a singlet at 11.9-12.5 ppm, and the C4 -OH occurred in the range 9.62-9.63 ppm; meanwhile, the pyran H10 methine exhibited chemical shifts at 4.46-5.08 ppm, and the amine protons resonated at 7.03-7.79 ppm. The singlet at 6.21-6.27 ppm corresponded to H6, while the remaining aromatic protons resonated further downfield between 6.74 and 8.08 ppm. As an example, the proton spectrum of 2a is shown in Figure 2. In the proton spectrum of Compound 2g, the methyl protons appeared at 0.98 ppm as a triplet, while the methylene chemical shift of the ethoxy group OCH 2 CH 3 ranged from 3.81 to 4.03 ppm. The 13 C-NMR spectra of the new molecules exhibited signals ranging from 78.8-80.2 ppm and 41.7-43.4 ppm that corresponded to C-2 and C-3, respectively, where the lower field signal was being assigned to the oxygenated C-2 carbon. The C-6 signal resonated at 94.8-96.8 ppm, whereas the B ring carbons C-2 , and C-6 showed up at 128.5-129.5 ppm with the equivalent C-3 and C-5 appearing at 115.9-116.1 ppm. The C-4 carbon, connected to the hydroxyl group, appeared at 157.9-158.9 ppm, and the signal at 128.4-132.8 ppm was ascribed to C-1 . The signal at 30.3-36.2 ppm corresponded to the C-10 of the pyran ring, while the quaternary carbon C-8 attached to amine group appeared in the range of 159.3-161.9 ppm. The cyanide functionality, which was a distinctive signal, resonated further downfield at 119.7-121.0 ppm, while the aromatic carbons showed signals between 162.9 and 102.8 ppm, with an additional signal for the C=O of the flavanone moiety at 198.0-198.9 ppm (Figure 3). The carbon signal for the alkoxy methyl group of 2g resonated at 15.0 ppm, the methylene carbon of -OCH 2 CH 3 had a chemical shift at 59.8 ppm, and the signal for (C=O ester) emerged at 168.7 ppm.

Computational Studies
The proposed molecules of flavanone-containing chromenes were evaluated for their in-silico bioactivity, physicochemical, pharmacokinetic/ADME, and drug likeness traits. The bioactivity scores were forecasted against six different preset protein structures within the Molinspiration software, namely the G Protein Coupled Receptors (GPCR) ligand, the ion channel modulator, the kinase inhibitor, the nuclear receptor ligand, and the protease and enzyme inhibition. The results are documented in Table 1. The obtained values indicated the binding affinity of the assessed compounds, 2a-2g, to the aforementioned enzymes and receptors, where the positive values suggested a greater affinity and the negative values implied a lower one. All the tested compounds showed low bioactivity towards the selected protein structures except for the nuclear receptor ligand.
Furthermore, the assorted physicochemical parameters like the number of rotatable bonds, the count of specific atom class, molar refractivity, lipophilicity, and water solubility were calculated. A very effective physiochemical variable, i.e., TPSA (topological polar surface area) was appraised for assessing the drug transport attributes. These physicochemical properties are tabulated in Table 2.  Table 2. Physicochemical properties of the selected compounds 2a-2g.
The predicted pharmacokinetic/ADME properties of the new series, 2a-2g, are given in Table 3. All of the examined molecules exhibited no gastrointestinal (GI) absorption and were P-gp (p-glycoprotein) non-inhibitors. None of these molecules were able to permeate through the blood-brain barrier (BBB). The forecast for the passive HIA (human gastrointestinal absorption), the BBB permeations, and the P-gp substrates was clubbed in an intuitive graphical classification model, namely the BOILED-Egg diagram as shown in Figure 4. Meanwhile, the examined series inhibited the cytochrome P450 isomers, i.e., CYP2C19, CYP2C9, and CYP3A4-except for Compound 2g, which did not inhibit CYP2C19. On the other hand, all the screened molecules emerged as non-inhibitors of the cytochromes CYP1A2 and CYP2D6. The skin permeability coefficient (log Kp; with Kp in cm/s) values that were evaluated for the flavanone/chromene compounds were discovered to be low skin permeable.  Drug likeness was deemed an imperative attribute that serves as a basis in order to establish whether the derivatives could be influential drug nominees. The Lipinski [47], Ghose [48], Veber [49], Egan [50], and Muegge [51] rules were implemented to appraise drug likeness and foretell whether a drug candidate was likely to be bioactive according to several vital criterion like molecular weight, LogP, and the number of hydrogen bond acceptors (HBA) as well as the number of hydrogen bond donors (HBD). The number of violations to the above-mentioned rules along with their bioavailability and drug likeness score are documented in Table 4. The Lipinski (Pfizer) sieve was the trendsetter rule-of-five (RO5), except for compounds 2c and 2g, which had one and two of Lipinski's violations, respectively; the rest of all the tested compounds were drug-like. The forecasting process with the Ghose rule flaunted that Compound 2c was discarded with one violation, compounds 2d and 2g were declined with two violations, and the rest of all the compounds upheld the rule. According to the appraisal procedure with the Veber and Egan rules, all compounds were alike except for compounds 2e and 2g, with one violation each. Moreover, the scrutinizing approach in accordance to the Muegge rules displayed that all the compounds satisfied the benchmark of the drug likeness assessment except for compounds 2d, 2e, and 2g, each with one violation. Meanwhile, these novel compounds exhibited a bioavailability score of 0.55, except for 2g, whose bioavailability score was 0.11. Furthermore, all the screened candidates exhibited good drug-likeness scores, ranging from 0.62 to 1.37, as presented in Figure 5.

Antimicrobial Screening
An in vitro antimicrobial assay was performed on the targeted molecules 2a-2g in order to evaluate their antibacterial, antifungal, and antimycobacterium characters through the agar diffusion-well method [52]. The activities of the novel derivatives were investigated against seven human pathogens, including four Gram-positive bacteria, three Gram-negative bacteria, four fungi, and Mycobacterium tuberculosis, Tables 5 and 6. ampicillin, gentamicin, amphotericin B, vancomycin, and isoniazid were exploited as control drugs [53,54]. The employment of the serial dilution procedure identified the inhibition zones and the minimum inhibitory concentrations (MIC), as shown in Figures 6 and 7. The values of the inhibition zone (IZ) and the minimum inhibitory concentrations (MIC) of the target compounds against Pseudomonas aeruginosa and E. coli point out a high inhibitory activity associated with derivatives 2a,2b and 2d-2g, as indicated by IZ values ranging from 18.3 to 24.6 mm and the MIC values from 0.49 to 3.9 µg/mL, as shown in Tables 5 and 6. Meanwhile, the results of the inhibition zone (IZ) and the minimum inhibitory concentrations (MIC) were discovered to be more effective against Salmonella typhimurium by the IZ value of 23.4-26.4 mm. Figures 6 and 7 display the aforementioned data. The antibacterial activity of most compounds was found to be comparably active to the standard drugs when evaluated against the examined gram-positive bacteria, with a MIC range of 0.49 to 3.9 µg/mL. Compounds 2b and 2e exhibited a mild inhibitory activity against the Methicillin-resistant Staphylococcus aureus (MRSA), as shown by the IZ value of 21.3-20.6 mm and the MIC value of 1.95-3.9 µg/mL. Meanwhile, most of the investigated derivatives were slightly more active against the Tuberculosis (TB) and the fungal species. Compound 2e demonstrated moderate activity in comparison to isoniazid. On the other hand, Compound 2c did not indicate any antimicrobial activity against the tested bacteria, fungi, and TB. In general, the antimicrobial activity of the new flavanone-containing chromene derivatives presented more potency than the reference drugs against Gram-negative bacteria and a relatively reduced activity towards Gram-positive bacteria, fungi, and TB.

Cytotoxic Screening
The in vitro cytotoxicity of the produced derivatives 2a-2g was tested with the 2-(4,5dimethylthiazol-2-yl)-3,5-diphenyl-2Htetrazol-3-ium bromide (MTT) method against the human colon carcinoma (HCT-116), human hepatocellular carcinoma (HepG-2), human breast adenocarcinoma (MCF-7), and adenocarcinoma human alveolar basal epithelial cell (A-549) cell lines [55,56]. The standard reference drug utilized was doxorubicin, and the inhibitory activities (IC 50 ) are provided in Table 7 and Figure 8. The compounds 2b and 2d-2g showed good cell growth inhibitory behavior against the HCT-116 cell line (IC 50 = 1.08-1.48 µg/mL). The IC 50 values of the assessed compounds against the HepG-2 and A-549 cell lines indicated that Compound 2e had a comparable activity with respect to the reference drug. By evaluating the inhibitory activity of the targeted molecules with that of doxorubicin against the MCF-7 cell line, it was determined that most of the compounds were less active than doxorubicin. Further research might lead to enhanced inhibitory behavior, especially for Compound 2e, against the HCT-116 cell line.  The cell viability of colon, breast, liver, and epithelial cell lines, following exposure to different concentrations of compounds 2a-2g, was assessed with the MTT method. Data are presented as IC 50 (µg/mL) values.

Docking Studies
A docking study was performed for the tested compounds 2a, 2b, 2d, and 2e in order to scrutinize their possible interactions with gyrase B (GyrB43) from E. coli (PDB code: 4PRV; resolution 2.00 Å) by employing the docking module that was implemented in the MOE software. The bacterial DNA gyrase has been reported as a good target for antibacterial agents and the assessment of potential antibacterial activity of new compounds [18]. Figure 9 presents the best docking poses for the novel flavanone bearing chromene moiety inside the GyrB binding pocket.   In order to verify the supreme in silico conformation, the molecular docking screenings of the novel derivatives were rendered with the cyclin-dependent kinase-2 (CDK2, PDB ID: 1FVV) as the target protein. To entertain this intent, a Lamarckian genetic algorithm docking program, AutoDock 4.0, was engaged where the flavanone chromene derivatives were docked on the target receptor. The docking scores of all ligands are documented in Table 9. The ligands unveiled low-to-moderate docking scores towards the target receptor CDK2 that ranged from −7.0 to −5.5. The docking pattern of the selected ligand derivative 2e, which exhibited the highest docking score, is illustrated in Figure 10.

Molecular Descriptors-Based SAR Analysis
The SAR analysis was implemented on a collection of molecules (2e, 2d, and 2a) that exhibited diverse activity profiles via the quantum mechanical calculations, and the analysis employed the Molecular Orbital PACkage (MOPAC) quantum engine in the MOE software [57]. For numerous pharmacological and chemical procedures, their significance was held within the energies of their frontier orbitals, which delivered data on the electron-donating and electron-withdrawing nature of derivatives with the formation of a charge transfer complex (CTC) [58], as illustrated in Table 10. Furthermore, the institution of the electron-accepting centers to the pursued moiety showed an encouraging impact against the antimicrobial behavior, specifically towards the Gram-negative bacteria, as established by the quantum estimates. As can be seen in Figure 11, the representative molecules demonstrating dissimilarities in the activity profiles was due to the electron density allocation of the Highest Occupied Molecular Orbital (HOMO) and the lowest Unoccupied Molecular Orbital (LUMO) surfaces. Regarding the newly active molecules, the substituent distribution resulted in a lower density quality in their HOMO in comparison to their LUMO analogue. Moreover, it was discovered that the compounds experiencing lower levels of activity possessed efficacious electron donors that interacted with several targets through the charge transfer mechanism prior to the attainment of the enzyme, and they could not pass through the bacterial cell membranes. The molecular parameters, including the number of atoms, orbitals, electrons, Self Consistent Field (SCF) energy, the dipole moment, and the heat of formation, were calculated from the Molecular Operating Environment (MOE) program. These values were reported for the representative derivatives of high activity (2e), medium activity (2a), and low activity (2f). Moreover, the electrostatic maps were analyzed against the molecular surfaces for the novel molecules (Figure 12), where the green regions show the hydrophobic moieties and the red/blue regions show the polar ones.

Method of Computation: In Silico Study
The bioactivity scores of the synthesized compounds, 2a-2g, were evaluated by utilizing the Molinspiration Cheminformatics server (http://www.molinspiration.com). The Molsoft server (http: //www.molsoft.com) was employed to find the drug likeness scores of the above-mentioned compounds. The molecular descriptors/physico-chemical and pharmaco-kinetic/ADME attributes of the synthesized compounds, 2a-2g, were determined with the SwissADME server (http://www.sib.swiss). The same web interface was used to carry out the investigations of the drug likeness violations of compounds 2a-2g.

Materials and Instrumentation
The chemicals and solvents were purchased from Sigma-Aldrich (Oakville, ON, Canada) and Alfa Aesar (Tewksbury, MA, USA), and they were used as received.
Aryl aldehyde (2.3 mmol) was added to a stirred solution that contained Compound 1 (2.3 mmol) in 5 ml of ethanol and malononitrile or ethyl cyanoacetate (2.3 mmol) with a few drops of piperidine. The reaction mixture was stirred at reflux. After the completion of the reaction (monitored by TLC), the mixture was kept at room temperature, and the formed solid product was collected by filtration and washed with ethanol and hexane to yield 2a-2g.

Antimicrobial Screening
The antimicrobial assay has been performed according to the preceding reports [46,60].

Molecular Modeling
The docking maneuver was assessed in order to dock the newly synthesized compounds into the crystal structure of the E. coli topoisomerase II DNA gyrase B (PDB code 4PRV). All the docking calculations were engineered by the MOE software [58], which was able to generate the docking input files and examine the docking outcomes. The protonation of the enzyme was carried out and energy was minimized by removing clorobiocin, all non-polar hydrogens, and crystal water molecules. In every case, the 100 docked structures were generated by implementing the genetic algorithm searches. The 3D structures of all the tested compounds were created in MOE, and the protonation of target ligands was performed. The energy minimization of the derivatives was done up to a 0.05 gradient, employing the GBVI/WSA dG force field. The obtained data were stored in a database as input files in MOE. The root-mean-square deviations (RMSD values) were calculated, and embryonic ligand binding fashion was plotted. The protein-ligand association plots were produced by utilizing MOE 2012.10. The MOE software was implemented to develop the surface molecular orbitals and to undertake the quantum mechanical calculations.
The in-silico docking tactics were executed to conduct structure-based drug designing in order to acquire the most potent inhibitor of CDK2 from the synthesized drug nominees. The Advanced Chemistry Development, Inc. ACD/Labs-Chemsketch program was exercised to construct the 3D atomic coordinates of the targeted ligands. The structure of CDK2 (PDB ID 1FVV) with crystallographic resolutions of less than 3.0 Å was procured from the Protein Data Bank (Source: www.rcsb.org/pdb/). The Dundee PRODRG2 server was employed to minimize the energy of the investigated ligands [63]. The autodock4 from "Auto-Dock Tools (ADT, 1.5.6)" is a graphical user interface program [64] that was utilized to prepare, run, and analyze the docking simulations. The docking stipulations were stationed to the software's default values, and a standard paradigm was preserved and escorted throughout the docking studies. The outcomes were explained based on the PDF file and created by the software by designating the different ligands with respect to the predicted binding energy. The cluster gaining the lowest energy was identified as the most accurate solution. The 3D visualization of the ligand protein interaction was done by utilizing UCSF Chimera 1.11.2 and mcule, a web interface which exploits the WebGL/Javascript-based molecule viewer of GLmol.

Conclusions
The present report details the synthesis of new flavanone/chromene molecules that were nominated for their confirmed drug-likeness capabilities through in silico studies and in vitro assessments of their antimicrobial activity and cytotoxic effects. The pursued derivatives were produced by the Knoevenagal condensation of an aldehyde, followed by the intramolecular Michael addition reaction of adduct for the 4 5,7-trihydroxy-flavanone. The structures of the aforementioned compounds were established under their spectral and analytical data. The antibacterial assay revealed that several molecules exhibited high inhibitory activity against P. aeruginosa and E. coli in comparison to the reference drugs. Additionally, the cytotoxicity investigations were assessed against four different human carcinoma cell lines and demonstrated strong effects of the molecules, particularly against the HCT-116 tumor cell line. The molecular modeling outcomes demonstrated a powerful binding interaction of the newly synthesized derivatives in the active site of the GyrB with the SAR analysis.