Synthesis and biological evaluation of coumarin-quinone hybrids as multifunctional bioactive agents doi: https://doi.org/10.5599/admet.1468 81 ADMET & DMPK 11(1) (2023) 81-96; doi: https://doi.org/10.5599/admet.1468 Open Access : ISSN : 1848-7718 http://www.pub.iapchem.org/ojs/index.php/admet/index Original scientific paper Synthesis and biological evaluation of coumarin-quinone hybrids as multifunctional bioactive agents Anees Pangal1,2 and Khursheed Ahmed1,2* 1 Department of Chemistry & Post Graduate Centre, Abeda Inamdar Sr. College of Arts, Science & Commerce (Autonomous), Camp, Pune – 411001, India 2 Advanced Scientific Research Laboratory, Azam Campus, Pune – 411001, India. *Corresponding Author: E-mail: khursheedahmed@azamcampus.org Received: July 22, 2022; Revised: September 29, 2022; Published: October 07, 2022 Abstract We report the synthesis, structural characterization and pharmaceutical activity of four coumarin-quinone hybrids. The compounds were significantly active against Staphylococcus aureus, Pseudomonas aeoginosa and Candida albicans. Promising antioxidant activity was observed when compared to ascorbic acid. Two compounds, DTBSB and DTBSN, also showed commendable in vitro antiproliferative activities against the cells of human cancer cell lines MCF-7, MDA-MB-231, COLO-205, HT-29 and A549 along with appreciable tumor selectivity with distinct selectivity index. Molecular docking studies using cyclooxygenase-2 (PDB ID: 6COX) revealed strong binding affinities for the COX-2 active site. Moreover, ADMET properties of the synthesized compounds were determined using the pKCSM and SwissADME online tools and all the compounds had accurate pharmacokinetic profiles. Hence, the new coumarin-quinone hybrids DTBSB and DTBSN can be considered for optimization and lead development. ©2022 by the authors. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). Keywords ADMET; Molecular Docking; Antiproliferative; Antimicrobial; Antioxidant; drug-likeness Introduction Natural and synthetic coumarins have gathered much attention based on a broad spectrum of pharmacological and biological properties. In the literature, coumarin and its derivatives exhibit comprehensive biological activities [1] like anticancer [2-5], antioxidant and anti-inflammatory [6], antimicrobial [7], antifungal [8] and anti-HIV [9] activities. Natural and synthetic coumarin compounds like esculetin and scopoletin have potential as anticancer agents. Naturally, coumarin displayed antiproliferative effects on various types of cancers such as prostate, renal, breast, laryngeal, lung, colon, CNS, leukemia and melanoma [10-11]. Coumarins are used in the treatment of different types of cancers like prostate cancer, renal cell carcinoma and leukemia and to inhibit the spread of tumors [12]. The wide scope of biological activities attributed to coumarins and their medicinal impact on various disorders have received considerable attention. Furthermore, the stability and solubility of coumarins are intriguing, which are important criteria for drug development [13]. https://doi.org/10.5599/admet.1468 https://doi.org/10.5599/admet.1468 http://www.pub.iapchem.org/ojs/index.php/admet/index mailto:khursheedahmed@azamcampus.org http://creativecommons.org/licenses/by/4.0/ A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 82 Natural quinones such as juglone and plumbagin exhibited growth inhibitory effects on microorganisms [14]. Benzoquinones play an important role in oxidative phosphorylation electron transfer processes and bioenergetic transport [15]. Quinones showed diverse pharmacological properties such as anti-inflammatory [16], antimicrobial [17] and anticancer [18-20]. 1,4-benzoquinone derivatives were applied as antibiotics [21- 22], antitumor [23-25], antimalarial [26] and anticoagulant compounds [27]. The anticancer properties of quinones are well described and there are several clinically important antitumor drugs based on quinone scaffolds, e.g., anthracyclines, mitoxantrones and saintopin [28]. Cheminformatic tools, including the Prediction of Activity Spectra for Substances (PASS), Lipinski’s rule of five, and ADMET (absorption, distribution, metabolism, and excretion – toxicity) predictions, are useful applications for the optimization of drug discovery [29]. ADMET, which constitutes the pharmacokinetic profile of a drug molecule, is essential for the evaluation of its pharmacodynamic properties [30]. ADMET Predictor is a program designed for the estimation of pharmacokinetic parameters or properties based on molecular structures of drug candidates [31]. The ideal oral drug is rapidly and completely absorbed by the gastrointestinal tract, is distributed specifically to its site of action in the body, is metabolized in a way that does not instantly diminish its activity, and is eliminated without causing harm. Therefore, ADMET properties are important determinants of the test compound for any future therapeutic application in humans [32]. In this work, we combined coumarin and quinone moieties to obtain new hybrid molecules with promising biological activities such as antimicrobial, antioxidant and anticancer properties. The interaction and binding affinities of the new test compounds with cyclooxygenase (COX) were determined via docking calculations. The drug-like potential of these hybrids was evaluated using in silico methods. Of the four synthesized coumarin-quinone hybrids, DTBSB and DTBSN were found to be more effective biological agents among the synthesized analogs. Experimental Materials Solvents were purchased from commercial sources and were dried by standard protocols. The starting materials such as ethyl 3-hydrazinyl-3-oxopropanoate, 2,6-di-tert-butyl-1,4-benzoquinone, 5- bromosalicylaldehyde, 5-chlorosalicylaldehyde, and 5-nitrosalicylaldehyde were obtained from Sigma- Aldrich, India. Salicylaldehyde, trifluoroacetic acid, piperidine, acetone, methanol, ethanol and dichloromethane were obtained from SD-FCL Chemical Limited, Mumbai, India. DMEM and FBS were purchased from Himedia, Mumbai. The MTT (3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide) reagent was obtained from G-Biosciences, USA. TLC was monitored using commercially available aluminium TLC plates coated with silica gel GF254, and the developed plates were visualized by UV light and iodine vapors. Melting points of synthesized compounds were determined with an open capillary tube using a VEEGO melting point apparatus. The HRMS, FTIR and NMR spectroscopic data were obtained from CIF, Savitribai Phule Pune University, Pune and CIF, IISc, Bangalore. The in vitro biological activities and in silico predictions were carried out at Advanced Scientific Research Laboratory, Abeda Inamdar Senior College, Pune. Synthesis of coumarin-quinone hybrids The procedure used for the synthesis of target coumarin-quinone hybrids compounds is illustrated in Figure 1. 2,6-di-tert-butyl-1,4-benzoquinone (1, 10 mmol) and ethyl 3-hydrazinyl-3-oxopropanoate (2, 10 mmol) was dissolved in ethanol. After complete dissolution, a few drops of trifluoroacetic acid were added and the mixture was refluxed for 2 hours. The reaction mixture was poured onto an ice/water mixture and ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 83 the separated product was collected, washed with cold water several times, and recrystallized from ethanol to obtain 2,6-di-tert-butyl-1,4-benzoquinone hydrazone (3). A mixture of (3) and substituted salicylaldehyde (4, 1eq) was dissolved in ethanol. A few drops of piperidine were added to the mixture, and the reaction mixture was stirred at room temperature until the reaction was completed, which was monitored by TLC. After completion of the reaction, the reaction mixture was neutralized with dil. HCl and formed coumarin-quinone hybrids (5) were isolated by filtration and recrystallized in ethanol. The detailed physical properties and spectral characterization data are given below. Ethyl 2-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dienylideneaminocarbamoyl)acetate (DTBH): Yellow solid (95 %), MP 164-166 °C, HRMS (EI): C19H29N2O4, [M+H] = 349.21, FTIR(cm-1): 3739.30 (N- H), 1744.30 (lactone C=O), 1683.55 (C=O), 1624.73 (C=O), 1536.02 (C=N), 1315.21 (C=C), 1141.65 - 1024.98 (C-O), , 1H-NMR (400MHz , d-DMSO, (δ,ppm): 1.23 (s, 18H), 4.10 (q, 2H), 3.74 (s, 2H), 1.21 (t, 3H), 6.82 d, 1H), 7.74 (d, 1H), 12.39 (s, 1H, –NH), 13C-NMR (125MHz, d-DMSO): 186.77, 166.03, 158.42, 154.57, 151.10, 150.61, 146.68, 135.22, 133.21, 130.26, 125.94, 118.52, 117.20, 116.13, 35.55, 29.46 N'-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)-2-oxo-2H-chromene-3-carbohydrazide (DTBSA): Light orange solid (85 %), MP 134-136 °C, HRMS (EI): C24H27N2O4, [M+H] = 407.20, FTIR(cm- 1): 3739.30 (N-H), 1712.48 (lactone C=O), 1683.15 (C=O), 1624.22 (C=O), 1525.42 (C=N), 1301.72 (Aromatic C=C),1202.40-1024.98 (C-O), 1H-NMR (400MHz, CDCl3) (δ, ppm,): 1.34 (s, 18H), 12.78 (s, 1H- NH), 9.15 (s, 1H), 7.40 to 7.79 (m, 4H), 8.5 (d, 1H), 7.04 (s, 1H), 6.98 (s, 1H), 13C-NMR (125MHz, CDCl3): 186.77, 166.03, 158.42, 154.57, 151.10, 150.61, 146.68, 135.22, 133.21, 130.26, 125.94, 118.52, 117.20, 116.13, 35.55, 29.46. N'-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)-6-chloro-2-oxo-2H-chromene-3- carbohydrazide (DTBSC): Orange solid (90 %), MP 186-188 °C, HRMS(EI): C24H26ClN2O4, [M+H] = 441.16, FTIR (cm-1): 3739.30 (N-H), 1712.48 (lactone C=O), 1525.42 (C=N), 1301.72 (Aromatic C=C), 1202.40- 1024.98 (C-O), 1H-NMR (400MHz, CDCl3) (δ, ppm,): 1.30 (s, 18H), 12.67 (s, 1H, -NH), 9.07 (s, 1H), 7.75 (d, J=7.69Hz, 1H), 7.69 (dd, J=7.69 and 8.8 Hz, 1H), 7.42 (d, J=8.8Hz, 1H), 7.02 (s, 1H), 6.96 (s, 1H), 13C-NMR (125MHz, CDCl3): 186.68, 167.08, 157.93, 154.41, 153.91, 150.52, 149.29, 146.97, 135.07, 133.29, 129.12, 118.37, 116.09, 115.62, 35.47, 29.44. N'-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)-6-bromo-2-oxo-2H-chromene-3- carbohydrazide (DTBSB): Brown solid (92 %), MP 152-156 °C, HRMS(EI): C24H26BrN2O4, [M+H] = 485.11, FTIR (cm-1):3745.08(N-H), 1712.48 (C=O), 1640.16 (C=O), 1525.10 (C=N) 1363.43 (C=C), 1197.58 - 1014.37 (C-O), 1H-NMR (400MHz , CDCl3) (δ, ppm,): 1.34 (s, 18H), 12.67 (s, 1H, -NH), 9.061 (s, 1H), 7.91 (s, 1H), 7.83 (d, J=8.8 Hz, 1H), 7.36 (d, J=8.8 Hz, 1H), 7.17 (s, 1H), 6.86 (s, 1H), 13C-NMR (125MHz, CDCl3): 186.71, 167.08, 161.55, 157.91, 154.41, 150.50, 149.18, 146.96, 137.85, 133.09, 132.76, 118.65, 116.36, 115.64, 36.38, 29.45. N'-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)-6-nitro-2-oxo-2H-chromene-3- carbohydrazide (DTBSN): Dark brown solid (92 %), MP 118-120 °C, HRMS(EI): C24H26N3O6, [M+H] = 452.18, FTIR (cm-1):3739.30(N-H), 1681.62 (C=O), 1337.39 to 1509.99 (Aromatic, -NO2), 1293.04 - 1020.16(C-O), 1H-NMR (400MHz, CDCl3) (δ, ppm,): 1.28 (s, 18H), 10.00 (s, 1H, -NH), 9.21 (s, 1H), 8.70 (d, J=2.4Hz, 1H), 8.07 (dd, J=2.4 and 2.8 Hz, 1H), 7.91 (d, J=2.8 Hz, 1H), 7.26 (s, 1H), 6.84 (s, 1H), 13C- NMR (125MHz, CDCl3): 186.74, 165.42, 159.32, 153.62, 151.61, 149.17, 144.96, 138.61, 136.54, https://doi.org/10.5599/admet.1468 A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 84 132.96, 128.04, 118.31, 116.85, 115.80, 34.38, 29.51. Antimicrobial activity The nutrient broth was prepared and autoclaved for 20 minutes at 120 psi. Cultures of Staphylococcus aureus NCIM 5021 and Pseudomonas aeruginosa NCIM 5029 were inoculated and incubated at 37 °C for 24 hours. Then, each well was inoculated with a microbial inoculum prepared in the same medium after dilution of standardized microbial suspension adjusted to 0.5 McFarland scale (108 CFU/mL). 180 µl of the cell suspension was seeded in each of the 96 well plates and 20 µl of different concentrations of the test compounds and the standard was added. The wells without test compound were considered as control and streptomycin was used as standard. After mixing, the 96-well plates were incubated at 37 °C for 24 hours. After incubation, the absorbance of each well was recorded at 620 nm using Readwell Touch Automatic Elisa Plate Reader (Robonik India Private Limited). All the experiments were performed in triplicates and the growth percentage was calculated using the formula: Percentage growth inhibition= Ti/C x 100 where Ti = Growth of the microorganisms in the presence of a drug, and C = Control growth. A similar procedure was applied for the antifungal activity test with slight changes. Potato dextrose broth (PDB) was used for fungal culture pre-enrichment, dilutions and inoculations. The antifungal activity was evaluated using the Candida albicans NCIM 3100 strain. 180 µl of the cell suspension was seeded in each of the 96-well plates and 20 µl of different concentrations of the test compounds and the standard was added to the respective wells in the plate. The wells without test compound were considered as control and itraconazole was used as standard. After mixing, the 96-well plates were incubated at 37 °C for 24 hours. After incubation, the absorbance of each well was recorded at 620 nm using Readwell Touch Automatic Elisa Plate Reader (Robonik India Private Limited). All the experiments were performed in triplicates and the growth percentage was calculated using the formula mentioned above. Antioxidant activity (DPPH scavenging activity) The DPPH free radicals scavenging activity was assessed using the microplate assay standard method with slight modifications. Drug stock solutions (1000 µg/ml) were diluted to final concentrations of 1, 5, 10, 20, 25, 40, 50, 60, 80, 100, 125 and 150 µg/ml in methanol. 0.004 g DPPH reagent was dissolved in 100 ml methanol. 50 µl of the sample and 150 µl of the DPPH solution were added to 96 well plates. The plate was incubated for 30 min at room temperature in the dark. The absorbance (Abs) was recorded at 520 nm wavelength with a microplate reader (Readwell Touch Automatic Elisa Plate Reader (Robonik India Private Limited) and converted to the percentages. Methanol was used as a solvent and ascorbic acid as standard. The percentage radical scavenging was calculated from the absorbance using the following formula: % Radical scavenging activity = ((Abs of control-Abs of sample))/(Abs of control) x 100 Cell viability inhibition assay (MTT Assay) The in vitro antiproliferative activities of the test compounds were evaluated against five human cancer cell lines, which include two human breast cancer cell lines (MCF-7 and MDA-MB-231), two human colon carcinoma cell lines (COLO-205 and HT-29), and one human lung carcinoma (A549) using the MTT assay. 5- Fluorouracil (5-FU) was used as a positive control. The tested cell lines were purchased from The National Centre for Cell Science (NCCS), Pune, and cultivated in the appropriate growth medium. The growth medium was supplemented with 100 mg/mL of streptomycin, 100 units/mL of penicillin, and 10 % of heat-inactivated fetal bovine serum in a humidified 5 % (v/v) CO2 atmosphere at 37 °C. Then 1x106 cells per well were seeded ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 85 into 96-well well plates. The medium was replaced after 24-48 hours with a fresh medium containing different dilutions of the test compounds (diluted using the DMEM). After 48 hours, 5 % MTT solution was added. After incubation for additional 4 hours, the formazan formed by metabolically viable cells was dissolved in DMSO, and after 10-20 minutes, absorbance was recorded at 570 nm using Readwell Touch Automatic Elisa Plate Reader (Robonik India Private Limited). The metabolic viability of cancer cells treated with test compounds was compared with the viability of untreated cells (taken as 100% viable). All experiments were performed in triplicates and the growth percentage was calculated using the formula: Percentage growth inhibition= Ti/C x 100 where, Ti = Growth of the microorganisms in the presence of test compound and C = Control growth. In vitro cytotoxicity assay against non-cancerous cells To study the toxicity against non-malignant cells, the compounds were tested against non-cancerous normal human peripheral blood mononuclear cells (PBMCs). Isolation of peripheral blood mononuclear cells was done using Ficoll-Hypaque according to the standard method [33] and an MTT assay was used to evaluate the cytotoxicity of the synthesized hydrazones. 1×106 cells per well were seeded in a 96-well plate before they were exposed to different concentrations of tested compounds for 48 hrs along with a control well. After 48 hrs, the culture medium containing hydrazones was removed by washing with PBS. Then 10 μl of MTT solution (5mg/ml) was added and incubated for 4 hours, followed by the addition of 100 μl of DMSO. After 10-20 minutes, absorbance was recorded at 570 nm using Readwell Touch Automatic Elisa Plate Reader (Robonik India Private Limited). Furthermore, the selectivity index was calculated by using the following formula. Selectivity index = IC50 value from PBMC/IC50 value of the same compound in cancer cells Molecular docking Molecular docking studies were carried out with the COX-2 protein model [34]. Essential hydrogen atoms, Kollman united atom type charges and salvation parameters were added with the aid of AutoDock 4.2 tools. Molecular docking was conducted in these protein cavities by using Autodock Vina. Auto Dock 4.2 (MGL tools- 1.5.6) was used to perform all docking calculations, and finally, Pymol viewer was used to visualize docking results. ADMET and pharmacokinetic studies ADMET and pharmacokinetic properties were determined using pkCSM (A Cambridge online source, link: http://biosig.unimelb.edu.au/pkcsm/prediction). The structures of all test compounds and their physicochemical properties were drawn and calculated using ChemDraw 12.0 software. Simultaneously, the SMILE file format of all compounds was obtained from ChemDraw 12.0 to obtain the drug-likeness data. pkCSM predictor provides information regarding absorption parameters like human intestinal absorption (HIA), oral bioavailability, Caco-2 permeability, distribution parameters like plasma protein binding (PPB), blood-brain barrier (BBB), metabolism parameters like cytochrome P450 2D6 (CYP2D6) inhibition and cytochrome P450 3A4 (CYP3A4) inhibition, excretion parameters like renal clearance, and toxicity parameters like organ toxicity and genomic toxicities. The pharmacological properties and drug-likeness of the test compounds were evaluated using the online source SwissADME (link: http://www.swissadme.ch/). Results and discussion Chemistry https://doi.org/10.5599/admet.1468 http://biosig.unimelb.edu.au/pkcsm/prediction http://www.swissadme.ch/ A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 86 The target compounds were synthesized in two steps, as shown in Figure 1. Initially, 2,6-di-tert-butyl-1,4- benzoquinone hydrazone (3) was prepared from the reaction of 2,6-di-tert-butyl-1,4-benzoquinone (1) with ethyl 3-hydrazinyl-3-oxopropanoate (2). The intermediate (3) was obtained as a yellow compound in high yield. The structure of (3) was confirmed based on its HRMS, IR, 1H-NMR and 13C-NMR spectra. Subsequently, the coumarin-quinone hybrids (5) were obtained from (3) and the corresponding salicylaldehyde (4) in the presence of a few drops of piperidine, followed by neutralization with diluted HCl. Four coumarin-quinone hybrids abbreviated as DTBSA, DTBSC, DTBSB and DTBSN were obtained and purified, followed by characterization using HRMS, FTIR, 1H-NMR and 13C-NMR spectroscopy. The HRMS (EI) spectra of all coumarin-quinone hybrids showed the major peaks corresponding to the expected M+1 or M+H fragment at 407.20, 441.16, 485.11 and 452.18, respectively. The IR spectra of these analogs showed characteristic peaks for –NH, lactone carbonyl and >C=O (amide). The IR spectrum of all analogs showed one peak between 3739.30 to 3745.08 cm-1 for –NH. The peaks at 1712 to 1714 cm-1 is due to >C=O (lactone moiety) and at 1624.73 to 1683.55 cm-1 are amide >C=O. The peak for the imine group was detected between 1525 to 1536 cm-1. The 1H-NMR spectra of the hybrid compounds showed the olefin proton of the coumarin ring as a sharp singlet at 9.06 to 9.5 ppm. The amide protons appeared as singlet from 10 to 12.78 ppm. The 13C-NMR of all these analogs exhibited signals for all aromatic carbon atoms in the estimated range and characteristic peaks of imine, lactone carbonyl, amide and ketone carbonyl carbons in the range of 153-154, 157-159, 165-167 and 186 ppm, respectively. O N H O CH3 O O CF3COOH EtOH, RT 1 H2N O N O N H O O O + N O N H O O O HO Piperidine EtOH, RT O N H O O H O X + X N O 3 DTBSA Where X = DTBSC DTBSB -NO2-Br-Cl-H DTBSN 2 3 4 5 Figure 1. Synthesis of coumarin-quinone hybrids (5) Antimicrobial activity The coumarin-quinone hybrids (5) were tested for their antimicrobial activity using Staphylococcus aureus NCIM 5021, Pseudomonas aeruginosa NCIM 5029 and Candida albicans NCIM 3100 strains. Different concentrations of the hybrids were used for screening. The obtained results were compared with the values produced from the standard drugs streptomycin (antibacterial) and itraconazole (antifungal). Growth curves are shown in Figure 2. Each compound showed plausible antimicrobial activity in a dose-dependent way. Among the synthesized derivatives, DTBSB was most active against Staphylococcus aureus, followed by DTBSN, DTBSA and DTBSC. DTBSB was most active against Gram-negative organism Pseudomonas aeruginosa ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 87 by 90 % at the highest concentration. DTBSC was found to be the least active analog, with about 20 % bacterial growth at higher concentrations. The screening data indicated that DTBSB showed significant activity against Candida albicans. Figure 2. Results of antimicrobial activity IC50 was calculated and tabulated in Table 1. In terms of the IC50 values, all the analogs have good to moderate antimicrobial activity against the three microorganisms. The standard compounds streptomycin (STR) and itraconazole (ITR) exhibited the IC50 value of 76.96 ± 4.46 μM and 56.49 ± 0.82 μM, respectively. Compared to STR, DTBSB exhibited good antibacterial activity against Gram-positive bacteria Staphylococcus aureus (IC50 = 107.28 ± 1.23 μM). In terms of the IC50 value, the analogs DTBSB was also most active against Pseudomonas aeruginosa (IC50 = 129.63 ± 2.50 μM), while DTBSC was the least active analog. The IC50 value of DTBSB was close to the IC50 value of the control compound STR. When compared with STR, the synthesized analogs exhibited good to moderate antibacterial potential against Gram-positive bacteria Pseudomonas aeruginosa. Further, all analogs possessed moderate antifungal activity against Candida albicans. Among the synthesized compounds, the most potent analog is DTBSB and exhibited an IC50 value of 121.04 ± 1.10 μM. The IC50 value of standard ITR was 56.49 ± 0.82 μM. The other derivative expressed higher IC50 values, which makes them less susceptible to Candida albicans. When compared with ITR, the new analogs have moderate antifungal potential. Table 1. IC50 concentration values of coumarin-quinone hybrids Microorganism Staphylococcus aureus Pseudomonas aeruginosa Candida albicans Compound IC50 Drug Concentrations (µM) DTBSA 236.42 ± 2.90 225.26 ± 3.08 260.19 ± 0.78 DTBSC 250.04 ± 3.37 275.70 ± 0.77 246.19 ± 8.18 DTBSB 107.28 ± 1.23 129.63 ± 2.50 121.04 ± 1.10 DTBSN 134.67 ± 2.94 172.59 ± 2.08 163.75 ± 2.58 STR 76.96 ± 4.46 93.14 ± 7.64 -- ITR -- -- 56.49 ± 0.82 The most active derivative, DTBSB, can be selected for further development and optimization as an antimicrobial agent can be selected for further development and optimization as an antimicrobial agent. Antioxidant activity All coumarin-quinone hybrids were evaluated for their antioxidant activity using the DPPH assay. The obtained results after drug treatment are depicted in Figure 3. The scavenging activity (in %) versus the concentration of test compounds was plotted and presented in Figure 3. The IC50 concentration values were determined from an online source (http://www.IC50.tk). The https://doi.org/10.5599/admet.1468 http://www.ic50.tk/ A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 88 results obtained were compared with the IC50 value of ascorbic acid (Standard/STD). The results revealed that DTBSB and DTBSN were highly active. The other analogs showed good antioxidant activity when compared with the standard. The scavenging effect of the test compounds increased in a dose-dependent manner. The IC50 values for the hybrids were 10.82, 19.20, 18.71, 11.63 and 13.90 μg/ml, respectively, which were comparable to the IC50 value of ascorbic acid. Among the new hybrid compounds, DTBSN exhibited the best antioxidant activity. Figure 3. Results of antioxidant activity (1=STD, 2=DTBSA, 3=DTBSC, 4=DTBSB, 5=DTBSN) Anticancer studies All coumarin-quinone hybrids were evaluated for their in vitro antiproliferative activity against a set of human cancer cell lines, which includes two breast cancer cell lines (MCF-7 and MDA-MB-231), two colon carcinoma cell lines (COLO-205 and HT-29) and one lung carcinoma (A549). All experiments were performed in triplicates and the obtained results are expressed as the percent growth (%) at different concentrations of test compounds expressed in μM. 5-Fluorouracil (5-FU) was used as standard. Drug concentration causing 50 % inhibition of cell growth was characterized as IC50 value. The results revealed that all coumarin-quinone hybrid compounds exhibited considerable activity against all tested cancer cell lines. Graphs of the dose- dependent effects of the hybrids on these cell lines are shown in Figure 4. Figure 4. Effect of coumarin-quinone hybrids concentration on cancer cell growth at the indicated doses, µM ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 89 From the antiproliferative screening data, it is apparent that with an increase in the concentrations of the tested compounds, the antiproliferative potential of the hybrids increases, too. The IC50 values were calculated using the graph in Figure 4. The results are shown in Table 2. The hybrids DTBSB and DTBSN exhibited good antiproliferative activity against all cancer cell lines. DTBSB was more active against MCF-7 and HT-29 cell lines showing remarkable IC50 values. However, DTBSN exhibited its highest potential against MDA-MB-231, COLO-205 and A-549 cancer cells. The IC50 values of both analogs were in the range of 50 to 100 µM making these compounds relevant for further lead development. Some of the IC50 values of DTBSB and DTBSN were comparable with the IC50 value of standard 5-FU. All the derivatives are active against all tested cancer cell lines. Table 2. Calculated IC50 values (µM) and Selectivity Index (SI) of coumarin-quinone hybrids Cell Lines MCF-7 MDA-MB-231 COLO-205 HT-29 A-549 PBMC Compounds IC50 Drug Concentrations DTBSA 120.5 ± 2.54 69.18 ± 6.45 109.99 ± 2.93 112.33 ± 1.58 103.30 ± 0.17 429.85 ± 3.63 DTBSC 107.88 ± 2.47 58.81 ± 7.38 108.93 ± 0.76 107.02 ± 2.43 88.50 ± 2.01 423.97 ± 2.06 DTBSB 63.93 ± 2.61 50.68 ± 4.31 78.18 ± 0.45 71.82 ± 3.61 65.62 ± 4.33 537.51 ± 5.37 DTBSN 76.84 ± 4.17 53.29 ± 2.22 78.19 ± 2.81 100.30 ± 1.97 66.12 ± 0.04 492.3 ± 4.75 5-FU 39.72 ± 1.68 46.76 ± 8.59 62.23 ± 2.04 56.46 ± 2.64 48.15 ± 1.56 --- Selectivity Index (SI) DTBSA 3.57 6.21 3.91 3.83 4.16 --- DTBSC 3.93 7.21 3.89 3.96 4.79 --- DTBSB 8.41 10.61 6.88 7.48 8.19 --- DTBSN 6.41 9.24 6.30 4.91 7.45 --- In addition, all hybrids were virtually non-toxic to human normal peripheral blood mononuclear cells (PBMCs), indicating a high selectivity of these compounds for cancer cells. The selectivity index (SI) of each test compound for every cancer cell line was determined. The higher the SI value, the more effective and safer a drug would be in future in vivo experiments. The SI of a compound is a widely accepted parameter used to express a compound’s in vitro efficacy in the inhibition of virus replication [35]. Here, the SI values for the hybrid molecules were calculated from the ratio of their IC50 values in tumor cells and that of normal PBMCsl (Table 2). The selectivity index indicates the selectivity of a given compound between normal and cancer cells. The higher the magnitude of the selectivity index, the greater its tumor selectivity is [36]. The highest SI values were calculated for DTBSB including MCF-7 (8.41), MDA-MB-231 (10.61), COLO-205 (6.88), HT-29 (7.48) and A549 (8.19). In general, all the derivatives showed certain selectivity (more than 2) and the SI values entail that the test compounds were more selective towards cancer cells than the non-malignant cells. Molecular docking Recently, benzopyran derivatives were investigated as potent COX-2 inhibitors and more specifically, coumarin derivatives were proved to possess potent anti-inflammatory effects and, thus, were evaluated as COX-2 inhibitors [37]. Our interest in the identification of new COX-2 inhibitors prompted us to explore the use of the coumarin framework for the design of this type of inhibitors [38]. Molecular docking was used for the exploration of the interaction between a drug and an enzyme. The determined binding energy (B. E.) values and the amino acid residues of COX-2 (PDB id: 6COX) are given in Table 3. The calculated binding energies reveal that all coumarin-quinone hybrids fit favorably into the COX-2 active site displaying hydrogen https://doi.org/10.5599/admet.1468 A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 90 bonding with various amino acid residues of the target protein. Table 3. Binding energies and the interacting surfaces of the compounds No. Code B.E. in kcal/mol Amino acid Residue Bond Length in Å 1 DTBSA -8.7 SER-471, ASN-43 3.2, 2.8, 3.4 2 DTBSC -11.1 CYS-47 3.0 3 DTBSB -11.1 CYS-47 3.0 4 DTBSN -11.3 CYS-47 2.8, 2.9 The docking ribbon structures of the COX-2 (6COX) protein with bound coumarin-quinone hybrids are given in Figure 5. The binding interactions for these hydrazones involve -NH functionalities. The best binding energy of -11.3 kcal/mol was exhibited by DTBSN followed by DTBSB, DTBSC and DTBSA. Thus, DTBSN has stronger binding interactions with COX-2 than the other derivatives. The compounds show hydrogen bonding interactions with amino acid residues and the hydrogen bond distances of 2.8 and 2.9 Å lengths indicate strong drug-enzyme interactions. These interactions lead to a stabilization of the bound compounds in the protein cavity. The docking results show that the hybrid compounds may have significant interactions with human COX-2 in vitro. Figure 5. Binding of coumarin-quinone hybrids into the active site of COX-2 (6COX) ADMET and pharmacokinetic studies ADMET Predictor is a computer program designed to predict pharmacokinetic parameters of drug-like compounds like absorption, distribution, metabolism, excretion and toxicity (ADMET) based on their molecular structures. An amenable pharmacokinetic profile with high bioactivity and low toxicities is essential for a compound, which should be investigated during drug discovery to reduce the wastage of time and resources [39-40]. The pharmacokinetic profile and drug-like properties of the new hybrid compounds were predicted using the online sources pkCSM and SwissADME to reassure the drug potential. The predicted values are shown in Table 4. The evaluated parameters showed that the molecules have considerable solubility in water. Log S (S in mol/L) is a parameter used to evaluate aqueous solubility. All compounds have good solubility values ranging from -5.287 to -5.938 mol/L. DTBSB is more soluble in water than all other analogs. A Papp coefficient greater than 0.90 indicates that that compound has high Caco-2 permeability and is easily absorbed in the ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 91 gastrointestinal tract. However, all test compounds exhibited lower Papp coefficients. DTBSN showed the highest value among all analogs, indicating a rather good absorption. Drugs with less than 30 % intestinal absorption are considered to be poorly absorbed in the intestine. All analogs were found to have good intestinal absorption, up to 94 %. With the log Kp > -2.5, the drug is considered to have relatively low skin permeability, and all analogs showed low skin permeability. Table 4. ADMET properties of coumarin-quinone hybrids calculated with pkCSM online tool Property Model Name DTBSA DTBSC DTBSB DTBSN Absorption Water solubilitya -5.287 -5.864 -5.938 -5.373 Caco-2 permeabilityb 0.597 0.611 0.602 0.632 Intestinal absorption (human)c 93.878 93.183 93.116 94.408 Skin permeabilityd -2.877 -2.876 -2.873 -2.754 Distribution VDss (human)e -0.01 -0.031 -0.021 -0.188 BBB permeabilityf 0.139 -0.015 -0.024 -0.227 CNS permeabilityg -1.665 -1.553 -1.531 -1.888 Metabolism CYP2D6 inhibitorh No No No No CYP3A4 inhibitorh Yes Yes Yes Yes Excretion Total clearancei 0.598 -0.373 -0.395 0.57 Toxicity Oral rat acute toxicityj 2.896 3.035 3.04 2.797 Oral rat chronic toxicityk 1.367 1.239 1.211 1.812 Hepatotoxicityh Yes Yes Yes Yes Skin sensitizationh No No No No a(log mol/L), b(log Papp in 10-6 cm/s), c(% Absorbed), d(log Kp), e(log L/kg), f(Fu), g(log PS), h(Yes/No), i(log ml/min/kg), j(LD50 in mol/kg), k(LOAEL in log mg/kg_bw/day) The hybrid DTBSN exhibited a distribution volume within the range (-0.15 to 0.45), which will allow a good distribution of this drug within tissues. The analog DTBSA can only cross the blood-brain barrier, while other analogs did not cross the membrane as the log BB is less than -1. The results also showed that the molecules could not inhibit CYP2D6, while all coumarin-quinone hybrids are good CYP3A4 enzyme inhibitors. This ability of the analogs indicates the ability of these compounds on the metabolism of xenobiotics in the body. The total clearance of DTBSA and DTBSN is high, while other analogs won’t be eliminated from the body. All analogs have LD50 values above 0.5 mM and, thus, they are non-toxic corroborating the in vitro results from PBMCs. The predicted results show that all analogs may cause hepatotoxicity and don’t have skin sensitization potential. These overall results of the ADMET studies disclosed that the compounds have good pharmacokinetic properties. The physicochemical properties of the hybrid compounds were predicted using the SwissADME website. The results are presented in Table 5. The bioavailabilities of all analogs are within the range (0.1 to 1). This profiling of the compounds brings out promising observations with respect to their pharmacological aspects. The drug-likeness of the test compounds was established based on their physicochemical properties to find oral drug candidates. There are five different rule-based filters [41] that are in practice to determine the drug-likeness of any compound. The results of drug-likeness evaluation of the hybrid compounds are shown in Table 6 https://doi.org/10.5599/admet.1468 A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 92 Table 5. Physicochemical properties of the new coumarin-quinone hybrids Properties DTBSA DTBSC DTBSB DTBSN Molecular weight (g/mol) 406.47 440.92 485.37 451.47 No. of heavy atoms 30 31 31 33 No. of arom. heavy atoms 10 10 10 10 No. of rotatable bonds 5 5 5 6 No. of H-Bond acceptors 5 5 5 7 No. of H-Bond donors 1 1 1 1 Molar refractivity 118.27 123.28 125.97 127.10 Total polar surface area Ų 88.74 88.74 88.74 134.56 Solubility log S (ESOL) -5.80 -6.40 -6.71 -5.88 log S (Ali) -7.22 -7.87 -7.93 -8.00 log S (SILICOS-IT) -7.04 -7.62 -7.81 -6.38 Lipophilicity MLOGP 3.11 3.59 3.69 2.23 WLOGP 4.41 5.06 5.17 4.31 XLOGP3 5.59 6.22 6.28 5.42 . Table 6. Drug likeness evaluation of the new coumarin-quinone hybrids Rule-based filters DTBSA DTBSC DTBSB DTBSN Lipinski violations 0 0 0 0 Ghose violations 0 0 0 0 Veber violations 0 0 0 0 Egan violations 0 0 0 1 (TPSA > 131.6) Muegge violations 1 (XLOGP3 >5) 1 (XLOGP3 >5) 1 (XLOGP3 >5) 1 (XLOGP3 >5) Bioavailability score 0.55 0.55 0.55 0.55 PAINS No. of alerts 1 (Quinone) 1 (Quinone) 1 (Quinone) 1 (Quinone) Brenk No. of alerts 3 (quinone, coumarin and imine) 3 (quinone, coumarin and imine) 3 (quinone, coumarin and imine) 5 (quinone, coumarin, imine, nitro group and N-O bond) Lead likeness No. of violations 2 (MW>350, XLOGP3>3.5) 2 (MW>350, XLOGP3>3.5) 2 (MW>350, XLOGP3>3.5) 2 (MW>350, XLOGP3>3.5) The predictions revealed that all test compounds have good drug similarity and can be suitable drug candidates for further study. They have no violation of drug-likeness according to the criteria defined by Lipinski, Ghose and Veber, but DTBSN exhibited one violation in the Egan filter due to a larger TPSA value. All analogs showed Muegge’s filter violations, corresponding to XLOGP3 > 5. According to the Five Laws, a molecule can be orally active/absorbent only if it does not violate two or more of the above rules [42]. All molecules resist Brenk’s rule due to the coumarin, quinone and imine fragments. All analogs contain a quinone moiety, which is responsible for one alert in PAINS. However, all compounds showed two violations in lead likeness due to large molecular weight (MW>350) and XLOGP3 values, which should be >3.5. Thus, ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 93 these preliminary results provide the lead for the design of more potent biologically active drugs with fewer toxicities. Conclusions Four new coumarin-quinone hybrids were synthesized from 3-acetylcoumarin and 2,6-di-tert-butyl-1,4- benzoquinone and tested for in vitro antimicrobial, antioxidant and anticancer activities. The results revealed that the analogs DTBSB and DTBSN were the more active antimicrobial agents when compared to the other analogs. DTBSN exhibited the best antioxidant activity and it may have a higher therapeutic potential as a chemoprotective agent against oxidative stress-related degenerative diseases. The toxicity of the synthesized hybrids was tested on human peripheral mononuclear cells (PBMCs), and they were found to be non-toxic to normal cells. The hybrids DTBSB and DTBSN exhibited good antiproliferative potential against all types of tested cancer cell lines. Compound DTBSB was more active against MCF-7 and HT-29 cells with remarkable IC50 values, while DTBSN exhibited its best potential against MDA-MB-231, COLO-205 and A-549 cancer cells. The IC50 values of both analogs are in the range of 50 to 100 µM making them suitable for further lead development. Furthermore, all derivatives showed a considerable selectivity index (more than 2), and the selectivity indexes entail that the synthesized compounds were more selective toward cancer cells than the non-malignant cells. It is appropriate to mention that antibiotics interfere with the normal functioning of living cells [43]. This property is useful for controlling the growth of microorganisms, but at the same time, it can act as a double-edged sword and can also interfere with the functioning of metabolically active, rapidly multiplying cancer cells [44]. The compounds in the present work have shown activity against the cancer cell lines as well as against microorganisms. The observed antioxidant property of these compounds enables them to reduce oxidative stress, play chemoprotective agents' role in the biological system, and protect cells from oxidative stress-induced neoplastic changes. The in vitro results appear to be in agreement with the observations of the molecular docking study. The pharmacokinetics and drug-likeness evaluation showed a high level of GI absorption of up to 94 %, while all analogs have good solubility in water. The VDss, BBB membrane permeability (log BB) and CNS permeability were used to characterize the distribution of the new compounds and all analogs have a fair distribution in the body. All analogs did not inhibit CYP2D6 and but they were good CYP3A4 inhibitors depicting the ability of these analogs to metabolize xenobiotics in the body. The predictions also underlined the non-toxic nature of these analogs, which is reflected through high values of total clearance, non-hepatotoxic nature and no skin sensitization. These results of ADMET studies revealed that the compounds have acceptable ADMET and pharmacokinetic properties. Furthermore, the drug-likeness study revealed that most of the compounds fulfilled all requirements of Lipinski, Ghose and Veber rules, only DTBSN exhibited one violation in the Egan filter due to a larger TPSA value. All analogs showed Muegge’s filter violations. The compounds possess a quinone moiety leading to one alert in PAINS. Further in vitro and in vivo studies will be necessary for the confirmation of the chemoinformatics investigation. These preliminary results may help get a lead structure with selective anticancer potential. Acknowledgements: We are thankful to the Department of Science and Technology, Govt. of India for providing financial assistance under DST-FIST (0 Level) to Abeda Inamdar Senior College, Pune vide letter number SR/FST/COLLEGE-277/2018 dated 20th December 2018. We are grateful to Dr. P. A. Inamdar, the President of MCE Society, Pune for providing the lab facilities. We are also thankful to Anti-Cancer Drug Screening Facility (ACDSF) at ACTREC, Tata Memorial Centre, Navi Mumbai. https://doi.org/10.5599/admet.1468 A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 94 Conflict of interest: The conflict of interest does not exist. References [1] Z.M. Nofal, M. I. El-Zahar, S.S. Abd El-Karim. Novel coumarin derivatives with expected biological activity. Molecules 5(2) (2000) 99-113. https://doi.org/10.3390/50200099. [2] A. Pangal, Y. Mujahid, B. Desai, J.A. Shaikh, K. Ahmed. Synthesis of 3-(2-(subsituted- (trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents. Current Chemistry Letters 11(1) (2022) 105–112. https://doi.org/10.5267/j.ccl.2021.8.004. [3] Y. Wu, J. Xu, Y. Liu, Y. Zeng, G. Wu. A review on antitumor mechanisms of coumarins. Front. Oncol. 10 (2020) 592853. https://doi.org/10.3389/fonc.2020.592853. [4] X.F. Song, J. Fan, L. Liu, X.F. Liu, F. Gao. Coumarin derivatives with anticancer activities: An update. Arch. Pharm. (Weinheim) 353 (2020) e2000025. https://doi.org/10.1002/ardp.202000025 [5] C. Kontogiorgis, D. Hadjipavlou-Litina. Biological evaluation of several coumarin derivatives designed as possible anti-inflammatory/antioxidant agents. .J Enzyme Inhib. Med. Chem. 18 (2003) 63-69. https://doi.org/10.1080/1475636031000069291 [6] D. Feng, A. Zhang,Y. Yang, P. Yang. Coumarin-containing hybrids and their antibacterial activities. Archiv der Pharmazie 353(6) (2020) e1900380. https://doi.org/10.1002/ardp.201900380 [7] Y.K. Al-Majedy, A.A.H. Kadhum, A.A. Al-Amiery, A.B. Mohamad. Coumarins: The antimicrobial agents. Sys. Rev. Pharm. 8(1) (2017) 24-30. http://dx.doi.org/10.5530/srp.2017.1.11 [8] Y. Wei, W. Peng, D. Wang, S.H. Hao, W. W. Li, F. Ding. Design, synthesis, antifungal activity, and 3D- QSAR of coumarin derivatives. J. Pestic. Sci. 43 (2018) 88-95. https://doi.org/10.1584%2Fjpestics.D17- 075 [9] Z. Xu, Q. Chen, Y. Zhang, C. Liang. Coumarin-based derivatives with potential anti-HIV activity. Fitoterapia 150 (2021) 104863. https://doi.org/10.1016/j.fitote.2021.104863 [10] H. Dai, M. Huang, J. Qian, J. Liu, C. Meng, Y. Li, G. Ming, T. Zhang, S. Wang, Y. Shi, Y. Yao, S. Ge, Y. Zhang, Y. Ling. Excellent antitumor and antimetastatic activities based on novel coumarin/pyrazole oxime hybrids. Eur. J. Med. Chem. 166 (2019) 470-479. https://doi.org/10.1016/j.ejmech.2019.01.070 [11] N. Bhattarai, A.A. Kumbhar, Y.R. Pokharel, P. N. Yadav. Anticancer potential of coumarin and its derivatives. Mini Rev. Med. Chem. 21 (2021) 2996-3029. https://doi.org/10.2174/1389557521666- 210405160323 [12] P.R. Finn. Motivation, working memory, and decision making: a cognitive-motivational theory of personality vulnerability to alcoholism. Behav. Cogn. Neurosci. Rev. 1 (2002) 183-205. https://doi.org/10.1177/1534582302001003001 [13] S.A. Behzadi, E. Sheikhhosseini, S.A. Ahmadi, D. Ghazanfari, M. Akhgar. Synthesis and characterization of novel biological tetracoumarin derivatives bearing ether moieties. Heterocyclic Comm. 26(1) (2020) 60-67. https://doi.org/10.1515/hc-2020-0009 [14] C. Asche. Antitumour quinones. Mini Rev. Med. Chem. 5 (2005) 449-467. https://doi.org/- 10.2174/1389557053765556 [15] A.A. Aly, A.A. Hassan, N.K. Mohamed, M. Ramadan, A.S. Abd El-Aal, S. Braese, M. Nieger. Synthesis of quinone-based heterocycles of broad-spectrum anticancer activity. J. Chem. Res. 45(5-6)(2021) 562- 571. https://doi.org/10.1177/1747519820959737 [16] H. Shaterzadeh-Yazdi, M.F. Noorbakhsh, F. Hayati, S. Samarghandian, T. Farkhondeh. Immunomodulatory and Anti-inflammatory Effects of Thymoquinone. Cardiovasc Hematol Disord Drug Targets 18 (2018) 52-60. https://doi.org/10.2174/1871529x18666180212114816 [17] K.W. Wellington, N.I. Kolesnikova, N.B.P. Nyoka, L.J. McGaw. Investigation of the antimicrobial and anticancer activity of aminonaphthoquinones. Drug Dev. Re.s 80 (2019) 138-146. https://doi.org/- 10.1002/ddr.21477 [18] K.W. Wellington. Understanding cancer and anticancer activities of naphthoquinones-a review. RSC Adv. 5 (2015) 20309-20338. https://doi.org/10.1039/C4RA13547D https://doi.org/10.3390/50200099 https://doi.org/10.5267/j.ccl.2021.8.004 https://doi.org/10.3389/fonc.2020.592853 https://doi.org/10.1002/ardp.202000025 https://doi.org/10.1080/1475636031000069291 https://doi.org/10.1002/ardp.201900380 http://dx.doi.org/10.5530/srp.2017.1.11 https://doi.org/10.1584%2Fjpestics.D17-075 https://doi.org/10.1584%2Fjpestics.D17-075 https://doi.org/10.1016/j.fitote.2021.104863 https://doi.org/10.1016/j.ejmech.2019.01.070 https://doi.org/10.2174/1389557521666210405160323 https://doi.org/10.2174/1389557521666210405160323 https://doi.org/10.1177/1534582302001003001 https://doi.org/10.1515/hc-2020-0009 https://doi.org/10.2174/1389557053765556 https://doi.org/10.2174/1389557053765556 https://doi.org/10.1177/1747519820959737 https://doi.org/10.2174/1871529x18666180212114816 https://doi.org/10.1002/ddr.21477 https://doi.org/10.1002/ddr.21477 https://doi.org/10.1039/C4RA13547D ADMET & DMPK 11(1) (2023) 81-96 Coumarin-quinone hybrids doi: https://doi.org/10.5599/admet.1468 95 [19] D. Bhasin, S.N. Chettiar, J.P. Etter, M. Mok, P.K. Li. Anticancer activity and SAR studies of substituted 1,4-naphthoquinones. Bioorg. Med. Chem. 21 (2013) 4662-4669. https://doi.org/10.1016%2Fj.bmc.- 2013.05.017 [20] M. Kadela-Tomanek, E. Bębenek, E. Chrobak, M. Latocha, S. Boryczka. Alkoxy and Enediyne Derivatives Containing 1,4-Benzoquinone Subunits-Synthesis and Antitumor Activity. Molecules 22 (2017) E447. https://doi.org/10.3390%2Fmolecules22030447 [21] I. Abraham, R. Joshi, P. Pardasani, R.T. Pardasani. Recent advances in 1,4-benzoquinone chemistry. J. Braz. Chem. Soc. 22(3) 2011 385-421. https://doi.org/10.1590/S0103-50532011000300002 [22] S.P. Gupta. Quantitative structure-activity relationship studies on anticancer drugs. Chem. Rev. 94 (1994) 1507–1551. https://doi.org/10.1021/cr00030a003 [23] A.J. M. da Silva, C.D. Netto, W. Pacienza-Lima, E.C. Torres-Santos, B. Rossi-Bergmann, S. Maurel, A. Valentind, P.R.R. Costa. Antitumoral, antileishmanial and antimalarial activity of pentacyclic 1,4- naphthoquinone derivatives. J. Braz. Chem. Soc. 20(1) (2009) 176-182. http://dx.doi.org/10.1590/- S0103-50532009000100026 [24] A.R. Amaro, G.G. Oakley, U. Bauer, H.P. Spielmann, L.W. Robertson. Metabolic activation of PCBs to quinones: reactivity toward nitrogen and sulfur nucleophiles and influence of superoxide dismutase. Chem. Re.s Toxicol. 9 (1996) 623-629. https://doi.org/10.1021/tx950117e [25] P.J. O'Brien. Molecular mechanisms of quinone cytotoxicity. Chem. Biol. Interact. 80 (1991) 1-41. https://doi.org/10.1016/0009-2797(91)90029-7 [26] T.S. Lin, L.Y. Zhu, S.P. Xu, A.A. Divo, A.C. Sartorelli. Synthesis and antimalarial activity of 2-aziridinyl- and 2,3-bis(aziridinyl)-1,4-naphthoquinonyl sulfonate and acylate derivatives. J. Med. Chem. 34 (1991) 1634-1639. https://doi.org/10.1021/jm00109a016 [27] A.J. Lin, B.J. Lillis, A.C. Sartorelli. Potential bioreductive alkylating agents. 5. Antineoplastic activity of quinoline-5,8-diones, naphthazarins, and naphthoquinones. J. Med. Chem. 18 (1975) 917-921. https://doi.org/10.1021/jm00243a012 [28] N.G. Deniz, C. Ibis, Z. Gokmen, M. Stasevych, V. Novikov, O. Komarovska-Porokhnyavets, M. Ozyurek, K. Guclu, D. Karakas, E. Ulukaya. Design, synthesis, biological evaluation, and antioxidant and cytotoxic activity of heteroatom-substituted 1,4-naphtho- and benzoquinones. Chem. Pharm. Bull. (Tokyo) 63(12) (2015) 1029-1039. https://doi.org/10.1248/cpb.c15-00607 [29] Y. Isyaku, A. Uzairu, S. Uba. Computational studies of a series of 2-substituted phenyl-2-oxo-, 2- hydroxyl- and 2-acylloxyethylsulfonamides as potent antifungal agents. Heliyon 6 (2020) e03724. https://doi.org/10.1016/j.heliyon.2020.e03724 [30] C.M. Nisha, A. Kumar, P. Nair, N. Gupta, C. Silakari, T. Tripathi, A. Kumar. Molecular docking and in silico ADMET study reveals acylguanidine 7a as a potential inhibitor of β-secretase. Adv. Bioinformatics 2016 (2016) 9258578. https://doi.org/10.1155/2016/9258578 [31] D.B. Singh, M.K. Gupta, D.V. Singh, S.K. Singh, K. Misra. Docking and in silico ADMET studies of noraristeromycin, curcumin and its derivatives with Plasmodium falciparum SAH hydrolase: a molecular drug target against malaria. Interdiscip. Sci. 5 (2013) 1-12. https://doi.org/10.1007/s12539- 013-0147-z [32] T. Żołek, D. Maciejewska. Theoretical evaluation of ADMET properties for coumarin derivatives as compounds with therapeutic potential. Eur. J. Pharm. Sci. 109 (2017) 486-502. https://doi.org/- 10.1016/j.ejps.2017.08.036 [33] M. Jenny, M. Klieber, D. Zaknun, S. Schroecksnadel, K. Kurz, M. Ledochowski, H. Schennach, D. Fuchs. In vitro testing for anti-inflammatory properties of compounds employing peripheral blood mononuclear cells freshly isolated from healthy donors. Inflamm. Res. 60 (2011) 127-135. https://dx.doi.org/10.1007/s00011-010-0244-y [34] O. Trott, A.J. Olson. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem. 31 (2010) 455-461. https://doi.org/10.1002%2Fjcc.21334 https://doi.org/10.5599/admet.1468 https://doi.org/10.1016%2Fj.bmc.2013.05.017 https://doi.org/10.1016%2Fj.bmc.2013.05.017 https://doi.org/10.3390%2Fmolecules22030447 https://doi.org/10.1590/S0103-50532011000300002 https://doi.org/10.1021/cr00030a003 http://dx.doi.org/10.1590/S0103-50532009000100026 http://dx.doi.org/10.1590/S0103-50532009000100026 https://doi.org/10.1021/tx950117e https://doi.org/10.1016/0009-2797(91)90029-7 https://doi.org/10.1021/jm00109a016 https://doi.org/10.1021/jm00243a012 https://doi.org/10.1248/cpb.c15-00607 https://doi.org/10.1016/j.heliyon.2020.e03724 https://doi.org/10.1155/2016/9258578 https://doi.org/10.1007/s12539-013-0147-z https://doi.org/10.1007/s12539-013-0147-z https://doi.org/10.1016/j.ejps.2017.08.036 https://doi.org/10.1016/j.ejps.2017.08.036 https://dx.doi.org/10.1007/s00011-010-0244-y https://doi.org/10.1002%2Fjcc.21334 A. Pangal and K. Ahmed ADMET & DMPK 11(1) (2023) 81-96 96 [35] N. Hashemi Goradel, M. Najafi, E. Salehi, B. Farhood, K. Mortezaee. Cyclooxygenase-2 in cancer: A review. J. Cell Physiol. 234 (2019) 5683-5699. https://doi.org/10.1002/jcp.27411 [36] K. Singh, A. Gangrade, A. Jana, B.B. Mandal, N. Das. Design, synthesis, characterization, and antiproliferative activity of organoplatinum compounds bearing a 1,2,3-triazole ring. ACS Omega 4 (2019) 835−841. https://doi.org/10.1021/acsomega.8b02849 [37] J.A. Badmus, O.E. Ekpo, A.A. Hussein, M. Meyer, D.C. Hiss. Cytotoxic and cell cycle arrest properties of two steroidal alkaloids isolated from Holarrhena floribunda (G. Don) T. Durand & Schinz leaves. BMC Complement. Altern. Med. 19 (2019) 112. https://doi.org/10.1186/s12906-019-2521-9 [38] D.H. Dawood, R.Z. Batran, T.A. Farghaly, M.A. Khedr, M.M. Abdulla. New coumarin derivatives as potent selective cox-2 inhibitors: synthesis, anti-inflammatory, QSAR, and molecular modeling studies. Arch. Pharm. (Weinheim) 348 (2015) 875-888. https://doi.org/10.1002/ardp.201500274 [39] F.M. Aqlan. Synthesis, ADMET and docking studies of novel pyrazoles incorporating coumarin moiety as tyrosine kinase (Src) inhibitors. Biointerface Res. Appl. Chem. 11(5) (2021) 13706-13714. https://doi.org/10.33263/BRIAC115.1370613714 [40] Y. Han, J. Zhang, C.Q. Hu, X. Zhang, B. Ma, P. Zhang. In silico ADME and toxicity prediction of ceftazidime and its impurities. Front. Pharmacol. 10 (2019) 434. https://doi.org/10.3389/fphar.2019.00434 [41] A. Daina, V. Zoete. A BOILED-Egg to predict gastrointestinal absorption and brain penetration of small molecules. Chem. Med. Chem. 11 (2016) 1117-1121. https://doi.org/10.1002/cmdc.201600182 [42] G.R. Bickerton, G.V. Paolini, J. Besnard, S. Muresan, A.L. Hopkins. Quantifying the chemical beauty of drugs. Nat. Chem. 4 (2012) 90-98. https://doi.org/10.1038%2Fnchem.1243 [43] J. Barrios-González, A. Mejýa. Production of Antibiotics and other Commercially Valuable Secondary Metabolites. In: Current Developments in Solid-state Fermentation A. Pandey, C. R. Soccol, C. Larroche. (eds)., Springer, New York, NY, USA, 2008, 302–336. https://doi.org/10.1007/978-0-387-75213-6_14 [44] D. Xia, X. Yang, W. Liu, F. Shen, J. Pan, Y. Lin, N. Du, Y. Sun, X. Xi. Over-expression of CHAF1A in Epithelial Ovarian Cancer can promote cell proliferation and inhibit cell apoptosis. Biochem. Biophys. Res. Commun. 486(1) (2017) 191-197. https://doi.org/10.1016/j.bbrc.2017.03.026 ©2022 by the authors; licensee IAPC, Zagreb, Croatia. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/) https://doi.org/10.1002/jcp.27411 https://doi.org/10.1021/acsomega.8b02849 https://doi.org/10.1186/s12906-019-2521-9 https://doi.org/10.1002/ardp.201500274 https://doi.org/10.33263/BRIAC115.1370613714 https://doi.org/10.3389/fphar.2019.00434 https://doi.org/10.1002/cmdc.201600182 https://doi.org/10.1038%2Fnchem.1243 https://doi.org/10.1007/978-0-387-75213-6_14 https://doi.org/10.1016/j.bbrc.2017.03.026 http://creativecommons.org/licenses/by/3.0/