Molecular Engineering of Curcumin, an Active Constituent of Curcuma longa L. (Turmeric) of the Family Zingiberaceae with Improved Antiproliferative Activity

Cancer is the world’s second leading cause of death, accounting for nearly 10 million deaths and 19.3 million new cases in 2020. Curcumin analogs are gaining popularity as anticancer agents currently. We reported herein the isolation, molecular engineering, molecular docking, antiproliferative, and anti-epidermal growth factor receptor (anti-EGFR) activities of curcumin analogs. Three curcumin analogs were prepared and docked against the epidermal growth factor receptor (EGFR), revealing efficient binding. Antiproliferative activity against 60 NCI cancer cell lines was assessed using National Cancer Institute (NCI US) protocols. The compound 3b,c demonstrated promising antiproliferative activity in single dose (at 10 µM) as well as five dose (0.01, 0.10, 1.00, 10, and 100 µM). Compound 3c inhibited leukemia cancer panel better than other cancer panels with growth inhibition of 50% (GI50) values ranging from 1.48 to 2.73 µM, and the most promising inhibition with GI50 of 1.25 µM was observed against leukemia cell line SR, while the least inhibition was found against non-small lung cancer cell line NCI-H226 with GI50 value of 7.29 µM. Compounds 3b,c demonstrated superior antiproliferative activity than curcumin and gefitinib. In molecular docking, compound 3c had the most significant interaction with four H-bonds and three π–π stacking, and compound 3c was found to moderately inhibit EGFR. The curcumin analogs discovered in this study have the potential to accelerate the anticancer drug discovery program.


Introduction
Natural products (NPs) have been used to treat human ailments since the dawn of medicine. NPs have historically been a highly prolific source of new medicines since the time immemorial in most of the civilizations. NPs continue to offer a diverse set of structural templates for drug discovery and development, which was heightened in the 1970s and 1980s [1,2]. Many of today's small molecule therapeutics can be traced back to NPs, which are anticipated to have provided or inspired the development of 50-70% of all agents currently in clinical use [3]. Studies focused on the isolation, structural elucidation, and biological activities of substances derived from NPs began around the end Plants 2021, 10, 1559 2 of 17 of the 18th century and introduction of column chromatography revolutionized an era of NP chemistry [4]. A number of anticancer drugs have been developed by chemically modifying plant NPs. Epothilone B, derived from Sorangiumcellulosum, has been chemically modified to Ixabepilone [5]. Camptothecin, an alkaloid derived from Camptotheca acuminate, has been modified into various anticancer agents including Karenitecin (BNP-1350), Diflomotecan (BN80915), and Gimatecanetc [6][7][8]. Tafluposide has been modified from Epipodophyllotoxin, an alkaloid derived from Podophyllum peltatum [9]. Acronycine is an alkaloid derived from Acronychiabaueri that has been modified to S23906-1 [10]. Combretastatin A-4 is an alkaloid derived from Combretum caffrum thathas been converted into anticancer agents such as Combretastatin A-4 phosphate, Combretastatin A-4 diphosphate and Ombrabulin (AVE8062) [11][12][13]. Terameprocol has been synthesized from 3 -Omethyl-nordihydroguaiaretic acid, a lignin isolated from Larreadivaricatta [14]. Daidzein, an isoflavone found in a variety of plants and herbs such as Pueraria Mirifica, soybeans, and soy products, has been converted to Triphendiol and Genistein [15,16].
Cancer is one of the most dreadful diseases and the leading cause of death today, with nearly 10 million deaths and 19.3 million new cases expected in 2020 [29]. Chemotherapy is the most commonly used method of cancer treatment, but it is always associated with a number of toxic side effects. As a result, we became more reliant on nature, because active constituents of natural origin are assumed to be safe. In some studies, curcumin analogs were also discovered to be an inhibitor of EGFR, one of the primary targets of many anticancer drugs [18,28]. Furthermore, many of the cancer cell lines, including breast (MDA-MB-231, MCF7, HS 578T, BT-549, T-47D MDA-MB-468, and MDA-MB-468), colon (HCT-116, HT-29, COLO 205, HCT 116, HT29, and SW620), non-small cell lung (A549, NCI-H460, and NCI-H322), renal (786-O), melanoma (SKMEL28), ovarian (SKOV3), and prostate (PC3) cancer cell lines, have been found to express varying levels of EGFR [30][31][32][33][34][35][36]. Inspired by their impressive biological activities, we reported herein the molecular docking, antiproliferative potential, and anti-EGFR activity of some of the prepared curcumin analogs (3a,b). In silico molecular docking analysis was carried out against EGFR through the Schrodinger's software. As molecular docking is now an integral part of computer-aided drug design (CADD), in which ligands with computed generated 3D structures are positioned into a receptor or biological target in a variety of orientations, conformations, and positions [37], it has numerous uses and applications in drug discovery, including structure-activity studies, lead optimization, and virtual screening to find potential leads [38]. Indeed, molecular docking has been used for more than three decades, and it has resulted in the discovery and development of a large number of new drugs [39].

Procurement of Chemicals and Crude Turmeric
All of the chemicals were obtained from a local vendor. The standard curcumin was obtained from Konark Herbals in India, and the remaining chemicals and reagents were obtained from Merck Chemicals, SD Fine, and CDH. All of the chemicals were either analytical or synthetic grades in nature. The dry turmeric was purchased from a local market and ground into powder.

Isolation of Curcumin
Eighty grams of ground turmeric was refluxed in 200 mL of dichloromethane for one hour with continuous stirring, followed by filtration under vacuum. The filtrate was concentrated under vacuum while the temperature was kept at 50 • C. The reddish yellow oily residue was triturated further with 80 mL of hexane to yield 2.47 g of solid residue. The resulting solid residue was dissolved in a small amount of dichloromethane/ methanol (99:1) and loaded into a column packed with silica gel. The column was eluted with the same mobile phase, and curucmin was isolated, collected, and analyzed using thin layer chromatography (TLC) with standard curcumin as a reference. For the isolation of curcumin the conventional method was used and with 80 g of curcumin powder nearly 244 mg of curcumin was isolated [40].

Preparation of Curcumin Analogues
The isolated curcumin was used as a starting compound for the preparation of curcumin analogues via chemical modification of curcumin according to the methods described [18,19]. Figure 1 depicts the chemical modification curcumin and curcumin analogues. An equimolar amount of curcumin (1) (0.25 mmol; 92 mg) and 3-chlorophenyl thiourea (2a) (0.25 mmol; 46 mg) in glacial acetic acid in 50 mL round-bottom flask placed in sand bath was heated at 80 • C with continuous stirring on magnetic stirrer for 10 h to obtain the compound 3a, while an equimolar amount of curcumin (1) (0.25 mmol; 92 mg) and N-(4-substitutedphenyl)hydrazine carboxamides (2b,c) (0.25 mmol) in glacial acetic acid in 50 mL round-bottom flask placed in sand bath was heated at 80 • C with continuous stirring for 8-10 h on magnetic stirrer to obtain the compound 3b,c. The completion of reaction was monitored throughout by thin layer chromatography using mobile phase, n-hexane: ethylacetate (6:4). The excess of solvent was removed under vacuum distillation. Cooled the reaction mixture to room temperature and poured into the crushed ice to obtain the crude product, filtered, and dried. The crude products were further re-crystallization with ethanol to obtain the compounds, 3a-c. The synthetic route followed is shown in Scheme 1.

Isolation of Curcumin
Eighty grams of ground turmeric was refluxed in 200 mL of dichloromethane for one hour with continuous stirring, followed by filtration under vacuum. The filtrate was concentrated under vacuum while the temperature was kept at 50 °C. The reddish yellow oily residue was triturated further with 80 mL of hexane to yield 2.47 g of solid residue. The resulting solid residue was dissolved in a small amount of dichloromethane/ methanol (99:1) and loaded into a column packed with silica gel. The column was eluted with the same mobile phase, and curucmin was isolated, collected, and analyzed using thin layer chromatography (TLC) with standard curcumin as a reference. For the isolation of curcumin the conventional method was used and with 80 g of curcumin powder nearly 244 mg of curcumin was isolated [40].

Preparation of Curcumin Analogues
The isolated curcumin was used as a starting compound for the preparation of curcumin analogues via chemical modification of curcumin according to the methods described [18,19]. Figure 1 depicts the chemical modification curcumin and curcumin analogues. An equimolar amount of curcumin (1) (0.25 mmol; 92 mg) and 3-chlorophenyl thiourea (2a) (0.25 mmol; 46 mg) in glacial acetic acid in 50 mL round-bottom flask placed in sand bath was heated at 80 °C with continuous stirring on magnetic stirrer for 10 h to obtain the compound 3a, while an equimolar amount of curcumin (1) (0.25 mmol; 92 mg) and N-(4-substitutedphenyl)hydrazine carboxamides (2b,c) (0.25 mmol) in glacial acetic acid in 50 mL round-bottom flask placed in sand bath was heated at 80 °C with continuous stirring for 8-10 h on magnetic stirrer to obtain the compound 3b,c. The completion of reaction was monitored throughout by thin layer chromatography using mobile phase, nhexane: ethylacetate (6:4). The excess of solvent was removed under vacuum distillation. Cooled the reaction mixture to room temperature and poured into the crushed ice to obtain the crude product, filtered, and dried. The crude products were further re-crystallization with ethanol to obtain the compounds, 3a-c. The synthetic route followed is shown in Scheme 1.

Isolation of Curcumin
Eighty grams of ground turmeric was refluxed in 200 mL of dichloromethane for one hour with continuous stirring, followed by filtration under vacuum. The filtrate was concentrated under vacuum while the temperature was kept at 50 °C. The reddish yellow oily residue was triturated further with 80 mL of hexane to yield 2.47 g of solid residue. The resulting solid residue was dissolved in a small amount of dichloromethane/ methanol (99:1) and loaded into a column packed with silica gel. The column was eluted with the same mobile phase, and curucmin was isolated, collected, and analyzed using thin layer chromatography (TLC) with standard curcumin as a reference. For the isolation of curcumin the conventional method was used and with 80 g of curcumin powder nearly 244 mg of curcumin was isolated [40].

Preparation of Curcumin Analogues
The isolated curcumin was used as a starting compound for the preparation of curcumin analogues via chemical modification of curcumin according to the methods described [18,19]. Figure 1 depicts the chemical modification curcumin and curcumin analogues. An equimolar amount of curcumin (1) (0.25 mmol; 92 mg) and 3-chlorophenyl thiourea (2a) (0.25 mmol; 46 mg) in glacial acetic acid in 50 mL round-bottom flask placed in sand bath was heated at 80 °C with continuous stirring on magnetic stirrer for 10 h to obtain the compound 3a, while an equimolar amount of curcumin (1) (0.25 mmol; 92 mg) and N-(4-substitutedphenyl)hydrazine carboxamides (2b,c) (0.25 mmol) in glacial acetic acid in 50 mL round-bottom flask placed in sand bath was heated at 80 °C with continuous stirring for 8-10 h on magnetic stirrer to obtain the compound 3b,c. The completion of reaction was monitored throughout by thin layer chromatography using mobile phase, nhexane: ethylacetate (6:4). The excess of solvent was removed under vacuum distillation. Cooled the reaction mixture to room temperature and poured into the crushed ice to obtain the crude product, filtered, and dried. The crude products were further re-crystallization with ethanol to obtain the compounds, 3a-c. The synthetic route followed is shown in Scheme 1.

Molecular Docking Studies
The docking was done against epidermal growth factor receptor (EGFR), which is one of the most appealing targets for many anticancer drugs. The protein data bank provided the EGFR (PDB:3W2R) X-ray crystal structure with a resolution of 2.05 Å; R-value 0.220 (observed) [41]. The ligands 3a-c were saved as mol files, and docking was performed according to the protocol described by Sogabe et al. (2013) [42].

Antiproliferative Activity
The antiproliferative activity of tested compounds was done against five dozen (60) cancer cell lines derived from nine different panels. All of the compounds were evaluated for antiproliferative activity in a single dose at 10 µM. Growth percent (GP) and percent growth inhibition (% GI) were used to calculate antiproliferative activity. The tested compounds that demonstrated significant activity were subjected to a five-dose assay (0.01 to 100 µM). The antiproliferative results of five-dose assay were calculated as three dose related parameters like, 50% growth inhibition (GI 50 ), 50% lethal concentration (LC 50 ), and total growth inhibition TGI [43][44][45][46][47].
Human tumor cell lines were grown in RPMI 1640 medium containing 5% fetal bovine serum and 2 mM L-glutamine. For a typical screening experiment, cells were inoculated into 96-well microtiter plates in 100 µL at plating densities ranging from 5000 to 40,000 cells/well, depending on the doubling time of individual cell lines. Two plates of each cell line were fixed in situ with trichloroacetic acid (TCA) after 24 h to represent a cell population measurement for each cell line at the time of drug addition (Ti). The experimental drugs were frozen after being solubilized in dimethyl sulfoxide at 400-fold the desired final maximum test concentration. An aliquot of frozen concentrate was thawed and diluted to twice the desired final maximum test concentration with medium containing 50 µg/mL gentamicin at the time of drug addition. Additional four, 10-fold, or 1 2 log serial dilutions serial dilutions were performed to provide a total of five drug concentrations plus the control. Aliquots of 100 µL of these different drug dilutions were added to the appropriate microtiter wells already containing 100 µL of medium, resulting in the required final drug concentrations. Following drug addition, the plates are incubated for an additional 48 h at 37 • C, 5% CO 2 , 95% air, and 100% relative humidity. For adherent cells, the assay is terminated by the addition of cold TCA. Cells are fixed in situ by the gentle addition of 50 µL of cold 50% (w/v) TCA (final concentration, 10% TCA) and incubated for 60 min at 4 • C. The supernatant is discarded, and the plates are washed five times with tap water and air dried. Sulforhodamine B (SRB) solution (100 µL) at 0.4% (w/v) in 1% acetic acid was added to each well, and plates were incubated for 10 min at room temperature. After staining, unbound dye was removed by washing five times with 1% acetic acid and the plates were air dried. Bound stain was subsequently solubilized with 10 mM trizma base, and the absorbance was read on an automated plate reader at a wavelength of 515 nm. For suspension cells, the methodology was the same except that the assay was terminated by fixing settled cells at the bottom of the wells by gently adding 50 µL of 80% TCA (final concentration, 16% TCA).

Anti-EGFR Activity
According to the reported method, a spectrophotometric assay for EGFR tyrosine kinase inhibition (absorbance at λ max 540 nm) was performed in human A431 cells, which express higher levels of EGFR protein [48].

Molecular Docking Studies
EGFR was chosen for docking studies because it is a potential target for many anticancer drugs, including gefitinib, erlotinib, cetuximab, and panitumumab [49]. Curcumin analogues have also been well studied as anti-EGFR agents [18,28]. The X-ray crystal structure of EGFR with PDB ID: 3W2R was retrieved from protein data bank [41]. The molecular docking score and types of interaction of curcumin analogs (3a-c) are given in Table 1 and binding mode of curcumin analogs are shown in Figure 2. Due to their large structure and high molecular weight, the curcumin analogs fit inside the active site of EGFR and showed various types of interaction including hydrophobic interaction, H-bond, and π-π stacking. The ligand 3a displayed only π-π stacking interaction with the amino acids Asp855, Asp800, and Leu718, while ligand 3b displayed two H-bond with the residues Leu718 and Asp800 and two π-π stacking with the residues Leu718 and Asp800 as showed in Figure 3. The ligand 3c displayed significant interaction within the active site of EGFR having three H-bonds with the residues Met793, Gln791, and Ser720, while three π-π stacking with the residues Asp855, Asp800, and Leu718 as shown in Figure 4. structure of EGFR with PDB ID: 3W2R was retrieved from protein molecular docking score and types of interaction of curcumin analo Table 1 and binding mode of curcumin analogs are shown in Figur structure and high molecular weight, the curcumin analogs fit ins EGFR and showed various types of interaction including hydrop bond, and π-π stacking. The ligand 3a displayed only π-π stackin amino acids Asp855, Asp800, and Leu718, while ligand 3b display the residues Leu718 and Asp800 and two π-π stacking with the Asp800 as showed in Figure 3. The ligand 3c displayed significant active site of EGFR having three H-bonds with the residues Met793 while three π-π stacking with the residues Asp855, Asp800, and Le ure 4.

Antiproliferative Activity
The ligands 3a-c demonstrated significant interactions (docking score: approximately−6.337 to 6.593 kcal/mol) in the molecular docking studies and were further tested for antiproliferative activity against five dozen (60) human cancer cell lines derived from nine different panels, including breast, colon, CNS, leukemia, melanoma, non-small cell lung, prostate, and renal cancer cell lines, according to National Cancer Institute (NCI US) protocols [43][44][45][46][47]. In a one-dose assay ( Figures S2-S4), compound 3a inhibited growth by more than 50% in three cancer cell lines-MOLT-4 (% GI = 53.78), HT29 (% GI = 53.43), and SR (% GI = 51.28), while the remaining cell lines (56 cell lines) inhibited growth by less than 50%. Compound 3b was found to be lethal against two cell lines-NCI-H522 and MDA-MB-435, with percent GIs of 113.52 and 136.25, respectively, whereas compound 3c had lethal effect against RPMI-8226 and HCT-116, with percent GIs of 100.21 and 153.67, respectively (shown in red bold font in the Table 2). The compound 3b was found to be active against 32 cell lines, while the compound 3c was found to be active against 25 cell lines with % GIs of ≥68% (shown in green bold font in the Table 2). The compound is supposed to be active if it inhibited the growth of cancer cell lines by ≥68 percent [50,51]. Compound 3b demonstrated >50% GIs (and <68% GIs) against 13 cell lines, while compound 3c demonstrated >50% GIs against 12 cell lines (shown in blue bold font in the Table 2). Compound 3b demonstrated <50% GIs against 9 cell lines, while compound 3c demonstrated <50% GIs against 17 cell lines (shown in black font in the Table 2). Curcumin was more antiproliferative than compound 3a. Compounds 3b demonstrated better inhibition than curcumin against 35 of the 56 cell lines in common, while compound 3c displayed better inhibition than curcumin against 27 of the 56 cell lines in common. Figure  5a,b shows a comparison of antiproliferative activity. The results of mean % GIs on each panel was compared, and it was found that compound 3b displayed better inhibition than curcumin against seven panels and better inhibition than gefitinib against six cell lines panels, while compound 3c displayed better inhibition than curcumin against the four cell lines panels and better inhibition than gefitinib against five cell lines panels in one dose assay at 10 µM (Table 3). The order of antiproliferative activity of curcumin analogues was found to be 3b > 3c > 3a. Compounds 3b,c demonstrated promising antiproliferative activity in a single dose assay and thus qualified for further evaluation in a five-dose assay (0.01, 0.10, 1, 10, and 100 µM).
Compounds 3b,c, which demonstrated promising antiproliferative activity against some of the cancer cell lines in a single dose assay with GIs of >68 (GP 32 percent), were

Antiproliferative Activity
The ligands 3a-c demonstrated significant interactions (docking score: approximately −6.337 to 6.593 kcal/mol) in the molecular docking studies and were further tested for antiproliferative activity against five dozen (60) human cancer cell lines derived from nine different panels, including breast, colon, CNS, leukemia, melanoma, non-small cell lung, prostate, and renal cancer cell lines, according to National Cancer Institute (NCI US) protocols [43][44][45][46][47]. In a one-dose assay ( Figures S2-S4), compound 3a inhibited growth by more than 50% in three cancer cell lines-MOLT-4 (% GI = 53.78), HT29 (% GI = 53.43), and SR (% GI = 51.28), while the remaining cell lines (56 cell lines) inhibited growth by less than 50%. Compound 3b was found to be lethal against two cell lines-NCI-H522 and MDA-MB-435, with percent GIs of 113.52 and 136.25, respectively, whereas compound 3c had lethal effect against RPMI-8226 and HCT-116, with percent GIs of 100.21 and 153.67, respectively (shown in red bold font in the Table 2). The compound 3b was found to be active against 32 cell lines, while the compound 3c was found to be active against 25 cell lines with % GIs of ≥68% (shown in green bold font in the Table 2). The compound is supposed to be active if it inhibited the growth of cancer cell lines by ≥68 percent [50,51]. Compound 3b demonstrated >50% GIs (and <68% GIs) against 13 cell lines, while compound 3c demonstrated >50% GIs against 12 cell lines (shown in blue bold font in the Table 2). Compound 3b demonstrated <50% GIs against 9 cell lines, while compound 3c demonstrated <50% GIs against 17 cell lines (shown in black font in the Table 2). Curcumin was more antiproliferative than compound 3a. Compounds 3b demonstrated better inhibition than curcumin against 35 of the 56 cell lines in common, while compound 3c displayed better inhibition than curcumin against 27 of the 56 cell lines in common. Figure 5a,b shows a comparison of antiproliferative activity. The results of mean % GIs on each panel was compared, and it was found that compound 3b displayed better inhibition than curcumin against seven panels and better inhibition than gefitinib against six cell lines panels, while compound 3c displayed better inhibition than curcumin against the four cell lines panels and better inhibition than gefitinib against five cell lines panels in one dose assay at 10 µM (Table 3). The order of antiproliferative activity of curcumin analogues was found to be 3b > 3c > 3a. Compounds 3b,c demonstrated promising antiproliferative activity in a single dose assay and thus qualified for further evaluation in a five-dose assay (0.01, 0.10, 1, 10, and 100 µM).  % GI = 100-GP; (-) = Not tested; Black font =< 50% GI; Bold & blue font = GIs > 50 (GPs < 50); Bold & green font = GIs > 68 (GPs < 32); Bold & red font = GIs >100 (GPs = < 0 means lethal effect) (One-dose assay); NSC Number: Originally known as Cancer Chemotherapy National Service Center number, and it is an identifying number assigned by Developmental therapeutics Program (DTP) to an agent or product (e.g., small molecule or biological agent); MID a and MID b were the mean GI 50 of 60 NCI cancer cell lines and the individual cancer cell line panels; Selectivity ration = MID a /MID b ; GI 50 , LC 50 and TGI stand for 50% growth inhibition, 50% lethal concentration, and total growth inhibition respectively.
lated and compared to that of curcumin. Except for the panel colon cancer by compound 3b, both the curcumin analogs (3b,c) demonstrated more promising antiproliferative activity with better inhibition than curcumin as shown in Figure 6. The antiproliferative activity of compounds 3c is shown in Figure 7, while antiproliferative activity of compound 3b against nine panels of 60 NCI cancer cell lines in terms of GP and Log10 molar concentration are shown in Figure S1 (In Supplementary Materials). In a 5-dose assay, the overall antiproliferative activity was 3c > 3b > curcumin. Curcumin molecular engineering into semi-synthetic curcumin analogues (3b,c) resulted in increased antiproliferative activity.
(a)   Compounds 3b,c, which demonstrated promising antiproliferative activity against some of the cancer cell lines in a single dose assay with GIs of >68 (GP 32 percent), were chosen for further evaluation in a five-dose assay [50,51]. The antiproliferative activity of compounds (3b,c) was represented as a three-dose-related parameter: GI 50 Table 2 summarizes the results of the 5-dose assay. The mean GI 50 of each panel was calculated and compared to that of curcumin. Except for the panel colon cancer by compound 3b, both the curcumin analogs (3b,c) demonstrated more promising antiproliferative activity with better inhibition than curcumin as shown in Figure 6. The antiproliferative activity of compounds 3c is shown in Figure 7, while antiproliferative activity of compound 3b against nine panels of 60 NCI cancer cell lines in terms of GP and Log10 molar concentration are shown in Figure S1 (In Supplementary Materials). In a 5-dose assay, the overall antiproliferative activity was 3c > 3b > curcumin. Curcumin molecular engineering into semi-synthetic curcumin analogues (3b,c) resulted in increased antiproliferative activity.  * Cur = Curcumin; The anticancer activity of curcumin was retrieved from NCI data-ware with NSC ID 32982 [43]; Bold font represents the best result; # The anticancer activity of gefitinib was retrieved from NCI data-ware with NSC ID 759856 [43].

Anti-EGFR Activity
The ligands (3b,c) with promising antiproliferative activity and displayed significant interaction within the active site of EGFR in molecular dockingwere then tested for anti-EGFR activity in human A431 cells, which express high levels of EGFR protein, using a spectrophotometric assay (absorbance at λmax 540 nm). Both the compounds (3b,c) moderately inhibited the EGFR with IC50 values of 3.89 and 4.18 µM, respectively, while the standard drug, gefitinib inhibited EGFR with IC50 value of 0.017 µM.

Discussion
Turmeric has been promoted as a therapeutic herb in the majority of indigenous traditional systems, including Ayurveda, Siddha, Unani, and Chinese medicine [52]. Turmeric's main active ingredient is curcumin, and its stability and bioavailability are the main issues, so it was modified into semi-synthetic analogs to make it more stable and potentiate its bioactivities [17]. Some of the curcumin analogues demonstrated superior antiproliferative activity than curcumin not only in the current study, but also in the previous study, where they demonstrated superior antiproliferative activity in single and five dose assays [18][19][20].
The molecular docking revealed that compound 3a exhibited two π-π stacking with the m-chlorophenyl moiety with the residues Asp800 and Leu718, as well as one π-π stacking between one of the methoxyphenyl moiety and the residue Asp855. Compound 3a demonstrated moderate antiproliferative activity with more than 50 percent sensitivity

Anti-EGFR Activity
The ligands (3b,c) with promising antiproliferative activity and displayed significant interaction within the active site of EGFR in molecular dockingwere then tested for anti-EGFR activity in human A431 cells, which express high levels of EGFR protein, using a spectrophotometric assay (absorbance at λ max 540 nm). Both the compounds (3b,c) moderately inhibited the EGFR with IC 50 values of 3.89 and 4.18 µM, respectively, while the standard drug, gefitinib inhibited EGFR with IC 50 value of 0.017 µM.

Discussion
Turmeric has been promoted as a therapeutic herb in the majority of indigenous traditional systems, including Ayurveda, Siddha, Unani, and Chinese medicine [52]. Turmeric's main active ingredient is curcumin, and its stability and bioavailability are the main issues, so it was modified into semi-synthetic analogs to make it more stable and potentiate its bioactivities [17]. Some of the curcumin analogues demonstrated superior antiproliferative activity than curcumin not only in the current study, but also in the previous study, where they demonstrated superior antiproliferative activity in single and five dose assays [18][19][20].
The molecular docking revealed that compound 3a exhibited two π-π stacking with the m-chlorophenyl moiety with the residues Asp800 and Leu718, as well as one π-π stacking between one of the methoxyphenyl moiety and the residue Asp855. Compound 3a demonstrated moderate antiproliferative activity with more than 50 percent sensitivity against MOLT-4 (% GI = 53.78), SR (% GI = 51.28), and HT29 (% GI = 53.43). The compound 3b displayed two H-bonds with the phenolic functions with the residues Asp800 and Leu718, as well as two π-π stacking one between the methoxyphenyl moiety and the residue Asp855 and another with one of the hydrogen of doubly bonded carbon (C=C). Compound 3b exhibited significant interaction within the active site of EGFR in molecular docking studies, and demonstrated better inhibition than curcumin against 35 of the 56 cell lines tested in common in single dose assay at 10 µM. Compound 3b inhibited leukemia cancer panel better with GI 50 values ranging from 1.52 to 3.38 µM, but the most promising inhibition with GI 50 of 1.25 µM was observed against MDA-MB-435, while the least sensitivity was found against OVCAR-5 with GI 50 value of 18.8 µM. Compound 3c displayed three H-bonds with the phenolic functions with the residues Met793, Ser720, and Gln791, as well as four π-π stacking three between the p-trifluoromethylphenyl moiety and the residues Leu718 and Asp800 and another one with the pyrazoline CH and residue Asp855. The p-trifluoromethyl phenyl function lies within the hydrophobic cavity containing important residues Leu844, Cys797, and Met793. Compound 3c inhibited leukemia cancer panel better with GI 50 values ranging from 1.48 to 2.73 µM, and the most promising inhibition with GI 50 of 1.25 µM was observed against SR, while the least inhibition was found against NCI-H226 with GI 50 value of 7.29 µM. The SI values indicated that both the curcumin analogues (3b,c) were found to be non-selective against all the nine panels tested.
The curcumin analogs (3a-c) demonstrated promising antiproliferative activity and significant interaction within the active site of EGFR in molecular docking. Previous research has shown that curcumin has anti-EGFR activity [53]. Furthermore, many of the cancer cell lines, including breast, colon, non-small cell lung, renal, melanoma, ovarian, and prostate cancer cell lines, have been found to express varying levels of EGFR; thus, it was worth testing their anti-EGFR activity [30][31][32][33][34][35][36]. Compounds (3a-c) were found to be moderately inhibited EGFR. Compound 3a had a higher docking score than compounds 3b,c, but it showed moderate antiproliferative and anti-EGFR activities. Compounds 3b,c, on the other hand, demonstrated significant antiproliferative and anti-EGFR activity, as we observed better interaction within the EGFR active site. Only π-π stacking interaction was observed with compound 3a, while H-bond and π-π stacking interactions were observed with compounds 3b,c.
In most of the cases, the chemical modifications of diketonic function of curcumin into pyrazole and primidinone analogues were found to be promising, whereas chemical modification of diketonic function that resulted in bigenelli-type curcumin compounds were found to be least significant [18][19][20]54]. Curcumin analogues previously reported in the literature demonstrated cytotoxicity on the CCGF-CEM cell line with IC 50 values ranging from 3.13 to 93.40 µM, whereas compounds (3b,c) were found to be much more potent than the reported curcumin analogues [55].

Conclusions
Three curcumin analogs were prepared and tested for antiproliferative activity (3a-c). Compounds (3a-c) had docking scores >−6.337 kcal/mol, indicating efficient binding to the active site of EGFR. Compounds 3b,c demonstrated promising antiproliferative activity in both one and five-dose assay. In a one-dose assay, compound 3b demonstrated the most promising antiproliferative activity with mean % GI of 66.46, while compound 3c demonstrated the most promising antiproliferative activity in five-dose assay with mean GI 50 value of 2.84 µM, but none of the compounds were found to be selective against any panel in five-dose assay, as indicated by their selectivity ratio values. Except for compound 3a, both compounds (3b,c) effectively inhibited the tested cancer cell lines in single and five dose assays. The curcumin analogues moderately inhibited the EGFR, a potential target for anticancer agents. Because the compounds demonstrated promising antiproliferative activity, the current report may lead to an expansion of the anticancer research development program in the future.