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Article

Synthesis, Anticancer Activity, and In Silico Studies of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine Analogs

by
Mohamed Jawed Ahsan
1,†,
Krishna Gautam
1,†,
Amena Ali
2,
Abuzer Ali
3,
Abdulmalik Saleh Alfawaz Altamimi
4,*,
Salahuddin
5,
Manal A. Alossaimi
4,
S. V. V. N. S. M. Lakshmi
6 and
Md. Faiyaz Ahsan
7
1
Department of Pharmaceutical Chemistry, Maharishi Arvind College of Pharmacy, Ambabari Circle, Jaipur 302039, Rajasthan, India
2
Department of Pharmaceutical Chemistry, College of Pharmacy, Taif University, Taif 21944, Saudi Arabia
3
Department of Pharmacognosy, College of Pharmacy, Taif University, Taif 21944, Saudi Arabia
4
Department of Pharmaceutical Chemistry, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia
5
Department of Pharmaceutical Chemistry, Noida Institute of Engineering and Technology (Pharmacy Institute), Knowledge Park-2, Greater Noida 201306, Uttar Pradesh, India
6
Department of Pharmacognosy, Vishnu Institute of Pharmaceutical Education & Research, Narsapur 502313, Medak Dist., Telangana, India
7
Department of Chemistry, Bihar National College, Patna 800004, Bihar, India
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2023, 28(19), 6936; https://doi.org/10.3390/molecules28196936
Submission received: 25 August 2023 / Revised: 30 September 2023 / Accepted: 2 October 2023 / Published: 5 October 2023
(This article belongs to the Special Issue Five and Six-Membered Heterocyclic Compounds and Their Therapeutic Potential II)
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Versions Notes

Abstract

:
In the current study, we described the synthesis of ten new 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine analogs (4a–j), as well as their characterization, anticancer activity, molecular docking studies, ADME, and toxicity prediction. The title compounds (4a–j) were prepared in three steps, starting from substituted anilines in a satisfactory yield, followed by their characterization via spectroscopic techniques. The National Cancer Institute (NCI US) protocol was followed to test the compounds’ (4a–j) anticancer activity against nine panels of 58 cancer cell lines at a concentration of 10−5 M, and growth percent (GP) as well as percent growth inhibition (PGI) were calculated. Some of the compounds demonstrated significant anticancer activity against a few cancer cell lines. The CNS cancer cell line SNB-75, which showed a PGI of 41.25 percent, was discovered to be the most sensitive cancer cell line to the tested compound 4e. The mean GP of compound 4i was found to be the most promising among the series of compounds. The five cancer cell lines that were found to be the most susceptible to compound 4i were SNB-75, UO-31, CCRF-CEM, EKVX, and OVCAR-5; these five cell lines showed PGIs of 38.94, 30.14, 26.92, 26.61, and 23.12 percent, respectively, at 10−5 M. The inhibition of tubulin is one of the primary molecular targets of many anticancer agents; hence, the compounds (4a–j) were further subjected to molecular docking studies looking at the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ) of tubulin. The binding affinities were found to be efficient, ranging from −6.502 to −8.341 kcal/mol, with two major electrostatic interactions observed: H-bond and halogen bond. Ligand 4i had a binding affinity of −8.149 kcal/mol with the tubulin–combretastatin A-4 binding site and displayed a H-bond interaction with the residue Asn258. The ADME and toxicity prediction studies for each compound were carried out using SwissADME and ProTox-II software. None of the compounds’ ADME predictions showed that they violated Lipinski’s rule of five. All of the compounds were also predicted to have LD50 values between 440 and 500 mg/kg, putting them all in class IV toxicity, according to the toxicity prediction. The current discovery could potentially open up the opportunity for further developments in cancer.

1. Introduction

Triazole, with the chemical formula C2H3N3, is one of the main heterocyclic compounds that has three nitrogen atoms in a five-membered ring. There are two potential isomers of triazole, 1,2,3 and 1,2,4-triazoles, depending on where the nitrogen atom is located within the five-membered ring (Figure 1A). It is possible to classify the 1,2,4-triazole ring as an ester, amide, carboxylic acid, or other heterocycle isostere. There may be equilibrium between the 1H-form and 4H-form for the 1,2,4-triazole ring (Figure 1B) [1,2]. The 1,2,4-triazole-containing ring system is a common pharmacophore incorporated into a wide range of therapeutically interesting active molecules [3]. A triazole heterocyclic ring is an effective and versatile moiety and is among the most studied chemotherapeutic prospects. The presence of numerous commercially available anticancer medications, including anastrozole, vorozole, and letrozole, which contain this scaffold as part of their structural makeup, supports the assertion that compounds possessing 1,2,4-triazoles stand out as the most promising anticancer agents among these two triazole structural isomers (Figure 1C) [3,4,5]. There have been numerous recent studies on 1,2,4-triazole-containing compounds acting as biologically active agents against various diseases, particularly as anticancer agents with apoptosis-inducing abilities [4]. Heterocyclic compounds have long been a fascinating topic due to the ever-increasing need for therapeutic chemicals. The 1H-1,2,4-triazole is a useful substitute in bioactive compounds with a variety of pharmacological actions due to its modest dipole character, stiffness, and stability in vivo [6]. Anticancer, antiprotozoal, antibacterial, antiproliferative, β-lactamase-inhibitory, anti-inflammatory, agrochemical, and material studies could all benefit from this moiety. The chemistry of 1,2,4-triazoles has received a lot of attention due to their synthetic utility and diverse range of biological activity. Numerous studies have demonstrated the potent biological properties of 1,2,4-triazoles, including their ability to be analgesic, antibacterial, antimicrobial, antifungal, anticancer, antitubercular, antinociceptive, antioxidant, anticonvulsant, antimycobacterial, antiviral, and anti-inflammatory, as well as show antimycotic activity [7,8,9,10,11,12,13,14,15,16,17,18,19].
Due to 1,2,4-triazole’s significance in biology, numerous techniques have been developed to create this scaffold, which possesses biological activity. Through multistep synthetic approaches, the synthetic methods documented to date give access to a variety of 1,2,4-triazoles. Surveys of the efficient synthetic techniques to create products containing 1,2,4-triazole systems have rapidly increased in recent studies, in response to the growing demand for the convenient and quick synthesis of heterocycles with biological activity [1]. Given the increasing significance of 1,2,4-triazole in emerging sciences, a thorough evaluation of this unique heterocyclic scaffold utilizing 1,2,4-triazole is required [1]. Due to their well-known pharmacologic efficacy, 1,2,4-triazoles have drawn the interest of numerous research teams looking to develop synthetic drugs with high bioavailability [20]. Compound I (reported as the most potent anticancer and anti-tubulin compound), IMC-038525 and FTAB (anticancer compounds), and the triazoles that we report on herein contain structural similarity, as shown in Figure 2 [21,22,23]. We further performed molecular docking studies with 3-Bromophenyl substitution at position 5 of the triazole ring and found efficient binding affinity with the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ), with the docking score ranging from −6.502 to −8.341 kcal/mol.
Cancer is ranked as one of the most aggressive and lethal diseases across the world. In 2020, GLOBOCAN reported nearly 10 million cancer deaths and approximately 19.3 million new cancer cases [24]. Cancer, if not treated correctly, is likely to become widespread in a large proportion of the world’s population. Existing chemotherapeutic drugs such as cisplatin, doxorubicin, chlorambucil, paclitaxel, and thiotepa fail to inhibit the growth of cancerous cells. This is primarily due to the fact that they are not selective against tumor cells, and secondarily because cancer cells develop resistance due to their unique structural and functional characteristics. In addition, the above-mentioned chemotherapeutic drugs have genotoxic and cytotoxic effects that are detrimental to human soft tissues, causing problems in cancer treatment. As a result, there is an urgent need for a new generation of versatile chemotherapeutic drugs. Thus, anticancer drug research strenuously continues to focus on finding new anticancer therapeutics with low toxicity and enhanced efficacy [6].

2. Results

2.1. Chemistry

Substituted aniline (1a–j) was allowed to react with sodium cyanate via stirring at room temperature to obtain substituted phenyl urea (2a–j) in the first step [25]. The substituted phenyl urea (2a–j) was refluxed with hydrazine hydrate in ethanol to obtain substituted phenyl semicarbazide (3a–j) in the second step [25] (Please refer Supplementary Materials for the general methods of synthesis for the intermediate compounds, 2a–j and 3a–j). In the final intermediate step, (3a–j) was treated with 3-bromobenzonitrile in n-butanol with an addition of potassium carbonate to obtain 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine (4a–j) [26,27]. The reaction was monitored via thin-layer chromatography (TLC) using eluent benzene/acetone (9:1). The synthetic protocols, reaction conditions, reagents, and yields in the individual steps are summarized in Scheme 1. The physical constants of the final compounds (4a–j) are summarized in Table 1. All of the prepared compounds were prepared in satisfactory yields (65 to 93%) and magnificently characterized via analytical techniques, including nuclear magnetic resonance (NMR), mass spectroscopy, and elemental analysis. The 1H NMR of the prototype compound 4a demonstrated a multiplet at δ ppm 7.39–7.44, corresponding to the H3 and H5 protons of a 4-fluorophenyl ring, two multiplets at δ ppm 7.70–7.73 and 7.76–7.97, corresponding to the H5 and H4 protons of a 3-Bromophenyl ring, respectively, a multiplet at δ ppm 8.04–8.08 for the two protons of the 4-fluorophenyl ring (H3 and H5), and one proton of 3-Bromophenyl (H6). A singlet peak at δ ppm 8.73 was observed for the ArNH, while a singlet at δ ppm 9.13 was observed for triazole NH. The 13C NMR revealed twelve different carbons at δ ppm 157.99, 157.53, 156.29, 134.57, 132.85, 131.86, 131.26, 128.62, 126.66, 122.68, 120.80, and 116.43. The ESI-MS of the compounds revealed (M+1)+ and (M+2)+ peaks at m/z, 333.01 and 333.99, corresponding to their molecular formula C14H10BrFN4. Please refer Supplementary Materials for the NMR and mass spectra of the compounds (Figures S1–S15).

2.2. Anticancer Activity

The compounds’ anticancer activity was observed in nine panels of 58 NCI cancer cell lines at a concentration of 10−5 M [28,29,30,31,32]. The anticancer activity was measured in terms of growth percent (GP) and percent growth inhibition (PGI), which are related as P G I = 100 − G P . The results of anticancer activity in terms of growth control (growth percent) are given in Table 2. The five cell lines that are most sensitive to each compound are shown in Table 3. The renal cancer cell line UO-31 was found to be the most sensitive against six compounds 4a, 4b, 4c, 4f, 4h, and 4j, with a PGI of 26.68, 31.14, 26.47, 37.17, 36.57, and 33.43 percent, respectively, while UO-31 was found to be the second most sensitive cell line against the compounds 4d, 4e, 4g, and 4i, with a PGI of 32.2, 28.47, 20.23, and 30.14, respectively. The non-small cell lung cancer cell line EKVX was the second most sensitive cell line against five compounds 4a, 4b, 4f, 4h, and 4j, with a PGI of 21.72, 19.83, 17.03, 24.56, and 24.57 percent, respectively. The CNS cancer cell line SNB-75 was found to be the most sensitive against the compounds 4e, 4g, and 4h, with a PGI of 41.25, 30.09, and 38.94 percent, respectively, while the breast cancer cell line MCF-7 was found to be the most sensitive cell line against compound 4d. The SNB-75 cancer cell line, which showed a PGI of 41.25 percent, was discovered to be the most sensitive cancer cell line to the tested compound 4e. The mean growth percent (GP = 97.48) of compound 4i was recorded as the most significant among the series of compounds and the five cell lines SNB-75, UO-31, CCRF-CEM, EKVX, and OVCAR-5 that showed maximum sensitivity with a PGI of 38.94, 30.14, 26.92, 26.61, and 23.12, respectively. Furthermore, the average PGIs of each cancer cell line panels were calculated and the anticancer activity was compared with the reference drug, imatinib. Compound 4i with the most significant anticancer activity among the series of ten compounds showed better anticancer activity than imatinib against CNS, melanoma, and ovarian cancer cell lines (Table 4). The anticancer data were retrieved form the National Cancer Institute website [28]. Please refer Supplementary Materials for the anticancer screening data of the compounds 4a–j at 10−5 M (Figures S16–S25). Compound 4i with 2,6-dimethyl substitution demonstrated good anticancer activity, followed by compound 4d with 4-methoxy substitution and compound 4e with 2-chloro substitution. The overall anticancer activity followed, with substitutions of 2,6-dimethyl < 4-methoxy < 2-chloro < 3-chloro-4-fluoro < 2,6-dimethyl < 4-fluoro < 4-chloro < 2-methyl < 4-methyl < 2-methoxy.

2.3. Molecular Docking Studies

One of the key molecular targets of many anticancer drugs is the inhibition of tubulin. Colchicine, combretastatin A-4, epothilones, nocodazole, vinca alkaloids, and taxanes are a few examples of tubulin inhibitors used in cancer chemotherapy [33]. The molecular docking of the ligands (4a–j) was carried out against the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ), and the results are given in Table 5. The docking scores ranged from −6.502 to −8.341 kcal/mol, with two major electrostatic interactions observed: H-bond and halogen bond. The ligands 4a, 4d, 4f, 4g, and 4i demonstrated a similar type of interaction and displayed a H-bond interaction with the residue Asn258 (Figure 3). The ligands 4e and 4j displayed a similar type of interaction, a H-bond interaction with the residue Asn258 and a halogen bond interaction with the residue Val315 (Figure 4), while ligand 4b demonstrated a H-bond interaction with the residue Asn258 and a halogen bond interaction with the residue Cys241 (Figure 5). The molecular docking studies showed that ligand 4i had a binding affinity of −8.149 kcal/mol and displayed a H-bond interaction with the residue Asn258. The two- and three-dimensional interactions of ligand 4i with the tubulin–combretastatin A-4 binding site are shown in Figure 5.

2.4. ADME and Toxicity Prediction Studies

Absorption, distribution, metabolism, and excretion, also known as ADME, are crucial variables to examine during the drug discovery process in order to reduce the likelihood of pharmacokinetics-related clinical failure [34]. The ADME prediction via SwissADME software [35] showed that all of the compounds followed Lipinski’s rule of five, with their molecular weight ranging from 329.19 to 367.6 (MW < 500), log p values ranging from 2.15 to 2.48 (log p < 5), number of hydrogen bond acceptors (HBAs) ranging from 2 to 3 (HBA < 10), and number of hydrogen bond donors (HBDs) being two (HBDs < 5) [36]. The percent absorption was calculated from the equation %   A b s = 109 ± [ 0.345 × T P S A ] , and was found to be 87.32 to 90.50 percent [37]. Lipinski’s rule of five is a general rule of thumb for evaluating druglikeness or determining whether a chemical compound with particular pharmacological or biological activity has physicochemical properties that would probably make it an orally active drug in humans. Furthermore, the compounds were found to be blood–brain barrier (BBB)-permeant in SwissADME prediction, as shown vis the boiled egg representation of compounds 4e, 4g, and 4i (Figure 6). The physicochemical space of molecules with the highest probability of entering the gastrointestinal tract is represented by the white region, and the physicochemical space of molecules with the highest probability of entering the brain is represented by the yellow region (yolk) [38]. The compounds 4e, 4g, and 4i were predicted to be highly absorbed from the gastrointestinal tract (GIT) and enter the BBB efficiently. Pharmaceutical companies experience significant financial losses as a result of post-marketing drug failure brought on by ADME and toxicity [39]. Toxicity prediction by ProTox-II predicted the toxicity with LD50 values between 440 and 500 mg/kg, putting them all in the class IV toxicity class (300 < LD50 ≤ 2000) [40]. The ADME and toxicity prediction of compounds (4a–j) are given in Table 6.

3. Discussion

5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine (4a–j) was prepared in three steps starting from substituted anilines (1a–j). Substituted phenyl urea (2a–j) and N-(substituted pheny)hydrazine carboxamide (3a–j) were prepared as intermediate compounds using a well-established synthetic procedure, as reported earlier [25]. The title compounds (4a–j) were prepared with a good yield and were thoroughly characterized using spectroscopic methods of analysis followed by their anticancer evaluation against 58 cancer cell lines in a one-dose assay at 10 µM. The CNS cancer cell line SNB-75 was found to be the most sensitive against compound 4e (PGI = 41.25). Compound 4i demonstrated the most significant anticancer activity with a mean GP of 97.48. SNB-75, UO-31, CCRF-CEM, EKVX, and OVCAR-5 were the five most sensitive cell lines to compound 4i, with PGIs of 38.94, 30.14, 26.92, 26.61, and 23.12, respectively. In comparison to the previously reported compound, the lead compound 4i had better anticancer effects on cancer cell lines. Because the prepared compounds shared the basic pharmacophore of previously reported anticancer and anti-tubulin compounds, tubulin was chosen as a plausible molecular target, and molecular docking against tubulin was examined to see whether any interactions could be observed. All of the compounds demonstrated efficient binding with the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ), with docking scores ranging from −6.502 to −8.341 kcal/mol and two major types of electrostatic interactions being observed: H-bond (with Asn258) and halogen bond (with Cys241 and Val315). The ADME studies are vital parameters to study during the drug discovery process in order to reduce the probability of pharmacokinetics-related clinical failure. Post-marketing drug failure brought on by ADME and toxicity results in significant financial losses for pharmaceutical companies. Therefore, when developing novel compounds with therapeutic value, ADME and toxicity studies should not be ignored. All of the compounds were consequently investigated for ADME and toxicity prediction. According to swissADME prediction, all of the compounds were found to be BBB-permeant. The compounds 4e, 4g, and 4i showed promising anticancer activity against the CNS cancer cell line SNB-75, and swissADME prediction studies revealed that these compounds are BBB-permeant. Lipinski’s rule of five is a general guideline for assessing druglikeness or determining whether a chemical compound has physicochemical properties that would probably make it an orally active drug in humans. According to the rule, a compound must meet five requirements in order to function as an oral drug: a molecular weight of ≤500, a log p of <5, an HBA of <10, and an HBD of <5. None of the compounds violated Lipinski’s rule of five, and ProTox-II predicted toxicity with LD50 values ranging from 440 to 500 mg/kg, putting them all in class IV toxicity. The current discovery could pave the way for the development of improved triazoles through chemical modification, leading to future advances in cancer therapeutics.

4. Materials and Methods

4.1. General Method for the Synthesis of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine analogs (4a–j)

Equimolar amounts of N-(substituted phenyl)hydrazine carboxamide (3a–j) (1 mmol) and 3-bromobenzonitrile (1 mmol; 182 mg) were dissolved in n-butanol (10 mL), and K2CO3 (1 g) was added and heated at 120 °C with continuous stirring via a magnetic stirrer for 8 h. Excess of solvent was removed, the reaction mixture was poured into the crushed ice, and the product was extracted in ethyl acetate; later, it was separated via filtration flask, obtained as a solid product of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine analogs (4a–j), and re-crystallized from petroleum ether [26,27].
5-(3-Bromophenyl)-N-(4-fluorophenyl)-4H-1,2,4-triazol-3-amine (4a): 1H NMR (300 MHz, DMSO-d6): δ ppm: 7.39–7.44 (m, 2H, ArH), 7.49 (s, 1H, ArH), 7.70–7.73 (m, 1H, ArH), 7.76–7.97 (m, 1H, ArH), 8.04–8.08 (m, 3H, ArH), 8.73 (s, 1H, ArNH), 9.13 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.99, 157.53, 156.29, 134.57, 132.85, 131.86, 131.26, 128.62, 126.66, 122.68, 120.80, 116.43; anal. calc. for C14H10BrFN4: C, 50.47; H, 3.03; N, 16.82 found: C, 50.30; H, 3.01; N, 16.75%. ESI-MS m/z = 333.01 (M+1)+, 333.99 (M+2)+.
5-(3-Bromophenyl)-N-(4-chlorophenyl)-4H-1,2,4-triazol-3-amine (4b): 1H NMR (300 MHz, DMSO-d6): δ ppm: 7.19 (d, J = 6.0 Hz, ArH), 7.39–7.43 (m, 2H, ArH), 7.49 (s, 1H, ArH), 7.70–73 (m, 1H, ArH), 7.76–7.97 (m, 1H, ArH), 8.04–8.08 (m, 3H, ArH), 8.73 (s, 1H, ArNH), 9.13 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.99, 157.39, 156.40, 134.64, 132.91, 131.93, 131.49, 128.48, 126.66, 122.68, 120.80, 116.43; anal. calc. for C14H10BrClN4: C, 48.10; H, 2.88; N, 16.03 found: C, 48.02; H, 2.86; N, 16.00%. ESI-MS m/z = 348.94 (M+1)+, 350.90 (M+3)+.
5-(3-Bromophenyl)-N-(p-tolyl)-4H-1,2,4-triazol-3-amine (4c): 1H NMR (300 MHz, DMSO-d6): δ ppm: 2.32 (s, 3H, CH3), 7.36–7.54 (m 1H, ArH), 7.59 (s, 1H, ArH), 7.83 (d, J = 12.3 Hz, 2H, ArH), 7.94 (d, J = 14.0 Hz, 2H, ArH), 8.01–8.11 (m, 2H, ArH), 8.32 (s, 1H, ArNH), 8.64 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 158.62, 156.63, 135.59, 132.90, 131.79, 131.54, 131.24, 129.89, 126.16, 126.65, 122.27, 120.34, 21.35; anal. calc. for C15H13BrN4: C, 54.73; H, 3.98; N, 17.02 found: C, 54.65; H, 3.95; N, 16.98%. ESI-MS m/z = 329.10 (M+1)+.
5-(3-Bromophenyl)-N-(4-methoxyphenyl)-4H-1,2,4-triazol-3-amine (4d): 1H NMR (300 MHz, DMSO-d6): δ ppm: 3.81 (s, 3H, ArH), 6.93 (d, J = 6.0 Hz, 2H, ArH), 7.77 (d, J = 6.3 Hz, 2H, ArH), 7.58 (s, 1H, ArH), 7.39–7.43 (m, 1H, ArH), 7.65–7.68 (m, 1H, ArH), 8.05–8.12 (m, 1H, ArH), 8.33 (s, 1H, ArNH), 8.89 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.91, 156.21, 153.93, 132.89, 131.79, 131.47, 131.19, 128.18, 126.57, 121.72, 115.16, 55.82; anal. calc. for C15H13BrN4O: C, 52.19; H, 3.80; N, 16.23 found: C, 52.09; H, 3.75; N, 16.18%. ESI-MS m/z = 345.24 (M+1)+.
5-(3-Bromophenyl)-N-(2-chlorophenyl)-4H-1,2,4-triazol-3-amine (4e): 1H NMR (300 MHz, DMSO-d6): δ ppm: 7.39–7.44 (m, 2H, ArH), 7.53 (s, 1H, ArH), 7.70–7.73 (m, 1H, ArH), 7.73–7.80 (m, 2H, ArH), 7.95–8.12 (m, 2H, ArH), 8.32 (s, 1H, ArNH), 8.55 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.62, 156.63, 136.79, 132.91, 131.71, 131.44, 130.27, 129.89, 128.33, 127.76, 126.51, 125.47, 122.94, 122.25; anal. calc. for C14H10BrClN4: C, 48.10; H, 2.88; N, 16.03 found: C, 48.03; H, 2.86; N, 15.99%. ESI-MS m/z = 348.94 (M+1)+, 350.90 (M+3)+.
5-(3-Bromophenyl)-N-(o-tolyl)-4H-1,2,4-triazol-3-amine (4f): 1H NMR (300 MHz, DMSO-d6): δ ppm: 2.12 (s, 3H, CH3), 7.35–7.44 (m, 2H, ArH), 7.48 (s, 1H, ArH), 7.70–7.73 (m, 1H, ArH), 7.84–7.94 (m, 2H, ArH), 8.04–8.07 (m, 2H, ArH), 8.30 (s, 1H, ArNH), 8.80 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.68, 156.69, 142.19, 132.91, 131.77, 131.49, 131.37, 129.09, 128.13, 126.96, 126.11, 123.97, 123.34, 122.29, 18.42; anal. calc. for C15H13BrN4: C, 54.73; H, 3.98; N, 17.02 found: C, 54.69; H, 3.96; N, 16.97%. ESI-MS m/z = 329.06 (M+1)+.
5-(3-Bromophenyl)-N-(2-methoxylphenyl)-4H-1,2,4-triazol-3-amine (4g): 1H NMR (300 MHz, DMSO-d6): δ ppm: 3.86 (s, 3H, OCH3), 6.97–7.21 (m, 4H, ArH), 7.39–7.42 (m, 1H, ArH), 7.58 (s, 1H, ArH), 7.72–7.75 (1H, m, ArH), 8.02–8.96 (m, 1H, ArH), 8.39 (s, 1H, ArNH), 9.989 (s, 1H, ArH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.72, 156.81, 147.52, 132.99, 132.27, 131.97, 131.57, 128.11, 126.89, 122.99, 122.14, 121.19, 113.89, 112.82, 56.62; anal. calc. for C15H13BrN4O: C, 52.19; H, 3.80; N, 16.23 found: C, 52.10; H, 3.76; N, 16.19%. ESI-MS m/z = 345.04 (M+1)+.
5-(3-Bromophenyl)-N-(2,4-dimethylphenyl)-4H-1,2,4-triazol-3-amine (4h): 1H NMR (300 MHz, DMSO-d6): δ ppm: 2.14 (s, 3H, CH3), 2.24 (s, 3H, CH3), 6.84–7.06 (m, 1H, ArH), 7.39–7.56 (m, 2H, ArH), 7.72 (d, J = 8.7 Hz, 1H, ArH), 7.87 (d, J = 7.8 Hz, 1H, ArH), 8.05 (s, 1H, ArH), 8.15 (s, 1H, ArH), 8.32 (s, 1H, ArNH), 9.65 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.99, 156.91, 139.19, 137.87, 132.97, 131.93, 131.59, 131.19, 128.91, 128.14, 126.89, 126.59, 116.82, 24.18, 18.42; anal. calc. for C16H15BrN4: C, 55.99; H, 4.41; N, 16.32 found: C, 55.89; H, 4.39; N, 16.28%. ESI-MS m/z = 343.05 (M+1)+.
5-(3-Bromophenyl)-N-(2,6-dimethylphenyl)-4H-1,2,4-triazol-3-amine (4i): 1H NMR (300 MHz, DMSO-d6): δ ppm: 2.12 (s, 6H, ArH), 7.04–7.14 (m, 3H, ArH), 7.38–7.41 (m. 1H, ArH), 7.59 (s, 1H, ArH), 7.71–7.74 (m, 1H, ArH), 8.04–8.06 (m, 1H, ArH), 8.37 (s, 1H, ArNH), 8.79 (s, 1H, NH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.99, 156.53, 137.88, 136.23, 132.91, 131.86, 131.49, 128.57, 128.33, 126.60, 122.83, 121.48, 18.57; anal. calc. for C16H15BrN4: C, 55.99; H, 4.41; N, 16.32 found: C, 55.90; H, 4.40; N, 16.29%. ESI-MS m/z = 343.06 (M+1)+.
5-(3-Bromophenyl)-N-(3-chloro-4-fluorophenyl)-4H-1,2,4-triazol-3-amine (4j): 1H NMR (300 MHz, DMSO-d6): δ ppm: 7.18–7.23 (m, 2H, ArH), 7.37, (s, 1H, ArH), 7.39–7.41 (m, 1H, ArH), 7.53 (s, 1H, ArH), 7.69–7.71 (m, 1H, ArH), 8.12–8.14 (m, 1H, ArH), 8.36 (s, 1H, NH), 8.89 (s, 1H, ArOH); 13C NMR (75 MHz, DMSO-d6): δ ppm: 157.99, 156.33, 148.88, 139.62, 132.62, 131.42, 128.70, 126.60, 122.83, 121.48, 118.92, 118.32, 114.55; anal. calc. for C14H9BrClFN4: C, 45.74; H, 2.47; N, 15.24 found: C, 45.70; H, 2.45; N, 15.19%. ESI-MS m/z = 367.60 (M+1)+, 369.60 (M+3)+.

4.2. Anticancer Activity

All of the title compounds were evaluated against 56 cancer cell lines derived from nine panels at 10 µM, as per the reported NCI US protocol [28,29,30,31,32]. A detailed methodology was described in our previous work [41].

4.3. Molecular Docking

The X-ray crystallographic structure of the tubulin–combretastatin A-4 complex, with a resolution of 2.40 Å and an R-value of 0.192 (observed), was obtained from the protein data bank (PDB ID: 5LYJ) [42]. The D-chain of the combretastatin A-4 binding site was selected for docking studies. The molecular docking was performed as explained in previous work [43,44].

4.4. ADME and Toxicity Prediction

The prediction of ADME was accomplished using SwissADME software available online [35]. The toxicity prediction in terms of LD50 and toxicity class was made using ProTox-II [40].

5. Conclusions

All of the compounds were successfully synthesized in satisfactory yields, characterized via a spectroscopic method of analysis, anticancer evaluation at 10 µM, and in silico studies. Some of the compounds demonstrated promising anticancer activity against a few cancer cell lines. The CNS cancer cell line SNB-75 was found to be the most sensitive against compound 4e (PGI = 41.25). With a mean GP of 97.48, the lead compound 4i showed the strongest anticancer activity. The five cell lines with the highest sensitivity to compound 4i were SNB-75, UO-31, CCRF-CEM, EKVX, and OVCAR-5, with PGIs of 38.94, 30.14, 26.92, 26.61, and 23.12, respectively. Compound 4i with 2,6-dimethyl substitution demonstrated good anticancer activity. The molecular docking of the compounds (4a–j) against the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ) was studied and the H-bond and halogen bond were the two main electrostatic interactions seen; the binding affinities were found ranging between −6.502 and −8.341 kcal/mol. The ADME prediction showed that all of the compounds followed Lipinski’s rule of five and were BBB-permeant. ProTox-II’s toxicity prediction indicated that the toxicity had LD50 values between 440 and 500 mg/kg, classifying them all as having class IV toxicity (300 > LD50 > 2000). The current discovery may pave the way to the chemical synthesis of improved triazoles, resulting in future advancements in cancer therapeutics.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/molecules28196936/s1: General method for the synthesis of intermediate compounds, 2a–j and 3a–j; Figures S1–S15: NMR and mass spectra of some of the compounds; Figures S16–S25: Anticancer data of compound 4a–j against 58 cancer cell lines at 10 µM.

Author Contributions

Conceptualization, M.J.A., S. and A.A. (Amena Ali); methodology, K.G., M.J.A. and A.A. (Abuzer Ali); software, A.A. (Amena Ali) and M.J.A.; validation, M.J.A. and A.S.A.A.; formal analysis, A.A. (Abuzer Ali) and A.S.A.A.; investigation, M.J.A.; resources, A.A. (Abuzer Ali) and M.F.A.; data curation, M.J.A., A.S.A.A. and M.F.A.; writing—original draft preparation, K.G., A.S.A.A., M.A.A., M.J.A., S.V.V.N.S.M.L. and A.A. (Amena Ali); writing—review and editing, A.S.A.A., M.J.A., M.F.A., S.V.V.N.S.M.L. and M.A.A.; visualization, M.J.A.; supervision, M.J.A.; project administration, M.J.A. and A.A. (Amena Ali); funding acquisition, A.A. (Amena Ali). All authors have read and agreed to the published version of the manuscript.

Funding

Amena Ali would like to acknowledge the Deanship of Scientific Research, Taif University, for funding this work.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The Supplementary Materials to this article contain information that supports the findings of this study.

Acknowledgments

The researchers would like to acknowledge the Deanship of Scientific Research, Taif University, for funding this work.

Conflicts of Interest

None of the authors have any scientific or financial conflicts of interest.

Sample Availability

Samples of the compounds are available from the authors.

References

  1. Nasri, S.; Bayat, M.; Kochia, K. Strategies for synthesis of 1,2,4-triazole-containing scaffolds using 3-amino-1,2,4-triazole. Mol. Divers. 2022, 26, 717–739. [Google Scholar] [CrossRef]
  2. Strzelecka, M.; Świątek, P. 1,2,4-Triazoles as Important Antibacterial Agents. Pharmaceuticals 2021, 14, 224. [Google Scholar] [CrossRef] [PubMed]
  3. Mahanti, S.; Sunkara, S.; Bhavani, R. Synthesis, biological evaluation and computational studies of fused acridine containing 1,2,4-triazole derivatives as anticancer agents. Synth. Comm. 2019, 49, 1729–1740. [Google Scholar] [CrossRef]
  4. Mohassab, A.M.; Hassan, H.A.; Abdelhamid, D.; Gouda, A.M.; Youssif, B.G.M.; Tateishi, H.; Fujita, M.; Otsuka, M.; Abdel-Aziz, M. Design and synthesis of novel quinoline/chalcone/1,2,4-triazole hybrids as potent antiproliferative agent targeting EGFR and BRAFV600E kinases. Bioorg. Chem. 2021, 106, 104510. [Google Scholar] [CrossRef] [PubMed]
  5. Wiseman, L.R.; Spencer, C.M. Vorozole. Drugs Aging 1997, 11, 245–250. [Google Scholar] [CrossRef]
  6. Tapera, M.; Kekeçmuhammed, H.; Tunç, C.; Kutlu, A.; Celik, I.; Zorlu, Y.; Aydin, O.; Saripinar, E. Design, synthesis, molecular docking and biological evaluation of 1,2,4 triazole derivatives possessing a hydrazone moiety as anti-breast cancer agents. New J. Chem. 2023, 47, 11602–11614. [Google Scholar] [CrossRef]
  7. Choudhary, S.K.; Gothwal, P.; Sogani, N.; Saini, A.; Swami, S. Rational Design, Synthesis, Characterization, and Antibacterial Activity of Urea Derivatives Bearing 1,2,4-Triazoles as Molecular Hybrid Scaffolds. Orient J. Chem. 2023, 39, 129–135. [Google Scholar] [CrossRef]
  8. Koparir, P.; Sarac, K.; Omar, R.A. Synthesis, Molecular Characterization, Biological and Computational Studies of New Molecule Contain 1,2,4- Triazole, and Coumarin Bearing 6,8-Dimethyl, 2021. Biointerface Res. Appl. Chem. 2022, 12, 809–823. [Google Scholar]
  9. Amin, N.H.; El-Saadi, M.T.; Ibrahim, A.A.; Abdel-Rahman, H.M. Design, synthesis and mechanistic study of new 1,2,4-triazole derivatives as antimicrobial agents. Bioorg. Chem. 2021, 111, 104841. [Google Scholar] [CrossRef]
  10. Bitla, S.; Gayatri, A.A.; Puchakayala, M.R.; Bhukya, V.K.; Vannada, J.; Dhanavath, R.; Kuthati, B.; Kothula, D.; Sagurthi, S.R.; Atcha, K.R. Design and synthesis, biological evaluation of bis-(1,2,3- and 1,2,4)-triazole derivatives as potential antimicrobial and antifungal agents. Bioorg. Med. Chem. Lett. 2021, 41, 128004. [Google Scholar] [CrossRef]
  11. Yusuf, S. Design and antiproliferative and antioxidant activities of furan-based thiosemicarbazides and 1,2,4-triazoles: Their structure-activity relationship and SwissADME predictions. Med. Chem. Res. 2021, 30, 1557–1568. [Google Scholar]
  12. El-Sebaey, S.A. Recent Advances in 1,2,4-Triazole Scaffolds as Antiviral Agents. ChemistrySelect 2020, 5, 11654–11680. [Google Scholar] [CrossRef]
  13. Vanjare, B.D.; Mahajan, P.G.; Dige, N.C.; Raza, H.; Hassan, M.; Han, Y.; Kim, S.J.; Seo, S.Y.; Lee, K.H. Novel 1,2,4-triazole analogues as mushroom tyrosinase inhibitors: Synthesis, kinetic mechanism, cytotoxicity and computational studies. Mol. Divers. 2020, 25, 2089–2106. [Google Scholar] [CrossRef]
  14. Nayak, S.; Poojary, B. Design, Synthesis, In Silico Docking Studies, and Antibacterial Activity of Some Thiadiazines and 1,2,4-Triazole-3-Thiones Bearing Pyrazole Moiety. Russ. J. Bioorg. Chem. 2020, 46, 97–106. [Google Scholar] [CrossRef]
  15. Pragathi, Y.J.; Sreenivasulu, R.; Veronica, D. Design, Synthesis, and Biological Evaluation of 1,2,4-Thiadiazole-1,2,4-Triazole Derivatives Bearing Amide Functionality as Anticancer Agents. Arab. J. Sci. Eng. 2021, 46, 225–232. [Google Scholar] [CrossRef]
  16. Sathyanarayana, R.; Poojary, B. Exploring recent developments on 1,2,4-triazole: Synthesis and biological applications. J. Chin. Chem. Soc. 2020, 67, 459–477. [Google Scholar] [CrossRef]
  17. Djemoui, A.; Naouri, A.; Ouahrani, M.R.; Djemoui, D.; Lahecen, S.; Lahrech, M.B.; Boukenna, L.; Albuquerque, H.M.T.; Saher, L.; Rocha, D.H.A.; et al. A step-by-step synthesis of triazole-benzimidazole-chalcone hybrids: Anticancer activity in human cells. J. Mol. Struct. 2019, 1204, 127487. [Google Scholar] [CrossRef]
  18. Chu, X.M.; Wang, C.; Wang, W.L.; Liang, L.L.; Liu, W.; Gong, K.K.; Sun, K.L. Triazole derivatives and their antiplasmodial and antimalarial activities. Eur. J. Med. Chem. 2019, 166, 206–223. [Google Scholar] [CrossRef]
  19. Alam, M.M.; Almalki, A.S.; Neamatallah, T.; Ali, N.M.; Malebari, A.M.; Nazreen, S. Synthesis of New 1, 3, 4-Oxadiazole-Incorporated 1, 2, 3-Triazole Moieties as Potential Anticancer Agents Targeting Thymidylate Synthase and Their Docking Studies. Pharmaceuticals 2020, 13, 390. [Google Scholar] [CrossRef]
  20. Zhao, J.W.; Wu, Z.H.; Guo, J.W.; Huang, M.J.; You, Y.Z.; Liu, H.M.; Huang, L.H. Synthesis and anti-gastric cancer activity evaluation of novel triazole nucleobase analogues containing steroidal/coumarin/quinoline moieties. Eur. J. Med. Chem. 2019, 181, 111520. [Google Scholar] [CrossRef]
  21. Ouyang, X.; Chen, X.; Piatnitski, E.L.; Kiselyov, A.S.; He, H.Y.; Mao, Y.; Pattaropong, V.; Yu, Y.; Kim, K.H.; Kincaid, J.; et al. Synthesis and structure-activity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors. Bioorg. Med. Chem. Lett. 2005, 15, 5154–5159. [Google Scholar] [CrossRef]
  22. Juszczak, M.; Matysiak, J.; Szeliga, M.; Pozarowski, P.; Niewiadomy, A.; Albrecht, J.; Rzeski, W. 2-Amino-1,3,4-thiadiazole derivative (FABT) inhibits extracellular signal-regulated kinase pathway and induces cell cycle arrest in human non-small lung carcinoma cells. Bioorg. Med. Chem. Lett. 2012, 22, 5466–5469. [Google Scholar] [CrossRef] [PubMed]
  23. Tuma, M.C.; Malikzay, A.; Ouyang, X.; Surguladze, D.; Fleming, J.; Mitelman, S.; Camara, M.; Finnerty, B.; Doody, J.; Che-kler, E.L.P.; et al. Antitumor activity of IMC-038525, a novel oral tubulin polymerization inhibitor. Trans. Oncol. 2010, 3, 318–325. [Google Scholar] [CrossRef] [PubMed]
  24. Sung, H.; Ferley, J.; Siegel, R.L.; Laversanne, M.; Soerjomartaram, I.; Jemal, A.; Bray, F. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef]
  25. Ahsan, M.J. Rationale design, synthesis and anticancer activity of 2,5-disubstituted-1,3,4-oxadiazole analogues. ChemistrySelect 2016, 1, 4713–4720. [Google Scholar] [CrossRef]
  26. Ahsan, M.J. Synthesis and anticancer activity of [(2,4-dichlorophenoxy)methyl]-5-aryl-1,3,4-oxadiazole/4H-1,2,4-triazole analogues. Turk. J. Chem. 2018, 42, 1334–1343. [Google Scholar] [CrossRef]
  27. Yeung, K.S.; Farkas, M.E.; Kadow, J.F.; Meanwell, N.A. A base-catalyzed, direct synthesis of 3,5-disubstituted 1,2,4-triazoles from nitriles and hydrazides. Tetrahedron Lett. 2005, 46, 3429–3432. [Google Scholar] [CrossRef]
  28. Development Therapeutic Program NCI/NIH. Available online: http://dtp.nci.nih.gov (accessed on 20 January 2022).
  29. Skehan, P.; Storeng, R.; Scudiero, D.; Monks, A.; McMahon, J.; Vistica, D.; Warren, J.T.; Bokesch, H.; Kenney, S.; Boyd, M.R.J. New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening. Natl. Cancer Inst. 1990, 83, 1107–11012. [Google Scholar] [CrossRef]
  30. Boyd, M.R.; Paull, K.D. Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen. Drug Dev. Res. 1995, 34, 91–109. [Google Scholar] [CrossRef]
  31. Monks, A.; Scudiero, D.; Skehan, P.; Shoemaker, R.; Paull, K.; Vistica, D.; Hose, C.; Langley, J.; Cronise, P.; Vaigro-Wolff, A.; et al. Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. Nat. Cancer Inst. 1991, 83, 757–766. [Google Scholar] [CrossRef]
  32. Shoemaker, R.H. The NCI60 human tumour cell line anticancer drug screen. Nat. Rev. Cancer 2006, 6, 813–823. [Google Scholar] [CrossRef]
  33. Arnst, K.E.; Banerjee, S.; Chen, H.; Deng, S.; Hwang, D.J.; Li, W.; Miller, D.D. Current advances of tubulin inhibitors as dual acting small molecules for cancer therapy. Med. Res. Rev. 2019, 39, 1398–1426. [Google Scholar] [CrossRef] [PubMed]
  34. Daina, A.; Michielin, O.; Zoete, V. SwissADME: A free web tool to evaluate pharmacokinetics, druglikeness and medicinal chemistry friendliness of small molecules. Sci. Rep. 2017, 7, 42717. [Google Scholar] [CrossRef]
  35. ADME Prediction. Available online: http://www.swissadme.ch/ (accessed on 20 August 2023).
  36. Lipinski, C.A.; Lombardo, L.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 2001, 46, 3–26. [Google Scholar] [CrossRef]
  37. Ertl, P.; Rohde, B.; Selzer, P. Fast calculation of molecular polar surface area as a sum of fragment-based contributions and its application to the prediction of drug transport properties. J. Med. Chem. 2000, 43, 3714–3717. [Google Scholar] [CrossRef]
  38. Daina, A.; Zoete, V. A BOILED-Egg To Predict Gastrointestinal Absorption and Brain Penetration of Small Molecules. ChemMedChem 2016, 11, 1117–1121. [Google Scholar] [CrossRef]
  39. Selick, H.E.; Beresford, A.P.; Tarbit, M.H. The emerging importance of predictive ADME simulation in drug discovery. Drug Discov. Today 2002, 7, 109–116. [Google Scholar] [CrossRef]
  40. Toxicity Prediction. Available online: https://tox-new.charite.de/protox_II/ (accessed on 20 August 2023).
  41. Ali, A.; Ali, A.; Tahir, A.; Bakht, M.A.; Salahuddin; Ahsan, M.J. Molecular Engineering of Curcumin, an Active Constituent of Curcuma longa L. (Turmeric) of the Family Zingiberaceae with Improved Antiproliferative Activity. Plants 2021, 10, 1559. [Google Scholar] [CrossRef]
  42. X-ray Crystallographic Structure of Tubulin-Combretastatin A4 Complex. Available online: https://www.rcsb.org/structure/5lyj (accessed on 12 January 2023).
  43. Gaspari, R.; Prota, A.E.; Bargsten, K.; Cavalli, A.; Steinmetz, M.O. Structural Basis of cis- and trans- Combretastatin Binding to Tubulin. Chem 2017, 2, 102–113. [Google Scholar] [CrossRef]
  44. Agarwal, M.; Afzal, A.; Salahuddin; Altamimi, A.S.A.; Alamri, M.A.; Alossaimi, A.A.; Sharma, V.; Ahsan, M.J. Design, Synthesis, ADME, and Anticancer Studies of Newer N-Aryl-5-(3,4,5-Trifluorophenyl)-1,3,4-Oxadiazol-2-Amines: An Insight into Experimental and Theoretical Investigations. ACS Omega 2023, 8, 26837–26849. [Google Scholar] [CrossRef] [PubMed]
Molecules 28 06936 g001
Figure 1. (A) Isomeric form of triazole, 1,2,3-triazole, and 1,2,4-triazole; (B) 4H and 1H-Tautomers of 1,2,4-triazole; (C) 1,2,4-triazole-containing anticancer agents.
Figure 1. (A) Isomeric form of triazole, 1,2,3-triazole, and 1,2,4-triazole; (B) 4H and 1H-Tautomers of 1,2,4-triazole; (C) 1,2,4-triazole-containing anticancer agents.
Molecules 28 06936 g001
Molecules 28 06936 g002
Figure 2. Design of new triazoles based on reported anticancer compounds.
Figure 2. Design of new triazoles based on reported anticancer compounds.
Molecules 28 06936 g002
Molecules 28 06936 sch001
Scheme 1. Reagents and conditions: (i). NaCNO, AcOH, 25 °C, 30 min, 82–94% yield; (ii). NH2NH2.H2O, C2H5OH, 80 °C, 24 h, 69–89%, yield (iii); n-Butanol, K2CO3, 120 °C, 8–10 h, 69–93% yield.
Scheme 1. Reagents and conditions: (i). NaCNO, AcOH, 25 °C, 30 min, 82–94% yield; (ii). NH2NH2.H2O, C2H5OH, 80 °C, 24 h, 69–89%, yield (iii); n-Butanol, K2CO3, 120 °C, 8–10 h, 69–93% yield.
Molecules 28 06936 sch001
Molecules 28 06936 g003
Figure 3. Three-dimensional interaction of ligands 4a, 4d, 4f, 4g, and 4i with the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ).
Figure 3. Three-dimensional interaction of ligands 4a, 4d, 4f, 4g, and 4i with the tubulin–combretastatin A-4 binding site (PDB ID: 5LYJ).
Molecules 28 06936 g003
Molecules 28 06936 g004
Figure 4. Three-dimensional interaction of ligands 4e and 4j with the tubulin–combretastatin A-4 binding site.
Figure 4. Three-dimensional interaction of ligands 4e and 4j with the tubulin–combretastatin A-4 binding site.
Molecules 28 06936 g004
Molecules 28 06936 g005
Figure 5. Two- and three-dimensional interaction of ligand 4i with the tubulin-combretastatin A-4 binding site.
Figure 5. Two- and three-dimensional interaction of ligand 4i with the tubulin-combretastatin A-4 binding site.
Molecules 28 06936 g005
Molecules 28 06936 g006
Figure 6. Boiled egg presentation of compounds 4e, 4g, and 4i using SwissADME software.
Figure 6. Boiled egg presentation of compounds 4e, 4g, and 4i using SwissADME software.
Molecules 28 06936 g006
Table 1. The physical constants and NSC code of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine analogs (4a–j).
Table 1. The physical constants and NSC code of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine analogs (4a–j).
Molecules 28 06936 i001
S. No.CompoundR% YieldMp (°C)Rf *
14a4-Fluoro69138–1400.58
24b4-Chloro93140–1420.66
34c4-Methyl82136–1380.73
44d4-Methoxy66146–1480.67
54e2-Chloro70152–1540.69
64f2-Methyl85144–1460.75
74g2-Methoxy65148–1500.62
84h2,4-Dimethyl71130–1320.70
94i2,6-Dimethyl89126–1280.68
104j3-Chloro-4-fluoro70128–1300.59
* Mobile phase, benzene/acetone (9:1).
Table 2. Anticancer activity of triazoles at 10−5 M.
Table 2. Anticancer activity of triazoles at 10−5 M.
PanelCell LinesGrowth Percentage (GP) of Cell Lines at 10−5 M
4a4b4c4d4e4f4g4h4i4j
LeukemiaCCRF-CEM108.27119.99108.68102.0994.53100.8889.67101.7673.0891.67
HL-60(TB)113.71114.64111.07112.68110.98110.97112113.2397.14114.35
K-562112.26109.82107.94103.69105.66102.97109.72103.2102.19103.41
MOLT-4107.03108.06111.15110.86113.17101.46110.07102.6397.5997.05
RPMI-8226105.59105.54100.4598.1598.41101.2595.4499.5695.6197.9
SR102.38101.3798.98101.01100.5899.66101.996.8195.0590.22
Non-small cell lung cancerA549/ATCC103.16103.69105.55100.8496.1100.9387.98104.3293.63106.05
EKVX78.2880.1782.0469.7179.1982.9788.7875.4473.3975.43
HOP-62101.0695.97101.2792.36100.4495.2105.9888.3684.3189.96
NCI-H22693.3197.92100.0795.5399.37104.72103.4594.9592.3398.69
NCI-H2388.792.0893.1690.0193.7792.05100.7185.1390.7286.94
NCI-H322M94.8198.59104.27102.66103.52104.54104.2990.5799.9799.48
NCI-H460107.43109.66106.66102.46105.58111.91106.39108.59100.48106.13
NCI-H52297.489495.7596.1594.51102.999.3899.5392.2296.13
Colon cancerCOLO 205110.19112.57110.57107.34110.79113.84112.68115.88107.53115.25
HCC-2998115.61110.62111.63119.85103.1108.79120.05109.12117.6107.2
HCT-11697.94111.89113.68107.29109.62110.01109.61112.05117.94108.97
HCT-15104.59102.35107.09101.37102.998.06107.29101.49105.4198.35
HT29105.5112.5108.16106.95108.98110.4109.4105.72109.17108.45
KM12105.22112.61105.97102.43100.98101.9104.3799.84106.7598.24
SW-620105.46104.34112.0896.23103.98103.77102.34108.9992.19107.34
CNS cancerSF-268106.54100.8497.7595.592.22106.799.08106.0495.37108.16
SF-29595.395.6695.5796.2696.7196.01101.3191.5497.6690.8
SF-539100.7799.9103.01103.1104.07102.34116.3495.16101.6497.27
SNB-19101.28104.36105.52102.63103.7197.3104.0294.5996.0493.01
SNB-7585.1294.9893.5774.1258.75105.169.9197.8661.0687.08
U251100.5198.72101.28103.9795.73101.07100.21103.1199.09103.42
MelanomaLOX IMVI102.66101.4101.31100.89102.4499.16104.892.9295.0594.16
MALME-3M98.54100.0296.3294.9392.7191.35100.5986.1790.3184.86
M14105.99108.76104.25112.38123.95105.19116.15105.298.01111.26
MDA-MB-435106.28107.8105.37104.17104.41110.41105.09108.55102.27108.5
SK-MEL-2113.88107.21103.44101.76103.4107.78108.78108.297.14103.77
SK-MEL-28113.3112.88118.51108.94120.72115.05120.5112.62112.3117.18
SK-MEL-599.698.9999.599.1299.9101.68101.97100.299.65100.08
UACC-257109.84114.31110.07103.1292.92103.8391.52103.591.31109.37
UACC-6286.6386.8889.286.3790.4791.6791.3986.8181.582.62
Ovarian cancerIGROV197.7993.46101.7396.31104.6993.62108.5398.0895.5395.01
OVCAR-3100.18100.05102.0297.2101.46108.69106.81105.94101.9114.63
OVCAR-4111.22110.06107.14106.18101.66114.27104.94117.35102.73114.79
OVCAR-597.8794.97107.49104.3114.17103.71110.58100.9276.8895.79
OVCAR-8106.58103.24106.89100.7896.44103.6799.3104.8797.38107.02
NCI/ADR-RES109.03107.66105.99105.54109.73105.49111.9103.85100.18103.94
SK-OV-3119.91111.75110.49102.74117.29103.01117.4486.5299.76104.47
Renal cancer786-0113.02103.97103.28108.45102.12106.4112100.76101.2398.23
A498135.1134.22128.18128.7111.35126.93121.95133.39116.19120.55
ACHN114.05106.61110.86102.05101.53111.23110.31108.6797.5106.13
CAKI-185.9382.7487.0982.8688.1793.4990.0894.1882.4497.73
RXF 393116.32117.62111.11130.25117.52108.82122.22108.85119.36115.41
SN12C102.39106.19107.4100.6798.2105.96103.3899.0698.1897.5
TK-10120.17137.39130.44157.41113.5127.11108.98126.78127.43144.83
UO-3173.3268.8673.5367.871.5362.8379.7763.4369.8666.57
Prostate cancerDU-195104.93109.62101.8499.1795.28114.08102.88117.08101.74107.28
Breast cancerMCF-787.7280.8481.8964.8188.9888.3792.8288.491.8875.48
MDA-MB-231/ATCC90.5689.4494.0488.2795.9591.7997.9188.6482.8488.16
HS 578T99.4399.85108.56100.8795105.7997.66113.2999.85105.98
BT-54995.99107.15119.87101.94108.77136.12122.63114.36116.88120.26
T-47D110.59111.95106.7492.699.07115.23104.25100.03103.99104.12
MDA-MB-468105.73108.68109.79104.93105.76105.16109.06101.61107.1696.56
Mean103.14103.75104.09100.88100.97103.89104.29101.4897.48101.19
Delta29.8234.8930.5636.0742.2241.0634.3838.0536.4234.62
Range61.7868.5356.9192.6065.2073.2952.7269.9666.3778.26
Table 3. The anticancer activity of the six most sensitive cell lines at 10−5 M.
Table 3. The anticancer activity of the six most sensitive cell lines at 10−5 M.
CompoundAnticancer Activity in One Dose (10−5 M Concentration)
The Most Sensitive Cell LinesGrowth Percent (GP)Percent Growth Inhibition (PGI)
4aUO-31 (renal cancer)73.3226.68
EKVX (non-small cell lung cancer)78.2821.72
SNB-75 (CNS cancer)85.1214.88
CAKI-1 (renal cancer)85.9314.07
UACC-62 (melanoma)86.6313.37
4bUO-31 (renal cancer)68.8631.14
EKVX (non-small cell lung cancer)80.1719.83
MCF-7 (breast cancer)80.8419.16
CAKI-1 (renal cancer)82.7417.26
UACC-62 (melanoma)86.8813.12
4cUO-31 (renal cancer)73.5326.47
MCF-7 (breast cancer)81.8918.11
EKVX (non-small cell lung cancer)82.0417.96
CAKI-1 (renal cancer)87.0912.91
UACC-62 (melanoma)89.210.8
4dMCF-7 (breast cancer)64.8135.19
UO-31 (renal cancer)67.832.2
EKVX (non-small cell lung cancer)69.7130.29
SNB-75 (CNS cancer)74.1225.88
CAKI-1 (renal cancer)82.8617.14
4eSNB-75 (CNS cancer)58.7541.25
UO-31 (renal cancer)71.5328.47
EKVX (non-small cell lung cancer)79.1920.81
CAKI-1 (renal cancer)88.1711.83
MCF-7 (breast cancer)88.9811.02
4fUO-31 (renal cancer)62.8337.17
EKVX (non-small cell lung cancer)82.9717.03
MCF-7 (breast cancer)88.3711.63
MALME-3M (melanoma)91.358.65
UACC-62 (melanoma)91.678.33
4gSNB-75 (CNS cancer)69.9130.09
UO-31 (renal cancer)79.7720.23
A549/ATCC (non-small cell lung cancer)87.9812.02
EKVX (non-small cell lung cancer)88.7811.22
CCRF-CEM (leukemia)89.6710.33
4hUO-31 (renal cancer)63.4336.57
EKVX (non-small cell lung cancer)75.4424.56
NCI-H23 (non-small cell lung cancer)85.1314.87
MALME-3M (melanoma)86.1713.83
SK-OV-3 (ovarian cancer)86.5213.48
4iSNB-75 (CNS cancer)61.0638.94
UO-31 (renal cancer)69.8630.14
CCRF-CEM (leukemia)73.0826.92
EKVX (non-small cell lung cancer)73.3926.61
OVCAR-5 (ovarian cancer)76.8823.12
4jUO-31 (renal cancer)66.5733.43
EKVX (non-small cell lung cancer)75.4324.57
MCF-7 (breast cancer)75.4824.52
UACC-62 (melanoma)82.6217.38
MALME-3M (melanoma)84.8615.14
Table 4. The average percent growth inhibition of the triazoles (4a–j) and imatinib at 10 µM.
Table 4. The average percent growth inhibition of the triazoles (4a–j) and imatinib at 10 µM.
Panels4a4b4c4d4e4f4g4h4i4jImatinib
Leukemia−8.21−9.90−6.38−4.75−3.89−2.86−3.13−2.866.560.99
Non-small cancer cell4.473.491.406.283.440.600.386.649.125.1515.68
Colon cancer−6.36−9.55−9.88−5.92−5.76−6.68−9.39−7.58−8.08−6.265.34
CNS cancer1.750.920.554.078.13-1.421.521.958.193.385.8
Melanoma−4.08−4.25−3.11−1.30−3.43−2.90−4.53−0.463.61−1.31−0.87
Ovarian cancer−6.08−3.03−5.96−1.86−6.49−4.64−8.5−2.503.66−5.09−7.16
Renal cancer−7.54−7.2−6.48−9.77−0.49−5.35−6.08−4.39−1.52−5.873.25
Prostate cancer−4.93−9.62−1.840.834.72−14.08−2.88−17.08−1.74−7.2812.5
Breast cancer1.660.35−3.487.761.078−7.08−4.05−1.05−0.431.5712.15
Bold font represents the best result.
Table 5. Molecular docking studies of oxadiazoles against tubulin.
Table 5. Molecular docking studies of oxadiazoles against tubulin.
S. No.CompoundPDB ID: 5LYJ
Docking ScoreEmodel ScoreInteraction
14a−7.582−61.616H-bond (Asn258, 2.47 Å)
24b−7.172−61.018H-bond (Asn258, 2.33 Å); halogen bond (Cys241, 3.09 Å)
34c−7.688−62.646−
44d−6.502−58.514H-bond (Asn258, 2.36 Å)
54e−7.899−65.212H-bond (Asn258, 2.34 Å); halogen bond (Val315, 3.47 Å)
64f−8.264−66.047H-bond (Asn258, 2.72 Å)
74g−8.341−74.031H-bond (Asn258, 2.76 Å)
84h−7.788−57.121−
94i−8.149−64.382H-bond (Asn258, 2.43 Å)
104j−7.912−61.999H-bond (Asn258, 2.38 Å); halogen bond (Val315, 3.47 Å)
Table 6. ADME and toxicity prediction studies of triazoles (4a–j).
Table 6. ADME and toxicity prediction studies of triazoles (4a–j).
S. No.Compound% ABSVolumeTPSANROTBHBA (<10)HBD (<5)Log p (<5)MW (500)BBB PermeabilityLipinski’s Violation (≤1)LD50 (mg/kg)Toxicity Class
14a90.49238.7553.633222.15333.16Yes05004
24b90.50247.3653.63222.33349.6Yes05004
34c90.50250.3853.63222.17329.19Yes05004
44d87.32259.3762.834322.2345.19Yes04404
54e90.50247.3653.63222.44349.6Yes05004
64f90.50250.3853.63222.34329.19Yes05004
74g87.32259.3762.834322.37345.19Yes04404
84h90.50266.9453.63222.48343.22Yes05004
94i90.50266.9453.63222.36343.22Yes05004
104j90.50252.2953.63222.36367.6Yes05004
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Ahsan, M.J.; Gautam, K.; Ali, A.; Ali, A.; Altamimi, A.S.A.; Salahuddin; Alossaimi, M.A.; Lakshmi, S.V.V.N.S.M.; Ahsan, M.F. Synthesis, Anticancer Activity, and In Silico Studies of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine Analogs. Molecules 2023, 28, 6936. https://doi.org/10.3390/molecules28196936

AMA Style

Ahsan MJ, Gautam K, Ali A, Ali A, Altamimi ASA, Salahuddin, Alossaimi MA, Lakshmi SVVNSM, Ahsan MF. Synthesis, Anticancer Activity, and In Silico Studies of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine Analogs. Molecules. 2023; 28(19):6936. https://doi.org/10.3390/molecules28196936

Chicago/Turabian Style

Ahsan, Mohamed Jawed, Krishna Gautam, Amena Ali, Abuzer Ali, Abdulmalik Saleh Alfawaz Altamimi, Salahuddin, Manal A. Alossaimi, S. V. V. N. S. M. Lakshmi, and Md. Faiyaz Ahsan. 2023. "Synthesis, Anticancer Activity, and In Silico Studies of 5-(3-Bromophenyl)-N-aryl-4H-1,2,4-triazol-3-amine Analogs" Molecules 28, no. 19: 6936. https://doi.org/10.3390/molecules28196936

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