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Article

Dihydropyrimidone Derivatives as Thymidine Phosphorylase Inhibitors: Inhibition Kinetics, Cytotoxicity, and Molecular Docking

by
Tian-Meng Cui
1,
Muhammad Altaf
2,
Abdu Aldarhami
3,*,
Abdulrahman S. Bazaid
4,
Nizar H. Saeedi
5,
Almohanad A. Alkayyal
5,
Fahad M. Alshabrmi
6,
Farman Ali
7,
Mohammed Aladhadh
8,
Muhammad Yasir Khan
9,10,
Ahad Amer Alsaiari
11 and
Yue-Rong Ma
1,*
1
School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China
2
Department of Biochemistry, Federal Urdu University of Arts, Sciences and Technology, Karachi 75300, Pakistan
3
Department of Medical Microbiology, Qunfudah Faculty of Medicine, Umm Al-Qura University, Al-Qunfudah 21961, Saudi Arabia
4
Department of Medical Laboratory Science, College of Applied Medical Sciences, University of Ha’il, Hail 55476, Saudi Arabia
5
Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, University of Tabuk, Tabuk 71491, Saudi Arabia
6
Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah 51452, Saudi Arabia
7
Department of Chemistry, Federal Urdu University of Arts, Sciences and Technology, Karachi 75300, Pakistan
8
Department of Food Science and Human Nutrition, College of Agriculture and Veterinary Medicine, Qassim University, Buraydah 51452, Saudi Arabia
9
Department of Biology, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia
10
Vaccine and Immunotherapy Unit, King Fahad Medical Research Center, King Abdulaziz University, Jeddah 21589, Saudi Arabia
11
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, Taif 21944, Saudi Arabia
 
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*
Authors to whom correspondence should be addressed.
Molecules 2023, 28(8), 3634; https://doi.org/10.3390/molecules28083634
Submission received: 5 March 2023 / Revised: 6 April 2023 / Accepted: 18 April 2023 / Published: 21 April 2023
(This article belongs to the Special Issue Five and Six-Membered Heterocyclic Compounds and Their Therapeutic Potential)
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Abstract

:
Overexpression of the thymidine phosphorylase (TP) enzyme induces angiogenesis, which eventually leads to metastasis and tumor growth. The crucial role of TP in cancer development makes it an important target for anticancer drug discovery. Currently, there is only one US-FDA-approved drug, i.e., Lonsurf, a combination of trifluridine and tipiracil, for the treatment of metastatic colorectal cancer. Unfortunately, numerous adverse effects are associated with its use, such as myelosuppression, anemia, and neutropenia. Since the last few decades, the discovery of new, safe, and effective TP inhibitory agents has been rigorously pursued. In the present study, we evaluated a series of previously synthesized dihydropyrimidone derivatives 1–40 for their TP inhibitory potential. Compounds 1, 12, and 33 showed a good activity with IC50 = 314.0 ± 0.90, 303.5 ± 0.40, and 322.6 ± 1.60 µM, respectively. The results of mechanistic studies revealed that compounds 1, 12, and 33 were the non-competitive inhibitors. These compounds were also evaluated for cytotoxicity against 3T3 (mouse fibroblast) cells and were found to be non-cytotoxic. Finally, the molecular docking suggested the plausible mechanism of non-competitive inhibition of TP. The current study thus identifies some dihydropyrimidone derivatives as potential inhibitors of TP, which can be further optimized as leads for cancer treatment.

Graphical Abstract

1. Introduction

Angiogenesis is the process by which new blood vessels form from pre-existing ones. It is a crucial process in normal development and tissue repair, but it can also be exploited by cancer cells to support their growth and spread. Tumors require a blood supply to deliver oxygen and nutrients, and angiogenesis provides a means for this. Additionally, angiogenesis can allow cancer cells to escape from the primary tumor and travel to distant sites in the body to form new tumors. There has been significant interest in targeting angiogenesis as a strategy to treat cancer [1,2]. While anti-angiogenic therapies have shown promise in treating some types of cancer, there are still challenges to be addressed.
Thymidine phosphorylase (TP) is an enzyme that plays a crucial role in the process of angiogenesis, which is the formation of new blood vessels. TP is over-expressed in many types of cancer, and its expression is associated with tumor growth, invasion, and metastasis. TP catalyzes the breakdown of thymidine into the following two products: thymine and 2′-deoxy-D-ribose-1-phosphate. The latter product, 2′-deoxy-D-ribose-1-phosphate, is then dephosphorylated to produce 2′-deoxy-D-ribose [3]. This molecule can stimulate the production of vascular endothelial growth factor (VEGF), a protein that plays a critical role in angiogenesis. VEGF activates endothelial cells, which line the walls of blood vessels and promotes their proliferation and migration. This process is further facilitated by the secretion of matrix metalloproteinases (MMPs), which are enzymes that break down extracellular matrix proteins and facilitate the remodeling of tissues. Together, these processes lead to the formation of new blood vessels, which can supply nutrients and oxygen to cancer cells and facilitate their spread to other parts of the body [4].
TP is a highly conserved enzyme that has been found in a wide range of organisms, including bacteria, plants, and animals. The primary amino acid sequence of TP is generally well conserved across different species, suggesting that the enzyme has an important and conserved biological function. It has been reported that TP from mammalian sources, such as humans, has a high degree of sequence similarity with TP from other mammals. Interestingly, TP from mammalian sources also shares a sequence similarity with TP from bacteria, including Escherichia coli. The amino acid sequence of TP from E. coli has been reported to be up to 39% identical to that of TP from mammals [5]. The active site of mammalian TP enzyme also shares around 65–70% sequence similarity with the active site residues of E. coli TP enzyme [6].
Since TP inhibition modulates the formation of a key product, i.e., 2′-deoxy-D-ribose, which leads to tumor growth suppression [7]. TP inhibition is thus a vital approach against angiogenesis and cancer. Lonsurf (trifluridine and tipiracil) and 5-fluorouracil are currently the only FDA-approved drugs for the treatment of metastatic colorectal cancer that has progressed after standard therapies [8]. Like many cancer drugs, Lonsurf can cause side effects, and some of the common side effects of this drug include anemia, neutropenia, and myelosuppression. Other less common side effects may include fatigue, nausea, vomiting, and loss of appetite. Hence, there is an urgent need for novel, safe, and effective TP inhibitory agents [9]. A pyrimidine analog known as TPI (5-chloro-6-[1-(2-iminopyrrolidinyl) methyl] uracil hydrochloride) was identified as the most potent inhibitor of human TP till date. In addition to it, 7-deazaxanthine (a purine analog) is a commonly used reference compound for in vitro TP inhibitory assay [10,11]. Previously, different analogs of triazines, i.e., 5-chlorouracil-linked-pyrazolo [1,5-α] [1,3,5] triazines, 1,2,4-triazolo [1,5-a] [1,3,5] triazin-5,7-dione, and 1,3,5-triazin-2,4-dione were described by different researchers for their inhibitory potential against TP enzyme [12,13,14]. Previously, the dihydropyrimidone derivatives also showed significant activity against TP [15]. Since the last decade, our research group has focused on the discovery of leads against thymidine phosphorylase. In continuation of our studies, we report here the TP inhibitory activity of a previously synthesized series of dihydropyrimidone derivatives [16].
Keeping in view the extensive medicinal importance of dihydropyrimidones, as well as their structural similarity with 7-deazaxanthine, a class of dihydropyrimidones derivatives was synthesized and previously reported by our research group [16]. In this manuscript, we report the in vitro TP inhibitory activity of 40 different dihydropyrimidones derivatives. Potent compounds of the series were also subjected to cytotoxicity evaluation against the 3T3 (mouse fibroblast) cell line using MTT (3-[4,5-dimethylthiazole-2-yl]-2,5-diphenyl-tetrazolium bromide) spectrophotometric assay [17]. Kinetic studies were also performed to identify the mode of action of active compounds. The Kinetic studies revealed that the most active compounds were non-competitive inhibitors of TP. We also performed the molecular docking study to rationalize the mechanism of TP inhibition.

2. Results and Discussion

2.1. In Vitro Study

Differently substituted dihydropyrimidone derivatives 1–40 were screened; among them, twenty-one compounds exhibited some level of activity against the TP enzyme (showed more than 50% inhibition) (Table 1). Compound 12 (IC50 = 303.5 ± 0.42 µM), 1 (IC50 = 314.3 ± 0.93 µM), and 33 (IC50 = 322.6 ± 1.68 µM) showed a significant activity when compared with standard inhibitors of the study, i.e., 7-deazaxanthine (IC50 = 41.0 ± 1.63 µM) and tipiracil-HCl (IC50 = 0.014 ± 0.04 µM).
To understand the structure–activity relationship (SAR), we considered compound 1 as the parent compound (i.e., with unsubstituted benzene ring) on which different substitutions made resulting compounds active, weakly active, or inactive. Results revealed that compound 1 was the second most potent compound of the series with an IC50 value of 314.3 ± 0.9 µM; however, when we compared it with standard inhibitors of the study, i.e., tipiracil-HCl (IC50 = 0.014 ± 0.04 µM) and 7-deazaxanthine (IC50 = 41.0 ± 1.63 µM), it was found to be weakly active and thus need structural optimization. To characterize the mechanism of enzyme inhibition, compound 1 was subjected to kinetic studies. Results revealed that compound 1 was a non-competitive type of inhibitor with Ki = 326.3 ± 0.002 µM (Table 2; Figure 1), while the dose–response curve of compound 1 with standard deviation is provided in the Supplementary File Figure S1. From these results, it is suggested that compound 1 might interact with non-active site amino acid residues of the enzyme and thus inhibit its activity. These interactions might be through hydrogen bonding or hydrophobic interactions.
Compound 12 was found to be the most active analog of this series with IC50 = 303.5 ± 0.42 µM. It has a NO2 group at the para position of the phenyl ring. On the other hand, when the position of NO2 was changed from para to meta, as is the case of compound 38, it became inactive (showed less than 50% inhibition). This indicates that the para position of the NO2 group is crucial for TP inhibitory activity. When subjected to mechanistic studies, compound 12 showed a non-competitive type inhibition with Ki = 297.6 ± 0.006 µM (Table 2; Figure 2), suggesting its interaction with amino acid residues other than the active site of the TP enzyme. The dose–response curve of compound 12 with standard deviation is provided in the Supplementary File Figure S1.
Compound 33 was found to be the third most active analog of the series with IC50 = 322.6 ± 1.60 µM. It has a trifluoromethyl moiety at the para position of the phenyl ring. On the other hand, when a single fluorine atom was substituted at the ortho position of the phenyl ring (i.e., compound 35), the activity was lost. Mechanistic studies revealed that compound 33 was a non-competitive inhibitor with Ki = 311.4 ± 0.004 µM (Table 2; Figure 3), while the dose–response curve of compound 33 with standard deviation is provided in Supplementary File Figure S1. In compound 34, the chloro group was substituted at the para position of the phenyl ring and showed IC50 = 443.9 ± 0.9 µM, less active than compound 33. Mono-O-Cl, di-O-Cl, and di-m-Cl substituted analogs, i.e., compounds 6, 18, and 39, were inactive. Compounds with para-bromo substitution (i.e., compound 37) also showed less than 50% inhibition (i.e., considered as inactive). Interestingly the presence of the bromo group, along with the methoxy group, makes the compound active, as in the case of compound 22 (IC50 = 394.3 ± 4.3 µM). Compound 22 has meta, para-di-chloro, and meta-bromo moieties in its skeleton.
Substitution of alkyl groups at the C-4 of the pyrimidine skeleton showed a weak inhibition, as were shown by compounds 10 and 21. Compound 10 (IC50 = 389.0 ± 0.6 µM) possess a butyl group at C-4 of the pyrimidine skeleton, while compound 21 possesses an isobutyl group at C-4 of the pyrimidine skeleton. From these results, it was observed that inhibitory activity increases when the compound possesses an isobutyl group (Compound 21; IC50 = 345.4 ± 0.5 µM). Substitution of the dimethyl amino group at the para position of the phenyl ring, as in compound 26, a weak activity (IC50 = 349.9 ± 3.7 µM) was observed.
All active derivatives of the current study were finally subjected to cytotoxicity evaluation. In vitro spectrophotometric assay was employed with a 3T3 (mouse fibroblast) cell line. Results revealed that all active compounds were non-toxic to the cells (Table 1).

2.2. In Silico Study

Molecular docking is routinely used to predict the binding mode and binding affinity of a small molecule with a receptor protein and to determine the plausible mechanism of observed experimental activities [18,19,20]. Thus, to rationalize the plausible mechanism of observed TP inhibition by dihydropyrimidone derivatives, molecular docking studies were performed using the crystal structure of TP. The details of the selection of the protein target and validation of the docking protocol are provided in the Supplementary File. The binding site was defined on a specific allosteric pocket identified by Bronckaers and co-workers and site map analysis, which is proximal to the catalytic site (Figure S1, Supplementary Materials) [21]. All the selected compounds (1, 12, 33, and 7-deazaxanthine) were significantly bound to the allosteric pocket of TP with a binding score in the range of −6.19 kcal/mol to −5.11 kcal/mol (Figure 4, Table 3). The 5′-O-tritylinosine (KIN59), a non-competitive inhibitor of human and E. coli TP was also docked into the defined binding site. Interestingly, the selected compounds and KIN59 get complexed in the same binding site (Figure S2). As expected, the KIN59 showed the highest binding score of −6.56 kcal/mol in comparison to selected compounds.
Insight into the binding mode of compound 1, it was observed that the dihydropyrimidone scaffold resides well into the loop region of the binding site, consisting of Gly122, Asp125, Lys126, Asn252, Val363, and Val364 (Figure 4A). Whereas the substituted phenyl ring bends towards the Gly116 and Arg370 by mediating hydrophobic interaction. The carbonyl group and the two nitrogen atoms of the pyrimidine ring were involved in the hydrogen bond contacts with Gly116, Gly122, Asp125, Lys126, Gly251, and Asn252 at a distance of 2.8 Å, 1.7 Å, 2.3 Å, 3.3 Å, 2.7 Å, and 2.2 Å, respectively. Compound 12 exhibited a binding mode comparable to that of compound 1 (Figure 4B). Similarly, a dihydropyrimidone scaffold sandwich between the allosteric loop and an alpha helix consists of Gly122, Asn252, Gly360, and Val363. Similarly, the substituted nitrophenyl ring stacked between the Gly116, Leu117, Asp125, and Arg370 by mediating electrostatic and hydrophobic interactions. In addition, the nitrogen of the pyrimidine ring and ester group substituted on the ring formed hydrogen bonds with Gly360 and Asn252 at a distance of 2.9 Å and 2.2 Å, respectively. In the case of compound 33, the observed binding mode was also similar to that of compounds 1 and 12 (Figure 4C). The dihydropyrimidone scaffold is stacked between the Gly89, Gly91, Gly121, Lys126, Asn252, and Gly360. Among which Gly89, Gly91, Asn252, and Gly360 were observed to mediate hydrogen bonds with oxygen and nitrogen elements of dihydropyrimidone scaffold at a distance of 3.2 Å, 3.2 Å, 2.7 Å, and 2.7 Å, respectively while rest of the residues were involved in hydrophobic interactions. Whereas the substituted trifluoromethyl moiety at the para position of the phenyl ring bends towards the Gly116, Val363, and Asp370 by mediating the hydrophobic interactions. In the case of 7-deazaxanthine, the pyrimidine ring mediates significant electrostatic and hydrophobic interactions with Gly116, Gly122, Asp125, and Asn252 (Figure 4D). Similarly, the pyrrole ring moves towards the Gly116, Asp125, and Arg370. The nitrogen of pyrimidine and pyrrole ring establishes hydrogen bonds with Gly116, Gly122, Asp125, Asn252, and Arg370 at a distance of 3.2 Å, 3.2 Å, 2.1 Å, 3.2 Å, and 3.7 Å, respectively.
Furthermore, the ADME profile of the dihydropyrimidone derivatives (1, 12, and 33) was evaluated using an online server, SwissADME, to identify the most promising compounds with good pharmacokinetic profiles and the best chances of success in the later phases of drug development [22,23]. Only most potential dihydropyrimidone derivatives have been considered for ADME analysis. Based on six physiochemical properties (solubility, polarity, flexibility, lipophilicity, insaturation, and size) represented in Figure 5, the selected compounds exhibit good oral absorption with good bioavailability scores (0.55) and TPSA (topological polar surface area) values less than 115 Å2, implying that they will be anticipated to be orally absorbed. In terms of pharmacokinetics, all of the selected compounds displayed high gastrointestinal absorption (GI). High GI absorption refers to a prediction that these compounds are likely to be absorbed efficiently from the gastrointestinal tract into the bloodstream after oral administration.

3. Material and Methods

Thymidine phosphorylase (source: E. coli, EC Number 2.4.2.4), thymidine (substrate), and potassium phosphate monobasic (as buffer) were acquired from Sigma Aldrich, USA. The 7-deazaxanthine (standard inhibitor) was acquired from Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA. Dimethylsulfoxide (DMSO), used as a solvent, was obtained from Fisher Scientific, Schwerte, Germany.

3.1. Thymidine Phosphorylase Inhibition Assay

Reaction was performed in 96-well plates and in triplicates. The 200 µL reaction mixture was comprised of 10 µL of the test compound (0.5 mM; dissolved in DMSO), 150 µL of potassium phosphate buffer (pH 7.0, 50 mM), and 20 µL of TP enzyme (0.058 unit/well). The 96-well plate containing all these reagents was then incubated at 30 °C for 10 min. After 10 min, 20 µL of 1.5 mM substrate, i.e., thymidine was added, and changes in O.D. (optical density) were recorded at 290 nm for 10 min by using microtiter plate reader (SpectraMax 384, Molecular Devices, San Jose, CA, USA) [24].

3.2. Mechanistic Studies

Kinetic studies are used for the investigation of chemical reactions in terms of their reaction rates, reaction mechanisms, and the factors that affect these parameters [25,26]. Herein, it is used determine the type/mechanism of inhibition of dihydropyrimidone derivatives. In mechanistic studies, TP (0.058 U/200 µL) was incubated with test compounds (200–500 µM) at 30 °C for 10 min. The reaction was then initiated with the addition of different concentrations of thymidine (ranging between 0.1875 and 1.5 mM). Cleavage of thymidine was monitored continuously for 10 min, at 290 nm, by using ELISA plate reader (SpectraMax 384, Molecular Devices, San Jose, CA, USA).

3.3. Cytotoxicity

Cytotoxicity of active compounds were evaluated employing a standard MTT calorimetric assay [27]. Mouse fibroblast (3T3 cell line) acquired from American Type Culture Collection (ATCC), Virginia, USA, was cultured in DMEM (Dulbecco’s modified eagle medium). In total, 5% FBS (fetal bovine serum), penicillin (100 IU/mL), and streptomycin (100 mg/mL) were then added to the medium in 75 cm3 flasks, and kept in a CO2 incubator at 37 °C. The harvested cell was then diluted with a specific medium. Haemocytometer was used for the quantification of cells. After that, the culture of cell having concentration of 5x104 (cells/mL) was prepared, inoculated into 96-well plates (100 µL/well), and then incubated overnight. After incubation, the old medium was removed, and fresh medium (200 µL) was added. Then different concentrations of test compounds (ranging from 1 to 30 µM) were added. After incubation of 48 h, each well received 200 µL of MTT dye (0.5 mg/mL), and further incubated for a duration of 4 h. After 4 h, 100 µL of DMSO was introduced into each well of the 96-well plate. The reduction of MTT to formazan was measured by recording absorbance at 540 nm with the help of a microplate reader (SpectraMax 384, Molecular Devices, San Jose, CA, USA).

3.4. Statistical Analysis

SoftMax Pro 4.8 software (Molecular Devices, San Jose, CA, USA) was used to analyse the results. Percent inhibition was calculated by using Microsoft Excel by applying the following formula:
%   I n h i b i t i o n = 100 − ( O . D . T e s t   c o m p o u n d / O . D . C o n t r o l ) × 100
where O.D. represented the optical density.
Results were presented as means ± SEM (standard error of mean) (n = 3). EZ-FIT, enzyme kinetics software (Perrella Scientific, Inc., Amherst, GA, USA) was used to calculate the IC50 values. In order to analyse the kinetic parameter, Grafit version 7.0 (Erithacus Software Ltd., Horley, UK) was used.

3.5. Molecular Docking Studies

Molecular docking study was conducted to investigate the potential mechanism of TP inhibition. The crystal structure of Thymidine Phosphorylase in complex with an inhibitor, 3′-azido-2′-fluoro-2′,3′-dideoxyuridine reported by Timofeev and co-workers was used as a target protein (PDB ID 4EAD) [28]. The compounds of interest were sketched in MOE v.2019 using the Builder module and then subjected to structure correction, protonation, and energy minimization using the MMFF94x force field. The crystal structure of the target protein was retrieved from the RCSB Protein Data Bank and prepared for docking by placing hydrogens and assigning ionization states and then minimizing the structure using Amber99 force field. The results of kinetic studies showed that the most potential inhibitors displayed a non-competitive mode of inhibition. Therefore, to investigate potential allosteric sites for these inhibitors, site map analysis was conducted using the Site Finder module of MOE. Site map analysis involves the use of computational methods to predict potential binding sites on a protein based on its structure and electrostatic properties. The site map analysis identified 26 potential allosteric sites on thymidine phosphorylase and the site with the highest PLB (propensity for ligand binding) score was selected for further analysis. Finally, the ligands were docked into the selected allosteric site to investigate their binding interactions and potential as inhibitors of thymidine phosphorylase. Previously utilized protocol by Uddin and co-workers for the docking studies of inhibitors of TP was utilized [29]. Therefore, Triangular Matcher was used as a placement method with London dG and GBVI/WSA dG as scoring and rescoring functions, respectively. For each compound, ten conformations were generated and five best were retained for analysis. All the graphics were rendered using Chimera software (UCSF, San Francisco, CA, USA) [30].

3.6. ADME Analysis

SwissADME (Swiss Institute of Bioinformatics (SIB), Geneva, Switzerland) is an online server that predicts several ADME (absorption, distribution, metabolism, and excretion) properties of small molecules [31]. The server provides estimates of physicochemical properties, lipophilicity, drug-likeness, and pharmacokinetic properties of small molecules. Herein, the SwissADME server was utilized to predict the ADME profile of potential dihydropyrimidone derivatives (compound 1, compound 12, and compound 33). In this regard, the canonical SMILES of selected compounds were subjected to the server.

4. Conclusions

Present study has identified dihydropyrimidone derivatives as potential inhibitors of thymidine phosphorylase enzyme. Among different derivatives, compounds 1, 12, and 33 showed inhibition of thymidine phosphorylase with non-competitive mode. Additionally, these compounds were found to be non-toxic to 3T3 (mouse fibroblast) cell line. Furthermore, molecular docking studies inferred that the dihydropyrimidone derivatives significantly reside well into the binding site of TP, which is proximal to catalytic site. In addition, ADME analysis of dihydropyrimidone derivatives suggested the good oral bioavailability and high gastrointestinal absorption. However, these initial hits need to be structurally optimized to improve their potency and selectivity for thymidine phosphorylase inhibition. Once optimized, these compounds could potentially be studied for their effect on angiogenesis, which is an important process in tumor growth and metastasis. Overall, this study provides a promising starting point for the development of new inhibitors of thymidine phosphorylase and highlights the potential of dihydropyrimidone derivatives as a class of compounds with therapeutic activity.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28083634/s1, Figure S1: Dose response curve of compounds with standard deviation; Figure S2: Comparison of allosteric sites and binding modes of compounds on human and E. coli Thymidine Phosphorylase. References [32,33,34] are cited in the Supplementary Materials.

Author Contributions

Conceptualization, T.-M.C. and A.S.B.; methodology, N.H.S., F.A. and A.A.A. (Almohanad A. Alkayyal); software, A.A., F.M.A., M.A. (Muhammad Altaf), M.Y.K. and M.A. (Mohammed Aladhadh); validation, A.A. and Y.-R.M.; data curation, A.S.B.; writing—original draft preparation, T.-M.C., F.A., A.S.B., N.H.S., A.A.A. (Ahad Amer Alsaiari) and A.A.A. (Almohanad A. Alkayyal); writing—review and editing, A.A. and Y.-R.M.; funding acquisition, A.A. and Y.-R.M. All authors have read and agreed to the published version of the manuscript.

Funding

The authors would like to thank the Deanship of Scientific Research at Umm Al-Qura University for supporting this work by Grant Code: (23UQU4420118DSR001).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors would like to thank the Deanship of Scientific Research at Umm Al-Qura University for supporting this work by Grant Code: (23UQU4420118DSR001).

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the compounds are not available from the authors.

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Molecules 28 03634 g001 550
Figure 1. The inhibition of thymidine phosphorylase (TP) by compound 1. (A) Lineweaver–Burk plot presented 1/V on their Y-axis while that of reciprocal of the substrate (thymidine) on their X-axis. Order of the concentrations of inhibitor included in the absence of compound 1 (■), in the presence of 300 µM (□), 400 µM (●), and 500 µM (○) of compound 1. (B) Secondary replot of Lineweaver–Burk was plotted between the slopes (Km/Vmax) on Y-axis and 1/Inhibitor on X-axis, and (C) Dixon plot presented 1/V on Y-axis, while 1/Inhibitor on X-axis.
Figure 1. The inhibition of thymidine phosphorylase (TP) by compound 1. (A) Lineweaver–Burk plot presented 1/V on their Y-axis while that of reciprocal of the substrate (thymidine) on their X-axis. Order of the concentrations of inhibitor included in the absence of compound 1 (■), in the presence of 300 µM (□), 400 µM (●), and 500 µM (○) of compound 1. (B) Secondary replot of Lineweaver–Burk was plotted between the slopes (Km/Vmax) on Y-axis and 1/Inhibitor on X-axis, and (C) Dixon plot presented 1/V on Y-axis, while 1/Inhibitor on X-axis.
Molecules 28 03634 g001
Molecules 28 03634 g002 550
Figure 2. The inhibition of thymidine phosphorylase by compound 12. (A) Lineweaver–Burk plot presented 1/V (velocities) on their Y-axis while that of reciprocal of the substrate (thymidine) on their X-axis. Order of the concentrations of inhibitor included in the absence of compound 12 (∆), in the presence of 200 µM (■), 300 µM (□), 400 µM (●), and 500 µM (○) of compound 12. (B) The secondary replot of Lineweaver–Burk was plotted between the slopes (Km/Vmax) on Y-axis and 1/Inhibitor on X-axis, and (C) Dixon plot presented 1/V on Y-axis, while 1/Inhibitor on X-axis.
Figure 2. The inhibition of thymidine phosphorylase by compound 12. (A) Lineweaver–Burk plot presented 1/V (velocities) on their Y-axis while that of reciprocal of the substrate (thymidine) on their X-axis. Order of the concentrations of inhibitor included in the absence of compound 12 (∆), in the presence of 200 µM (■), 300 µM (□), 400 µM (●), and 500 µM (○) of compound 12. (B) The secondary replot of Lineweaver–Burk was plotted between the slopes (Km/Vmax) on Y-axis and 1/Inhibitor on X-axis, and (C) Dixon plot presented 1/V on Y-axis, while 1/Inhibitor on X-axis.
Molecules 28 03634 g002
Molecules 28 03634 g003 550
Figure 3. The inhibition of thymidine phosphorylase by compound 33. (A) Lineweaver–Burk plot presented 1/V (velocities) on their Y-axis, while that of reciprocal of the substrate (thymidine) on their X-axis. Order of the concentrations of inhibitor included in the absence of compound 33 (■), in the presence of 300 µM (□), 400 µM (●), and 500 µM (○) of compound 33. (B) The secondary replot of Lineweaver–Burk was plotted between the slopes (Km/Vmax) on Y-axis and 1/Inhibitor on X-axis, and (C) Dixon plot presented 1/V on Y-axis, while 1/Inhibitor on X-axis.
Figure 3. The inhibition of thymidine phosphorylase by compound 33. (A) Lineweaver–Burk plot presented 1/V (velocities) on their Y-axis, while that of reciprocal of the substrate (thymidine) on their X-axis. Order of the concentrations of inhibitor included in the absence of compound 33 (■), in the presence of 300 µM (□), 400 µM (●), and 500 µM (○) of compound 33. (B) The secondary replot of Lineweaver–Burk was plotted between the slopes (Km/Vmax) on Y-axis and 1/Inhibitor on X-axis, and (C) Dixon plot presented 1/V on Y-axis, while 1/Inhibitor on X-axis.
Molecules 28 03634 g003
Molecules 28 03634 g004 550
Figure 4. The binding mode of (A) compound 1 (B) compound 12 (C) compound 33, and (D) 7-deazaxanthine with the allosteric site of TP enzyme predicted by site map analysis. The TP residues are shown in dark grey sticks, while ligands are shown in different color sticks. The red dotted lines represented the hydrogen bond contacts.
Figure 4. The binding mode of (A) compound 1 (B) compound 12 (C) compound 33, and (D) 7-deazaxanthine with the allosteric site of TP enzyme predicted by site map analysis. The TP residues are shown in dark grey sticks, while ligands are shown in different color sticks. The red dotted lines represented the hydrogen bond contacts.
Molecules 28 03634 g004
Molecules 28 03634 g005 550
Figure 5. ADME profile of dihydropyrimidone derivatives (1, 12, and 33) predicted by SwissADME server. The pink region represents the optimal region for each physiochemical property.
Figure 5. ADME profile of dihydropyrimidone derivatives (1, 12, and 33) predicted by SwissADME server. The pink region represents the optimal region for each physiochemical property.
Molecules 28 03634 g005
Table
Table 1. Thymidine phosphorylase (TP) inhibitory activity of dihydropyrimidone (1–40).
Table 1. Thymidine phosphorylase (TP) inhibitory activity of dihydropyrimidone (1–40).
Molecules 28 03634 i001
Compound
Number		RThymidine Phosphorylase
Inhibitory Activity		Cytotoxicity Studies
% InhibitionIC50 ± SEM
(µM)		Cell
Viability (%)		IC50 ± SD
(µM)
1Molecules 28 03634 i002
Methyl 6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate		84.0314.3 ± 0.957NC
2Molecules 28 03634 i003
Methyl 4-(4-ethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		78.2389.2 ± 6.267NC
3Molecules 28 03634 i004
Methyl 6-methyl-4-(naphthalen-2-yl)-2-oxo- 1,2,3,4-tetrahydropyrimidine-5-carboxylate		38.1N/ANCNC
4Molecules 28 03634 i005
Methyl 4-ethyl-6-methyl-2-oxo-1,2,3,4- tetrahydropyrimidine-5-carboxylate		46.8N/ANCNC
5Molecules 28 03634 i006
Methyl 4-(4-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		52.9387.4 ± 2.072NC
6Molecules 28 03634 i007
Methyl 4-(2-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−65.3N/ANCNC
7Molecules 28 03634 i008
Methyl 4-(2-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−19.3N/ANCNC
8Molecules 28 03634 i009
Methyl 6-methyl-4-(naphthalen-2-yl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−10.3N/ANCNC
9Molecules 28 03634 i010
Methyl 4-(furan-2-yl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		78.9373.6 ± 2.272NC
10Molecules 28 03634 i011
Methyl 4-butyl-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		92.7389.0 ± 0.666NC
11Molecules 28 03634 i012
Methyl 6-methyl-4-(5-methylfuran-2-yl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		76.9386.0 ± 0.677NC
12Molecules 28 03634 i013
Methyl 6-methyl-4-(4-nitrophenyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		91.5303.5 ± 0.457NC
13Molecules 28 03634 i014
Methyl 4-(4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		56.2448.9 ± 4.172NC
14Molecules 28 03634 i015
Methyl 4-(2-fluoro-4-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		68.4397.1 ± 0.171NC
15Molecules 28 03634 i016
Methyl 4-(3-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		38.9NANCNC
16Molecules 28 03634 i017
Methyl 4-(4-fluoro-3-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		47.8NANCNC
17Molecules 28 03634 i018
Methyl 4-(2,5-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		46.5NANCNC
18Molecules 28 03634 i019
Methyl 4-(2,6-dichlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−15.4NANCNC
19Molecules 28 03634 i020
Methyl 4-(4-isopropylphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−18.5NANCNC
20Molecules 28 03634 i021
Methyl 4-(2,3-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		67.8414.7 ± 1.662NC
21Molecules 28 03634 i022
Methyl 4-isobutyl-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		90.7345.4 ± 0.555NC
22Molecules 28 03634 i023
Methyl 4-(3-bromo-4,5-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		61.9394.3 ± 4.376NC
23Molecules 28 03634 i024
Methyl 4-(3-(benzyloxy)-4-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		7.5NANCNC
24Molecules 28 03634 i025
Methyl 6-methyl-2-oxo-4-(thiophen-3-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate		79.6350.6 ± 0.682NC
25Molecules 28 03634 i026
Methyl 4-(3,4-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		59.0424.1 ± 0.999NC
26Molecules 28 03634 i027
Methyl 4-(4-(dimethylamino) phenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		92.3349.9 ± 3.757NC
27Molecules 28 03634 i028
Methyl 6-methyl-2-oxo-4-(thiophen-2-yl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate		47.1NANCNC
28Molecules 28 03634 i029
Methyl 4-(3-chloro-4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		67.5404.6 ± 1.095NC
29Molecules 28 03634 i030
Methyl 4-(4-acetoxy-3-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		76.0400.5 ± 0.680NC
30Molecules 28 03634 i031
Methyl 4-(4-hydroxy-3,5-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		69.6396.7 ± 1.575NC
31Molecules 28 03634 i032
Methyl 4-(3-(benzyloxy) phenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−41.9NANCNC
32Molecules 28 03634 i033
Methyl 6-methyl-4-(5-methylthiophen-2-yl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		58.3485.7 ± 1.585NC
33Molecules 28 03634 i034
Methyl 6-methyl-2-oxo-4-(4-(trifluoromethyl) phenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate		73.6322.6 ± 1.661NC
34Molecules 28 03634 i035
Methyl 4-(4-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
66.3443.9 ± 0.972NC
35Molecules 28 03634 i036
Methyl 4-(2-fluorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		9.6NANCNC
36Molecules 28 03634 i037
Methyl 4-(2-(benzyloxy) phenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		5.3NANCNC
37Molecules 28 03634 i038
Methyl 4-(4-bromophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		15.7NANCNC
38Molecules 28 03634 i039
Methyl 6-methyl-4-(3-nitrophenyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−23.1NANCNC
39Molecules 28 03634 i040
Methyl 4-(2,4-dichlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−1.8NANCNC
40Molecules 28 03634 i041
Methyl 4-(4-(benzyloxy) phenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate		−273.6NANCNC
Standard*Molecules 28 03634 i042
7-Deazaxanthine		82.041.0 ± 1.6NCNC
Standard*Molecules 28 03634 i043
Tipiracil-HCl		92.00.014 ± 0.04NCNC
Standard**Molecules 28 03634 i044
Cycloheximide		NDND300.8 ± 0.2
SEM: standard error of the mean (n = 3); SD: standard deviation; NA: not active; NC: non-cytotoxic; ND: not determine; Standard*: used as reference compound for in vitro assay; Standard**: used as standard in cytotoxicity assay.
Table
Table 2. Kinetics parameters of selected potent compounds.
Table 2. Kinetics parameters of selected potent compounds.
CompoundKi ± SEM (µM)Type of Inhibition
1326.3 ± 0.002Non-Competitive
12297.6 ± 0.006Non-Competitive
33311.4 ± 0.004Non-Competitive
7-deazaxanthine45.0 ± 0.003Non-Competitive
7-deazaxanthine: standard; SEM: standard error of the mean; Ki: dissociation constant.
Table
Table 3. Detail of results of molecular docking studies including docking scores, type of interactions, and interacted residues.
Table 3. Detail of results of molecular docking studies including docking scores, type of interactions, and interacted residues.
CompoundDocking Score (kcal/mol)Type of Interactions
Hydrophobic InteractionsHydrogen Bonding
1−6.19Gly116, Gly122, Asp125, Lys126, Asn252, Arg370, Val363, and Val364Gly116, Gly122, Asp125, Lys126, and Asn252
12−5.60Gly116, Leu117, Gly122, Asp125, Asn252, Gly360, Arg370, and Val363Asn252 and Gly360
33−5.11Gly116, Gly121, Lys126, Asn252, Val363, and Asp370Gly89, Gly91, Asn252, and Gly360
7-deazaxanthine−5.23Gly116 and Gly122Gly116, Gly122, Asp125, Asn252, and Arg370
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Cui, T.-M.; Altaf, M.; Aldarhami, A.; Bazaid, A.S.; Saeedi, N.H.; Alkayyal, A.A.; Alshabrmi, F.M.; Ali, F.; Aladhadh, M.; Khan, M.Y.; et al. Dihydropyrimidone Derivatives as Thymidine Phosphorylase Inhibitors: Inhibition Kinetics, Cytotoxicity, and Molecular Docking. Molecules 2023, 28, 3634. https://doi.org/10.3390/molecules28083634

AMA Style

Cui T-M, Altaf M, Aldarhami A, Bazaid AS, Saeedi NH, Alkayyal AA, Alshabrmi FM, Ali F, Aladhadh M, Khan MY, et al. Dihydropyrimidone Derivatives as Thymidine Phosphorylase Inhibitors: Inhibition Kinetics, Cytotoxicity, and Molecular Docking. Molecules. 2023; 28(8):3634. https://doi.org/10.3390/molecules28083634

Chicago/Turabian Style

Cui, Tian-Meng, Muhammad Altaf, Abdu Aldarhami, Abdulrahman S. Bazaid, Nizar H. Saeedi, Almohanad A. Alkayyal, Fahad M. Alshabrmi, Farman Ali, Mohammed Aladhadh, Muhammad Yasir Khan, and et al. 2023. "Dihydropyrimidone Derivatives as Thymidine Phosphorylase Inhibitors: Inhibition Kinetics, Cytotoxicity, and Molecular Docking" Molecules 28, no. 8: 3634. https://doi.org/10.3390/molecules28083634

APA Style

Cui, T. -M., Altaf, M., Aldarhami, A., Bazaid, A. S., Saeedi, N. H., Alkayyal, A. A., Alshabrmi, F. M., Ali, F., Aladhadh, M., Khan, M. Y., Alsaiari, A. A., & Ma, Y. -R. (2023). Dihydropyrimidone Derivatives as Thymidine Phosphorylase Inhibitors: Inhibition Kinetics, Cytotoxicity, and Molecular Docking. Molecules, 28(8), 3634. https://doi.org/10.3390/molecules28083634

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