Table of Contents Author Guidelines Submit a Manuscript
BioMed Research International
Volume 2013, Article ID 154856, 9 pages
Research Article

1-Aryl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]ureas as VEGFR-2 Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Molecular Modelling Studies

1Centro de Química, Escola de Ciências, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal
2CIQ/Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal
3Departamento de Bioquímica (U38-FCT), Faculdade de Medicina, Universidade do Porto, 4200-319 Porto, Portugal
4Centro de Investigação de Montanha (CIMO), Escola Superior Agrária, Instituto Politécnico de Bragança, Campus de Santa Apolónia, Apartado 1172, 5301-855 Bragança, Portugal

Received 7 April 2013; Revised 12 June 2013; Accepted 13 June 2013

Academic Editor: Carmen Domene

Copyright © 2013 Pedro Soares et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The vascular endothelial growth factor receptor-2 (VEGFR-2) is a tyrosine kinase receptor involved in the growth and differentiation of endothelial cells that are implicated in tumor-associated angiogenesis. In this study, novel 1-aryl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]ureas were synthesized and evaluated for the VEGFR-2 tyrosine kinase inhibition. Three of these compounds showed good VEGFR-2 inhibition presenting low IC50 values (150–199 nM) in enzymatic assays, showing also a significant proliferation inhibition of VEGF-stimulated human umbilical vein endothelial cells (HUVECs) at low concentrations (0.5–1 µM), using the Bromodeoxyuridine (BrdU) assay, not affecting cell viability. The determination of the total and phosphorylated (active) VEGFR-2 was performed by western blot, and it was possible to conclude that the compounds significantly inhibit the phosphorylation of the receptor at 1 µM pointing to their antiproliferative mechanism of action in HUVECs. The molecular rationale for inhibiting the tyrosine kinase domain of VEGFR-2 was also performed and discussed using molecular docking studies.

1. Introduction

Angiogenesis is the process of new blood vessel formation from preexisting vascular networks by capillary sprouting [1] and plays an important role in the pathogenesis of several disorders including cancer, vasculoproliferative ocular disorders, and rheumatoid arthritis [2]. A key regulatory pathway of angiogenesis is mediated by the vascular endothelial growth factor (VEGF), involved in the vascular permeability and an inducer of endothelial cell proliferation, migration, and survival [3], and its cell membrane tyrosine kinase receptor VEGFR-2 (also known as KDR) [4]. Upon ligand binding, VEGFR-2 undergoes autophosphorylation, triggering signaling pathways leading to endothelial cell proliferation and subsequent angiogenesis. Small molecule inhibitors act by competing with ATP for its binding site of the VEGFR-2 intracellular tyrosine kinase domain, thereby preventing the signaling pathways that lead to angiogenesis [5]. Several small molecule VEGFR-2 inhibitors have emerged as promising antiangiogenic agents for possible treatment against a wide variety of cancers (Figure 1). Sunitinib was approved for the treatment of renal cell carcinoma and gastrointestinal stromal tumor, and Sorafenib was approved for the treatment of primary kidney cancer and hepatocellular carcinoma [6]. Recently, two new VEGFR-2 inhibitors have been approved for the treatment of advanced renal cell carcinoma: axitinib [7] and pazopanib [8]. A number of thienopyridines and thienopyrimidines ureas have also shown potent VEGFR-2 inhibition activity [9, 10] including arylether derivatives [1113].

Figure 1: Competitive inhibitors of VEGFR-2 in clinical use against several cancers: sunitinib (Sutent, C. P. Pharmaceuticals International, NY, USA), soranefib (Nexavar, Bayer, Germany), axitinib (Inlyta, Pfizer), and pazopanib (Votrient, GlaxoSmithKline).

In this report, we describe an ongoing effort to develop novel small molecules as VEGFR-2 inhibitors, based on the aryletherthieno[3,2-d]pyrimidine arylurea scaffold. The synthesis of the compounds and the VEGFR-2 tyrosine kinase phosphorylation inhibition evaluation using either enzymatic or cellular assays including the determination of the total and of the phosphorylated VEGFR-2 by western blot were performed. The probable binding mode of the 1-aryl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]ureas with the receptor using docking studies is also presented and discussed.

2. Materials and Methods

2.1. Synthesis

Melting points (°C) were determined in a Stuart SMP3 and are uncorrected. and NMR spectra were recorded on a Varian Unity Plus at 300 and 75.4 MHz, respectively, or on a Bruker Avance III at 400 and 100.6 MHz, respectively. Two-dimensional 1H-13C correlations were performed to attribute some signals. Mass spectra (MS) EI-TOF or ESI-TOF and HRMS on the M+, [M + H]+ or on [M + Na]+, were performed by the mass spectrometry service of the University of Vigo, C.A.C.T.I., Spain.

The reactions were monitored by thin layer chromatography (TLC) using Macherey-Nagel precoated aluminium silica gel 60 sheets (0.20 mm) with UV254 indicator. Column chromatography was performed on Panreac, silica gel 60, 230–400 mesh.

2.1.1. General Procedure for the Synthesis of Compounds and

In a flask with 5 mL of DMF, thienopyrimidine (1 equiv.), 4-aminophenol (1 equiv.), and K2CO3 (4 equiv.) were heated at 140°C for 2 h. After cooling, water (5 mL) and ethyl acetate (5 mL) were added. The phases were separated, and the aqueous phase was extracted with more ethyl acetate (2 × 5 mL). The organic phase was dried (MgSO4) and filtered. The solvent was evaporated under reduced pressure giving a solid which was submitted to column chromatography.

4-(Thieno[3,2-d]pyrimidin-4-yloxy)aniline 1a. 4-Chlorothieno[3,2-d]pyrimidine (242 mg, 1.42 mmol) and 4-aminophenol (155 mg, 1.42 mmol) were heated, and the reaction mixture was treated according to the general procedure. Column chromatography using ethyl acetate gave compound 1a as a yellow solid (290 mg, 91%), m.p. 115.8–116.5°C. NMR (300 MHz, DMSO-): δ 5.15 (s, 2H, NH2), 6.60 (d, = 9.0 Hz, 2H, 2 and 6-H), 6.95 (d, = 9.0 Hz, 2H, 3 and 5-H), 7.62 (d, = 5.6 Hz, 1H, HetAr), 8.40 (d, = 5.6 Hz, 1H, HetAr), 8.66 (s, 1H, 2′-H) ppm. NMR (75.4 MHz, DMSO-): δ 114.2 (2 and 6-CH), 116.6 (C), 122.3 (3 and 5-CH), 124.1 (CH), 137.1 (CH), 141.7 (C), 146.9 (C), 154.2 (2′-CH), 162.9 (C), 164.3 (C) ppm. MS (EI-TOF) (%): 243.05 (M+, 100) HRMS (EI-TOF): calcd for C12H9N3OS [M+] 243.0466, found 243.0467.

4-(7-Methylthieno[3,2-d]pyrimidin-4-yloxy)aniline 1b. 4-Chloro-7-methylthieno[3,2-d]pyrimidine (242 mg, 1.31 mmol) and 4-aminophenol (143 mg, 1.31 mmol) were heated, and the reaction mixture was treated according to the general procedure. Column chromatography using ethyl acetate gave compound 1b as a yellow solid (310 mg, 92%), m.p. 167.8–168.6°C. NMR (300 MHz, DMSO-): δ 2.40 (s, 3H, CH3), 5.13 (s, 2H, NH2), 6.61 (d, = 9.0 Hz, 2H, 2 and 6-H), 6.93 (d, = 9.0 Hz, 2H, 3 and 5-H), 8.01 (s, 1H, 6′-H), 8.67 (s, 1H, 2′-H) ppm. NMR (75.4 MHz, DMSO-): δ 12.5 (CH3), 114.2 (2 and 6-CH), 116.8 (C), 122.3 (3 and 5-CH), 131.4 (6′-CH), 132.6 (C), 141.7 (C), 146.8 (C), 153.9 (2′-CH), 161.8 (C), 164.3 (C) ppm. MS (EI-TOF) (%): 257.06 (M+, 100) HRMS (EI-TOF): calcd for C13H11N3OS [M+] 257.0623, found 257.0621.

2.1.2. General Procedure for the Synthesis of 1,3-Diarylureas

Compounds 1a or 1b and different arylisocyanates (1 equiv.) in 6 mL CH2Cl2 : THF (1 : 1) were left stirring at room temperature for 16 h. If a precipitate does not come out after this time, hexane (3–5 mL) is added to the mixture to precipitate the product. This was filtered under vacuum to give the corresponding 1,3-diarylureas.

1-Phenyl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]urea 2a. From compound 1a (100 mg, 0.410 mmol), and phenylisocyanate (0.0400 mL, 0.410 mmol) compound 2a was isolated as a white solid (117 mg, 79%), m.p. 237.3–238.7°C. NMR (400 MHz, DMSO-): δ 6.95–6.99 (m, 1H, Ar-H), 7.24–7.30 (m, 4H, Ar-H), 7.45–7.47 (m, 2H, 2 × Ar-H), 7.54 (d, = 9.0 Hz, 2H, 2 × Ar-H), 7.65 (d, = 5.2 Hz, 1H, HetAr), 8.45 (d, = 5.2 Hz, 1H, HetAr), 8.68 (s, 1H, NH), 8.69 (s, 1H, -H), 8.78 (s, 1H, NH) ppm. NMR (100.6 MHz, DMSO-): δ 116.8 (C), 118.2 (2 × CH), 119.2 (2 × CH), 121.8 (CH), 122.3 (2 × CH), 124.2 (CH), 128.8 (2 × CH), 137.2 (CH), 137.6 (C), 139.6 (C), 146.0 (C), 152.6 (C), 154.1 (-CH), 163.0 (C), 163.8 (C) ppm. MS (ESI-TOF) (%): 363.09 ([M + H]+, 100) HRMS (ESI-TOF): calcd for C19H15N4O2S [M + H]+ 363.0910, found 363.0909.

1-(4-Methoxyphenyl)-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]urea 2b. From compound 1a (100 mg, 0.410 mmol), and 4-methoxyphenylisocyanate (0.0500 mL, 0.410 mmol) compound 2b was isolated as a white solid (145 mg, 90%), m.p. 247.2–248.3°C. 1H NMR (400 MHz, DMSO-): δ 3.71 (s, 3H, OCH3), 6.86 (d, = 9.0 Hz, 2H, 3′ and 5′-H), 7.23 (d, = 9.0 Hz, 2H, 2 × Ar-H), 7.36 (d, = 9.0 Hz, 2H, 2′ and 6′-H), 7.53 (d, = 9.0 Hz, 2H, 2 × Ar-H), 7.65 (d, = 5.6 Hz, 1H, HetAr), 8.44 (d, = 5.6 Hz, 1H, HetAr), 8.50 (s, 1H, NH), 8.69 (s, 1H, -H), 8.70 (s, 1H, NH) ppm. NMR (100.6 MHz, DMSO-): δ 55.1 (OCH3), 114.0 (3′ and 5′-CH), 116.8 (C), 119.1 (2 × CH), 120.1 (2′ and 6′-CH), 122.3 (2 × CH), 124.2 (CH), 132.7 (C), 137.2 (CH), 137.8 (C), 145.9 (C), 152.8 (C), 154.1 (-CH), 154.5 (C), 163.0 (C), 163.8 (C) ppm. MS (ESI-TOF) (%): 393.08 ([M+H]+, 39) HRMS (ESI-TOF): calcd for C20H17N4O3S [M+H]+ 393.1016, found 393.1026.

1-(4-Cyanophenyl)-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]urea 2c. From compound 1a (100 mg, 0.410 mmol) and 4-cyanophenylisocyanate (59.0 mg, 0.410 mmol), compound 2c was isolated as a white solid (111 mg, 70%), m.p. 245.5–247.2°C. RMN (300 MHz, DMSO-): δ 7.26 (d, = 9.2 Hz, 2H, 2 × Ar-H), 7.55 (d, = 9.2 Hz, 2H, 2 × Ar-H), 7.62–7.66 (m, 3H, 2′ and 6′-H and HetAr), 7.73 (d, = 9.2 Hz, 2H, 3′ and 5′-H), 8.45 (d, = 5.2 Hz, 1H, HetAr), 8.69 (s, 1H, -H), 8.99 (s, 1H, NH), 9.24 (s, 1H, NH) ppm. NMR (75.4 MHz, DMSO-): δ 103.3 (C), 116.8 (C), 118.0 (2′ and 6′-CH), 119.3 (C), 119.7 (2 × CH), 122.4 (2 × CH), 124.3 (CH), 133.3 (3′ and 5′-CH), 137.0 (C), 137.2 (CH), 144.2 (C), 146.5 (C), 152.2 (C), 154.1 (-CH), 163.0 (C), 163.8 (C) ppm. MS (ESI-TOF) (%): 388.09 ([M + H]+, 100) HRMS (ESI-TOF): calcd for C20H13N5O2S [M + H]+ 388.0863, found 388.0861.

1-Phenyl-3-[4-(7-Methylthieno[3,2-d]pyrimidin-4-yloxy)phenyl]urea 2d. From compound 1b (100 mg, 0.389 mmol) and phenylisocyanate (0.0400 mL, 0.389 mmol), compound 2d was isolated as a white solid (121 mg, 83%), m.p. 285.7–287.3°C. NMR (400 MHz, DMSO-): δ 2.43 (s, 3H, CH3), 6.96 (m, 1H, Ar-H), 7.23–7.29 (m, 4H, Ar-H), 7.46 (m, 2H, 2 × Ar-H), 7.53 (d, = 9.2 Hz, 2H, 2 × Ar-H), 8.10 (s, 1H, -H), 8.70 (s, 1H, NH), 8.71 (s, 1H, -H), 8.78 (s, 1H, NH) ppm. NMR (100.6 MHz, DMSO-): δ 12.5 (CH3), 116.9 (C), 118.2 (2 × CH), 119.2 (2 × CH), 121.8 (C), 122.3 (2 × CH), 128.8 (2 × CH), 131.5 (-CH), 132.7 (C), 137.6 (C), 139.6 (C), 146.1 (C), 152.6 (C), 153.9 (-CH), 161.9 (C), 163.9 (C) ppm. MS (ESI-TOF) (%): 377.10 ([M + H]+, 100) HRMS (ESI-TOF): calcd for C20H17N4O2S [M + H]+ 377.1067, found 377.1064.

1-(4-Methoxyphenyl)-3-[4-(7-methylthieno[3,2-d]pyrimidin-4-yloxy)phenyl]urea 2e. From compound 1b (100 mg, 0.389 mmol) and 4-methoxyphenylisocyanate (0.0500 mL, 0.389 mmol), compound 2e was isolated as a white solid (131 mg, 83%), m.p. 248.4–249.6°C. NMR (400 MHz, DMSO-): δ 2.43 (s, 3H, CH3), 3.71 (s, 3H, OCH3), 6.86 (d, = 9.2 Hz, 2H, 3′ and 5′-H), 7.22 (d, = 9.2 Hz, 2H, and -H), 7.36 (d, = 9.2 Hz, 2H, 2′ and 6′-H), 7.52 (d, = 9.2 Hz, 2H, and -H), 8.06 (s, 1H, -H), 8.49 (s, 1H, NH), 8.69 (s, 1H, NH), 8.70 (s, 1H, -H) ppm. NMR (100.6 MHz, DMSO-): δ 12.5 (CH3), 55.2 (OCH3), 114.0 (3′ and 5′-CH), 116.9 (C), 119.1 ( and -CH), 120.1 (2′ and 6′-CH), 122.2 ( and -CH), 131.5 (-CH), 132.7 (C), 137.8 (C), 146.0 (C), 152.8 (C), 153.9 (-CH), 154.5 (C), 161.9 (C), 163.9 (C) ppm. MS (ESI-TOF) (%): 407.12 ([M + H]+, 100) HRMS (ESI-TOF): calcd for C21H19N4O3S [M + H]+ 407.1172, found 407.1182.

1-(4-Cyanophenyl)-3-[4-(7-methylthieno[3,2-d]pyrimidin-4-yloxy)phenyl]urea 2f. From compound 1b (100 mg, 0.389 mmol) and 4-cyanophenylisocyanate (56.0 mg, 0.389 mmol), compound 2f was isolated as a white solid (128 mg, 82%), m.p. 246.7–248.2°C. NMR (400 MHz, DMSO-): δ 2.42 (s, 3H, CH3), 7.25 (d, = 9.2 Hz, 2H, and -H), 7.54 (d, = 9.2 Hz, 2H, and -H), 7.64 (d, = 9.2 Hz, 2H, 2′ and 6′-H), 7.72 (d, = 9.2 Hz, 2H, 3′ and 5′-H), 8.06 (s, 1H, -H), 8.70 (s, 1H, -H), 8.97 (s, 1H, NH), 9.23 (s, 1H, NH) ppm. NMR (100.6 MHz, DMSO-): δ 12.5 (CH3), 103.3 (C), 117.0 (C), 118.1 (2′ and 6′-CH), 119.3 (C), 119.7 ( and -CH), 122.4 ( and -CH), 131.5 (-CH), 132.7 (C), 133.3 (3′ and 5′-CH), 137.0 (C), 144.2 (C), 146.6 (C), 152.2 (C), 153.9 (-CH), 162.0 (C), 163.8 (C) ppm. MS (ESI-TOF) (%): 402.10 ([M + H]+, 100) HRMS (ESI-TOF): calcd for C21H16N5O2S [M + H]+ 402.1019, found 402.1029.

2.2. VEGFR-2 Enzymatic Inhibition Assay

The compounds were assessed for VEGFR-2 inhibition activity using the -LYTE-Tyr1 Peptide assay kit (according to the procedures recommended by the manufacturer Invitrogen, Cat. PV3190) [14]. Briefly, assays were performed in a total of 20 μL in 384-well plates using fluorescence resonance energy transfer technology. A Tyr1 substrate (coumarin-fluorescein double-labeled peptide) at 1.0 μM was incubated for 1 h with 4 μg/mL VEGFR-2, 10 μM ATP, and inhibitors at room temperature in 50 mM Hepes/Na (pH 7.5), 10 mM MgCl2, 2.0 mM MnCl2, 2.5 mM DTT, 0.10 mM orthovanadate, and 0.01% bovine serum albumin. The wells were incubated at 25°C for 1 hour and 5.0 μL of the development reagent was added to each well. After a second incubation of 1 hour, a stop reagent was added to each well. Using a Biotek FLX800 microplate, the fluorescence was read at 445 nm and 520 nm (excitation 400 nm), and Gen5 Software was used for data analysis. The validation assay was performed using Staurosporine that presented a IC50 value 6 nM that compares to the one reported in the literature (IC50 7 nM) [14].

2.3. Cell Culture Experiments Using HUVECs
2.3.1. Cell Cultures

Human umbilical vein endothelial cells (HUVECs) were obtained from the ScienceCell Research Labs (San Diego, CA, USA), HUVECs were seeded on plates coated with 0.2% gelatin (Sigma-Aldrich, Sintra, Portugal) and cultured in M199 medium (Sigma-Aldrich, Sintra, Portugal) supplemented with 20% fetal bovine serum (FBS) (Invitrogen Life Technologies, Scotland, UK), 1% penicillin/streptomycin (Invitrogen Life Technologies), 0.01% heparin (Sigma-Aldrich), and 30 mg/mL endothelial cell growth supplement (Biomedical Technologies Inc., MA, USA) and maintained at 37°C in a humidified 5% carbon dioxide atmosphere. Cells were kept between passages 3 and 8 for every experiment. The test compounds were dissolved in DMSO and added to cell cultures at a concentration of 0.1–10 μM. Incubations were performed for 24 h in medium supplemented with 2% FBS, 1% penicillin/streptomycin, and 60 ng/mL of the vascular endothelial growth factor (Sigma-Aldrich, Sintra, Portugal). Control cells were incubated with vehicle (DMSO at 0.1% in every culture).

2.3.2. MTS Toxicity Assay

HUVECs (2 × 105 cells/mL) were allowed to grow for 24 h and then incubated with the test compounds at a range concentration between 0.1 and 10 μM or control (0.1% DMSO) for 24 h. After the incubation period, cells were washed and their viability was assessed using Cell Titer 96 Aqueous ONE Solution Reagent MTS [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium] colorimetric assay (Promega, Madison, USA), according to the instructions provided by the manufacturer and as previously described [15]. Optical density was measured at 492 nm. Three independent experiments were performed, and the results were expressed as mean ± SEM.

2.3.3. BrdU Incorporation Assay

HUVECs (6 × 104 cells/mL) were grown during 24 h and then were incubated with the compounds at 0.1–10 μM or control (0.1% DMSO) for 24 h. Cells were also incubated with 5′-bromodeoxyuridine (BrdU), a thymidine analogue which incorporates into DNA of dividing cells. After incubation with BrdU solution at a final concentration of 0.01 mM during the treatment period, the optical density of proliferating cells (positive for BrdU) after ELISA assay using anti-BrdU-specific antibodies (Roche Diagnostics, Mannheim, Germany) was evaluated at the microplate reader according to the manufacturer’s instructions and as previously reported [16]. The results are given as percentage versus control group (100%).

2.3.4. Cell Apoptosis

HUVECs (6 × 104 cells/mL) were grown for 24 h on glass coverslips and incubated with different concentrations (0.1–1 μM) of the tested compounds. TUNEL assay was performed using the In Situ Cell Death Detection kit (Roche Diagnostics, Mannheim, Germany), according to the manufacturer’s instruction and as previously reported [16]. Immunofluorescence was visualized under a fluorescence microscope (Olympus, BH-2, UK). The percentage of stained cells was evaluated by counting the cells stained with TUNEL (apoptotic cells) divided by the total number of nuclei counterstained with DAPI (Invitrogen, CA, USA) at a 200x magnification field. One thousand nuclei were evaluated. Results were expressed as percentage of control (100%).

2.3.5. Western Blotting Analyses

Proteins were isolated from HUVEC lysates using RIPA (Chemicon International, CA, USA). Proteins were quantified using a spectrophotometer (Jenway, 6405 UV/vis, Essex, UK), and 20 μg of protein were subjected to 8% SDS-PAGE with a 5% stacking gel. After electrophoresis, proteins were blotted into a Hybond nitrocellulose membrane (Amersham, Arlington, VA, USA). Immunodetection for total VEGFR-2 (1 : 1000; Cell Signaling, MA, USA), phosphorylated (activated) VEGFR-2 (1 : 750; Santa Cruz Biotechnology, CA, USA), and β-actin (1 : 3000; Abcam, Cambridge, UK) was accomplished with enhanced chemiluminescence (ECL kit, Amersham, Arlington, USA). The phosphorylated antibody recognizes Tyr951 kinase insert domain, a major site of VEGFR-2 phosphorylation particularly involved in angiogenic processes. The relative intensity of each protein blotting analysis was measured using a computerized software program (Bio-Rad, CA, USA), and the expression of activated and total VEGFR-2 were normalized with total VEGFR-2 and β-actin bands, respectively, to compare the expression of proteins in different treatment groups.

2.3.6. Statistical Analyses

All experiments were performed at least in three independent experiments. Quantifications are expressed as mean ± SEM. Statistical significance of difference between the distinct groups was evaluated by analysis of variance (ANOVA) followed by the Bonferroni test. A difference between experimental groups was considered significant with a confidence interval of 95%, whenever .

2.4. Docking Simulations Using AutoDock4

A VEGFR-2 crystal structure (PDB: 2XIR) was extracted from the Protein Data Bank (PDB) ( The cocrystallized ligand was extracted from the PDB file, and AutoDockTools was used to assign polar hydrogens and Gasteiger charges to the compounds [17]. AutoGrid4 was used to create affinity grid maps for all the atom types. The affinity grids enclosed an area of 100 × 100 × 100 with 0.375 Å spacing, centered on the coordinates . AutoDock4 (version 4.1) with the Lamarckian genetic algorithm was used with the following docking parameters: 100 docking runs, population size of 200, random starting position and conformation, translation step ranges of 2.0 Å, mutation rate of 0.02, crossover rate of 0.8, local search rate of 0.06, and 2.5 million energy evaluations [17]. The entire virtual screening experiment was performed on a cluster of 8 Intel Dual-Core 2.8 GHz computers using MOLA software [18]. Inhibition constants for all ligands were calculated by AutoDock4 as follows: = , where is the binding energy, cal is 1.98719, and TK is 298.15. All figures with structure representations were prepared using PyMOL software [19].

3. Results and Discussion

3.1. Synthesis

We were able to promote the regioselective attack of the hydroxyl group of the 4-aminophenol in the chlorine nucleophilic displacement of two commercial 4-chlorinated thieno[3,2-d]pyrimidines, using stoichiometric amounts of the reagents, in the synthesis of the aminated compounds 1a and 1b in excellent yields (Scheme 1). This regioselectivity constitutes an important achievement that avoids the reaction of 4-nitrophenols followed by reduction of the nitro compounds to the corresponding amino compounds, as often described in the literature [12, 13]. With 4-aminophenol as a reagent, it is possible to use DMF as solvent and heat only at 140°C instead of diphenylether at 180°C which is needed for the nucleophilic displacement of the chlorine using 4-nitrophenol. The amino compounds 1a and 1b, obtained in one step, were then reacted with different arylisocyanates to give the corresponding new 1-aryl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]ureas 2a2f in high yields (Scheme 1). Compounds 1a, b, and 2a2f were fully characterized by m.p., , NMR, and mass spectrometry including HRMS.

Scheme 1: Synthesis of 1-aryl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]ureas 2a2f. The yields are presented as % of pure compounds.
3.2. Biological Evaluation
3.2.1. Enzymatic Assays

The synthesized thieno[3,2-d]pyrimidine ureas 2af were evaluated for their ability to interact with the VEGFR2 tyrosine kinase domain (Table 1), using an enzymatic FRET-based assay. Compounds 2a, 2b, and 2c displayed the highest inhibition with IC50 values of 199, 188, and 150 nM, respectively. The presence of a methoxy group in the para position of the phenyl ring (2b) did not show a significant increase in VEGFR-2 inhibition activity relative to 2a, while the presence of a nitrile group in the same position (2c) promoted a small increase in VEGFR-2 inhibition activity. These findings appear to suggest that the presence of small substituents in the para position of the phenyl group will not have a significant effect on VEGFR-2 potency of the compounds. When a methyl group is present in position 7 of the thieno[3,2-d]pyrimidine moiety (compounds 2df), no VEGFR-2 inhibition activity was observed. This finding indicates that substitutions on the mentioned position are not favorable for this series of thieno[3,2-d]pyrimidine ureas, when considering VEGFR-2 inhibition activity.

Table 1: Results of the VEGFR2 enzymatic inhibition assay using compounds 2af.
3.2.2. Cellular Assays

The best compounds in enzymatic assays (2a, 2b, and 2c) were studied at cellular level. Cell cytotoxicity was first analyzed by MTS assay in the HUVEC cultures upon treatment with 0.10–10 μM of compounds 2ac (Figure 2(a)). Viability of HUVEC decreased at the highest concentration of 2c ( O.D.) and at concentrations of 5.0 and 10 μM for 2a ( O.D. and O.D., resp.) and for 2b ( O.D. and O.D., resp.) versus control ( O.D.).

Figure 2: (a) Cell viability was evaluated in HUVECs upon treatment with 2a, 2b, and 2c at 0.10, 0.50, 1.0, 5.0 and 10 μM, or untreated (control, 0.1% DMSO) using MTS assay. (b) Cell proliferation was assessed by BrdU incorporation assay. Bars represent the percentage of proliferating cells when compared to control group, after incubation with anti-BrdU antibody by ELISA assay. (c) Apoptosis was assessed in HUVECs by TUNEL assay using 2a, 2b, and 2c at 0.1, 0.5, and 1 μM. Bars represent the percentage of apoptotic cells evaluated by the ratio between TUNEL-stained cells and DAPI-stained nuclei in every culture. Results are expressed as mean ± SEM of three independent experiments (). * versus control.

Then, the ability of compounds 2ac to inhibit VEGF-stimulated proliferation of HUVECs was evaluated using the BrdU incorporation assay (Figure 2(b)). Inhibition of the VEGFR-2 activity was strongly reflected at the cellular level, with all the three compounds showing a statistical significant inhibition activity against VEGF-stimulated HUVEC proliferation at 0.5 μM (% for 2a; % for 2b, and % for 2c) when comparing to control, which is consider to be %.

The number of proliferating HUVECs decreased in a dose-dependent manner (Figure 2(b)).

Interestingly, incubation of HUVECs with compounds 2a, 2b, and 2c for 24 h with concentrations 0.1, 0.5, and 1 μM (due to cytotoxic effect for higher concentrations, Figure 2(a)) using the TUNEL assay resulted in an increase in apoptosis, reaching statistical significance only for 2a at the highest concentration tested (% increase) comparing with untreated cells (Figure 2(c)).

To investigate the cellular inhibition of VEGFR-2 by the compounds in HUVEC cultures, immunoblotting assays for total and phosphorylated (active) VEGFR-2 were performed (Figure 3(a)). As illustrated in Figure 3(b), incubation with compounds 2a and 2b significantly decrease the formation of the active form of the receptor at 1 μM concentration, when comparing with the expression of VEGFR-2 (*). Compound 2c did not significantly inhibit the activation of the VEGFR-2, although a dose-dependent decrease was observed.

Figure 3: (a) Evaluation of phosphorylated and total VEGFR-2 expression in HUVECs after incubation with compounds 2a, 2b, and 2c by western blotting. Representative bands obtained after immunostaining are shown. (b) Quantification of densitometry and mean relative intensity by comparison of the relative intensity of activated VEGFR-2 after normalization with total VEGFR-2 intensity. Data presented as mean ± SEM of two independent experiments. * versus control.

VEGF signaling pathway through the VEGFR-2 activation displays a crucial role in endothelial cells, namely, survival, proliferation, invasion, and apoptosis. Our data suggest that compounds 2ac exert direct actions in HUVECs by inhibiting their growth mainly at 0.5 and 1 μM, slightly increasing the percentage of apoptotic cells without cytotoxic effects at the same range of concentrations. The referred cellular-based results are triggered by the inhibition of the phosphorylation (activation) of the VEGFR-2, which is overexpressed in several pathological conditions, such as cancer.

3.3. Molecular Modelling Studies

To better understand the molecular basis of compounds 2 observed VEGFR-2 inhibition activity, docking simulations using AutoDock4 [17] were carried out against the VEGFR-2 kinase domain (PDB code 2XIR).

Figure 4(a) displays the superimposition of the best docked poses obtained for the most potent thieno[3,2-d]pyrimidine derivatives 2ac. They present similar docking poses, with the binding conformation stabilized mainly by the formation of a network of four H-bonds. The two N–H of the urea group form two H-bonds with the Glu885 carboxyl group, while the C=O bond of the urea group forms a third H-bond with the backbone N–H of Asp1046. These H-bonds are similar to the ones observed with other known VEGFR-2 inhibitors presenting a biphenyl urea moiety, including the drug Soranefib (Figure 1). A fourth H-bond is predicted between the N atom in position 4 of the thieno[3,2-d]pyrimidine moiety and the backbone N–H of Cys919.

Figure 4: (a) Superimposition of the docking poses at the VEGFR-2 kinase domain for compounds: 2a (cyan), 2b (green) and 2c (orange). (b) Surface representation of the VEGFR-2 kinase hinge with the docking poses of compounds 2c (orange)and 2f (light grey). H-bonds are depicted in dashed yellow lines (distances between 2.9 and 3.3 Å) and hydrophobic interactions are depicted in dashed white lines (distances between 3.5 and 4.0 Å). Important residues are drawn in sticks. Figures were prepared using PyMOL [19].

The terminal aryl group is positioned in a hydrophobic region formed by several hydrophobic residues (Ile888, Leu889, Ile892, Val898, Val 899, and Leu1019). From Figure 4(a), it is clearly observed that the 4-methoxyphenyl and 4-cyanophenyl substituents occupy part of a large hydrophobic pocket that is able to accommodate them, providing an explanation for compounds 2b and 2c being almost equipotent to 2a that bears no substituents in the phenyl ring. Substitutions of hydrophobic groups in ortho or meta positions of the phenyl ring will probably be worth exploring for synthesis of even more potent compounds in this series.

The lack of inhibition by compounds 2df for VEGFR-2 was analysed by superimposing the docked pose of compound 2c (the most potent in the enzymatic assays, 150 nM) and the corresponding 7-methylated compound 2f (Figure 4(b)). The methyl group seems to displace the thieno[3,2-d]pyrimidine ring away from Cys919. This displacement probably interferes with the formation of the H-bond between the N atom in position 4 of the thieno[3,2-d]pyrimidine ring and the backbone N–H of Cys919 (Figure 4(b)). These results demonstrate that this H-bond is an absolute requirement for VEGFR-2 inhibition potency of this thieno[3,2-d]pyrimidine series, and the methyl group in position 7 of compounds 2df promotes loss of VEGFR-2 inhibition activity by impairing H-bond formation. We can also infer that other substitutions in position 7 of the thieno[3,2-b]pyridine are probably not desirable as they will also impair H-bond formation.

4. Conclusion

In conclusion, we reported the synthesis of novel 1-aryl-3-[4-(thieno[3,2-d]pyrimidin-4-yloxy)phenyl]ureas 2a2f in high yields in two steps: the regioselective nucleophilic displacement of chlorine on two 4-chlorothieno[3,2-d]pyrimidines using 4-aminophenol and the reaction of the resultant 4-(thieno[3,2-d]pyrimidin-4-yloxy)anilines with arylisocyanates. Compounds 2ac, without the methyl group in position 7, were shown to be the most potent VEGFR-2 inhibitors presenting IC50 values between 150–199 nM in enzymatic assays. The cell culture assays enable us to identify the angiogenic steps targeted by the compounds 2ac. In fact, compounds were evaluated using a cell-based HUVEC assay and showed activity at the same concentration range (0.5–1 μM) without affecting cell viability, inhibiting cell proliferation, and avoiding the formation of active VEGFR-2 specially in the case of compounds 2a and 2b, thus showing their anti-angiogenic potential. Compound 2a increases also apoptosis at the highest concentration tested (1 μM) using the TUNEL assay. By performing docking studies, the binding conformation and H-bond network of the most promising compounds 2ac were predicted. Based on these molecular modelling studies, several suggestions can be done for the synthesis of even more potent compounds.

Conflict of Interests

The authors declare that they have no conflict of interests.


The authors would like to acknowledge Foundation for the Science and Technology (FCT Portugal) for financial support through the NMR Portuguese network (Bruker 400 Avance III-Univ Minho). FCT and European Fund for Regional Development (FEDER)-COMPETE-QREN-EU for financial support through the research unities PEst-C/QUI/UI686/2011, PEst-OE/SAU/UI0038/2011, and PEst-OE/AGR/UI0690/2011, the research project PTDC/QUI-QUI/111060/2009, and the post-Doctoral Grant attributed to Ricardo C. Calhelha (SFRH/BPD/68344/2010) also financed by Human Potential Operational Programme (POPH) and Social European Fund (FSE).


  1. S. Patan, “Vasculogenesis and angiogenesis as mechanisms of vascular network formation, growth and remodeling,” Journal of Neuro-Oncology, vol. 50, no. 1-2, pp. 1–15, 2000. View at Publisher · View at Google Scholar · View at Scopus
  2. J. Folkman and Y. Shing, “Angiogenesis,” The Journal of Biological Chemistry, vol. 267, no. 16, pp. 10931–10934, 1992. View at Google Scholar · View at Scopus
  3. N. Ferrara, H.-P. Gerber, and J. LeCouter, “The biology of VEGF and its receptors,” Nature Medicine, vol. 9, no. 6, pp. 669–676, 2003. View at Publisher · View at Google Scholar · View at Scopus
  4. M. A. Lemmon and J. Schlessinger, “Cell signaling by receptor tyrosine kinases,” Cell, vol. 141, no. 7, pp. 1117–1134, 2010. View at Publisher · View at Google Scholar · View at Scopus
  5. S. Baka, A. R. Clamp, and G. C. Jayson, “A review of the latest clinical compounds to inhibit VEGF in pathological angiogenesis,” Expert Opinion on Therapeutic Targets, vol. 10, no. 6, pp. 867–876, 2006. View at Publisher · View at Google Scholar · View at Scopus
  6. A. Eichholz, S. Merchant, and A. M. Gaya, “Anti-angiogenesis therapies: their potential in cancer management,” Oncology Targets Therapy, vol. 3, pp. 69–82, 2010. View at Google Scholar
  7. D. D. Hu-Lowe, H. Y. Zou, M. L. Grazzini et al., “Nonclinical antiangiogenesis and antitumor activities of axitinib (AG-013736), an oral, potent, and selective inhibitor of vascular endothelial growth factor receptor tyrosine kinases 1, 2, 3,” Clinical Cancer Research, vol. 14, no. 22, pp. 7272–7283, 2008. View at Publisher · View at Google Scholar · View at Scopus
  8. L. Cowey, G. Sonpavde, and T. E. Hutson, “New advancements and developments in treatment of renal cell carcinoma: focus on pazopanib,” OncoTargets and Therapy, vol. 3, pp. 147–155, 2010. View at Google Scholar
  9. Y. Dai, Y. Guo, R. R. Frey et al., “Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors,” Journal of Medicinal Chemistry, vol. 48, no. 19, pp. 6066–6083, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. H. R. Heyman, R. R. Frey, P. F. Bousquet et al., “Thienopyridine urea inhibitors of KDR kinase,” Bioorganic and Medicinal Chemistry Letters, vol. 17, no. 5, pp. 1246–1249, 2007. View at Publisher · View at Google Scholar · View at Scopus
  11. S. Claridge, F. Raeppel, M.-C. Granger et al., “Discovery of a novel and potent series of thieno[3,2-b]pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases,” Bioorganic and Medicinal Chemistry Letters, vol. 18, no. 9, pp. 2793–2798, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. S. Raeppel, S. Claridge, O. Saavedra et al., “N-(3-fluoro-4-(2-arylthieno[3,2-b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors,” Bioorganic and Medicinal Chemistry Letters, vol. 19, no. 5, pp. 1323–1328, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. O. Saavedra, S. Claridge, L. Zhan et al., “N3-Arylmalonamides: a new series of thieno[3,2-b]pyridine based inhibitors of c-Met and VEGFR2 tyrosine kinases,” Bioorganic and Medicinal Chemistry Letters, vol. 19, no. 24, pp. 6836–6839, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. “Staurosporine IC50 calculated by Invitrogen with the same FRET-based VEGFR-2 enzymatic kit used in this study,”
  15. R. Costa, Â. Carneiro, A. Rocha et al., “Bevacizumab and ranibizumab on microvascular endothelial cells: a comparative study,” Journal of Cellular Biochemistry, vol. 108, no. 6, pp. 1410–1417, 2009. View at Publisher · View at Google Scholar · View at Scopus
  16. A. Rocha, I. Azevedo, and R. Soares, “Anti-angiogenic effects of imatinib target smooth muscle cells but not endothelial cells,” Angiogenesis, vol. 10, no. 4, pp. 279–286, 2007. View at Publisher · View at Google Scholar · View at Scopus
  17. G. M. Morris, H. Ruth, W. Lindstrom et al., “Software news and updates AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility,” Journal of Computational Chemistry, vol. 30, no. 16, pp. 2785–2791, 2009. View at Publisher · View at Google Scholar · View at Scopus
  18. R. M. V. Abreu, H. J. C. Froufe, M. J. R. P. Queiroz, and I. C. F. R. Ferreira, “MOLA: a bootable, self-configuring system for virtual screening using AutoDock4/Vina on computer clusters,” Journal of Cheminformatics, vol. 2, no. 1, article 10, 2010. View at Publisher · View at Google Scholar · View at Scopus
  19. “The PyMOL Molecular Graphics System, Version 1.3, Schrödinger, LLC,” September 2012,