BioMed Research International

BioMed Research International / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 3941242 | 13 pages |

Antimicrobial Activity of 4-Chlorocinnamic Acid Derivatives

Academic Editor: Francesca Mancianti
Received07 Mar 2019
Revised06 Apr 2019
Accepted14 Apr 2019
Published23 Apr 2019


The microbial resistance of fungi and bacteria is currently considered a major public health problem. Esters derived from cinnamic acid have a broad spectrum of pharmacological properties that include antimicrobial activity. In this study, a collection of structurally related 4-chlorocinnamic acid esters was prepared using Fischer esterification reactions, alkyl or aryl halide esterification, and Mitsunobu and Steglich reactions. All of the esters were submitted to antimicrobial tests against strains of the species Candida albicans, Candida glabrata, Candida krusei, Candida guilliermondii, Pseudomonas aeruginosa, and Staphylococcus aureus. The compounds also were subjected to molecular docking study with the enzyme 14α-demethylase. Twelve esters derived from 4-chlorocinnamic acid were obtained, with yields varying from 26.3% to 97.6%, three of which were unpublished. The ester methyl 4-chlorocinnamate (1) presented activity against S. aureus at the highest concentration tested. In the antifungal evaluation, all of the esters were bioactive, but methoxyethyl 4-chlorocinnamate (4) and perillyl 4-chlorocinnamate (11) were the most potent (MIC = 0.13 and 0.024 μmol/mL, respectively). The data of molecular docking suggested that all the compounds present good affinity towards the active site related to antifungal activity. Therefore, the esters tested may be inhibitors of the enzyme 14α-demethylase. In addition, the results demonstrate that substituents of short alkyl chains with presence of heteroatom, such as oxygen, or those with a perillyl type terpenic substructure promote better antifungal profiles.

1. Introduction

Infectious diseases caused by microorganisms such as bacteria and fungi remain a prominent global health problem, especially in developing and low-income countries [1, 2]. Bacteria are becoming highly drug resistant, creating a growing problem in medicine. Several types of resistant bacterial infections are ever more difficult to treat, increasing morbidity and mortality and causing high health care costs [3]. Similarly, fungal infections also pose a challenge to medical practice; significant increases in indicators of morbidity and mortality have been observed, especially in hospitalized immunocompromised individuals [4, 5].

Of the most common fungal infections, the most frequent etiological agent is C. albicans. However, other species of the Candida genus can also be included such as C. guilliermondii, C. parapsilosis, C. stellatoidea, C. tropicalis, C. glabrata, and C. krusei, which are recognized for resistance to antifungal drugs, particularly azole derivatives [6, 7]. Usually, clinical manifestations of fungal infection occur as localized in the mucosa, yet these may become disseminated infections which can involve multiple organs [8]. The reduced number of antifungals available at market, together with the high frequency of their use, has made treatment of fungal infections more complex, since many etiological agents have already acquired resistance to the few drugs available [911].

Phenylpropanoic derivatives, especially cinnamic acid derivatives, form a group of substances with varied pharmacological and biological properties. They are found in nature in various forms, such as acids, esters, and amides. Due to their therapeutic potential, studies have been carried out to develop methods of preparation [12]. In addition, certain halogenated derivatives present antifungal activity [13]. Therefore, in the present work we aimed to prepare a collection of twelve esters derived from 4-chlorocinnamic acid to evaluate their antimicrobial potential against the microorganism strains: Candida albicans ATCC 90028; Candida glabrata ATCC 90030; Candida krusei ATCC 34125; Candida guilliermondii 207; Pseudomonas aeruginosa ATCC 8027; Pseudomonas aeruginosa 102; Staphylococcus aureus ATCC 25925; and Staphylococcus aureus 47. A molecular docking study using the enzyme 14α-demethylase as possible site of antifungal action and the structure-activity relationships of the prepared compounds were also performed.

2. Experimental Section

2.1. Chemistry
2.1.1. Materials

Structural identification of the compounds was performed from 1H and 13C Nuclear Magnetic Resonance spectra analyses obtained using a MERCURY-VARIAN spectrometer operating at 200 MHz for NMR of 1H and 50 MHz for 13C NMR, a VARIAN-NMR SYSTEM operating at 500 MHz for NMR of 1H and 125 MHz for 13C NMR, and an ASCEND-BRUKER system operating at 400 MHz (1HNMR) and 100 MHz (13CNMR). As the solvent, small amounts of the compounds in deuterated chloroform (CDCl3) from MERCK were used. The chemical shifts (δ) were expressed in parts per million (ppm) over tetramethylsilane (TMS), which was used as the internal standard. Melting points were recorded on a GEHAKA apparatus, model PF 1500. Infrared spectra were performed using an IRPrestige-21 FTIR spectrophotometer, Shimadzu. Potassium bromide tablets (KBr) were used with frequencies measured in cm−1. The unpublished compounds were also analyzed using High Resolution Mass Spectrometry where measurements were performed using a TOF/TOF Ultraflex II mass spectrometer equipped with a high performance solid state laser (λ = 355 nm) and reflector. The system was operated using the FlexControl 2.4 (Bruker Daltonics GmbsH, Bremen, Germany) software package. Reactions were monitored and purity was checked using analytical thin-layer chromatography plates.

2.1.2. General Synthesis Method for Ester Derivatives of 4-Chlorocinnamic Acid 1-6

To a solution of 4-chlorocinnamic acid (0.1 g, 0.547 mmol) in 20 mL of alcohol, 0.2 mL of concentrated sulfuric acid (H2SO4) was slowly added. The reaction mixture was refluxed with magnetic stirring for 3-24 hours and monitored using silica gel thin-layer chromatography (TLC) and a mixture of hexane and ethyl acetate as eluent. The solvent was partially evaporated by about half, under reduced pressure. Extraction was performed by adding 15 mL of distilled water; the extractive solvent used was ethyl acetate (3 x 10 mL). The resulting organic phases were joined and neutralized with 5% sodium bicarbonate (NaHCO3), washed with 10 mL of distilled water, and dried with anhydrous sodium sulfate (Na2SO4) and then filtered, and the solvent evaporated with a rotary evaporator. For ester 6, the purification was carried out using a chromatographic column on silica gel 60 using hexane and ethyl acetate (9:1) as eluents. This procedure was also monitored using TLC [15].

2.1.3. General Method for Synthesis of Esters 710

4-Chlorocinnamic acid (0.1 g, 0.547 mmol) was dissolved in 14 mL of anhydrous acetone. To this solution was added 0.3 mL of triethylamine (2.188 mmol) and halide (0.563 mmol). The flask was then coupled to a reflux condenser. The reaction mixture was refluxed with magnetic stirring for 24-48 hours until consumption of the starting material; this was monitored using TLC. After formation of the product, the solvent was partially evaporated in a rotary evaporator. Subsequently, the reaction product was extracted from 15 mL of distilled water with dichloromethane (3 x 10 mL). The organic phases were joined and treated with 10 mL of 5% sodium bicarbonate (NaHCO3). It was then washed with 10 mL of distilled water and dried with anhydrous sodium sulfate (Na2SO4). Subsequently, filtration was performed and the solvent was evaporated with the aid of a rotary evaporator. The residue was purified using a chromatographic column on silica gel 60 with hexane/ethyl acetate as eluent, in an increasing polar gradient (95:05 – 90:10) [16, 17].

2.1.4. Method for Synthesis of Ester 11

4-Chlorocinnamic acid (0.1 g, 0.547 mmol) and perillyl alcohol (0.09 mL, 0.547 mmol) were solubilized in 2 mL tetrahydrofuran (THF). The reaction mixture was placed under magnetic stirring at 0°C for about 30 minutes. Diisopropyl azodicarboxylate (0.12 mL, 0.55 mmol) and triphenylphosphine (0.144 g, 0.547 mmol) were then added, maintaining stirring at room temperature for 72 hours and monitoring with TLC. The solvent was then partially evaporated in a rotary evaporator. Extraction was performed with 10 mL of distilled water and ethyl acetate (3 x 10 mL). The resulting organic layers were joined and neutralized with 5% sodium bicarbonate solution (3 x 10 mL). The reaction mixture was then dried with anhydrous sodium sulfate and filtered, and finally the solvent was evaporated. The product was isolated in a silica gel 60 chromatographic column using hexane/ethyl acetate (9:1) as eluent [18].

2.1.5. Method for Synthesis of Ester 12

4-Chlorocinnamic acid (0.1 g, 0.547 mmol), 4-(dimethylamino)pyridine (DMAP) (0.00669 g, 0.0547 mmol), and lauryl alcohol (0.245 mL, 1.095 mmol) were dissolved in dichloromethane (4 mL). Dicyclohexylcarbodiimide (DCC) (0.124 g, 0.602 mmol) dissolved in dichloromethane (6 mL) was then added dropwise. The reaction occurred under magnetic stirring at room temperature and monitored with TLC for 72 hours. After filtration, the reaction product was extracted with 10 mL of distilled water and dichloromethane (3 x 10 mL). The resulting organic phase was treated with 5% hydrochloric acid solution (10 mL). Subsequently a 5% sodium bicarbonate solution (10 mL) was added, followed by 10 mL of distilled water. The solution was dried over anhydrous sodium sulfate, filtered, and rotated to reduce the solvent volume. The product was then purified using column chromatography on silica gel 60 using hexane/ethyl acetate as eluents in increasing order of polarity (100:00-95:05) [19].

Methyl 4-Chlorocinnamate (1). White crystals; Yield 97.6% (105.7 mg); m.p.: 71–72°C; IR (KBr, cm−1): 3035 (C-H sp2), 2949 (C-H sp3), 1705 (C=O), 1631 and 1431 (aromatic C=C bending), 1273 and 1166 (C-O stretching), 1004; 1H NMR (200 MHz, CDCl3): 7.61 (d, J = 16.0 Hz, 1H, H-7); 7.43 (d, J = 7.8 Hz, 2H, H-2, H-6); 7.33 (d, J = 7.8 Hz, 2H, H-3, H-5); 6.38 (d, J = 16.0 Hz, 1H, H-8); 3.79 (s, 3H, H-1′) ppm; 13C NMR (50 MHz, CDCl3): 167.1 (C=O); 143.4 (C-7); 136.2 (C-4); 132.8 (C-1); 129.3 (C-2, C-6); 129.1 (C-3, C-5); 118.2 (C-8); 51.8 (C-1′) ppm.

Ethyl 4-Chlorocinnamate (2). Yellow amorphous solid; Yield 89.0% (102.7 mg); IR (KBr, cm−1): 3066 (C-H sp2), 2981(C-H sp3), 1710 (C=O), 1639 and 1448 (aromatic C=C bending), 1311 and 1172 (C-O stretching), 1037; 1H NMR (400 MHz, CDCl3): 7.61 (d, J = 15.7 Hz, 1H, H-7); 7.43 (d, J = 8.8 Hz, 2H, H-2, H-6); 7.34 (d, J = 8.4 Hz, 2H, H-3, H-5); 6.39 (d, J = 16.0 Hz, 1H, H-8); 4.25 (q, J = 7.1 Hz, 2H, H-1′); 1.32 (t, J = 6.9 Hz, 3H, H-2′) ppm; 13C NMR (100 MHz, CDCl3): 166.8 (C=O); 143.3 (C-7); 136.2 (C-4); 133.2 (C-1); 129.3 (C-2, C-6); 129.2 (C-3, C-5); 119.0 (C-8); 60.7(C-1′); 14.4 (C-2′) ppm.

Propyl 4-Chlorocinnamate (3). Yellow amorphous solid; Yield 88.5% (109 mg) ); m.p.: 34–36°C; IR (KBr, cm−1): 3035 (C-H sp2), 2956 (C-H sp3), 1705 (C=O), 1635 and 1409 (aromatic C=C bending), 1317 and 1087 (C-O stretching), 1004; 1H NMR (200 MHz, CDCl3): 7.61 (d, J = 16.0 Hz, 1H, H-7); 7.44 (d, J = 8.5 Hz, 2H, H-2, H-6); 7.33 (d, J = 8.6 Hz, 2H, H-3, H-5); 6.40 (d, J = 16.0 Hz, 1H, H-8); 4.15 (t, J = 6.7 Hz, 2H, H-1′), 1.71 (m, J = 7.2 Hz, 2H, H-2′); 0.97 (t, J = 7.3 Hz, 3H, H-3′) ppm; 13C NMR (50 MHz, CDCl3): 166.8 (C=O); 143.1 (C-7); 136.1 (C-4); 132.8 (C-1); 129.2 (C-2, C-6); 129.1 (C-3, C-5); 118.7 (C-8); 66.2 (C-1′); 22.0 (C-2′); 10.3 (C-3′) ppm.

Isopropyl 4-Chlorocinnamate (4). Yellow solid; Yield 91.2% (112.4 mg); m.p.: 34 – 35°C; IR (KBr, cm−1): 3049 (C-H sp2), 2980 (C-H sp3), 1710 (C=O), 1639 and 1462 (aromatic C=C bending), 1309 and 1109 (C-O stretching); 1H NMR (200 MHz, CDCl3): 7.54 (d, J = 16.0 Hz, 1H, H-7); 7.36 (d, J = 7.8 Hz, 2H, H-2, H-6); 7.30 (d, J = 7.8 Hz, 2H, H-3, H-5), 6.32 (d, J = 16.0 Hz, 1H, H-8); 5.07 (m, 1H, H-1′), 1.25 (d, J = 5.8 Hz, 6H, H-2′, H-3′) ppm; 13C NMR (50 MHz, CDCl3): 166.2 (C=O); 142.8 (C-7); 135.9 (C-4); 131.0 (C-1); 129.2 (C-2, C-6); 129.1 (C-3, C-5); 119.3 (C-8); 67.9 (C-1′); 22.1 (C-2′, C-3′) ppm.

Butyl 4-Chlorocinnamate (5). Brown amorphous solid; Yield 87.4% (115.3 mg); m.p.: 30 - 32°C; IR (KBr, cm−1): 3034 (C-H sp2), 2960 (C-H sp3), 1712 (C=O), 1637 and 1473 (aromatic C=C bending), 1313 and 1172 (C-O stretching), 1010; 1H NMR (200 MHz, CDCl3): 7.61 (d, J = 16.0 Hz, 1H, H-7); 7.44 (d, J = 7.9 Hz, 2H, H-2, H-6); 7.34 (d, J = 7.9 Hz, 2H, H-3, H-5); 6.40 (d, J = 16.0 Hz, 1H, H-8); 4.20 (t, J = 6.2 Hz, 2H, H-1′); 1.69 (quint, J = 6,7 Hz, 2H, H-2′); 1.42 (sex, J = 7.1 Hz, 2H, H-3′); 0.95 (t, J = 7,0 Hz, 3H, H-4′) ppm; 13C NMR (50 MHz, CDCl3):166.8 (C=O); 143.1 (C-7); 136.0 (C-4); 132.9 (C-1); 129.2 (C-2, C-6); 129.1 (C-3, C-5); 118.8 (C-8); 64.5 (C-1′); 30.7 (C-2′); 19.2 (C-3′); 13.7 (C-4′) ppm.

2-Methoxyethyl 4-Chlorocinnamate (6). Yellow oil; Yield 36.0% (47.6 mg); IR (KBr, cm−1):3068 (C-H sp2), 2927 (C-H sp3), 1714 (C=O), 1639 and 1452 (aromatic C=C bending), 1313 and 1170 (C-O stretching), 1039; 1H NMR (400 MHz, CDCl3): 7.67 (d, J = 16.0 Hz, 1H, H-7); 7.46 (d, J = 8.8 Hz, 2H, H-2, H-6); 7.36 (d, J = 9.7 Hz, 2H, H-3, H-5), 6.47 (d, J = 16.0 Hz, 1H, H-8); 4.38 (t, J = 5.4, 2H, H-1′); 3.68 (t,J = 4.7, 2H, H-2′); 3.43 (s, 3H, H-3′) ppm; 13C NMR (100 MHz, CDCl3): 166.8 (C=O); 143.8 (C-7); 136.3 (C-4); 133.0 (C-1); 129.4 (C-2, C-6); 129.3 (C-3, C-5); 118.5 (C-8); 70.64 (C-1′); 63.7 (C-2′); 59.1 (C-3′) ppm; HRMS (MALDI) calculated or C12H13ClO3[M + Na]+: 263.6722; encountered: 263.6333.

Pentyl 4-Chlorocinnamate (7). White amorphous solid; Yield 55.6% (77 mg); m.p.: 38 – 39°C; IR (KBr, cm−1): 3035 (C-H sp2), 2958 (C-H sp3), 1703 (C=O), 1635 and 1492 (aromatic C=C bending), 1311 and 1172 (C-O stretching), 1083; 1H NMR (400 MHz, CDCl3): 7.61 (d, J = 16.0 Hz, 1H, H-7); 7.44 (d, J = 8.6 Hz, 2H, H-2, H-6); 7.34 (d, J = 8.5 Hz, 2H, H-3, H-5 ); 6.40 (d, J = 16.0 Hz, 1H, H-8); 4.19 (t, J = 6.8 Hz, 2H, H-1′); 1.69 (quint, J = 6.9 Hz, 2H, H, 2′); 1.37 (m, 4H, H-3′, H-4′), 0.92 (t,J= 7.0 Hz, 3H, H-5′) ppm; 13C NMR (100 MHz, CDCl3): 166.8 (C=O); 143.1 (C-7); 136.1 (C-4); 133.0 (C-1); 129.2 (C-2, C-6); 129.1 (C-3, C-5); 118.9 (C-8); 63.8 (C-1′); 28.4 (C-2′); 28.1 (C-3′); 22.4 (C-4′); 14.0 (C-5′) ppm.

Decila 4-Chlorocinnamate (8). Yellow oil; Yield 30.6% (54.2 mg); IR (KBr, cm−1):3066 (C-H sp2), 2926 (C-H sp3), 1710 (C=O), 1637 and 1465 (aromatic C=C bending), 1311 and 1168 (C-O stretching), 1012; 1H NMR (400 MHz, CDCl3): 7.62 (d, J = 16.0 Hz, 1H, H-7); 7.45 (d, J = 8.4 Hz, 2H, H-2, H-6); 7.35 (d, J = 8.5 Hz, 2H, H-3, H-5); 6.41 (d, J = 16.0 Hz, 1H, H-8); 4.19 (t, J = 6,7 Hz, 2H, H-1′); 1.68 (quint, J = 6.6 Hz, 2H, H-2′), 1.40 – 1.24 (m, 14H, H-3′, H-4′, H-5′, H-6′, H-7′, H-8′, H-9′); 0.88 (t, J = 6.7 Hz, 3H, H-10′) ppm.13C NMR (100 MHz, CDCl3): 166.9 (C=O); 143.1 (C-7); 136.0 (C-4); 133.0 (C-1); 129.2 (C-2, C-6); 129.1 (C-3, C-5); 118.7 (C-8); 64.8 (C-1′); 32.0 (C-2′); 29.5 (C-3′); 29.3 (C-4′); 29.2 (C-5′); 28.7 (C-6′); 26.0 (C-7′); 22.7 (C-8′, C-9′); 14.0 (C-10′) ppm.

Chemical shift for carbons.

4-Chlorobenzyl 4-Chlorocinnamate (9). White solid; Yield 61.6% (103.5 mg);m.p.: 131 – 133°C; IR (KBr, cm−1): 3057 (C-H sp2), 2949 (C-H sp3), 1701 (C=O), 1653 and 1450 (aromatic C=C bending), 1273 and 1188 (C-O stretching), 1010 (C-Cl stretching); 1H NMR (500 MHz, CDCl3): 7.66 (d, J = 16.0 Hz, 1H, H-7); 7.44 (d, J = 8.8 Hz, 2H, H-2, H-6), 7.36 (d, J =7.1 Hz, 6H, H-3, H-5, H-3′, H-4′, H-6′, H-7′); 6.44 (d, J = 16.0 Hz, 1H, H-8); 5.21 (s, 2H, H-1′) ppm;13C NMR (125 MHz, CDCl3): 166.3 (C=O); 144.0 (C-7); 136.3 (C-2′); 134.5 (C-4); 134.2 (C-1); 132.7 (C-5′); 129.6 (C-3′, C-7′); 129.2 (C-2, C-6); 129.2 (C-4′, C-6′); 128.8 (C-3, C-5); 118.2 (C-8); 65.6 (C-1′) ppm; HRMS (MALDI) calculated for C16H12Cl2O2[M +Na]+: 330.161; encountered 330.1609.

4-Methoxybenzyl 4-Chlorocinnamate (10). White amorphous solid; Yield 39.3% (65.1 mg); m.p.: 80 – 83°C; IR (KBr, cm−1): 3035 (C-H sp2), 2960 (C-H sp3), 1712 (C=O), 1610 and 1442 (aromatic C=C bending), 1261 and 1159 (C-O stretching), 1014; 1H NMR (500 MHz, CDCl3): 7.66 (d, J = 16.5 Hz, 1H, H-7); 7.44 (d, J = 8.5 Hz, 2H, H-2, H-6); 7.35 (d, J = 5.1 Hz, 4H, H-3, H-5, H-2′, H-6′); 6.92 (d, J = 8.7 Hz, 2H, H-3′, H-5′); 6.44 (d, J = 16.0 Hz, 1H, H-8); 5.19 (s, 2H, H-7′), 3.82 (s, 3H, H-8′) ppm; 13C NMR (125 MHz, CDCl3): 166,6 (C=O); 159.7 (C-4′); 143.5 (C-7); 136.2 (C-4); 132.9 (C-1); 130.1 (C-2′, C-6′);129.2 (C-2, C-6); 129.1 (C-3, C-5); 128.1 (C-1′); 118.6 (C-8); 114.0 (C-3′, C-5′); 66.3 (C-7′); 55.1 (C-8′) ppm.

Perillyl 4-Chlorocinnamate (11). Yellow oil; Yield 30.7% (53.6 mg); IR (KBr, cm−1): 3070 (C-H sp2), 2926 (C-H sp3),1712 (C=O), 1637 and 1406 (aromatic C=C bending), 1273 and 1166 (C-O stretching), 1012; 1H NMR (400 MHz, CDCl3): 7.64 (d, J = 16.0 Hz, 1H, H-7); 7.45 (d, J = 8.4 Hz, 2H, H-2, H-6); 7.35 (d, J = 8.5 Hz, 2H, H-3, H-5); 6.43 (d, J = 16.0 Hz, 1H, H-8); 5.81 (s, 1H, H-2′); 4.73 (s, 2H, H-10′), 4.60 (s, 2H, H-7′); 2.20 (m, 1H, H-3′); 2.16 (m, 1H, H-4′); 2.15 – 2.10 (m, 2H, H-6′); 2.03 – 1.96 (m, 1H, H-3′); 1.90 – 1.84 (m, 1H, H-5′); 1.76 – 1.72 (m, 3H, H-9′), 1.56 – 1.46 (m, 1H, H-5′) ppm; 13C NMR (100 MHz, CDCl3): 166.7 (C=O); 149.6 (C-8′); 143.4 (C-7); 136.2 (C-4); 132.9 (C-1); 132.6 (C-1′); 129.2 (C-2, C-6); 129.1 (C-3, C-5); 126.0 (C-2′); 118.7 (C-8); 108.5 (C-10′); 68.7 (C-7′); 40.8 (C-4′); 30.5 (C-3′); 27.2 (C-5′); 26.4 (C-6′); 20.6 (C-9′) ppm; HRMS (MALDI) calculated for C19H21ClO2 [M + Na]+: 339.8121; encountered 339.8119.

Dodecyl 4-Chlorocinnamate (12). Colorless oil; Yield 26.3% (115.2 mg); IR (KBr, cm−1): 3068 (C-H sp2), 2926 (C-H sp3), 1714 (C=O), 1639 and 1465 (aromatic C=C bending), 1271 and 1168 (C-O stretching), 1012; 1H NMR (400 MHz, CDCl3): 7.62 (d, J = 16.0 Hz, 1H, H-7); 7.45 (d, J = 8.4 Hz, 2H, H-2, H-6); 7.35 (d, J = 8.5 Hz, 2H, H-3, H-5); 6.41 (d, J = 16,0 Hz, 1H, H-8); 4.20 (t, J = 6,7 Hz, 2H, H-1′); 1.69 (quint, J = 6.7 Hz, 2H, H-2′); 1.26 (m, 8H, H-3′, H-4′, H-5′, H-6′, H-7′, H-8′, H-9′, H-10′, H-11′); 0.89 (t, J = 6.7 Hz, 3H, H-12′) ppm; 13C NMR (100 MHz, CDCl3): 166.9 (C=O); 143.1 (C-7); 136.1 (C-4); 133.0 (C-1); 129.2 (C-2, C-6); 129.2 (C-3, C-5); 118.9 (C-8); 64.9 (C-1′); 31.9 (C-2′); 29.7 (C-3′); 29.6 (C-4′); 29.6 (C-5′); 29.5 (C-6′); 29.4 (C-7′); 29.3 (C-8′); 28.7 (C-9′); 25.9 (C-10′); 22.7 (C-11′); 14.2 (C-12′) ppm.

2.2. Antimicrobial Activity
2.2.1. Antifungal Activity

The antifungal activity of the prepared compounds was assessed against four selected fungus groups: reference strains of Candida spp. which were obtained from the American Type Culture Collection (ATCC), C. albicans ATCC 90028; C. glabrata ATCC 90030; C. krusei ATCC 34125; and C. guilliermondii ATCC 22017.

(1) Compound Preparation for Testing. To analyze antifungal activity in fungal yeast strains, the compounds were submitted to biological assays. They were solubilized in dimethylsulfoxide (DMSO) (final concentration ≤ 5%) and then in sterile distilled water (completing to 1.0 mL) [2023].

(2) Determination of Minimum Inhibitory Concentrations (MICs). The MIC was determined using the microdilution technique, as previously described by the CLSI [24]. Briefly, microtiter plates with 96 U-bottom wells were used, and serial dilutions of the test substance, culture medium, and fungal inoculum (2.5 103 CFU/mL, 530 nm, abs 0.08 to 0.1) were added to the plates. The plates were incubated for 24 h at 35°C, and the results were read by visual observation of cell aggregates at the bottom of the wells. Nystatin (Sigma-Aldrich, São Paulo, SP) was used as a positive control. Controls for strain viability and medium sterility, DMSO (dimethyl sulfoxide) (Sigma-Aldrich, São Paulo, Brazil) used for compound preparation, were performed simultaneously with the assay. TTC (2,3,5-triphenyl tetrazolium chloride) dye was added to each well in order to confirm the presence of viable microorganisms [25]. The MIC was defined as the lowest concentration of the test substance inhibiting microbial growth.

(3) Determination of the Minimum Fungicide Concentrations (MFCs). Onto Petri dishes containing Sabouraud Dextrose Agar (SDA) (KASVI®, KasvImport and Distribution of Laboratory Products LTDA, Curitiba, Brazil) 50 μL well aliquots corresponding to MIC and two concentrations above (2 MIC and 4 MIC) were plated. The plates were incubated for 24 h at 35°C, and the reading was performed by visual observation of fungal growth on the solid medium. The MFC was defined as the lowest concentration inhibiting visible growth on solid medium [26]. The MFC/MIC ratio was calculated to determine whether the substance presented fungistatic (MFC/MIC ≥ 4) or fungicidal (MFC/MIC < 4) activity [14].

2.2.2. Antibacterial Activity

Antibacterial activity was assessed for the prepared compounds against Gram-positive and Gram-negative bacteria from the American Type Culture Collection (ATCC) and also from clinical origins, namely, Pseudomonas aeruginosa ATCC 8027; Pseudomonas aeruginosa 102; Staphylococcus aureus ATCC 25925; and Staphylococcus aureus 47. The bacteria were cultured in a medium consisting of yeast extract (HIMEDIA) 5 g, peptone (MERCK) 10 g, NaCl (MERCK) 5 g, KH2 PO4 (MERCK) 1.5 g, and (NaHPO4) 12H2O (MERCK) 9 g solubilized in 1 L of distilled water and sterilized using autoclaving at 121°C and 1 atm for 20 minutes.

(1) Compound Preparation for Testing. To prepare the twelve esters for antibacterial testing, a 10 mg/ml solution of each of the substances was made using 25% DMSO in sterile distilled water.

(2) Determination of Minimum Inhibitory Concentration (MIC). MIC determination was performed using microdilution technique and 96-well plates for each of the strains tested, as described by Gerhardt et al. (1994) [27]. For this, 100 μL of the culture medium was distributed to all of the wells, except those of the first and second columns that received 150 μL. Subsequently, 50 μL of the 10 mg/mL solution of each of the substances was added to the 1st and 2nd well columns. From the second column serial dilution was performed in halves, obtaining the final concentrations of 500-15.6 μg/mL for each of the substances tested. The volume was completed with 100 μL of the bacterial culture making up the final volume at 200 μL. To test 1000 μg of each of the substances, larger volumes (1 mL) were used in Eppendorf tubes to keep DMSO to a concentration which would not affect the bacteria (≤ 8%).

The plates and tubes were incubated at 37°C for 24 h for further reading, which was performed with the addition of 20 μL of a 0.01% (w/v) solution of resazurin sodium (SIGMA), a colorimetric indicator of metabolic activity. The MIC was considered to be the lowest concentration that completely inhibited bacterial growth.

2.3. Docking Study

The experimental in vitro anti-Candida activity of 4-chlorocinnamic acid derivatives was explored and correlated via molecular docking study, which involves study of possible interactions with cytochrome P450 14α-sterol demethylase from C. albicans (EC:; Candida P450DM).

2.3.1. Ligand Preparation

Chem sketch (Version 12.01) was used for the generation of 2D structure of the synthesized derivatives which were further converted to 3D structures. The structures were further energetically minimized and saved in MDL MolFiles.

2.3.2. Docking Procedure

Molegro Virtual Docker (MVD 2010.4.1.0) program was used for the docking analysis of the synthesized compounds using cytochrome P450 14α-demethylase from Candida albicans (Candida P450DM) with ID 1EA1. The hydrogen atoms were added in the structure followed by assigning bond orders. Further, the potential binding sites were determined by refining the structure using grid based cavity prediction algorithm. The site possessing highest number of amino acid residues, i.e., 189.44 amino acids, and nearest to heme cofactor was chosen as active site [28].

3. Results and Discussion

3.1. Chemistry

Compounds 1-6 were prepared by Fischer esterification, and reaction times were from 3-24 hours, with satisfactory yields (36.0-97.6%). For compounds 7-10 the alkyl or aryl halide esterification methods were employed, and reactions times were from 24 to 48 hours with yields of 30.6-61.6%. Compound 11 was prepared via the Mitsunobu reaction, with a reaction time of 72 hours and a yield of 30.7%. The Steglich esterification methodology was used to obtain the ester 12; reaction time was 72 hours with a yield of 26.3% (Scheme 1).

The infrared spectra of the 4-chlorocinnamic acid analogs presented absorption bands at 3000 relative to the C-H sp2 stretch, with C=C ring stretch absorption bands occurring in pairs in the 1600 and 1475 cm−1 regions; C=O stretch bands occurred in the 1750-1735 cm−1 range; C-O stretch assigned to C-O bonds in the ester appears with two bands in the range of 1300 to 1000 cm−1; and C-Cl stretch occurred in the 1010-1000 range. Alkyl analogs exhibit alkane (sp3) C-H stretching bands at about 3000 cm−1, methylene groups with angular deformation absorption at 1465 cm −1, and methyl groups at 1375 cm−1. In aryl derivatives, a strong folding vibration band was found at the para position in the region of 800-850 cm−1, a characteristic absorption for its para-substituent.

In 1H and 13C NMR of the prepared products, six hydrogens can be observed in common (H-2, H-3, H-5, H-6, H-7, and H-8), where four are from the aromatic ring and two from the side chain attached to the carbonyl. In the hydrogen (CDCl3, 400 MHz, ppm) spectral data for ester 6 olefinic hydrogens were observed which are presented as two doublets in δ 7.67 (d, J = 16.0 Hz, 1H) and 6.47 (d, J = 16.0 Hz, 1H), given, respectively, to the hydrogens H-7 and H-8; the coupling constant is equal (J = 16.0 Hz). For the aromatic hydrogens we observed two doublets each, referring to two hydrogens 7.46 (d, J = 8.8 Hz, 2H) and 7.36 (d, J = 9.7 Hz, 2H), belonging to hydrogens H-2, H-6, H-3, and H-5, respectively.

There were also nine carbons in common for all of the analogs (C-1, C-2, C-3, C-4, C-5, C-6, C-7, C-8, C=O), six from the aromatic ring and three from the side chain with the presence of the ester carbonyl. In the 13C NMR (CDCl3, 400 MHz, ppm) spectral data of ester 6 presented peaks at 166.8 (C=O of esters), 143.8 from C-7, 136.3 from C-4, and 133.0 attributed to carbon C-1 and a peak at 129.4 corresponding to carbons C-2 and C-6 and also occurring for the 129.3 peaks of carbons C-3 and C-5. The peak at 118.5 refers to the C-8.

3.2. Biology
3.2.1. Bioactivity of the Tested Compounds against Pathogenic Fungi of the Candida Genus

The microorganisms used in this study are associated with infections in humans and are related to high rates of morbidity and mortality, especially in debilitated and immunocompromised individuals. C. albicans is the most common species in patients with fungal infections and presents a remarkable ability to develop virulence factors while C. glabrata and C. krusei are especially resistant to azole antifungals [29, 30]. C. guilliermondii has been reported in patients diagnosed with candidemia [31].

Twelve ester derivatives of 4-chlorocinnamic acid were prepared and tested against strains of the genus Candida. Analysis of the structure-activity relationships of 4-chlorocinnamic acid-derived esters was based on the minimum inhibitory concentration (MIC) results against the Candida genus fungal strains tested. The preparation of the structurally similar compounds and changes in the size of the alkyl group or the types of substituents on the aromatic ring (such as electron donors or attractors) can promote significant changes in the properties of the compounds and thus result in distinct antifungal potencies.

The antifungal activity results for esters 1 to 12 under the CLEELAND, SQUIRES (1991), and NCCLS/CLSI (2002) [20, 24] protocols are presented in Tables 1 and 2. All of the compounds presented bioactivity; however some did not present bioactivity against all of the strains tested. Regarding the assays against strains of Candida albicans ATCC 90028 and according to the results presented in Table 1, esters 1, 2, 6, 8, 11, and 12 were bioactive; the others were inactive. It was observed that the ester methyl 4-chlorocinnamate (1), structurally the simplest ester of all the preparations (MIC = 5.09 μmol/mL), presented antifungal activity at its highest tested concentration, an activity reported by [32]. Substitution using an ethyl group produced a slight increase in antifungal activity against this strain. Compound ethyl 4-chlorocinnamate (2) presented a MIC = 4.75 μmol/mL, as compared with compound 1, presenting slightly higher activity. There was loss of biological activity when increasing alkyl side chain length as seen in esters 3, 4, and 5, which suggests that increasing alkyl side chain length when formed by three or four carbon atoms results in inactivity.

CompoundsCandida albicansCandida glabrataCandida kruseiCandida guilliermondii
ATCC 90028ATCC 90030ATCC 34135ATCC 22017

15.09 μmol/mL5.09 μmol/mL+1.27 μmol/mL

24.75 μmol/mL4.75 μmol/mL4.75 μmol/mL1.19 μmol/mL

3+++2.22 μmol/mL

4+++2.22 μmol/mL

5+4.19 μmol/mL+2.09 μmol/mL

62.08 μmol/mL2.08 μmol/mL4.16 μmol/mL0.13 μmol/mL

7+3.96 μmol/mL+1.98 μmol/mL

83.10 μmol/mL3.10 μmol/mL3.10 μmol/mL1.55 μmol/mL

9+++0.40 μmol/mL

10+++0.41 μmol/mL

111.58 μmol/mL1.58 μmol/mL0.78 μmol/mL0.024 μmol/mL

122.85 μmol/mL2.85 μmol/mL2.85 μmol/mL1.42 μmol/mL

Control of the environment----

Nystatin0.00043 μmol/mL0.00043 μmol/mL0.00043 μmol/mL0.00043μmol/mL

Control of the microorganism++++

(+) indicates growth of the microorganism; (-) no growth microorganism.

CompoundsCandida albicansCandida glabrataCandida kruseiCandida guilliermondi
(ATCC 90028)(ATCC 90030)(ATCC 34135)(ATCC 22017)













(+) The compounds present no MFC.
MFC/MIC relation ≥ 4: fungistatic activity. MFC/MIC < 4: fungicidal activity [14].
MFC: minimal fungicidal concentration; MIC: minimum inhibitory concentration.

The ester 2-methoxyethyl 4-chlorocinnamate (6) contains in its side chain a heteroatom presenting a MIC = 2.08 μmol/mL. When comparing this compound with ester 2 it can be inferred that the presence of a heteroatom in the lateral alkyl chain results in better bioactivity. No activity was observed for the ester pentyl 4-chlorocinnamate (7), in which the lateral alkyl chain was lengthened, formed by five carbon atoms. An increase in lipophilicity resulted in the inactivity for the molecule. Yet with a ten-carbon chain, the ester decyl 4-chlorocinnamate (8) at its highest concentration, MIC = 3.10 μmol/mL, inhibited growth of the tested strain. Comparing compound 8 with 4′-chlorobenzyl 4-chlorocinnamate (9) and with 4′-methoxybenzyl 4-chlorocinnamate (10) which presented no bioactivity suggests that exchanging a ten-carbon chain with an aromatic ring does not result in antifungal activity.

The perillyl 4-chlorocinnamate ester (11) presented a MIC = 1.58 μmol/mL, the best result against the C. albicans tested strain. This is due to the presence of the terpenic substructure. It is reported that terpenes present a good antifungal profile [3335]. Comparing ester 11 to dodecyl 4-chlorocinnamate (12), MIC = 2.85 μmol/mL, it can be inferred that exchanging an unsaturated alicyclic with a saturated acyclic chain diminishes the bioactivity of the compound. According to the results of the MFC/MIC ratio esters 1, 2, 6, 8, 11, and 12 possess fungicidal activity, as seen in Table 2.

Considering the results against Candida glabrata strain (ATCC 90030) of the twelve esters tested, compounds 1, 2, 5, 6, 7, 8, 11, and 12 present bioactivity against the strain. Using compound 1 as a base, presenting fungal inhibition at its highest concentration tested (MIC = 5.09 μmol/mL), compound 2 was also bioactive at its highest concentration tested (MIC = 4.75 μmol/mL). Yet side chains containing three carbon atoms such as in esters 3 and 4, respectively, either straight or branched chains, present no bioactivity.

Comparing the nonactive propyl 4-chlorocinnamate (3) with butyl 4-chlorocinnamate (5) it can be inferred that the slight increase of CH2 in the side chain of compound 5 provided bioactivity, suggesting that the increase from three to four carbon atoms in the side chain resulted in increased lipophilicity; i.e., the substance may bind to cell membrane sterols and thus cause outflows of cellular constituents and even cell death. This assertion, however, applies only to specific carbon chain lengths, depending on several factors involving both the molecule and the microorganism tested.

Considering ester 5 as compared to ester 6, it may be suggested that the presence of a heteroatom such as an oxygen on the side chain of the compound results in greater bioactivity, since compound 6 presented a MIC = 2.08 μmol/mL, being 1/2 that of 5 (MIC = 4.19 μmol/mL), thus more potency. The activity decreases when a heteroatom containing side chain is exchanged for chains with five or ten carbons, as was the case for compounds 7 and 8 (presenting MICs = 3.96 μmol/mL and 3.10 μmol/mL, respectively), suggesting that the presence of an oxygen in the side chain of the ester provides it with a better antifungal profile.

Comparing compound 8 with the ester 4-chlorobenzyl 4-chlorocinnamate (9) and with 4-methoxybenzyl 4-chlorocinnamate (10), the two aromatic esters were inactive against this C. glabrata strain. When comparing to alkyl esters, we infer that the aryl esters tested for presenting a voluminous group close to the carbonyl present no antifungal activity; interaction of the aryl esters with their biological target is more difficult. When comparing compound 11 (presenting the best bioactivity in relation to the C. glabrata strain and obtaining a MIC = 1.58 μmol/mL) to compound 12 (presenting decreased activity) and exchanging an unsaturated alicyclic substituent (a terpenic substructure) with a saturated acyclic chain, compound 12 bioactivity decreased, presenting a MIC of 2.85 μmol/mL. For this C. glabrata strain, the compounds that presented bioactivity were 1, 2, 5, 6, 7, 8, 11, and 12, all of which presented the ability to inhibit the growth of the strain as well as exhibiting fungicidal activity according to their MFC/MIC ratio.

Of the results involving the Candida krusei strain (ATCC 34135), the compounds that presented bioactivity were 2, 6, 8, 11, and 12. Comparing compounds 1 and 2, compound 1 presented no activity against this strain. Addition of a methylene group in the side chain conferred bioactivity (at highest concentration for compound 2). However, carbon chain increases such as in 3, 4, and 5 resulted in inactivity against this C. krusei strain. When a heteroatom was added to the molecule as in compound 6, bioactivity was observed at the highest concentration tested, MIC = 4.16 μmol/mL. Such activity does not occur when a lateral chain formed by five carbon atoms is present, as in compound 7, which is inactive against the C. krusei strain. Comparing 7 and 8 it can be observed that substitution of a five-carbon atom side chain with a ten-carbon atom side chain yields antifungal activity MIC = 3.10 μmol/mL. While comparing ester 8 with 9 and 10, there was loss of bioactivity (as occurred in the two previous strains). Exchanging a linear alkyl side chain using aryl groups resulted in an inactive compound. Analyzing compounds 10 and 11 against the C. krusei strain, when exchanging an aryl substituent with an unsaturated alicyclic substituent (for compound 11; MIC = 0.78 μmol/mL), the derivative presented the best antifungal activity of all the esters tested. In analyzing esters 11 and 12, it was observed that substitution of the unsaturated alicyclic chain with a linear saturated acyclic chain generates diminished biological potency (about three times smaller). The presence of a terpenic substructure potentiates antifungal action. In relation to the C. krusei strain tested, the esters that presented activity were 2, 6, 8, 11, and 12. In addition, inhibiting fungal growth, they obey the MFC/MIC ratio to present fungicidal activity.

In the present work, Candida guilliermondii ATCC 22017 was the most susceptible microorganism; thus all of the esters tested were bioactive. Esters 1 (MIC = 1.27 μmol/mL) and 2 (MIC = 1.19 μmol/mL) presented similar antifungal potency. Comparing compound 2 with 3, 4, and 5, we observed a decline in activity, MIC = 2.22 μmol/mL, for compounds 3 and 4, and for compound 5 the MIC = 2.09 μmol/mL. Comparing compound 5 with 6, we note a bioactivity increase (lowering MIC to 0.13 μmol/mL), which is the second best result of the study. It can be inferred that the exchange of a methylene group with oxygen gives the molecule greater antifungal potency, possibly by increasing electronic affinity, which can be considered a main factor in determining better antimicrobial activity [36].

Analyzing ester compound 6 with compounds 7 and 8, it was observed that more extensive carbon side chains (of five and ten carbon atoms, respectively) and absence of a heteroatom diminished compound activity, MICs of 1.98 μmol/mL and 1.55 μmol/mL, respectively. Comparing compound 8 with 9 and 10, it was observed that converting an extended alkyl chain to para-chlorinated aromatic ring or to para-methoxylated aromatic ring yields molecules with better bioactivity (MICs = 0.40 and 0.41 μmol/mL, respectively), roughly four times more active than compound 8.

Ester 11 presented the best activity of all the tested compounds, obtaining a MIC = 0.024 μmol/mL against the C. guilliermondii strain. This may be due to the fact that the substance presents a terpenic substructure, which conferred greater antifungal activity than all of the other tested compounds. It has been reported that terpenes present good antifungal profiles [3335]. Comparing the results of 11 and 12, the latter presenting a MIC = 1.42 μmol/mL, it was noted that the presence of a terpenic group made the compound more active against the C. guilliermondii strain, than if a saturated acyclic side chain was present. Thus, analyzing the results against the C. guilliermondii strain, it was observed that all twelve esters presented inhibitory activity. However, compounds 7 and 12 presented no fungicidal activity (Table 2).

3.2.2. Bioactivity of Tested Compounds against the Pathogenic Bacteria.

The use of Pseudomonas aeruginosa and Staphylococcus aureus in this study is justified because they are associated with infection in a hospital environment [37]. According to the antibacterial assays performed with the twelve esters derived from 4-chlorocinnamic acid, only the ester methyl 4-chlorocinnamate (1) was able to inhibit the growth of the S. aureus ATCC 25925 strain (at the highest concentration tested), MIC = 5.09 μmol/mL. It has been reported by TONARI et al. (2002) [38] that 4-chlorocinnamic acid presents activity against bacterial strains. However, a slight increase in the lipophilicity of the molecule resulted in activity loss; for esters 2 through 12, inhibitory action was not observed, as seen in Table 3.

CompoundsPseudomonas aeruginosaPseudomonas aeruginosaStaphylococcus aureusStaphylococcus aureus
ATCC 8027102ATCC 2592547

1++5.09 μmol/mL+












Control of the environment----

Chloramphenicol0.3095 μmol/mL0.3095 μmol/mL0.3095 μmol/mL0.3095 μmol/mL

Control of the microorganism++++

(+) indicates growth of the microorganism; (-) no microorganism growth.
3.3. Molecular Modelling

The antifungal potency of the 4-chlorocinnamic acid esters was investigated using the chimeric enzyme. The modeled structure was energetically minimized and was subjected to molecular docking analysis using Molegro Virtual Docker (MVD 2010.4.1.0).

The chimeric enzyme along with ligand, heme cofactor, and water molecules was imported in the MVD software. The site having ligand, nearer to heme cofactor, was preferred as the best region for the binding of the prepared compounds. Docking was carried out involving 10 independent docking runs for each compound on the active site of 14α-demethylase [28].

The protein-ligand interaction was screened via the docking score function, i.e., Mol Dock Score, PLANTS Score, and Rerank Score. The predicted binding energy and other docking results of the esters are tabulated in Table 4 and Figure 1.

CompoundsPLANT ScoreM. Dock ScoreRerank ScoreAmino acidGroup involvedDistance (Å)

1-76.5806-92.0557-65.2081H2O175 (O)CO(O)3.11

2-71.2322-98.2911-32.276Thr 260 (O)CO(O)3.22
H2O87 (O)CO(O)2.66

3-78.216-93.7199-71.2272H2O87 (O)CO(O)3.01

4-73.6695-95.7275-61.0177H2O87 (O)CO(O)3.08
Thr 260 (O)CO(O)3.07

5-82.0128-105.117-76.2732H2O87 (O)CO(O)3.00
Thr 260 (O)CO(O)2.98

6-77.3574-93.9184-71.3815H2O175 (O)CO(O)2.76
H2O87 (O)O-22.87

7-83.0449-118.622-86.715H2O87 (O)CO(O)2.96

8-92.9589-140.652-102.107Thr 260 (O)CO(O)2.97
H2O87 (O)CO(O)3.00
H2O87 (O)O3.34

9-84.0241-108.849-84.857H2O175 (O)CO(O)2.82

10-77.7839-113.068-59.4905Gln 72 (N)CO(O)2.69
H2O175 (O)CO(O)3.12
H2O175 (O)O-13.31
H2O87 (O)O-23.52

11-85.142-115.206-85.2394Gln 72 (N)CO(O)2.98
H2O175 (O)O3.09

12-81.6806-131.112-91.5155H2O175 (O)O3.59

The docking scores indicated that the esters can act as potential inhibitors of 14α-demethylase enzyme. The molecular modeling studies depicted that most of the synthesized derivatives exhibited interaction with the protein residue and two protein residues were necessary for ligand binding, namely, Gln 72 and Thr 260. The protein-ligand interaction is attributed to the binding potency of ligand with the protein. The molecular docking results confirmed the interactions of synthesised 4-chlorocinnamic acid esters with the active site of cytochrome P450 14α-demethylase and depicted that the esters can be further explored for antifungal potency. In fact, the use of this enzyme as a possible site of antifungal action has virtually confirmed the bioactivity of several chemical classes, for example, 2-mercaptoimidazoles [28]. Figure 2 shows a summary of the main aspects of the antimicrobial structure-activity relationship of the twelve esters tested.

4. Conclusion

Of the twelve esters prepared, only the structurally simpler compound, methyl 4-chlorocinnamate (1), presented activity against S. aureus strain ATCC 25925 at the highest concentration tested. For antifungal activity, all of the compounds were active. Considering the four strains tested: Candida albicans ATCC 90028, Candida glabrata ATCC 90030, Candida krusei ATCC 34125 and Candida guilliermondii 207, compounds 6 and 11 presented good activity against all strains tested as highlighted, especially for C. guilliermondii 207. The molecular modeling study revealed good affinity of the esters with the possible biological target related to anti-Candida activity. The presence of a heteroatom in the carbon chain, or a terpenic substructure, results in esters with better antifungal profiles. Thus, esters prepared from 4-chlorocinnamic acid may be employed for antifungal compound studies.

Data Availability

The article data used to support the findings of this study titled “Antimicrobial Activity of 4-Chlorocinnamic Acid Derivatives” have been deposited in the Federal University of Paraíba repository

Conflicts of Interest

The authors declare that they have no conflicts of interest.


This work was supported by the Brazilian agencies: Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES).


  1. I. C. Bygbjerg, “Double burden of noncommunicable and infectious diseases in developing countries,” Science, vol. 337, no. 6101, pp. 1499–1501, 2012. View at: Publisher Site | Google Scholar
  2. R. J. Coker, B. M. Hunter, J. W. Rudge, M. Liverani, and P. Hanvoravongchai, “Emerging infectious diseases in southeast Asia: regional challenges to control,” The Lancet, vol. 377, no. 9765, pp. 599–609, 2011. View at: Publisher Site | Google Scholar
  3. Y. Nakajima, J. Ishibashi, F. Yukuhiro, A. Asaoka, D. Taylor, and M. Yamakawa, “Antibacterial activity and mechanism of action of tick defensin against Gram-positive bacteria,” Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 1624, no. 1-3, pp. 125–130, 2003. View at: Publisher Site | Google Scholar
  4. B. M. De Almeida, G. L. Breda, F. Queiroz-Telles, and F. F. Tuon, “Positive tip culture with candida and negative blood culture: To treat or not to treat? A systematic review with meta-analysis,” Infectious Diseases, vol. 46, no. 12, pp. 854–861, 2014. View at: Publisher Site | Google Scholar
  5. T. P. McCarty and P. G. Pappas, “Invasive candidiasis,” Infectious Disease Clinics of North America, vol. 30, no. 1, pp. 103–124, 2016. View at: Publisher Site | Google Scholar
  6. T. Wang, J. Shao, W. Da et al., “Strong synergism of palmatine and fluconazole/itraconazole against planktonic and biofilm cells of candida species and efflux-associated antifungal mechanism,” Frontiers in Microbiology, vol. 9, 2018. View at: Publisher Site | Google Scholar
  7. Y.-L. Yang, “Virulence factors of Candida species,” Journal of Microbiology, Immunology and Infection, vol. 36, no. 4, pp. 223–228, 2003. View at: Google Scholar
  8. R. L. F. Silva, “Chapter 8 - Fungal infections in immunocompromised patients,” Jornal Brasileiro de Pneumologia, vol. 36, no. 1, pp. 142–147, 2010. View at: Publisher Site | Google Scholar
  9. J. C. De Araujo, E. De O. Lima, B. S. O. de Ceballos, K. R. de L. Freire, E. L. de Souza, and L. Santos Filho, “Ação antimicrobiana de óleos essenciais sobre microrganismos potencialmente causadores de infecções oportunistas,” Revista de Patologia Tropical, vol. 33, no. 1, pp. 55–64, 2007. View at: Publisher Site | Google Scholar
  10. R.-J. Bensadoun, L. L. Patton, R. V. Lalla, and J. B. Epstein, “Oropharyngeal candidiasis in head and neck cancer patients treated with radiation: update 2011,” Supportive Care in Cancer, vol. 19, no. 6, pp. 737–744, 2011. View at: Publisher Site | Google Scholar
  11. A. L. Colombo, T. Guimarães, L. F. A. Camargo et al., “Brazilian guidelines for the management of candidiasis - a joint meeting report of three medical societies: Sociedade Brasileira de Infectologia, Sociedade Paulista de Infectologia and Sociedade Brasileira de Medicina Tropical,” The Brazilian Journal of Infectious Diseases, vol. 17, no. 3, pp. 283–312, 2013. View at: Publisher Site | Google Scholar
  12. J.-R. Ioset, A. Marston, M. P. Gupta, and K. Hostettmann, “Antifungal and larvicidal compounds from the root bark of Cordia alliodora,” Journal of Natural Products, vol. 63, no. 3, pp. 424–426, 2000. View at: Publisher Site | Google Scholar
  13. R. Montes, A. Perez, C. Medeiros et al., “Synthesis, antifungal evaluation and in silico study of n-(4-halobenzyl)amides,” Molecules, vol. 21, no. 12, p. 1716, 2016. View at: Publisher Site | Google Scholar
  14. Z. N. Siddiqui, F. Farooq, T. N. M. Musthafa, A. Ahmad, and A. U. Khan, “Synthesis, characterization and antimicrobial evaluation of novel halopyrazole derivatives,” Journal of Saudi Chemical Society, vol. 17, no. 2, pp. 237–243, 2013. View at: Publisher Site | Google Scholar
  15. M. O. De Farias, T. C. Lima, A. L. A. L. Pérez et al., “Antifungal activity of ester derivatives from caffeic acid against Candida species,” International Journal of Pharmacy & Pharmaceutical Research, vol. 7, no. 1, pp. 151–159, 2016. View at: Google Scholar
  16. P. Boeck, M. M. Sá, B. S. De Souza et al., “A simple synthesis of kaurenoic esters and other derivatives and evaluation of their antifungal activity,” Journal of the Brazilian Chemical Society, vol. 16, no. 6 B, pp. 1360–1366, 2005. View at: Publisher Site | Google Scholar
  17. X. Li, W. Eli, and G. Li, “Solvent-free synthesis of benzoic esters and benzyl esters in novel Brønsted acidic ionic liquids under microwave irradiation,” Catalysis Communications, vol. 9, no. 13, pp. 2264–2268, 2008. View at: Publisher Site | Google Scholar
  18. J. G. Handique, D. Mahanta, A. Devi, and M. P. Boruah, “Synthesis and electrochemical behavior of some dendritic polyphenols as antioxidants,” Letters in Organic Chemistry, vol. 10, no. 1, pp. 53–59, 2013. View at: Publisher Site | Google Scholar
  19. B. Neises and W. Steglich, “Simple method for the esterification of carboxylic acids,” Angewandte Chemie International Edition, vol. 17, no. 7, pp. 522–524, 1978. View at: Publisher Site | Google Scholar
  20. R. Cleland and E. Squires, “Evalution of new antimicrobials in vitro and in experimental animal infections,” in Antibiotics in Laboratory Medicine, V. M. D. Lorian, Ed., pp. 739–788, Willians & Wilkins, 1991. View at: Google Scholar
  21. P. F. Nascimento, A. C. Nascimento, C. S. Rodrigues et al., “Atividade antimicrobiana dos óleos essenciais: uma abordagem multifatorial dos métodos,” Revista Brasileira de Farmacognosia, vol. 17, no. 1, pp. 108–113, 2007. View at: Publisher Site | Google Scholar
  22. O. P. Fde, J. M. Mendes, I. O. Lima, K. S. Mota, W. A. Oliveira, and O. L. Ede, “Antifungal activity of geraniol and citronellol, two monoterpenes alcohols, against Trichophyton rubrum involves inhibition of ergosterol biosynthesis,” Pharmaceutical Biology, vol. 53, no. 2, pp. 228–234, 2015. View at: Publisher Site | Google Scholar
  23. L. R. Peixoto, P. L. Rosalen, G. L. S. Ferreira et al., “Antifungal activity, mode of action and anti-biofilm effects of Laurus nobilis Linnaeus essential oil against Candida spp,” Archives of Oral Biolog, vol. 73, pp. 179–185, 2017. View at: Publisher Site | Google Scholar
  24. Clinical and Laboratory Standards Institute (CLSI), Protocol M27-A2. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts, NCCLS, Pa, USA, 2nd edition, 2002.
  25. D. P. Deswal and U. Chand, “Standardization of the tetrazolium test for viability estimation in rice bean (Vigna umbellate T.),” Seed Science and Technology, vol. 25, pp. 409–417, 1997. View at: Google Scholar
  26. I. Rasooli and M. R. Abyaneh, “Inhibitory effects of Thyme oils on growth and aflatoxin production by Aspergillus parasiticus,” Food Control, vol. 15, no. 6, pp. 479–483, 2004. View at: Publisher Site | Google Scholar
  27. P. Gerhardt, R. G. E. Murray, W. A. Wood, and N. R. Krieg, “Methods for general and molecular bacteriology, Washington,” American Society for Microbiology, p. 791, 1994. View at: Google Scholar
  28. N. Rani and R. Singh, “Molecular modeling investigation of some new 2-mercaptoimidazoles,” Current Computer-Aided Drug Design, vol. 13, no. 1, pp. 48–56, 2017. View at: Publisher Site | Google Scholar
  29. P. Pais, M. Galocha, R. Viana, M. Cavalheiro, D. Pereira, and M. C. Teixeira, “Microevolution of the pathogenic yeasts Candida albicans and Candida glabrata during antifungal therapy and host infection,” Microbial Cell, vol. 6, no. 3, pp. 142–159, 2019. View at: Publisher Site | Google Scholar
  30. A. L. Colombo, J. N. D. A. Júnior, and J. Guinea, “Emerging multidrug-resistant Candida species,” Current Opinion in Infectious Diseases, vol. 30, no. 6, pp. 528–538, 2017. View at: Publisher Site | Google Scholar
  31. T. M. Wozniak, E. J. Bailey, and N. Graves, “Health and economic burden of antimicrobial-resistant infections in Australian hospitals: a population-based model,” Infection Control & Hospital Epidemiology, vol. 40, no. 3, pp. 320–327, 2019. View at: Publisher Site | Google Scholar
  32. T. C. Lima, A. R. Ferreira, D. F. Silva, E. O. Lima, and D. P. de Sousa, “Antifungal activity of cinnamic acid and benzoic acid esters against Candida albicans strains,” Natural Product Research (Formerly Natural Product Letters), vol. 32, no. 5, pp. 572–575, 2018. View at: Publisher Site | Google Scholar
  33. R. D. Castro, Atividade antifúngico do óleo essencial de Cinnamomum zeylanicum Blume (Canela) e de sua associação com antifúngicos sintéticos sobre espécies de Candida, Tese. Universidade Federal da Paraíba, João Pessoa, 2010.
  34. A. Saad, M. Fadli, M. Bouaziz, A. Benharref, N.-E. Mezrioui, and L. Hassani, “Anticandidal activity of the essential oils of Thymus maroccanus and Thymus broussonetii and their synergism with amphotericin B and fluconazol,” Phytomedicine, vol. 17, no. 13, pp. 1057–1060, 2010. View at: Publisher Site | Google Scholar
  35. A. G. Tempone, P. Sartorelli, D. Teixeira et al., “Brazilian flora extracts as source of novel antileishmanial and antifungal compounds,” Memórias do Instituto Oswaldo Cruz, vol. 103, no. 5, pp. 443–449, 2008. View at: Publisher Site | Google Scholar
  36. B. Narasimhan, D. Belsare, D. Pharande, V. Mourya, and A. Dhake, “Esters, amides and substituted derivatives of cinnamic acid: Synthesis, antimicrobial activity and QSAR investigations,” European Journal of Medicinal Chemistry, vol. 39, no. 10, pp. 827–834, 2004. View at: Publisher Site | Google Scholar
  37. S. Z. Sadrossadati, M. Ghahri, A. A. Fooladi, S. Sayyahfar, S. Beyraghi, and Z. Baseri, “Phenotypic and genotypic characterization of Candida species isolated from candideamia in Iran,” Current Medical Mycology, vol. 4, no. 2, 2018. View at: Publisher Site | Google Scholar
  38. K. Tonari, K. Mitsui, and K. Yonemoto, “Structure and antibacterial activity of cinnamic acid related compounds,” Journal of Oleo Science, vol. 51, no. 4, pp. 271–273, 2002. View at: Publisher Site | Google Scholar

Copyright © 2019 Rayanne H. N. Silva 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.

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