Design, synthesis, and antimelanogenic effects of (2-substituted phenyl-1,3-dithiolan-4-yl)methanol derivatives

Contact: Audrey Hu Whatsapp/hp: 0086 13880143964 Email: audrey.hu@wecistanche.com

Do Hyun Kim1 Su Jeong Kim1 Sultan Ullah1 Hwi Young Yun1 Pusoon Chun2 Hyung Ryong Moon1

Abstract: The authors designed and synthesized 17 (2-substituted phenyl-1,3-dithiolan-4-yl) methanol (PDTM) derivatives to find a new chemical scaffold, showing excellent tyrosinase-inhibitory activity. Their tyrosinase-inhibitory activities were evaluated against mushroom tyrosinase at 50 μM, and five of the PDTM derivatives (PDTM3, PDTM7–PDTM9, and PDTM13) were found to inhibit mushroom tyrosinase more than kojic acid or arbutin, the positive controls. Of seventeen PDTMs, PDTM3 (half-maximal inhibitory concentration 13.94±1.76 μM), with a 2,4-dihydroxyphenyl moiety, exhibited the greatest inhibitory effects (kojic acid half-maximal inhibitory concentration 18.86±2.14 μM). Interestingly, PDTM compounds with no hydroxyl group, PDTM7–PDTM9, also had stronger inhibitory activities than kojic acid. In silico studies of interactions between tyrosinase and the five PDTMs suggested their binding affinities were closely related to their tyrosinase-inhibitory activities. Cell-based experiments performed using B16F10 mouse-skin melanoma cells showed that PDTM3 effectively inhibited melanogenesis and cellular tyrosinase activity. A cell-viability study conducted using B16F10 cells indicated that the antimelanogenic effect of PDTM3 was not attributable to its cytotoxicity. Kinetic studies showed PDTM3 competitively inhibited tyrosinase, indicating binding to the tyrosinase-active site. We found that PDTM3 with a new chemical scaffold could be a promising candidate for skin-whitening agents and that the 1,3-dithiolane ring could be used as a chemical scaffold for potent tyrosinase inhibition.Keywords: tyrosinase inhibitor, melanogenesis, 1,3-dithiolane, PDTM

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Introduction

For the past few decades, tyrosinase inhibitors have been of considerable interest, due to the key role played by tyrosinase in melanogenesis. Melanin is produced using a combination of enzymatically catalyzed and chemical reactions. The biosynthetic pathway responsible for melanin production was initially elucidated by Raper1 and Mason2 and recently modified by Cooksey et al3 and Schallreuter et al.4 Melanogenesis is initiated by the enzyme tyrosinase, which catalyzes the first two oxidative steps in the melanin biosynthetic pathway: the oxidations of l-tyrosine to l-dopa followed by l-dopa to l-dopaquinone (Figure 1). These two steps are also the rate-determining steps in melanin biosynthesis because physiological pH can continue spontaneously subsequent steps.5 The dopaquinone produced in the second step is converted to cysteinyldopa by glutathione or cysteine, and finally to pheomelanin, which is responsible for yellow to red colors of mammal skin, or to dopachrome by auto-oxidation and finally eumelanin, which is responsible for brown/black colors of mammal skin (Figure 1). Melanin protects human skin from harmful ultraviolet radiation and also determines the phenotypic appearance. On the other hand, excessive melanin accumulation in the skin can cause hyperpigmentation-associated diseases and cosmetic problems, such as freckles, melasma, and senile lentigines.

Tyrosinase is widely distributed in bacteria, fungi, insects, plants, and animals, including humans, and is responsible for the colors of human skin and hair and the undesirable browning of fruit and vegetables.6 Undesirable enzymatic browning and diseases associated with hyperpigmentation in the skin have encouraged scientists to seek novel potent tyrosinase inhibitors for use as skin-whitening and antibrowning agents. Many tyrosinase inhibitors have been discovered to date,7–9 but relatively few have been approved as skin-whitening materials, due to safety concerns or weak whitening effects.

In our previous studies, on the basis of structures of l-tyrosine and l-dopa, natural substrates of tyrosinase, we designed two potential tyrosinase inhibitors with a thiazolidine ring (MHY384 and MHY794; Figure 1) and synthesized them by condensation of an appropriate benzaldehyde and l-cysteine or cysteamine hydrochloride. These two compounds were identified to be potent competitive tyrosinase inhibitors and to effectively reduce melanogenesis in HRM2 hairless mice.10,11 In addition to directly inhibiting tyrosinase activity, MHY384 inhibited tyrosinase expression by suppressing the cyclic adenosine monophosphate–PKA10 and NO-induced cyclic guanosine monophosphate–PKG12,13 pathways, and MHY794 also suppressed tyrosinase expression induced by NO-mediated melanogenesis signaling.11 These positive results and the fact that divalent –S– is a classical isostere of divalent –NH– encouraged us to synthesize derivatives with a dithiolane ring as a surrogate for the thiazolidine ring commonly existing in MHY384 and MHY794, in order to find novel tyrosinase inhibitors.

In the present study, as part of our ongoing efforts to find a new and strong chemical scaffold for inhibition of tyrosinase and develop new tyrosinase inhibitors, we synthesized a class of structurally novel (2-substituted phenyl-1,3-dithiolan-4-yl) methanol (PDTM) derivatives (Figure 1) and investigated their antimelanogenic effects using mushroom tyrosinase and cell-based assays. In this study, kojic acid and arbutin were used as a positive control for tyrosinase-inhibitory activity, because kojic acid is one of the most commonly used positive controls for the evaluation of tyrosinase inhibition and arbutin is clinically used as a whitening agent.

Materials and methods

Materials

Unless otherwise noted, all commercially available reagents – l-tyrosine (code T3754), l-dopa (code PHR1271), kojic acid (code K3125), MTT (3-(4,5-dimethyl-2-thiazolyl)- 2,5-diphenyl-2H-tetrazolium bromide) (code M2128), PMSF (phenylmethylsulfonyl fluoride) (code P7626), Triton X-100 (4-(1,1,3,3-tetramethylbutyl)phenylpolyethylene glycol) (code T8787), potassium hydrogen phosphate (code P9666), potassium dihydrogen phosphate (code PHR1330), 2,3-dimercapto-1-propanol (code 64046), 1,4-dioxane (code 296309), sulfuric acid (code 339741), and benzaldehydes – were purchased from Sigma-Aldrich (St Louis, MO, USA). Fetal bovine serum, Dulbecco’s Modified Eagle’s Medium, phosphate-buffered saline (PBS), penicillin, streptomycin, and trypsin were purchased from Thermo Fisher Scientific (Waltham, MA, USA). Mushroom tyrosinase (code T3824) and α-melanocyte-stimulating hormone (α-MSH; code M4135) were also purchased from Sigma-Aldrich. 1 H and 13C nuclear magnetic resonance (NMR) spectra were recorded on Varian Unity Inova 400 and Varian Unity AS 500 instruments (Agilent Technologies, Santa Clara, CA, USA). Low-resolution mass spectrometry (MS) and high-resolution MS data were obtained on an Expression CMS (Advion, Ithaca, NY, USA) and a 6530 Accurate Mass quadrupole time-of-flight liquid-chromatography mass spectrometer (Agilent), respectively. Synthesis of PDTM1–PDTM17 was accomplished in our laboratory.

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General procedure for the synthesis of PDTM1–PDTM17

To a stirred solution of 2,3-dimercapto-1-propanol (100 mg, 0.80 mmol) in 1,4-dioxane (1 mL) were added a solution of sulfuric acid (0.1 equivalence) in 1,4-dioxane (1 mL) and an appropriate benzaldehyde (1.1 equivalence) subsequently. After being stirred at room temperature for 10 minutes, the reaction mixture was stirred at 70°C for 40 minutes to 1 hour. The mixture was then partitioned between ethyl acetate and water, and the organic layer was dried over anhydrous MgSO4, filtered, and evaporated. The residue obtained was purified using silica-gel column chromatography to give pure PDTM products: PDTM1–PDTM17.14 Structural characterization (1 H and 13C NMR and mass data of all PDTMs and 1-D and 2-D NMR spectra of some PDTMs) of synthesized compounds are provided in Supplementary materials.

Inhibition of mushroom tyrosinase by PDTM1–PDTM17

The inhibitory effects of PDTM analogues on mushroom tyrosinase were explored with minor modifications, as described previously in our work.15 Each compound (10 μL, final concentration 50 μM) was mixed with substrate solution (170 µL), prepared from 14.7 mM potassium phosphate buffer (pH 6.5) and 293 µM l-tyrosine solution (1:1, v/v), in each well of a 96-well plate. To each well, mushroom tyrosinase solution (20 μL, 1,000 U/mL) was added and incubated for 30 minutes at 37°C. Contents of dopachrome formed in wells were determined by measuring optical densities at 475 nm using a VersaMax microplate reader (Molecular Devices, Sunnyvale, CA, USA). Kojic acid and arbutin were used as positive controls. All experiments were performed in triplicate. Inhibition rates of tyrosinase were calculated thus:

Inhibition (%) = × 100 [ ( 1 − A B/ )] (1)

where A indicates the optical density of the test compound and B represents the optical density of the control.

Half-maximal inhibitory concentration (IC50) is the concentration of a compound that inhibits a standard 50% response. IC50 is derived from the x-axis on an inhibitor-concentration versus product-formation curve and is determined from the alignment of the dose-response curve on the dependent y-axis. In the present study, dose-dependent inhibition experiments were performed in triplicate to determine the IC50 of compounds. According to the inhibition percentage of five doses (final concentration 10, 20, 30, 40, and 50 µM) in each experiment, the log-linear curves and their equations were determined. Individual IC50 values were then calculated as the concentration when the y-axis equaled 50% inhibition. The results from the three experiments are shown.

Analysis of the nature of mushroom tyrosinase inhibition

To elucidate the nature of the inhibitory effect of PDTM3 on mushroom tyrosinase, kinetic studies were performed. PDTM3 (10 μL [0, 5, 10, or 25 μM final concentration]) was added to 170 µL l-tyrosine solution (0.5, 1, 2, or 4 mM final concentration) and then mixed with mushroom tyrosinase solution (20 μL, 1,000 U/mL) in each well of a 96-well plate. After the mixture was incubated for 30 minutes at 37°C, the contents of dopachrome produced in wells were determined by measuring optical densities at 475 nm using a microplate reader. All experiments were carried out in triplicate. For the determination of the nature of inhibition, a Lineweaver–Burk plot was used.

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Docking simulation of PDTM3 or kojic acid with tyrosinase

The in silico docking simulation of protein-ligand was performed with AutoDock Vina using a systematic search technique and the 3-D structure of Agaricus bisporus tyrosinase (Protein Data Bank ID 2Y9X).16,17 In the crystal structure of tyrosinase, the binding site of l-tyrosine was used as a docking pocket. Simulation results were obtained from docking between tyrosinase and synthetic compounds (PDTM3, PDTM7, PDTM8, PDTM9, and PDTM13) or kojic acid. Before performing docking simulation with the compounds, 2-D structures of compounds were transformed into 3-D structures, charges of compounds were determined, and hydrogen atoms were inserted using ChemOffice. LigandScout 3.1.2 was used for the prediction of possible interactions between ligands and tyrosinase and the identification of pharmacophores. Docking-simulation images of 17 PDTMs are provided in Supplementary materials.

Determination of melanogenesis level in B16F10 cells

Melanin-content assays with minor modifications were used in B16F10 cells for the inhibitory effects of PDTM3 on melanogenesis.19 Cells seeded at a density of 5×104 cells/well in a 24-well plate were allowed to adhere at 37°C in a humidified atmosphere containing 5% CO2 overnight. The following day, the cells were exposed to α-MSH (1 µM) and PDTM3 (0, 5, 10, or 25 μM) or kojic acid (25 μM), and the plate was incubated for 24 hours under the same conditions. After being washed twice with PBS, the cells were detached by incubation at 60°C in 200 μL of 1 N NaOH for 1 hour. The lysates were moved to a 96-well plate and optical densities were measured at 405 nm by an enzyme-linked immunosorbent assay reader for calculation of mean percentage inhibitions of kojic acid and PDTM3. All experiments were carried out in triplicate.

Tyrosinase-activity assay in B16F10 cells

By estimating the oxidation rate of l-dopa, tyrosinase activities were evaluated with minor modifications, as described in the previous work.20 Cells seeded at a density of 5×104 cell/well in a 24-well plate were allowed to adhere at 37°C in a humidified atmosphere containing 5% CO2 for 24 hours. The cells were exposed to α-MSH (1 µM) and PDTM3 (0, 5, 10, or 25 μM) or kojic acid (25 μM), and the plate was incubated under the same conditions for 24 hours. After being rinsed twice with PBS, the cells were lysed with 100 μL lysis buffer containing 0.1 mM PMSF (5 μL), 50 mM PBS (90 μL, pH 6.8), and 1% Triton X-100 (5 μL) and frozen at -80°C for 30 minutes. Lysates were thawed and centrifuged at 12,000 g for 30 minutes at 4°C and supernatants (80 μL) were combined with 10 mM l-dopa (20 μL) in a 96-well plate, which was then incubated for 30 minutes at 37°C. Optical densities were calculated at 500 nm, and the inhibitory activities of tyrosinase were determined thus:

Inhibition (%) = × 100 ([A−B] − [C−D] /[ A−B ] ) (2)

where B and A are the optical densities of the blank before and after incubation, respectively, and D and C are the optical densities of the test compound before and after incubation, respectively.

Statistical analysis

One way analysis of variance followed by Dunnett’s test was used to determine whether group means differed significantly from those of controls. Welch’s unpaired t-test was used to determine whether the effects of PDTM3 and kojic acid were significantly different. Statistical analysis was performed using GraphPad (GraphPad Software, La Jolla, CA, USA). All results are indicated as means ± standard error of three independent experiments. Two-sided P-values of, 0.05 were considered statistically significant.

Results and discussion

Preparation of PDTM1–PDTM17 PDTM1–PDTM17 were synthesized as shown in Scheme 1. Heating 2,3-dimercapto-1-propanol and numerous suitably substituted benzaldehydes (1–17) in 1,4-dioxane in the presence of sulfuric acid afforded the desired PDTM products as solids or sticky oil. The structures of the final products were confirmed by 1 H and 13C NMR, correlation spectroscopy, heteronuclear single-quantum correlation spectroscopy, heteronuclear multiple-bond correlation spectroscopy, and low- and high-resolution MS. The presence of the singlet corresponding to the –SCH(Ph)S– proton at δ=6.09–5.56 ppm in 1 H NMR spectra confirmed the formation of a dithiolane ring between benzaldehydes and 2,3-mercapto-1-propanol. In 1 H NMR spectroscopic data of PDTMs, the 2-H peak appeared more downfield than the peaks of protons attached to sp3 carbon atoms, and the 4-H exomethylene and 5-H2 peaks were observed more upfield in named order. In 13C NMR spectroscopic data, apart from peaks from the phenyl ring, the carbon peak of exomethylene (~64 ppm) was most downfield, followed in order by 4-C (~58 ppm), 2-C (~55.3 ppm), and 5-C (~41 ppm). Four products – PDTM6, PDTM12, PDTM13, and PDTM15 – were each obtained as a single racemate, whereas the others were obtained as a mixture of two racemates ([2R,4R]/[2S,4S] and [2R,4S]/ [2S,4R], 1:1–1:1.5), the ratios of which were calculated using 1 H NMR spectroscopic data. The phenomenon in the product formation could not be explained simply by steric, electronic, and/or stereoelectronic effects. The tyrosinase-inhibition assay was performed without the separation of the racemates.

Inhibitory effects of PDTM1–PDTM17 on mushroom tyrosinase

The potentials of the 17 synthesized products, PDTM1– PDTM17, to inhibit mushroom tyrosinase activity were examined using kojic acid22 and arbutin23 as positive controls. Inhibitions were determined using 293 µM l-tyrosine as the substrate and synthetic compounds at a concentration of 50 µM. Tyrosinase inhibitions by kojic acid and arbutin were determined at 50 and 500 µM, respectively.

Three compounds – PDTM11 (3,4,5-trimethoxyphenyl), PDTM15 (4-hydroxy-3-methylphenyl), and PDTM17 (3,5-di-t-butyl-4-hydroxymethyl) – inhibited tyrosinase to the same extent as kojic acid and inhibited it more than arbutin (Table 1). Five PDTM derivatives – PDTM3 (2,4- dihydroxyphenyl), PDTM7 (4-methoxyphenyl), PDTM8 (3,4- dimethoxyphenyl), PDTM9 (2,4-dimethoxyphenyl), and PDTM13 (3-bromo-4-hydroxyphenyl) – inhibited tyrosinase more potently than kojic acid. IC50 values of these compounds were examined: 13.94±1.76 µM (PDTM3), 16.47±2.36 µM (PDTM7), 16.97±2.99 µM (PDTM8), 27.85±1.47 µM (PDTM9), and 15.57±3.31 µM (PDTM13). The low IC50 values of PDTM3, PDTM7, PDTM8, and PDTM13 indicated that potency was stronger than that of kojic acid (18.86±2.14 µM) and arbutin (381.26±3.22 µM), which were used as positive controls. Interestingly, this result concurs with our previous finding that many analogues with a 2,4-dihydroxyphenyl moiety possess higher tyrosinase-inhibitory activity than kojic acid.10,13,24–32

The remaining PDTM derivatives had no (PDTM1 and PDTM2) or low inhibitory effect (PDTM4, PDTM5, PDTM6, PDTM10, PDTM12, PDTM14, and PDTM16) compared with kojic acid. According to our accumulated structure-activity relationship data, analogues with at least one hydroxyl group were more capable of inhibiting tyrosinase. Somewhat surprisingly, four PDTM derivatives with no hydroxyl group inhibited tyrosinase activity as much or more effectively than kojic acid. These were PDTM7 (4-methoxyphenyl), PDTM8 (3,4-dimethoxyphenyl), PDTM9 (2,4-dimethoxyphenyl), and PDTM11 (3,4,5-trimethoxyphenyl). Compounds (PDTM1-2, PDTM4-5, and PDTM12) with only a 4-hydroxyl group on the phenyl ring or an alkoxy or hydroxyl group at position 3 with a 4-hydroxyl group had low or no activity, whereas compounds (PDTM13–PDTM17) with an alkyl or bromo group at position 3 with a 4-hydroxyl group showed moderate-high tyrosinase-inhibitory activity. These structure-activity relationship results support the hypothesis that the tyrosinase inhibitory activity of compounds with a 4-hydroxyl group is greatly affected by the type of 3-substituent.

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Mode of mushroom tyrosinase inhibition by PDTM3

Since PDTM3 inhibited mushroom tyrosinase most, a Lineweaver–Burk plot was used to determine the nature of its inhibitory effect. As depicted in Figure 2, a double-reciprocal plot was obtained, and all lines with different slopes intersected the y-axis at the same point. Therefore, Km (Michaelis constant) values increased gradually with the concentration of PDTM3. Detailed kinetic-parameter values are shown in Table 2. On the other hand, maximum reaction velocity (Vmax) was not affected by PDTM3 concentration. These findings demonstrate PDTM3 dose-dependently and competitively inhibited tyrosinase.

In silico docking simulations of association of tyrosinase with PDTM3, PDTM7–PDTM9, PDTM13, and kojic acid

AutoDock Vina was utilized to determine whether the synthesized PDTM analogs directly inhibited tyrosinase through binding to its active site. Kojic acid and five PDTM analogs (PDTM3, PDTM7–PDTM9, and PDTM13), which were found to have potent mushroom tyrosinase-inhibitory activity, were used as ligands for the docking simulation. Each of these PDTM analogs could have four stereoisomers, and the binding energies of the stereoisomers are indicated in Figure 3A. All five PDTM analogs were found to have a similar or higher affinity for the active site of tyrosinase compared to kojic acid (-5.4 kcal/mol), and PDTM3 demonstrated the greatest affinity. This result indicated that the strong inhibitory effects of these five PDTM derivatives were attributable to their binding affinity with tyrosinase, and showed a close relationship between binding affinity, as determined by docking simulation, and tyrosinase inhibition.

LigandScout 3.1.2 was used to identify tyrosinase amino acid residues that interact with PDTM analogs. As shown in Figures 3B and C, the 4-hydroxyl group on the phenyl ring of PDTM3 interacted with His85 of tyrosinase through hydrogen bonding, and the phenyl ring interacted with Val283 and Ala286 through hydrophobic interactions and with His263 through π–π stacking interaction. Hydrogen bonding between the alcoholic hydroxyl group and amino acid residues of tyrosinase was detected only for PDTM7 and PDTM8. However, the alcoholic hydroxyl group of both PDTM analogues interacted with different amino acid residues, eg, PDTM7 interacted with His244 and Asn260, whereas PDTM8 interacted with Gly281. Furthermore, Val283 of tyrosinase was involved in hydrophobic interactions with all five analogs.

Melanin-content assays

B16F10 cells were used to evaluate the depigmenting activities of the PDTM analogues. PDTM3 was chosen for the cell-based experiments, due to its potent mushroom tyrosinase-inhibitory effect and its lack of toxicity to B16F10 cells. PDTM3 was evaluated for its inhibitory effect against α-MSH-stimulated melanogenesis in B16F10 cells by determining melanin levels in the cells. Melanin levels were significantly reduced after cells were cotreated with PDTM3 and α-MSH compared with cells treated with α-MSH alone. Over the concentration range 0–25 μM, PDTM3 exhibited a significant and dose-dependent antimelanogenic effect. Furthermore, at a concentration of only 10 μM, PDTM3 showed higher inhibitory potency than kojic acid at 25 μM, as depicted in Figure 5. These results indicated the antimelanogenic effect of PDTM3 in B16F10 cells was not related to cytotoxicity.

Tyrosinase-activity assay in B16F10 cells

The inhibitory effect of PDTM3 on cellular tyrosinase activity was examined in B16F10 cells prestimulated with α-MSH. PDTM3 dose-dependently inhibited tyrosinase activity over the concentration range 0–25 μM (Figure 6). Furthermore, these results matched melanin content results well, which suggested that the antimelanogenic effect of PDTM3 was attributable to the inhibition of tyrosinase.

Conclusion

In this work, a variety of PDTM analogs were synthesized and evaluated for their effects on melanogenesis and tyrosinase activity in B16F10 cells. Eight analogs exhibited as much or more potent inhibition against mushroom tyrosinase than kojic acid, and PDTM3 had the greatest inhibitory activity. In B16F10 cells, PDTM3 significantly inhibited melanin biosynthesis in a dose-dependent manner and tyrosinase activity over the concentration range 0–25 μM with no cytotoxic effect. At a concentration of 10 μM, PDTM3 reduced melanin biosynthesis and tyrosinase activity significantly more than kojic acid at 25 μM. In view of our observation that many PDTM analogs showed potent tyrosinase-inhibitory activities, we suggest that 1,3-dithiolane be considered an appropriate scaffold for tyrosinase-inhibitory activity. Now, we are looking for separation conditions of each PDTM mixture of two racemates, and the separation conditions and antimelanogenic effect of every single racemate will be reported in due course.

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