Synthesis, H2S releasing properties, antiviral and antioxidant activities and acute cardiac effects of nucleoside 5’-dithioacetates

doi:10.21203/rs.3.rs-4869589/v1

Download PDF

Article

Synthesis, H2S releasing properties, antiviral and antioxidant activities and acute cardiac effects of nucleoside 5’-dithioacetates

https://doi.org/10.21203/rs.3.rs-4869589/v1

This work is licensed under a CC BY 4.0 License

You are reading this latest preprint version

Hydrogen sulfide (H₂S) is an endogenous gasotransmitter with cardioprotective and antiviral effects. In this work, new cysteine-selective nucleoside-H₂S-donor hybrid molecules were prepared by conjugating nucleoside biomolecules with a thiol-activatable dithioacetyl group. 5'-Dithioacetate derivatives were synthesized from the canonical nucleosides (uridine, adenosine, cytidine, guanosine and thymidine), and the putative 5'-thio metabolites were also produced from uridine and adenosine. According to our measurements made with an H₂S-specific sensor, nucleoside dithioacetates are moderately fast H₂S donors, the guanosine derivative showed the fastest kinetics and the adenosine derivative the slowest. The antioxidant activity of 5'-thionucleosides is significantly higher than that of trolox, but lower than that of ascorbic acid, while intact dithioacetates have no remarkable antioxidant effect. In human Calu cells, the guanosine derivative showed a moderate anti-SARS-CoV-2 effect which was also confirmed by virus yield reduction assay. Dithioacetyl-adenosine and its metabolite showed similar acute cardiac effects as adenosine, however, it is noteworthy that both 5'-thio modified adenosines increased left ventricular ejection fraction or stroke volume, which was not observed with native adenosine.

nucleoside

dithioacetate

H2S donor

H2S release kinetics

antioxidant

antiviral

SARS-CoV-2

Hydrogen sulfide (H₂S) is known as a highly toxic foul-smelling compound, on the other hand, it is an important endogenous gasotransmitter, that plays a critical role in a wide range of biological processes.¹ Endogenous H₂S is largely produced from cysteine and homocysteine as a metabolite of the transsulfuration pathway by the action of three enzymes, cystathionine β-synthase, cystathionine γ-lyase and 3-mercaptopyruvate sulfur transferase. H₂S is involved in several signaling patwhways, including the regulation of cell proliferation by inducing apoptosis through increased p53 tumorsupressor gene expression.² However, in some cell lines, such as endothelial cells, overproduction of H₂S can stimulate cell proliferation through kinase activation leading to angiogenesis.³ Low H₂S levels can be observed in some neurological diseases (Parkinson’s or Alzheimer’s disease) demonstrating the neuromodulating effect of hydrogen sulfide.⁴ H₂S has been shown to have anti-inflammatory and immunomodulating effects, and to protect against multiple stresses, including oxidative stress.^4–6. It can induce vasodilation by activating potassium channels.⁷ H₂S shows significant activity against numerous fungi, including the human pathogen C. albicans,⁸ and also inhibits the replication of a wide range of RNA viruses, such as the causative agent of COVID-19, SARS-CoV-2, presumably by preventing the pathogens from interacting with their receptors on the cell surface.^9–12

Based on these various biological effects, H₂S is a promising molecular entity in the prevention and treatment of several diseases. However, administering a highly toxic and extremely unpleasant-smelling gas poses a real challenge. Therefore, it is preferable to use H₂S donor molecules rather than hydrogen sulfide itself. The simplest of such compounds are inorganic sulfide, polysulfide and hydrogene-sulfide salts, although the H₂S releasing profile of these compounds is not ideal as they release a high amount of H₂S in a short period, causing short-lived effect¹³. To overcome this problem, several small-molecule organic H₂S donors have been developed that release hydrogen upon hydrolysis, endogenous triggers (usually thiols), or external stimuli.^13–14 Some key representatives of organic H₂S donors include 1,2-dithiol-3-thiones, arylthioamides, aryl isothiocyanates and Lawesson reagent-based molecules such as GYY4137.^4,13–15

The hydrogen sulfide-releasing structures is often conjugated to nonsteroidal anti-inflammatory or other drugs or to different biomolecules to obtain H₂S-donor hybrid molecules that combine the beneficial therapeutic effects of the parent compound and H₂S.^16–19 Recently, we synthesized the H₂S-donor hybrid molecules EV-34¹⁸ and BM-88¹⁹ from the commonly used nonsteroidal anti-inflammatory drug ibuprofen (Fig. 1, A), the former being a formaldehyde O,S-acylal, which is a hydrolysis-based H₂S donor,²⁰ while BM-88 is a dithioacetic acid ester that is activated by the endogenous trigger, cysteine.²¹ We also produced a dithioacetate-containing H₂S donor hybrid, BM-164, from the well-known antioxidant ascorbic acid (vitamin C).²¹ All three compounds showed excellent hydrogen sulfide-releasing properties, and BM-88 and BM-164 also exhibited remarkable cardioprotective effects.

Nucleosides are important biomolecules, and their synthetic analogs are widely used in the anticancer and antiviral chemotherapy.^23,24 Albeit sporadically, nucleosides have already been used to construct hydrogen sulfide donors, which always contain the H₂S-releasing group in the 5' position (Fig. 1, B). Among them, compound 1 is an aryl-thioamide-type H₂S donor, which is connected to adenosine with a non-hydrolyzable ether bond,²⁵ while derivatives 2 and 3 are nucleoside monophosphorothioates, which can be enzymatically converted into AMP and GMP, respectively, while hydrogen sulfide is released.^26,27 Adenosine 1 significantly reduced infarct size when administered at the end of sustained ischemia and showed enhanced cardioprotection compared to adenine.²⁵ Phosphorothioates 2 and 3 were reported to restore the anti-contractile effects of perivascular adipose tissue in obese rats through efficient H₂S release.²⁶

It is also worth mentioning that 5'-thio-modified nucleosides have significant bioactivity and therapeutic potential. Notably, 5'-thioadenosine derivatives exert significant antiprotozoal activity against P. falciparum,^28,29 and 5'-thiothymidine was shown to be a strongly binding allosteric ligand of the SARS-CoV-2 NSP15 endonuclease.³⁰ 5’-Cysteine and homocysteine derivatives of nucleosides and homonucleosides have been prepared and tested against S-adenosyl-homocysteine hydrolase and also used as monomer building blocks in the synthesis of peptide nucleic acids.^31,32 Moreover, S-adenosylmethionine (SAM) is a well-known biomolecule that serves as a methyl donor in methyl transfer reactions.³³

Inspired by the literature results, we envisaged the synthesis of new cysteine-selective nucleoside-H₂S-donor hybrid molecules, which release H₂S in the body in a controllable manner, while being transformed into the corresponding 5'-thionucleoside (Fig. 1, C). In this work, we describe the synthesis, H₂S-releasing and antioxidant properties as well as antiviral effect against SARS-CoV-2 of the 5'-dithioacetate derivatives of the four canonical nucleosides (uridine, adenosine, cytidine, guanosine) and the deoxynucleoside thymidine. As reference compounds for the biological assays, the putative 5'-thio metabolites were also produced from uridine and adenosine. Given that adenosine plays a critical role in the regulation of heart function, we also studied the cardiac effects of the 5'-dithioacetyl adenosine derivative in a rat model.

Synthesis

The synthesis of nucleoside 5'-dithioacetates was performed from properly protected nucleosides containing a leaving group in the 5'-position. Tosyl (Ts) was chosen as the leaving group, isopropylidene acetal was used to protect the 2' and 3' hydroxyl groups, while the exocyclic amino group of adenosine, guanosine and cytidine was protected with a triphenylmethyl (Trt) group (Fig. 2). Uridine was converted to 5’-tosylate 5 in two steps by isopropylidenation (4) followed by treatment with TsCl in pyridine.³⁴ Adenosine, guanosine and cytidine were acetalated according to the literature method.³⁵ Compounds 6, 10 and 14 were O,N-ditritylated, followed by selective O-detritylation, using a cocktail of hexafluoroisopropanol (HFIP), and boron trifluoride diethyl etherate (BF₃.Et₂O) as Brönsted and Lewis acids, respectively, and triethylsilane (Et₃SiH) as reducing agent.³⁶ The free 5'-OH of the resulting 8, 12 and 16 was tosylated to obtain the fully protected 5'-tosylates 9³², 13 and 17.

The required tosylate was prepared from the deoxynucleoside thymidine in one step without the use of any protecting group. By reacting thymidine with TsCl in pyridine at room temperature, only the 5',3'-ditosylate was obtained. Repeating the reaction at 0 ^oC, the desired 5'-O-monotosyl derivative (18)³⁷ was formed as the main product.

Next, the dithioacetate group was introduced into the 5'-position of the nucleoside using a one-pot reaction. First, the Mg salt of dithioacetic acid was produced in situ by the reaction of carbon disulfide and methyl magnesium bromide, using a modified version of the method described by Maeda et al.³⁸ (Fig. 3, A). Nucleoside tosylate was then added to the reaction mixture and reacted with the dithioacetate at 80 ^oC. After 5 hours, completion of the reaction and the formation of a uniform product was observed by TLC. Unfortunately, however, NMR spectra showed that the chromatographically uniform product was an inseparable 1:1.4 mixture of the desired 5'-dithioacetate (21) and a side product. We assumed that 5'-deoxy-5'-bromouridine (20) is formed as an undesired product, and to prove this, the presumed bromo derivative was synthesized from 5, using tetrabutylammonium bromide at 80 ^oC. By comparing the NMR spectra of the obtained 5’-bromouridine 20 and the mixture (Fig. 3, B), it was confirmed that the impurity is indeed the the 5’-bromo derivative. The rapid conversion of tosylate to bromouridine (2.5 hours) and the high proportion of the latter in the mixture after 5 hours indicate that the bromo derivative is is formed first, which is converted to dithioacetate in a slow reaction. Accordingly, the reaction was repeated with an extended reaction time of 18 h. In this case, only the desired 5’-dithioacetate was obtained with good yield (80%).

Based on the above, nucleoside 5'-tosylates 9, 13, 17 and 18 were reacted with 3 equiv. of dithioacetate salt in an 18-hour reaction at 80 ^oC to obtain the desired 23, 28 and 30. In the case of the guanosine derivative, only the 5’-bromoderivative 25 was formed under the above conditions, which could be converted to the desired 26 in 85% yield with a large excess of dithioacetate salt during a 28-hour reaction. Adenosine dithioacetate 23 was formed with CH₃CSSMgBr in an exceptionally low yield of 28%, which significantly increased to 72% when the reaction was performed with potassium dithioacetate obtained in two steps from the magnesium salt.

The trityl and isopropylidene protecting groups were removed in one step with 90% trifluoroacetic acid, using triethylsilane as a reducing agent in the presence of trityl group. (Fig. 4, A).

It is assumed, that in a biological milieu, the synthesized 5'-dithioacetyl nucleosides are converted to the corresponding 5'-thionucleosides triggering by the endogenous thiol cysteine. Thus, the assumed metabolites of 5'-dithioacetyl-adenosine and -uridine were also synthesized for biological study. Uridine and adenosine were converted into 5’-acetylthio derivatives 31 and 33 in a Mitsunobu-like reaction, then the S-acetyl group was cleaved, using sodium methylate to obtain the desired thiols 32 and 34 in good yields. (Fig. 4, B).

Evaluation of H₂S releasing profile of the compounds

The H₂S release of compounds 22, 24, 27, 29 and 30 was detected in Dulbecco's modified Eagle's medium with an amperometric, H₂S-specific sensor. The gas release reached the maximum level after 10–20 min and remained at a measurable level even after two hours. On the other hand, the base clearly also has a role in the kinetics of the process. The guanosine derivative 27 releases a large amount of H₂S relatively quickly, while adenosine and thymidine release H₂S more slowly than the other nucleosides, and adenosine has the longest-lasting effect. (Fig. 5. A-E). We also studied the H₂S emissions of two known H₂S donors as references, the fast-release NaHS and the slow-release GYY4137 (Figur 5, F). With the latter, there was no measurable H₂S release, which is in line with the literature data, according to which GYY4137 requires the presence of a high concentration of cysteine (4 mM) for detectable generation of H₂S.⁷ Based on the comparison with the reference compounds, it can be concluded that nucleoside dithioacetates can be considered H₂S donors with a medium release rate.

Antioxidant assays

Oxidative stress arises from an imbalance between increased reactive oxygen species (ROS) production and diminished antioxidant host defenses. Growing evidence suggests that this condition significantly contributes to the pathogenesis of several human diseases, including SARS-CoV-2 infection.³⁹ With the 5’-dithioacetate derivatives and their synthetic 5’-SH metabolites in hand, the antioxidant activities of compounds 22, 24, 32, and 34 were estimated in the DPPH radical scavenging assay. The resulting inhibition ratios were then compared with those obtained for the precursor uridine or adenosine, as well as the positive control (ascorbic acid).

Figure 6 depicts the correlations between the concentrations (mM) and DPPH inhibition ratios (%) of the compounds tested immediately and after 30 min of incubation. Remarkable differences in the inhibition ratios were observed in both time- and concentration-dependent manners.

As shown in Fig. 6, immediate antioxidant activity was observed in all compounds. The 5’-SH metabolites 32 and 34 demonstrated notably higher antioxidant activity than the corresponding 5’-dithioacetate derivatives (22 and 24), achieving an inhibition ratio of 70–80% and 90% immediately and after 30 min incubation, respectively, when employed at a concentration of 2 mM.

The IC₅₀ values of the synthesized compounds deviated significantly from that belonging to the reference compounds, with the 5’-SH analogues 32 and 34 as the most active. However, the observed activity was 10 times lower than that achieved with ascorbic acid.

Furthermore, we compared the antioxidant activity of dithioacetate derivatives and 5'-SH metabolites using ABTS (2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid)) assay, which showed a similar activity pattern to the DPPH assay. Among the molecules the 5'-SH metabolites 32 and 34 showed higher antioxidant activity than the parent dithioacetate derivatives 22 and 24. (Fig. 6, panel D)

Cell viability

In order to evaluate the biocompatibility of the new compounds, MTT assays were carried out in the presence of different concentrations of 5'-dithioacetate derivatives and their synthetic 5'-SH metabolites on H9c2 cells. None of the molecules showed cell toxicity in a physiologically relevant concentration range (Figure S1).

Antivirals results

To determine H₂S releasing effect of nucleoside 5’-dithioacetates on SARS-CoV-2 replication, we added compounds to Calu-3 lung epithelial cells two hours after infection and washing virus away. As the release of H₂S is relatively short-lived we evaluated anti-SARS-CoV-2 effect of compounds already two days after infection in cytopathic-effect-based assay using sensitive CellTiter-Glo luminescent cell viability assay. Only compounds 24 and 27 exhibited moderate anti-SARS-CoV-2 activity in Calu-3 cells with an EC₅₀ of 173 ± 24 µM and 158 ± 34 µM, respectively (Table 1). Next, the virus yield reduction assay was performed to ascertain if there is direct effect on the released SARS-CoV-2 virions into media. The medium after two days infection of Calu-3 cells was analyzed in Vero E6 cells using plaque assay. Only compound 27 very slightly reduced the SARS-CoV-2 titer by 0.38 log₁₀ PFU/mL.

Table 1

Anti-SARS-CoV-2 activities (EC₅₀), cytotoxicity in Calu-3 cells (CC₅₀) and virus yield reduction assay for nucleoside 5’-dithioacetates.
Compound	EC50 ± SE [µM]	CC50 ± SE [µM]	SARS-CoV-2 titer reduction [log₁₀ PFU/mL]
22	> 1000	> 1000	0.02
24	173 ± 24	~ 1000	0
27	158 ± 34	> 1000	0.38
29	> 1000	> 1000	0.13
30	621 ± 181	764 ± 82	0.01
Remdesivir	0.5 ± 0.26	> 10	7.1

Results of in vivo experiments

The cardiac effects of 5’-dithioacetyl uridine and adenosine (22 and 24), 5’-thioadenosine (34) and adenosine as a reference compound were evaluated in rat model. Adenosine at a dose of 2 mg/kg induced heart block, and heart rate (HR) remained significantly lower 30 seconds post-administration compared to baseline; however, this negative chronotropic effect dissipated within approximately 60 seconds. None of the new compounds (22, 24, and 34) induced complete heart block or pauses, but adenosine derivatives 24 and 34 significantly reduced HR relative to baseline values (p = 0.0162; and p = 0.0010, respectively). Although the negative chronotropic effect of compounds 24 and 34 was less pronounced than that of adenosine, their duration of action was longer. The uridine-based compound 22 did not produce notable changes in HR, though a non-significant reduction was observed (p = 0.0562).

Neither the new compounds nor adenosine significantly affected the ECG PR interval in anesthetized rats. Adenosine significantly prolonged the QT interval (p = 0.0062 vs. baseline), and both compounds 24 and 34 similarly extended the QT interval compared to their corresponding baseline values (p = 0.0035 and p = 0.0034, respectively), akin to the parent compound adenosine. Compound 22 did not alter PR or QT intervals but slightly decreased ejection fraction (EF) 30 seconds after administration (p = 0.0208 vs. baseline). Adenosine and compound 34 tended to increase EF (p = 0.189 and p = 0.0757 vs. baseline, respectively), whereas compound 24 significantly increased EF (p = 0.0302 vs. baseline). Interestingly, stroke volume (SV) remained unchanged following administration of adenosine or compound 22, but both compounds 24 and 34 increased SV (p = 0.0811 and p = 0.0068, respectively; Fig. 7).

By optimizing the synthesis steps, we developed an efficient route for the synthesis of new hydrogen sulfide donor nucleosides containing a dithioacetyl group. Using amperometric, H₂S-specific sensor measurements, we established that dithioacetate nucleosides are medium-speed H₂S donors, and nucleobases also have an effect on the kinetics of hydrogen sulfide release. DPPH and ABTS assays were used to determine the antioxidant profile of the hydrogen sulfide donor uridine and adenosine and their 5'-thio metabolites.

In the antiviral tests against SARS-CoV-2, both adenosine and guanosine derivatives 24 and 27 showed an antiviral effect, but surprisingly, only the fastest hydrogen sulfide-releasing guanosine derivative 27 measurably reduced the virus titer.

In the in vivo experiments, administration of 2 mg/kg adenosine resulted in a significant reduction in heart rate (negative chronotropy) accompanied by a marked prolongation of the ECG QT interval, consistent with literature reports^40–41. Interestingly, the effects of the novel adenosine-based compounds 24 and 34 were less pronounced in terms of negative chronotropy and QT prolongation when administered at the same dose (2 mg/kg). However, the heart rate-lowering effect of compound 34 did not significantly differ from that of adenosine. Notably, the duration of the negative chronotropic effect was longer for compounds 24 and 34 compared to the parent compound. The ECG PR interval, indicative of AV nodal conduction, remained unchanged following drug administration. The uridine-based compound 22 produced a non-significant reduction in heart rate without altering other ECG parameters. Regarding left ventricular systolic parameters, compound 22 slightly decreased ejection fraction. Interestingly, both compounds 24 and 34 increased left ventricular ejection fraction and stroke volume, an effect not observed with adenosine, suggesting this phenomenon warrants further investigation.

General informations

Compounds 5³⁴, 9³², 10³⁵, 14³⁵and 18³⁷ were prepared according to literature procedures. Nucleosides and reagents were purchased from Sigma-Aldrich Chemical Co. and used without further purification. The optical rotation values of the nucleoside derivatives were determined on a Perkin-Elmer 241 automatic polarimeter. The reactions were monitored by thin-layer chromatography (TLC) on Kieselgel 60 F254 (Merck), detection was done with UV light (254 nm) and by immersion in sulfuric acid ammonium molybdate solution or 5% ethanolic sulfuric acid, followed by heating. Purification was performed by flash chromatography on a silica gel 60 column (Merck, 0.040–0.063 mm). The organic solutions were dried over over anhydrous Na₂SO₄ or MgSO₄, and solvents were evaporated in vacuo. The NMR and MS analysis of the compounds was performed as previously described.^32,34 Briefly, ¹H NMR (360 and 400 MHz) and ¹³C NMR (90 and 100 MHz) spectra were recorded with Bruker DRX-360 and Bruker DRX-400 spectrometers at 25°C, chemical shifts are referenced to Me₄Si (0.00 ppm 1H) and residual solvent signals (CDCl₃: 77.2, DMSO-d₆: 39.5, CD₃OD: 49.0 for ¹³C). Two-dimensional COSY and ¹H−¹³C HSQC experiments were used to assist NMR assignments. MALDI-TOF MS analyses of the compounds were carried out in the positive reflectron mode using a Bruker Autoflex Speed mass spectrometer equipped with a time-of-flight (TOF) mass analyzer (Bruker, Germany). 2,5-Dihydroxybenzoic acid (DHB) was used as matrix and F₃CCOONa as cationising agent in DMF.

Synthesis of the compounds

2’,3’- O -Isopropylidene-5’- O -tosyl-2- N -trityl-guanosine (13): Compound 12 (1.5 g, 2.65 mmol) was dissolved in dry pyridine (20 mL), TsCl (657 mg, 3.45 mmol, 1.3 equiv.) was added and stirred at rt overnight. Because of the low conversion, another portion of TsCl (657 mg, 3.45 mmol, 1.3 equiv.) was added and stirred for another night. Next day, the reaction mixture was evaporated, the residue was dissolved in CH₂Cl₂ (350 mL) and extracted with 10% aq. Na₂HSO₄ solution and brine. The organic phase was dried over Na₂SO₄, filtered and evaporated under reduced pressure. The crude product was purified by flash column chromatography (gradient elution CH₂Cl₂/MeOH 98:2 →97:3→95:5) to give 13 (558 mg, 29%) as a white foam. [α]_D = + 19.05 (c = 0.21, CHCl₃), Rf = 0.17 (CH₂Cl₂/MeOH 95/5), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 7.77 (s, 1H), 7.64 (d, J = 8.3 Hz, 2H), 7.29 (dd, J = 15.7, 7.8 Hz, 8H), 7.12 (dt, J = 23.7, 7.1 Hz, 9H), 6.96 (s, 1H), 5.36 (d, J = 2.1 Hz, 1H), 4.85–4.80 (m, 1H), 4.18 (d, J = 4.7 Hz, 2H), 3.85 (dd, J = 10.7, 3.6 Hz, 1H), 3.74 (dd, J = 10.7, 6.2 Hz, 1H), 2.41 (s, 3H, Ts CH₃), 1.43, 1.19 (2 x s, 2 x 3H, i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 158.6 (1C, C-6), 151.5, 149.7, 145.6, 144.5, 132.3 (7C, C-2, C-4, Ts C-1, Ts C-4, 3 x Trt arom C_q), 130.1, 128.9, 127.9, 127.9, 127.1 (19C, arom.), 118.4 (1C, C-5), 114.3 (1C, i-propylidene C_q), 90.7 (1C, C-1’), 83.3, 82.3, 80.9 (3C, C-2’, C-3’, C-4’), 71.3 (1C, N-TrtC_q), 68.9 (1C, C-6’), 27.3, 25.9 (2C, 2 x i-propylidene CH₃), 21.8 (1C, Ts CH₃). MALDI ToF MS: m/z calcd for C₃₉H₃₇N₅NaO₇S [M + Na]⁺ 742.231, found 742.241.

2’,3’-O-Isopropylidene- O,N -ditrityl-cytidine (15): 2’,3’-O-Isopropylidene-cytidine 14 (0.927 g, 3.27 mmol) was dissolved in dry pyridine (10 mL). TrtCl (3.7 g, 13.08 mmol, 4.0 equiv.) was added and the rection mixture was stirred at 60 ^oC for 3 days. Since the conversion was not complete, another portion of TrtCl (462 mg, 0.5 equiv.) and DMAP (20 mg, 0.05 equiv) was added and the solution was stirred at 60 ^oC for 4 days. The solvent was evaporated in vacuo. The crude product was purified by flash column chromatography (gradient elution CH₂Cl₂→ CH₂Cl₂:MeOH 98:2) to give 15 (1.30 g, 39%) as a white solid. [α]_d = -8.75 (c = 0.40, CHCl₃), Rf = 0.63 (CH₂Cl₂/MeOH 98/2), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 8.58 (d, J = 4.2 Hz, 1H, NH), 7.35–7.09 (m, 31H, arom.), 6.89 (s, 1H, H-6), 5.90 (d, J = 1.6 Hz, 1H, H-1’), 4.87 (dd, J = 6.2, 1.7 Hz, 1H, H-2’), 4.77 (d, J = 3.4 Hz, 1H, H-5), 4.75 (d, J = 4.5 Hz, 1H, H-3’), 4.29 (dd, J = 7.0, 4.1 Hz, 1H, H-4’), 3.44 (dd, J = 10.7, 4.6 Hz, 1H), 3.36 (dd, J = 10.7, 2.4 Hz, 1H), 1.53, 1.32 (2 x s, 2 x 3H, 2 x i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm)165.65 (1C, C-4), 155.00 (1C, C-2), 143.92, 143.24 (6C, arom. C_q), 141.90 (1C, C-6), 128.69, 128.66, 128.36, 127.90, 127.57, 127.21 (30C, arom.), 113.78 (1C, i-propylidene C_q), 87.27 (1C, O-Trt C_q), 94.47, 93.36, 86.43, 85.76, 80.50 (5C, C-1’, C-2’, C-3’, C-4’, C-5), 70.85 (1C, N-Trt C_q), 63.78 (1C, C-5’), 27.32, 25.48 (2C, 2x i-propylidene CH₃), MALDI-ToF MS: m/z calcd for C₅₀H₄₅N₃NaO₅ [M + Na]⁺ 790.33, found 790.43.

2’,3’- O -Isopropylidene- N -trityl-cytidine (16): Compound 15 (500 mg, 0.651 mmol) was added to the mixture of HFIP (6.5 mL), Et₃SiH (395 µL, 2.47 mmol, 3.8 equiv.) and BF₃.Et₂O (10.4 µL, 0.0846 mmol, 0.13 equiv). When the yellow colour of the solution was disappeared the reaction was monitored by TLC (hexane/acetone 65/35 R_f=0.19). After complete conversion of the starting compound (1 h) the reaction was quenched by saturated aq. solution of NaHCO₃ (0.5 mL). The solvent was evaporated in vacuo and the residue was purified by flash column chromatography (gradient elution hexane:acetone 65:35→6:4→1:1) to give 16 (315 mg = 92%) as a white solid. [α]_d = -46.0 (c = 0.25, CHCl₃), Rf = 0.19 (hexane/acetone 65/35), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 7.41–7.15 (m, 15H, arom.), 7.02 (d, J = 7.5 Hz, 1H, H-6), 5.09 (d, J = 2.7 Hz, 1H, H-1’), 5.05 (d, J = 7.5 Hz, 1H, H-5), 4.38 (s, 0.5H), 4.27 (d, J = 2.2 Hz, 1H), 3.88 (d, J = 12.2 Hz, 1H), 3.75 (d, J = 10.6 Hz, 1H), 1.52, 1.33 (2 x s, 2 x 3H, 2 x i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 166.02 (1C, C-4), 155.22 (1C, C-2), 144.73 (1C, C-6), 143.68 (3C, arom C_q), 128.67, 128.50, 127.75 (15C, arom.), 113.84 (1C, i-propylidene C_q), 99.07, 94.98, 87.81, 83.32, 80.54 (C-1’, C-2’, C-3’, C-4’, C-5), 71.07 (1C, N-TrtC_q), 62.83 (1C, C-5’), 27.27, 25.24 (2C, 2x i-propylidene CH₃). MALDI-ToF MS: m/z calcd for C₃₁H₃₁N₃NaO₅ [M + Na]⁺ 548.22, found 548.38.

2’,3’- O -Isopropyliden-5’- O -tosyl- N -trityl-cytidine (17): Compound 16 (1.86 g, 3.5 mmol) was dissolved in dry pyridine (10 mL) and TsCl (1.33 g, 7.0 mmol, 2.0 equiv.) was added and stirred overnight. Next day, water was added to the reaction mixture and stirred for an hour. The solvent was evaporated under educed pressure and the residue was dissolved in CH₂Cl₂ (300 mL). The organic phase was extracted with satd. aq. NaHCO₃, 10% aq. NaHSO₄ and water, then dried over Na₂SO₄, filtered and evaporated in vacuo. The crude product was purified by flash chromatography (hexane:acetone 75:25) to give 17 (303 mg, 13%) as a white foam. [α]_d = + 37.7 (c = 0.13, CHCl₃), Rf = 0.37 (hexane/acetone 6/4), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 7.75 (d, J = 8.3 Hz, 1H), 7.56 (d, J = 8.1 Hz, 1H), 7.38–7.14 (m, 23H), 7.02 (d, J = 8.0 Hz, 1H), 6.92 (d, J = 7.6 Hz, 1H), 5.35 (s, 1H), 5.07 (s, 1H), 5.00 (s, 1H), 4.81 (d, J = 6.4 Hz, 1H), 4.77 (d, J = 2.1 Hz, 1H), 2.42 (s, 3H, Ts CH₃), 1.48, 1.28 (2 x s, 2 x 3 H, 2 x i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ 166.1 (1C, C-4), 154.6 (1C, C-2), 144.9 (1C, C-6), 144.1, 143.8, 142.8, 132.9 (5C, Ts C-1, Ts C-4, 3 x Trt arom C_q), 129.9, 129.1, 128.7, 128.5, 128.4, 128.0, 127.8, 127.0, 126.2 (19C, arom.), 113.9 (1C, i-propylidene C_q), 97.8, 94.8, 86.6, 84.7, 81.9 (5C, C-1’, C-2’, C-3’, C-4’, C-5), 71.1, 70.3 (2C, C-5’, N-Trt C_q), 27.0, 25.2, 21.7 (3C, Ts CH_3, i-propylidene CH₃), MALDI-ToF MS: m/z calcd for C₃₈H₃₇N₃NaO₇S [M + Na]⁺ 702.2, found 702.4.

5’-Bromo-5’-deoxy-2’,3’- O -isopropylidene-uridine (20)⁴²: Compound 5 (6.6 g, 15.1 mmol), and Bu₄NBr (6.3 g 19.6 mmol, 1.3 equiv.) were dissolved in acetone (50 mL) and stirred for 2.5 h at 80 ^oC. The solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography (hexane:acetone 7:3) to give 20 (5 g, 94%) as white foam. [α]_d = + 12.92 (c = 0.48, CHCl₃), Rf = 0.22 (hexane/acetone 7/3), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 10.13 (s, 1H, NH), 7.37 (d, J = 8.0 Hz, 1H, H-6), 5.78 (dd, J = 8.0, 1.2 Hz, 1H, H-5), 5.67 (d, J = 2.1 Hz, 1H, H-1’), 5.04 (dd, J = 6.5, 2.1 Hz, 1H, H-2’), 4.90 (dd, J = 6.5, 3.7 Hz, 1H, H-3’), 4.38 (td, J = 5.8, 3.8 Hz, 1H, H-4’), 3.69 (dd, J = 10.6, 6.4 Hz, 1H, H-5’a), 3.57 (dd, J = 10.6, 5.4 Hz, 1H, H-5’b), 1.58 (s, 3H, i-propylideneCH₃), 1.37 (s, 3H, i-propylideneCH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 164.0, 150.2 (2C, C-2, C-4), 142.9 (1C, C-6), 114.8 (1C, i-propylideneC_q), 102.9 (1C, C-5), 95.3 (1C, C-1’), 86.8, 84.5, 83.2 (3C, C-2’, C-3’, C-4’), 32.4 (1C, C-5’), 27.1, 25.3 (2C, 2x i-propylideneCH₃). MALDI ToF MS: m/z calcd for C₁₂H₁₅BrN₂NaO₅ [M + Na]⁺ 369.006, found 369.010.

S -(2’,3’- O -Isopropylidene-uridine-5’-yl)-dithioacetic acid (21): Method A: CS₂ (91 µL, mmol, 3.0 equiv.) was dissolved in dry THF (4 mL) under Ar and MeMgBr 3 M solution in diethyl ether (0.5 mL, 1.5 mmol, 3.0 equiv.) was added and stirred overnight. Next day, compound 5 (219 mg, 0.5 mmol) was added and stirred at 80 ^oC for 5 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (hexane:acetone 85:15→7:3) to give 152 mg of the unseparable mixture of 20 and 21 with approximately 1.4:1 ratio, as a yellow foam. Method B: CS₂ (1.0 mL, 17.1 mmol, 3.0 equiv.) was dissolved in dry THF (46 mL) under Ar and MeMgBr (3 M solution, in diethyl ether, 5.7 mL, 17.1 mmol, 3.0 equiv.) was added and stirred overnight. Next day, compound 5 (2.5 g, 5.7 mmol) was added and stirred at 80 ^oC for 18 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (hexane:acetone 85:15→7:3) to give 21 (1.63 g, 80%) as a yellow foam. [α]_D = + 33.0 (c = 0.20, CHCl₃), Rf = 0.28 (hexane/acetone 7/3), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 9.92 (s, 1H, NH), 7.23 (d, J = 8.0 Hz, 1H, H-6), 5.76 (d, J = 8.0 Hz, 1H, H-5), 5.53 (d, J = 1.4 Hz, 1H, H-1’), 5.09 (dd, J = 6.5, 1.6 Hz, 1H, H-2’), 4.82 (dd, J = 6.4, 4.1 Hz, 1H, H-3’), 4.32 (td, J = 6.6, 4.2 Hz, 1H, H-4’), 3.72–3.60 (m, 2H, H-5’ab), 2.86 (s, 3H, thioAc CH₃), 1.54 (s, 3H, i-propylidene CH₃), 1.35 (s, 3H, i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 232.1 (1C, CS), 163.8, 150.2 (2C, C-2, C-4), 143.3 (1C, C-6), 114.7 (1C, i-propylidene C_q), 102.8 (1C, C-5), 96.1 (1C, C-1’), 85.6, 84.7, 83.8 (3C, C-2’, C-3’, C-4’), 39.4 (1C, thioAc CH₃), 39.1 (1C, C-5’), 27.2, 25.3 (2C, 2 x i-propylidene CH₃). MALDI ToF MS: m/z calcd for C₁₄H₁₈N₂NaO₅S₂ [M + Na]⁺ 381.056, found 381.065.

S -(Uridine-5’-yl)-dithioacetic acid (22): Compound 21 (2.64 g, 7.36 mmol) was dissolved in 90% aq. TFA (20 mL) and stirred for 2 h at r.t. The solvent was evaporated under reduced pressure, and co-evaporated with toluene. The crude product was purified by flash column chromatography (CH₂Cl₂:MeOH 97.5:2.5→96:4→95:5) to give 22 (1.3 g, 57%) as yellow solid. [α]_D = + 22.0 (c = 0.10, DMSO), Rf = 0.60 (CH₂Cl₂/MeOH 9/1), ¹H NMR (400 MHz, MeOD) δ (ppm) 7.60 (d, J = 8.1 Hz, 1H, H-6), 5.79 (d, J = 4.8 Hz, 1H, H-1’), 5.74 (d, J = 8.1 Hz, 1H, H-5), 4.28 (t, J = 5.2 Hz, 1H, H-2’), 4.15–4.08 (m, 1H, H-4’), 4.03 (t, J = 5.3 Hz, 1H, H-3’), 3.76 (dd, J = 13.9, 5.1 Hz, 1H, H-5’a), 3.61 (dd, J = 13.9, 7.4 Hz, 1H, H-5’b), 2.85 (s, 3H, CH₃). ¹³C NMR (100 MHz, MeOD) δ (ppm) 234.2 (1C, CS), 166.0, 152.2 (2C, C-2, C-4), 142.8 (1C, C-6), 103.1 (1C, C-5), 91.9 (1C, C-1’), 82.7 (1C, C-4’), 74.5 (1C, C-1’), 74.1 (1C, C-3’), 40.2 (1C, C-5’), 39.5 (1C, CH₃). MALDI ToF MS: m/z calcd for C₁₁H₁₄N₂NaO₅S₂ [M + Na]⁺ 341.024, found 341.039.

S -(2’,3’- O -Isopropylidene- N -trityl-adenosine-5’-yl)-dithioacetic acid (23): Method A: CS₂ (257 µL, 4.26 mmol, 3.0 equiv.) was dissolved in dry THF (10 mL) under Ar and MeMgBr 3 M solution in diethyl ether (1.42 mL, 4.26 mmol, 3.0 equiv.) was added and stirred overnight. Next day, compound 9 (1.0 g, 1.42 mmol) was added and stirred at 80 ^oC for 18 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (hexane:acetone 9:1→8:2) to give 23 (251 mg, 72%) as a yellow foam. Method B: Compound 9 (100 mg, 0.142 mmol) was dissolved in acetone (5 mL) and potassium-dithioacetate (37 mg, 0.284 mmol, 2.0 equiv.) was added and stirred at r.t. overnight. The solvent was evaporated and the residue was dissolved in CH₂Cl₂ (150 mL) and extracted with H₂O (3 x 50 mL). The organic phase was dried over Na₂SO₄, filtered and evaporated under educed pressure. The crude product was purified by flash chromatography (hexane/acetone 85/15) to give 23 (64 mg, 72%) as a yellow foam. [α]_D = + 15.8 (c = 0.12, DMSO), Rf = 0.25 (hexane/acetone 8/2), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 8.03, 7.83 (2 x s, 2 x 1H, H-2, H-8), 7.34 (d, J = 7.0 Hz, 6H, arom.), 7.30–7.20 (m, 9H, arom.), 6.98 (s, 1H, NH), 6.02 (s, 1H, H-1’), 5.51 (d, J = 7.6 Hz, 1H, H-2’), 5.00 (dd, J = 6.2, 3.1 Hz, 1H, H-3’), 4.43 (dt, J = 6.8, 3.2 Hz, 1H, H-4’), 3.68 (dd, J = 13.8, 6.6 Hz, 1H, H-5’a), 3.58 (dd, J = 13.8, 7.2 Hz, 1H, H-5’b), 2.81 (s, 3H, thioAc CH₃), 1.57 (s, 3H, i-propylidene CH₃), 1.36 (s, 3H, i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 231.9 (1C, CS), 154.4, 148.2, 121.7 (3C, C-4, C-5, -6), 152.5 (1C, adenine CH), 145.0 (3C, 3 x Trt arom C_q), 129.1, 128.0, 127.1 (15C, arom.), 114.7 (1C, i-propylidene C_q), 91.1 (1C, C-1’), 84.8, 84.23, 84.1 (3C, C-2’, C-3’, C-4’), 39.3 (1C, thioAc CH₃), 39.2 (1C, C-5’), 27.2, 25.4 (2C, 2 x i-propylidene CH₃). MALDI ToF MS: m/z calcd for C₃₄H₃₃N₅NaO₃S₂ [M + Na]⁺ 646.192 found 646.204.

S -(Adenosine-5’-yl)-dithioacetic acid (24): Compound 23 (218 mg, 0.35 mmol) was dissolved in 90% aq. TFA (5 mL) Et₃SiH (167 µL, 1.05 mmol, 3.0 equiv.) was added and stirred for 2 h at r.t. The solvent was evaporated under reduced pressure, and co-evaporated with toluene. The crude product was purified by flash column chromatography (CH₂Cl₂:MeOH 98:2→97:3→95:5) to give 24 (76 mg, 64%) as yellow solid. [α]_D = -7.14 (c = 0.14, DMSO), Rf = 0.1 (CH₂Cl₂/MeOH 95/5), ¹H NMR (400 MHz, MeOD) δ (ppm) 8.23, 8.20 (2 x s, 2x 1 H, H-2, H-8), 5.97 (d, J = 5.3 Hz, 1H, H-1’), 4.92 (t, J = 5.3 Hz, 1H, H-2’), 4.31 (d, J = 4.3 Hz, 1H, H-3’), 4.28–4.21 (m, 1H, H-4’), 3.83 (dd, J = 13.9, 5.5 Hz, 1H, H-5’a), 3.72 (dd, J = 13.9, 7.3 Hz, 1H, H-5’b), 2.82 (s, 3H, thioAc CH₃). ¹³C NMR (100 MHz, MeOD) δ (ppm) 234.3 (1C, CS), 153.9 (1C, adenine CH), 90.4 (1C, C-1’), 83.5 (1C, C-4’), 74.6 (2C, C-3’, C-2’), 40.4 (1C, C-5’), 39.4 (1C, thioAc CH₃). MALDI ToF MS: m/z calcd for C₁₂H₁₅N₅NaO₃S₂ [M + Na]⁺ 364.041 found 364.077.

5’-Bromo-5’-deoxy-2’,3’- O -isopropylidene- N -trityl-guanosine (25): CS₂ (126 µL, 2.08 mmol, 3.0 equiv.) was dissolved in dry THF (5 mL) under Ar and MeMgBr 3 M solution in diethyl ether (126 µL, 2.08 mmol, 3.0 equiv.) was added and stirred overnight. Next day, compound 13 (500 mg, 0.6976 mmol) was added and stirred at 80 ^oC for 24 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (CH₂Cl₂:MeOH 98:2→97:3→96:4→95:5) to give 25 (335 mg, 77%) as a yellowish solid. [α]_D = + 39.1 (c = 0.32, CHCl₃), Rf = 0.3 (CH₂Cl₂/MeOH 9/1), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 11.69 (s, 1H, NH), 7.85 (s, 1H), 7.31 (t, J = 7.7 Hz, 8H, arom.), 7.16 (dt, J = 24.6, 7.4 Hz, 12H, arom.), 7.04 (s, 1H, arom.), 5.33 (d, J = 3.4 Hz, 1H, H-1’), 4.59 (dd, J = 5.9, 3.5 Hz, 1H), 4.19–4.10 (m, 2H), 2.94 (dd, J = 10.6, 5.9 Hz, 1H, H-5’a), 2.82 (dd, J = 10.5, 7.6 Hz, 1H, H-5’b), 1.46 (s, 3H, i-propylidene CH₃), 1.23 (s, 3H, i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 158.8, 151.4, 149.7, 118.6 (4C, C-2, C-4’, C-5, C-6), 144.5 (3C, 3 x Trt arom C_q), 128.9, 127.8, 126.9 (15C, arom.), 114.2 (1C, i-propylidene C_q), 90.9, 84.3, 82.6, 81.3 (4C, C-1’, C-2’, C-3’, C-4’), 71.0 (1C, Trt C_q), 31.5 (1C, C-5’), 27.4, 25.9 (2C, 2 x i-propylidene CH₃). MALDI ToF MS: m/z calcd for C₃₂H₃₀BrN₅NaO₄ [M + Na]⁺ 650.138 found 650.147.

S -(2’,3’- O -Isopropylidene- N -trityl-guanosine-5’-yl)-dithioacetic acid (26): CS₂ (173 µL, 2.86 mmol, 6.0 equiv.) was dissolved in dry THF (6 mL) under Ar and MeMgBr (3 M solution in diethyl ether, 0.95 mL, 2.86 mmol, 6.0 equiv.) was added and stirred overnight. Next day, compound 25 (300 mg, 0.477 mmol) was added and stirred at 80 ^oC for 28 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (CH₂Cl₂:MeOH 95:5) to give 26 (259 mg, 85%) as a yellow solid. [α]_D = + 39.1 (c = 0.32, CHCl₃), Rf = 0.3 (CH₂Cl₂/MeOH 9/1), ¹H NMR (400 MHz, DMSO) δ (ppm) 10.79 (s, 1H, NH), 7.76 (s, 1H), 7.72 (s, 1H), 7.36–7.22 (m, 15H, arom.), 5.51 (d, J = 3.3 Hz, 1H, H-1’), 4.76 (d, J = 5.7 Hz, 1H), 4.06 (s, 1H), 4.01 (t, J = 7.2 Hz, 1H), 3.14 (dd, J = 13.9, 6.3 Hz, 1H, H-5’b), 2.99 (dd, J = 13.7, 8.3 Hz, 1H, H-5’a), 2.79 (d, J = 13.6 Hz, 3H, thioAc CH₃), 1.36 (s, 3H, i-propylidene CH₃), 1.20 (s, 3H, i-propylidene CH₃). ¹³C NMR (100 MHz, DMSO) δ (ppm) 156.3, 151.2, 148.9, 118.1 (4C, C-2, C-4, C-5, C-6), 144.5 (3C, 3 x Trt arom C_q), 128.4, 127.9, 126.9 (15 C, arom.), 113.4 (1C, i-propylidene C_q), 89.3, 82.8, 81.1, 80.6 (4C, C-1’, C-2’, C-3’, C-4’), 70.3 (1C, Trt C_q), 39.2 (1C, thioAc CH₃), 39.1 (1C, C-5’), 27.0, 25.7 (2C, 2 x i-propylidene CH₃). MALDI ToF MS: m/z calcd for C₃₄H₃₃N₅NaO₄S₂ [M + Na]⁺ 662.1872 found 662.1876.

S -(Guanosine-5’-yl)-dithioacetic acid (27): Compound 26 (221 mg, 0.35 mmol) was dissolved in 90% aq. TFA (5 mL), Et₃SiH (167 µL, 1.05 mmol, 3.0 equiv.) was added and stirred for 2 h at r.t. The solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography (CH₂Cl₂:MeOH 9:1→85:15→8:2) to give 27 (89 mg, 72%) as yellow solid. [α]_D = -5.45 (c = 0.11, DMSO), Rf = 0.44 (CH₂Cl₂/MeOH 8/2), ¹H NMR (400 MHz, DMSO) δ (ppm) 10.80 (s, 1H, NH), 7.90 (s, 1H), 6.61 (s, 2H), 5.68 (d, J = 6.0 Hz, 1H, H-1’), 5.57 (d, J = 6.1 Hz, 1H, 2’-OH), 5.40 (d, J = 4.9 Hz, 1H, 3’-OH), 4.64 (dd, J = 11.3, 5.8 Hz, 1H, H-2’), 4.10–4.05 (m, 1H, H-3’), 4.02–3.97 (m, 1H, H-4’), 3.71 (dd, J = 13.7, 5.5 Hz, 1H, H-5’a), 3.59 (dd, J = 13.7, 8.0 Hz, 1H, H-5’b), 2.83 (s, 3H, thioAc CH₃). ¹³C NMR (100 MHz, DMSO) δ (ppm) 233.9 (1C, CS), 156.8, 153.8, 151.4, 116.9 (4C, C-2, C-4, C-5, C-6), 136.63*, 86.8 (1C, C-1’), 81.2 (1C, C-4’), 72.9, 72.6 (2C, C-2’, C-3’). * Can only be seen in HSQC. MALDI ToF MS: m/z calcd for C₁₂H₁₅N₅NaO₄S₂ [M + Na]⁺ 380.046 found 380.081.

S -(2’,3’- O -Isopropylidene- N -trityl-cytidine-5’-yl)-dithioacetic acid (28): CS₂ (692 µL, 11.4 mmol, 6.0 equiv.) was dissolved in dry THF (24 mL) under Ar and MeMgBr (3 M solution in diethyl ether, 3.82 mL, 11.4 mmol, 6.0 equiv.) was added and stirred overnight. Next day, compound 17 (1.3 mg, 1.91 mmol) was added and stirred at 80 ^oC for 18 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (CH₂Cl₂:MeOH 100:0.5→100:1→100:2) to give 28 (1 g, 95%) as a yellow solid. [α]_D = + 37.5 (c = 0.16, CHCl₃), Rf = 0.3 (hexane/acetone 6/4), ¹H NMR (400 MHz, CDCl₃) δ (ppm) 7.37–7.27 (m, 10H, arom.), 7.26–7.20 (m, 7H, arom.), 6.91 (6.92 (d, J = 7.6 Hz, 1H, H-6), 5.27 (s, 1H, H-1’), 5.25 (s, 1H, H-2’), 5.01 (d, J = 7.5 Hz, 1H, H-5), 4.93 (dd, J = 6.3, 3.5 Hz, 1H, H-3’), 4.30 (td, J = 6.8, 3.6 Hz, 1H, H-4’), 3.82–3.77 (m, 1H, H-5’a), 3.72 (dd, J = 13.7, 7.3 Hz, 1H, H-5’b), 2.83 (s, 3H, thioAc CH₃), 1.49 (s, 3H, i-propylidene CH₃), 1.32 (s, 3H, i-propylidene CH₃). ¹³C NMR (100 MHz, CDCl₃) δ (ppm) 232.3 (1C, CS), 166.1, 154.6 (2C, C-2, C-4), 144.5 (1C, C-6), 143.8 (3C, 3 x Trt arom C_q), 128.7, 128.5, 127.7 (15C, arom.), 113.7 (1C, i-propylidene C_q), 98.6 (1C, C-1’), 94.7 (1C, C-5), 86.6 (1C, C-4’), 84.9, 84.6 (2C, C-2’, C-3’), 71.1 (1C, Trt C_q), 39.3, 39.2 (1C, thioAc CH₃), 29.3 (1C, C-5’), 26.9, 25.1 (2C, 2 x i-propylidene CH₃). MALDI ToF MS: m/z calcd for C₃₃H₃₃N₃NaO₄S₂ [M + Na]⁺ 622.181 found 622.154.

S -(Cytidine-5’-yl)-dithioacetic acid (29): Compound 28 (1 g, 1.69 mmol) was dissolved in 90% aq. TFA (10 mL), Et₃SiH (808 µL, 5.07 mmol, 3.0 equiv.) was added and stirred for 2 h at r.t. The solvent was evaporated under reduced pressure, and co-evaporated with toluene. The crude product was purified by flash column chromatography (CH₂Cl₂:MeOH 9:1) to give 29 (379 mg, 73%) as yellow solid. [α]_D = + 40.8 (c = 0.12, CHCl₃), Rf = 0.18 (CH₂Cl₂/MeOH 9/1), ¹H NMR (400 MHz, MeOD) δ (ppm) 7.76 (d, J = 7.7 Hz, 1H, H-6), 6.06 (d, J = 7.6 Hz, 1H, H-5), 5.80 (d, J = 3.9 Hz, 1H, H-1’), 4.27 (d, J = 4.6 Hz, 1H, H-2’), 4.15 (dd, J = 12.7, 5.4 Hz, 1H, H-4’), 4.01 (t, J = 5.6 Hz, 1H, H-3’), 3.80 (dd, J = 13.9, 4.9 Hz, 1H, H-5’a), 3.63 (dd, J = 13.9, 7.6 Hz, 1H, H-5’b), 2.86 (s, 3H, thioAc CH₃). ¹³C NMR (100 MHz, MeOD) δ (ppm) 234.2 (1C, CS), 165.1 (2C, C-2, C-4), 144.3 (1C, C-6), 96.3, 92.9 (2C, C-1’, C-5), 82.8 (1C, C-4), 75.2, 74.1 (2C, C-2’, C-3’), 40.2 (1C, C-5’), 39.4 (1C, thioAc CH₃). MALDI ToF MS: m/z calcd for C₁₁H₁₅N₃NaO₄S₂ [M + Na]⁺ 340.0402 found 340.0556.

S -(Thymidine-5’-yl)-dithioacetic acid (30): CS₂ (457 µL, 7.6 mmol, 3.0 equiv.) was dissolved in dry THF (15 mL) under Ar and MeMgBr 3 M solution in diethyl ether (2.53 mL, 7.57 mmol, 3.0 equiv.) was added and stirred overnight. Next day, compound 18 (1.0 g, 2.52 mmol) was added and stirred at 80 ^oC for 18 h. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (CH₂Cl₂:MeOH 96:4→95:5) to give 30 (568 mg, 72%) as a yellow solid. [α]_D = + 42.7 (c = 0.36, DMSO), Rf = 0.44 (CH₂Cl₂/MeOH 95/5), ¹H NMR (400 MHz, DMSO) δ (ppm) 11.32 (s, 1H, NH), 7.46 (s, 1H, H-6), 6.17 (t, J = 6.9 Hz, 1H, H-1’), 5.46 (s, 1H, OH), 4.19 (s, 1H, H-3’), 3.89 (s, 1H, H-4’), 3.66 (dd, J = 13.6, 5.3 Hz, 1H, H-5’a), 3.53 (dd, J = 13.5, 7.8 Hz, 1H, H-5’b), 2.85 (s, 3H, thioAc CH₃), 2.29 (dt, J = 13.7, 6.9 Hz, 1H, H-2’a), 2.15–2.05 (m, 1H, H-2’b), 1.81 (s, 3H, thymine CH₃). ¹³C NMR (100 MHz, DMSO) δ (ppm) 233.9(1C, CS), 163.9, 150.7 (2C, C-2, C-4), 136.3 (1C, C-6), 110.1 (1C, C-5), 84.2 (1C, C-1’), 83.2 (1C, C-4’), 73.1 (1C, C-3’), 39.6 (1C, thioAc CH₃), 38.2 (1C, C-2’), 12.3 (1C, thymine CH₃). MALDI ToF MS: m/z calcd for C₁₂H₁₆N₂NaO₄S₂ [M + Na]⁺ 339.0449, found 339.0430.

5’- S -Acetyl-5’-thiouridine (31): PPh₃ (6.5 g, 24.6 mmol, 2.0 equiv.) was dissolved in dry THF (50 mL) and cooled to 0 ^oC. DIAD (5.0 mL, 24.6 mmol, 2.0 equiv.) was added dropwise and stirred for 30 min at 0 ^oC. Uridine (3.0 g, 12.3 mmol) and HSAc (1.8 mL, 24.6 mmol, 2.0 equiv.) were dissolved in dry DMF (50 mL) and added dropwisely to the reaction mixture and stirred for 30 min at 0 ^oC and 30 min at r.t. The solvent was evaporated under reduced pressure and the crude product was purified by flash column chromatography (gradient elution, CH₂Cl₂:MeOH 97.5:2.5→9:1→8:2) to give 31 (2.5 g, 70%) as a pale yellowish solid. [α]_D = + 17.8 (c = 0.23, DMSO), Rf = 0.16 (CH₂Cl₂/MeOH 95/5), ¹H NMR (400 MHz, DMSO) δ (ppm) 11.36 (s, 1H, NH), 7.63 (d, J = 8.1 Hz, 1H, H-6), 5.73 (d, J = 5.6 Hz, 1H, H-1’), 5.67 (dd, J = 8.0, 2.1 Hz, 1H, H-5), 5.43 (d, J = 5.6 Hz, 1H, 2’-OH), 5.29 (d, J = 4.5 Hz, 1H, 3’-OH), 4.14 (dd, J = 10.2, 5.1 Hz, 1H, H-2’), 3.87–3.78 (m, 2H, H-4’, H-3’), 3.27 (dd, J = 13.8, 5.0 Hz, 1H, H-5’a), 3.10 (dd, J = 13.8, 7.0 Hz, 1H, H-5’b), 2.36 (s, 3H, AcCH₃). ¹³C NMR (100 MHz, DMSO) δ (ppm) 194.8 (1C, AcCO), 163.1, 150.7 (2C, C-2, C-4), 141.2 (1C, C-6), 102.2 (1C, C-5), 88.4, 82.3, 72.3, 72.2 (4C, C-1’, C-2’, C-3’, C-4’), 31.0 (1C, C-5’), 30.5 (1C, AcCH₃). MALDI-ToF MS: m/z calcd for C₁₁H₁₄N₂NaO₆S [M + Na]⁺ 325.0470, found 325.0423.

5’-Thiouridine (32)⁴³: Compound 31 (2.4 g, 8.0 mmol) was dissolved in dry MeOH (50 mL) under Ar, and NaOMe (648 mg, 12 mmol, 1.5 equiv.) was added and stirred at r.t. for 1 h. The reaction mixture was neutralized with Amberlite IR 120 H⁺ ion exchanger resine, filtered off, and evaporated under reduced pressure. The crude product was purified by flash column chromatography (CH₂Cl₂:MeOH 9:1) to give 32 (1.47 g, 71%) as a white solid. [α]_D= -40.8 (c = 0.13, DMSO), Rf = 0.24(CH₂Cl₂/MeOH 95/5), ¹H NMR (400 MHz, DMSO) δ (ppm) 11.35 (s, 1H, NH), 7.67 (d, J = 8.1 Hz, 1H, H-6), 5.78 (d, J = 6.0 Hz, 1H, H-1’), 5.67 (d, J = 8.1 Hz, 1H, H-5), 5.41 (d, J = 5.8 Hz, 1H, 2’-OH), 5.22 (d, J = 5.0 Hz, 1H, 3’-OH), 4.13 (dd, J = 11.3, 5.7 Hz, 1H, H-2’), 3.92 (dd, J = 8.8, 4.6 Hz, 1H, H-3’), 3.85 (dd, J = 9.5, 5.8 Hz, 1H, H-4’), 2.81 (dd, J = 13.6, 5.5 Hz, 1H, H-5’a), 2.73 (dd, J = 13.8, 6.0 Hz, 1H, H-5’b), 2.48 (d, J = 19.6 Hz, 1H, SH). ¹³C NMR (100 MHz, DMSO) δ (ppm) 172.6, 160.3 (2C, C-2, C-4), 150.6 (1C, C-6), 111.7 (1C, C-5), 97.5, 94.1, 81.9, 81.0 (4C, C-1’, C-2’, C-3’, C-4’), 35.8 (1C, C-5’). MALDI-ToF MS: m/z calcd for C₉H₁₂N₂NaO₅S [M + Na]⁺ 283.0365, found 283.0306.

5’- S -Acetyl-5’-thioadenosine (33): PPh₃ (6.5 g, 24.6 mmol, 2.0 equiv.) was dissolved in dry THF (50 mL) and cooled to 0 ^oC. DIAD (5.0 mL, 24.6 mmol, 2.0 equiv.) was added dropwise and stirred for 30 min at 0 ^oC. Adenosine (3.3 g, 12.3 mmol) and HSAc (1.8 mL, 24.6 mmol, 2.0 equiv.) were dissolved in dry DMF (50 mL) and added dropwisely to the reaction mixture and stirred for 30 min at 0 ^oC and 90 min at r.t. The solvent was evaporated under reduced pressure and the crude product was purified by flash column chromatography (gradient elution, CH₂Cl₂MeOH 91→82) to give 33 (3.47 g, 87%) as a pale yellowish solid. [α]_D= -23.3 (c = 0.39, DMSO), Rf = 0.33 (CH₂Cl₂/MeOH 8/2), ¹H NMR (400 MHz, DMSO) δ (ppm) 8.35, 8.17 (2x s, 2x 1H, H-2, H-8), 7.33 (s, 2H, NH₂), 5.89 (d, J = 5.7 Hz, 1H, H-1’), 5.55 (d, J = 6.1 Hz, 1H, 2’-OH), 5.41 (d, J = 5.0 Hz, 1H, 3’-OH), 4.80 (dd, J = 11.2, 5.7 Hz, 1H, H-2’), 4.12 (dd, J = 8.9, 4.6 Hz, 1H, H-3’), 3.94 (dd, J = 9.2, 7.2 Hz, 1H, H-4’), 3.36 (dd, J = 13.8, 5.7 Hz, 1H, H-5’a), 3.18 (dd, J = 13.5, 7.8 Hz, 1H, H-5’b), 2.33 (s, 3H, AcCH₃). ¹³C NMR (100 MHz, DMSO) δ (ppm) 195.3 (1C, AcCO), 153.1 (2C, C-2, C-8), 156.6, 149.9 (2C, C-4, C-5), 119.7 (1C, C-6), 88.0, 83.3, 73.1 (4C, C-1’, C-2’, C-3’, C-4’), 31.7 (1C, C-5’), 30.9 (1C, AcCH₃). MALDI-ToF MS: m/z calcd for C₁₂H₁₅N₅NaO₄S [M + Na]⁺ 348.074, found 348.067.

5’-Deoxy-5’-thioadenosine (34)⁴³: Compound 33 (3.16 g, 9.7 mmol) was dissolved in dry MeOH (50 mL) under Ar, and NaOMe (787 mg, 14.5 mmol, 1.5 equiv.) was added and stirred at r.t. for 1 h. The reaction mixture was neutralized with AcOH and evaporated under reduced pressure. The crude product was purified by flash column chromatography (CH₂Cl₂:MeOH 9:1→8:2) to give 34 (2.11 g, 77%) as a white solid. [α]_D= -18.3 (c = 0.4, DMSO), Rf = 0.17 (CH₂Cl₂/MeOH 9/1), ¹H NMR (400 MHz, DMSO) δ (ppm) 8.37, 8.17 (2 x s, 2 x 1H, H-2, H-8), 7.32 (s, 2H, NH₂), 5.91 (d, J = 6.1 Hz, 1H, H-1’), 4.79 (t, J = 5.6 Hz, 1H, H-2’), 4.25–4.19 (m, 1H, H-3’), 3.99 (td, J = 6.1, 3.3 Hz, 1H, H-4’), 2.89 (dd, J = 13.7, 6.0 Hz, 1H, H-5’a), 2.78 (dd, J = 13.8, 6.3 Hz, 1H, H-5’b). ¹³C NMR (100 MHz, DMSO) δ (ppm) 156.1, 149.5 (2C, C-4, C-5), 152.7 (2C, C-2, C-8), 119.3 (1C, C-6), 87.4, 85.5, 72.7, 71.9 (4C, C-1’, C-2’, C-3’, C-4’), 26.6 (1C, C-5’). MALDI-ToF MS: m/z calcd for C₁₀H₁₃N₅NaO₃S [M + Na]⁺ 306.0637, found 306.0594.

Detection of H₂S release of 5’-dithioacetyl nucleosides

The H₂S-donating ability of compound 22, 24, 27, 29 and 30 (0.5 mg dissolved in 0.1 mL of DMSO) was detected in Dulbecco’s modified Eagle’s medium (DMEM) (4.9 mL) supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin. The released H₂S was detected by an amperometric, H₂S specific sensor (ISO-H2S-100, World Precision Instruments, Saratosa, FL, USA) connected to a WPI TBR 1025 One-Channel Free Radical Analyzer. The sensor was set to 10 nA range and poise voltage to + 150 mV. Before the measurements the sensor was polarized in phosphate buffered saline (PBS) for 12 hours.¹⁹ The H₂S-release of NaHS was detected in distilled water (0.1 mg in 5 mL of H₂O) and the H₂S-release of GYY4137 was measured in DMEM (0.5 mg of GYY4137 in 5 mL of medium).

Antioxidant assays

Determination of Antioxidant Activity by 2,2-diphenyl-1-picrylhydrazyl (DPPH) Assay

DPPH is a stable free radical with a deep violet color that changes to yellow when neutralized by an electron or hydrogen radical, indicating the antioxidant activity of the sample being tested. The DPPH radical scavenging abilities were investigated following the method outlined by Shimamura et al., with minor adjustments.⁴⁴ Briefly, 1 mL of DPPH solution was added to a mixture of 200 µL of the methanolic sample solution and 800 µL of 0.1 M Tris-HCl buffer (pH = 7.4). After mixing, the absorbance was promptly recorded, after which the solutions were incubated in the dark at room temperature for 30 min before the absorbance was measured again. The test samples were prepared and assayed at varying concentrations using a 2-fold serial dilution method, starting from a concentration of 2 mM. Each investigation was performed in triplicate, and the antioxidant activity was based on the absorbance recorded at 517 nm on a UV-1600PC VWR spectrophotometer (VWR, China). A mixture of 1.2 mL of methanol and 800 µL of 0.1 M Tris-HCl buffer served as a blank. Ascorbic acid (AA) and the unmodified nucleosides were used as positive control and reference compounds, respectively.

The inhibition ratio (IR) was calculated as follows:

$$\:Inhibition\:Ratio\:\left(\%\right)=\:\left(\frac{Ac-\:As}{Ac}\right)*100\:$$

Where Ac is the absorbance when methanol is added instead of the sample and As is the absorbance when the testing sample solution is added.

The antioxidant capacity was expressed as the concentration needed to achieve a 50% inhibition of the free radical (IC₅₀). The IC₅₀ values were calculated by plotting the percent of inhibition as a function of sample concentration.

ABTS decolorization assay

The ABTS decolorization assay was carried out as described by Szoke et al.⁴⁵ Briefly, the method is based on the scavenging of (2,2’-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) ABTS^•+ radical cation. The decolorization caused by the compound is compared to the decolorization induced by Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid), and expressed as Trolox equivalent antioxidant capacity (TEAC) value. TEAC values were expressed as Trolox equivalents calculated from (Ai − Af)antioxidant/(Ai − Af) Trolox at 0.1 mM concentrations. Briefly, a total of 10 µL sample, 20 µL of Myoglobin Working Solution, and 150 µL of ABTS Substrate Working Solution were mixed and incubated for 5 min at room temperature. At the end of incubation 100 mL of Stop Solution was added and endpoint absorbance at 405 nm was read. All experiments were performed in triplicates and repeated three times.

MTT assay

H9c2 viability was measured by MTT assay (3-(4,5-dimethylthiazol-2-yl)-2,5- (diphenyltetrazolium bromide)) on 96-well plates, according to the method described in the literature.⁴⁶ Briefly, H9c2 cells were plated at density of (3 × 10³ cells/well) and grown overnight in a humidified incubator with 5% CO2 at 37 ◦C for 24 h. For the determination of IC₅₀ values, cells were treated with the following conditions: fresh culture medium alone (control), fresh culture medium with compound 22, 24, 32 and 34 at concentrations ranging from 1 µM to 1000 µM for 24 h. After that, 20 µL of 5 mg/mL MTT solution was added to each well. The plate was again incubated for 3 h at 37°C. During incubation, a conversion of the water-soluble yellow dye MTT into an insoluble purple formazan by the action of mitochondrial reductase occurred. Formazan crystals were solubilized by adding 200 µL of isopropanol to each well. The concentrations were determined by optical density at 570 nm. The background absorbance was also recorded at 690 nm, which was subtracted. Cell viability was expressed as a percent of the cell viability of the untreated control cells. After 24 h, cells were treated with compound 22, 24, 32 and 34. On the next day, cell viability was measured by MTT assay as described previously.⁴⁶

Antiviral assay

Anti-SARS-CoV-2 activity and cytotoxicity determination in Calu-3 cells

The anti-SARS-CoV-2 activity was measured by determining the extent to which the compounds inhibited virus-induced cytopathic effect (CPE) in Calu-3 cells (ATCC). Briefly, 40,000 Calu-3 cells in a 96-well plate in DMEM medium with 2% FBS, 100 U of penicillin/mL and 100 µg of streptomycin/mL (all Merck) were infected with SARS-CoV-2 (strain hCoV-19/Czech Republic/NRL_6632_2/2020) at multiplicity of infection 0.3. After 2 hours, the medium was removed, cells were washed two times with 1X DMEM and two-fold fold serial dilutions of compounds from 1000 µM were added in triplicate. Following two days incubation at 37°C in 5% CO₂ the cell viability was determined by adding CellTiter-Glo luminescent cell reagent (Promega) using Tempest liquid dispenser (Formulatrix). The luminescent signal produced by ATP-dependent oxidation of luciferin by viable cells was measured using EnVision plate reader (Perkin Elmer). Drug concentrations required to reduce viral cytopathic effect by 50% (EC50) were calculated using nonlinear regression from plots of percentage cell viability versus log₁₀ drug concentration using GraphPad Prism v.9.5.1 (GraphPad Software).

Cytotoxicity was evaluated by incubating the same two-fold serial dilutions of each compound with Calu-3 cells as above in the absence of the virus. Following two days incubation at 37°C in 5% CO₂, the cell viability was determined as above. The compound concentrations resulting in 50% reduction of cell viability (CC₅₀) were calculated from plots of percentage of luminescence versus log₁₀ drug concentration as above. Remdesivir was used as control in both assays.

Virus yield reduction assay

The reduction in virus titer was assessed in medium after 2 days infection of Calu-3 in the Vero E6 cells by plaque assay. Briefly, 50 µl of medium from Calu-3 cells infected in the presence of the highest compound concentration was mixed with DMEM medium followed by 10-fold dilution, mixed with Vero E6 cells, added to 24-well plate and incubated for 4 hours at 37°C in 5% CO₂. Next, the mixture was overlaid with 500 µl of 3% carboxymethyl cellulose (Merck) and incubated for 5 days at 37°C in 5% CO₂. Remdesivir was included as control. After incubation, the cells were washed once with 1xPBS, stained with naphthalene black (Merck), washed with water and air-dried. Plaques were counted and expressed as log₁₀ plaque forming units (PFU) per mL.

In vivo studies

The cardiac effects of adenosine, compound 22, 24 and 34 were assessed with electrocardiography (ECG) and echocardiography on anaesthetized Sprague-Dawley rats (weighing 600–800 g, Charles River Laboratories) as described previously.⁴⁷ The animals received humane care, and all experimental procedures were carried out in accordance with the “Principles of Laboratory Animal Care” by EU Directive 2010/63/EU. All experimental protocols were approved by the local Ethics Committee of University of Debrecen (25/2023/DEMÁB). Animal experiments are reported in compliance with the ARRIVE guidelines.⁴⁸ Anesthesia was carried out using ketamine/xylazine mixture (100/10 mg/kg, i.m.). The chest was shaved and the animal was placed onto a heated pad (VisualSonics SR200, VisualSonics, Amsterdam, The Netherlands). The lateral tail vein was cannulated using a heparinized 26G i.v. cannula (BD Neoflon, BD Medical, NJ, USA). B-mode and M-mode echocardiography was carried out before and 30 seconds after the intravenous administration of the compounds. A high-resolution ultrasound machine (Vevo 3100 Imaging Station, VisualSonics, Amsterdam, The Netherlands) equipped with a 21 Hz transducer (MX201) was used for assessing cardiac parameters. Traces were obtained from the parasternal long axis view (PLAX). A B-mode video and an M-mode trace was recorded, and the following parameters were then offline analysed: left ventricle (LV) end-systolic and end-diastolic volume (LVESV, LVEDV, respectively) fractional shortening (FS) and ejection fraction (EF) and stroke volume (SV).

A 3-channel ECG was continuously recorded during the experiments (Vevo monitor ECG, VisualSonics, Amsterdam, The Netherlands). On the recorded ECG data, RR, PR and QT intervals, and heart rate (HR) were determined before and 30 seconds after the administration of the drugs, and 6 consecutive cardiac cycles were averaged for each parameter.

Statistical analyses for the in vivo studies were carried out using the GraphPad Prism 9.0 software (GraphPad Software, San Diego, CA, USA). Data distribution was assessed by the Shapiro-Wilk normality test, and paired t-test were used to determine the differences between the baseline (drug free) and endpoint (treated) parameters in each group. A multiple comparison was also carried out between the treatment groups by using one-way ANOVA with Tukey multiple comparison test. Data was shown as mean ± SD, and differences with p < 0.05 were considered significant.

A, adenine; ABTS, 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid); Ac, acetyl; Bu₄NBr, tetrabutyl ammonium bromide; C, cytosine; DIAD, diisopropyl azodicarboxylate; DMF, dimethylformamide; DPPH, 2,2-Diphenyl-1-picrylhydrazyl; G, guanine; HFIP, hexafluoro isopropanol; HSAc, thioacetic acid; MeOH, methanol; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5- (diphenyltetrazolium bromide); NaOMe, sodium methylate; PPh₃, triphenyl phosphine; TFA, trifluoroacetic acid; THF, tetrahydrofuran; TLC, thin layer chromatography; Trt, triphenylmethyl; TrtCl, triphenylmethyl chlorid; Ts, p-toluenesulfonyl; TsCl, p-toluenesulfonyl chloride; TsOH, p-toluenesulfonic acid; U, uridine.

Associated content

Supporting Information.

Antiviral EC50 and CC50 graphs, HPLC chromatograms and NMR spectra of the compounds. A listing of the contents of each file supplied as Supporting Information should be included. For instructions on what should be included in the Supporting Information as well as how to prepare this material for publications, refer to the journal’s Instructions for Authors.The following files are available free of charge. brief description (file type, i.e., PDF) brief description (file type, i.e., PDF)

Author information

Corresponding Author

*Anikó Borbás ([email protected]) and

Miklós Bege ([email protected])

Author Contributions

Synthesis of the compounds: M.B. and M.L. NMR characterization: M. B. MALDI characterization and H2S releasing measurements: I.B. Antiviral assays: J.H. and J.W. DPPH antioxidant assay: R.G.K. ABTS and MTT assays: I.L, R. K. and S. E. HPLC measurments: L. N. In vivo experiments: D.P. and B.B. Conceptualisation and supervision: A.B. and P.H. The main manuscript text was written by M.B., R.G.K., D.P., J.W. and A.B. All authors reviewed the manuscript and all authors have given approval to the final version of the manuscript.

Data availability statement

Data is provided within the manuscript or supplementary information files.

Competing interest statement

The authors declare no competing interests.

Acknowledgements

This research was conducted with the support of the National Academy of Scientist Education Program of the National Biomedical Foundation under the sponsorship of the Hungarian Ministry of Culture and Innovation. Chemical synthesis work was funded by the National Research, Development and Innovation Office of Hungary (K 132870 and FK 142315) and by the University of Debrecen Scientific Research Bridging Fund (DETKA). The research was also supported by the EU and co-financed by the European Regional Development Fund under the project GINOP-2.3.4-15-2020-00008. Antiviral tests were funded by the project National Institute Virology and Bacteriology (Programme EXCELES, Project No. LX22NPO5103) - Funded by the European Union - Next Generation EU.

Gadalla, M.M.; Snyder, S.H.; Hydrogen sulfide as a gasotransmitter, J. Neurochem. 113, 14 – 26 (2010) DOI: 10.1111/j.1471-4159.2010.06580.x C.
Baskar, R.; Bian, J.; Hydrogen sulfide gas has cell growth regulatory role, Eur J. Pharmacol.656, 5-9 (2011) DOI: 10.1016/j.ejphar.2011.01.052
Hellmich, M.R.; Coletta, C.; Chao, C.; Szabo, Cs.; The therapeutic potential of cystathionine β-synthetase/hydrogen sulfide inhibition in cancer, Antioxid. Redox. Signal.22, 424-448 (2015) DOI: 10.1089/ars.2014.5933
Zaorska, E.; Tomasova, L.; Koszelewski, D.; Ostaszewski, R.; Ufnal, M.; Hydrogen sulfide in pharmacotherapy, beyond the hydrogen sulfide-donors, Biomolecules, 10, 323-348 (2020) DOI: 10.3390/biom10020323
Aroca, A.; Gotor, C.; Bassham, D.C.; Romero, L.C.; Hydrogen sulfide: from a toxic molecule to a key molecule of cell life, Antioxidants. 9, 621-644 (2020) DOI: 10.3390/antiox9070621
Wallace, J.L. et al. A proof‐of‐concept, Phase 2 clinical trial of the gastrointestinal safety of a hydrogen sulfide‐releasing anti-inflammatory drug, Br. J. Pharmacol.177, 769-777 (2020) DOI: 10.1111/bph.14641
Citi, V. et al. Searching for novel hydrogen sulfide donors: The vascular effects of two thiourea derivatives, Pharmacol. Res.159, 105039-105048 (2020) DOI: 10.1016/j.phrs.2020.105039
Fu, L. et al. An antifungal role of hydrogen sulfide on the postharvest pathogens Aspergillus niger and Penicillium italicum, PLoS One, 9, e104206; (2014) DOI: 10.1371/journal.pone.0104206
Yang, G.; H₂S as a potential defense against COVID-19?, Am. J. Physiol. Cell Physiol.319, C244-C249 (2020) DOI: 10.1152/ajpcell.00187.2020
Evgen’ev, M.B.; Frenkel, A.; Possible application of H₂S-producing compounds in therapy of coronavirus (COVID-19) infection and pneumonia, Cell Stress Chaperones. 25, 713-715 (2020) DOI: 10.1007/s12192-020-01120-1
Dai, J.; Teng, X.; Jin, S.; Wu, Y.; The antiviral roles of hydrogen sulfide by blocking the interaction between SARS-CoV-2 and its potential cell surface receptors, Oxid. Med. Cell Longev. 2021, Article ID 7866992 (2021) DOI: 10.1155/2021/7866992
Bazhanov, N.; Escaffre, O.; Freiberg, A.N.; Garofalo, R.P.; Casola, A.; Broad-Range antiviral activity of hydrogen sulfide against highly pathogenic RNA viruses, Sci. Rep. 7, Article number: 41029 (2017) DOI: 10.1038/srep41029
Powell, C.R.; Dillon, K.M.; Matson, J.B.; A review of hydrogen sulfide (H₂S) donors: Chemistry and potential therapeutic applications, Biochem. Pharmacol. 149, 110-123 (2018) DOI: 10.1016/j.bcp.2017.11.014
Levinn, C.M.; Cerda, M.M.; Pluth, M.D.; Activatable small-molecule hydrogen sulfide donors, Antioxid. Redox. Signal. 32, 96-109 (2020), DOI: 10.1089/ars.2019.7841
Kashfi, K.; Olson, K.R.; Biology and therapeutic potential of hydrogen sulfide and hydrogen sulfide-releasing chimeras, Biochem. Pharmacol.85, 689-703 (2013) DOI: 10.1016/j.bcp.2012.10.019
Antoniadou, I. et al. Novel H₂S-releasing bifunctional antihistamine molecules with improved antipruritic and reduced sedative actions, J. Med. Chem.66, 9607-9621 (2023) doi: 10.1021/acs.jmedchem.3c00321
Song, Z-L. et al. Progress and perspective on hydrogen sulfide donors and their biomedical applications, Med. Res. Rev. 42, 1930-1977 (2022) DOI: 10.1002/med.21913
Gyöngyösi, A. et al. Pharmacological characterization of EV-34, a new H₂S-releasing ibuprofen derivative, Molecules, 26, 599-611 (2021) DOI: 10.3390/molecules26030599
Vass, V. et al. Reperfusion-induced injury and the effects of the dithioacetate type hydrogen sulfide donor ibuprofen derivative, BM-88, in isolated rat hearts, Eur. J. Pharm. Sci. 185, 106449-106463 (2023) DOI: 10.1016/j.ejps.2023.106449
Liu, R.; Orgel, L.E.; Oxidative acylation using thioacids, Nature, 389, 52-54 (1997) DOI: 10.1038/37944
Cerda, M.M.; Newton, T.D.; Zhao, Y.; Collins, B.K.; Hendon, C.H.; Pluth, M.D.; Dithioesters: simple, tunable, cysteine-selective H₂S donors, Chem. Sci.10, 1773-1779 (2019) DOI: 10.1039/C8SC04683B
Tánczos, B. et al. Effects of H₂S-donor ascorbic acid derivative and ischemia/reperfusion-induced injury in isolated rat hearts, Eur. J. Pharm.Sci. 195, 106721-106736 (2024) DOI: 10.1016/j.ejps.2024.106721
Guinan, M.; Benckendorff, C.; Smith, M.; Miller, G.J.; Recent advances in the chemical synthesis and evaluation of anticancer nucleoside analogues, Molecules, 25, 2050-2075 (2020) DOI: 10.3390/molecules25092050
Seley-Radtke, K.L.; Yates, M.K.; The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold, Antiviral Res. 154, 66-86 (2018) DOI: 10.1016/j.antiviral.2018.04.004
Lougiakis, N. et al. Synthesis and pharmacological evaluation of novel adenine-hydrogen sulfide slow release hybrids designed as multi-target cardioprotective agents, J. Med. Chem. 59, 1776-1790 (2016) DOI: 10.1021/acs.jmedchem.5b01223
Beltowski, J.; Guranowski, A.; Jamroz-Wisniewska, A.; Wolski, A.; Halas, K.; Hydrogen sulfide (H₂S)-mediated vasodilatory effect of nucleoside 5′-monophosphorothioates in perivascular adipose tissue, Can. J. Physiol. Pharmacol.93, 585-595 (2015) DOI: 10.1139/cjpp-2014-0543
Beltowski, J.; Guranowski, A.; Jamroz-Wisniewska, A.; Nucleoside monophosphorothioates as the new hydrogen sulfide precursors with unique properties, Pharmacol. Res. 81, 34-43 (2014) DOI: 10.1016/j.phrs.2014.01.003
Zheng, Z. et al. Novel nucleoside-based antimalarial compounds, Bioorg. Med. Chem. Lett. 26, 2861-2865 (2016) DOI: 10.1016/j.bmcl.2016.04.053
Bege, M. et al. In vitro and in vivo antiplasmodial evaluation of sugar-modified nucleoside analogues, Sci. Rep.13, 12228; 10.1038/s41598-023-39541-4 (2023)
Godoy, A. S. et al. Allosteric regulation and crystallographic fragment screening of SARS-CoV-2 NSP15 endoribonuclease, Nucleic Acids Res. 51, 5255-5270 (2023) DOI: 10.1093/nar/gkad314
Miles, R.W.; Nielsen, L.P.C.; Ewing, G.J.; Yin, D.; Borchardt, R.T.; Robins, M.J.; S-Homoadenosyl-L-cysteine and S-homoadenosyl-L-homocysteine. Synthesis and binding studies of non-hydrolyzed substrate analogues with S-adenosyl-L-homocysteine Hydrolase, J. Org. Chem. 67, 8258-8260 (2002) DOI: 10.1021/jo020478g
Bege, M. et al. Synthesis and oligomerization of cysteinyl nucleosides, Org. Biomol. Chem.18, 8161-8178 (2020) DOI: 10.1039/d0ob01890b
Friedel, H.A.; Goa, K.L.; Benfield, P.; S-Adenosyl-L-methionine. A review of its pharmacological properties and therapeutic Potential in liver dysfunction and affective disorders in relation to its physiological role in cell metabolism, Drugs. 38, 389-416 (1989) DOI: 10.2165/00003495-198938030-00004
Bege, M. et al. A low-temperature, photoinduced thiol-ene click reactio: a mild and effort for the synthesis of sugar-modified nucleosides, Org. Biomol. Chem. 15, 9226-9233 (2017) DOI: 10.1039/C7OB02184D
Tomasz, J.; in Nucleic Acid Chemistry Part Two (eds. L.B. Townsend, R. S. Tipson) 765-769 (John Wiley & Sons, 1978)
Kicsák, M. et al. A three-component reagent system for rapid and mild removal of O-, N- and S-trityl protecting groups, Org. Biomol. Chem. 14, 3190-3192 (2016) DOI: 10.1039/C6OB00067C
Debreczeni, N. et al. Tightly linked morpholino-nucleoside chimeras: new, compact cationic oligonucleotide analogues, Org. Biomol. Chem. 19, 8711-8721 (2021) DOI: 10.1039/D1OB01174J
Sugihara, S.; Konegawa, N.; Maeda, Y.; HCl·Et₂O-Catalyzed metal-free RAFT cationic polymerization: one pot transformation from metal-free living cationic polymerization to RAFT radical polymerization, Macromolecules, 48, 5120-5131 (2015) DOI: 10.1021/acs.macromol.5b01071
Gain, C.; Song, S.; Angtuaco, T.; Satta, S.; Kelesidis, T. The role of oxidative stress in the pathogenesis of infections with coronaviruses. Front. Microbiol. 13, 1111930; 10.3389/fmicb.2022.1111930 (2023)
Alvarado-Tapias, E. et al. Adenosine induces ventricular arrhythmias in hearts with chronic chagas cardiomyopathy. Rev Esp Cardiol (Engl Ed).63, 478-482 (2010) DOI: 10.1016/S1885-5857(10)70097-9
Guideri, F. et al. QTc interval prolongation during infusion with dipyridamole or adenosine. Int. J. Cardiol. 48, 67-73 (1995) DOI: 10.1016/0167-5273(94)02209-2
Fujisawa, Y.; Mitsunobu, O.; Preparation of Deoxyhalogenouridines, J. Chem. Soc. Chem. Commun. 1973, 201-201 (1973) DOI: 10.1039/C39730000201
Marriott, J.H.; Mottahedeh, M.; Reese, C.B. 9-(4-Methoxyphenyl)xanthen-9-thiol: a useful reagent for the preparation of thiols, Tetrahedron Lett.31, 7485-7488 (1990) DOI: 10.1016/S0040-4039(00)88523-8
Shimamura, T. et al. Applicability of the DPPH assay for evaluating the antioxidant capacity of food additives-inter-laboratory evaluation study. Anal. Sci. 30, 717-721 (2014) DOI: 10.2116/analsci.30.717
Szőke, K. et al. Pharmacological evaluation of newly synthesized cannabidiol derivates on H9c2 cells. Antioxidants, 12, 1714-1729 (2023) DOI: 10.3390/antiox12091714
Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol. Methods. 65, 55-63 (1983). DOI: 10.1016/0022-1759(83)90303-4. PMID: 6606682.
Vecsernyes, M. et al. Alpha–Melanocyte-stimulating Hormone Induces Vasodilation and Exerts Cardioprotection Through the Heme-Oxygenase Pathway in Rat Hearts. J. Cardiovasc. Pharmacol. 69, 286-297 (2017)| DOI: 10.1097/FJC.0000000000000472
Percie du Sert. N.; Hurst, V.; Ahluwalia, A.; Alam, S.; Avey, M.T.; Baker, M. et al. The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research. PLoS Biol. 18(7), e3000410 (2020). DOI: 10.1371/journal.pbio.3000410

No competing interests reported.

8.png
Graphical abstract
SIfinal.docx

Download PDF

Reviews received at journal
14 Sep, 2024
Reviewers agreed at journal
14 Sep, 2024
Reviewers agreed at journal
02 Sep, 2024
Reviewers invited by journal
21 Aug, 2024
Editor assigned by journal
20 Aug, 2024
Editor invited by journal
12 Aug, 2024
Submission checks completed at journal
12 Aug, 2024
First submitted to journal
06 Aug, 2024

You are reading this latest preprint version

Synthesis, H2S releasing properties, antiviral and antioxidant activities and acute cardiac effects of nucleoside 5’-dithioacetates

Status:

Version 1

Abstract

Figures

Introduction

Results and discussion

Synthesis

Evaluation of H₂S releasing profile of the compounds

Antioxidant assays

Cell viability

Antivirals results

Results of in vivo experiments

Conclusions

Experimental methods

General informations

Synthesis of the compounds

Detection of H₂S release of 5’-dithioacetyl nucleosides

Antioxidant assays

Determination of Antioxidant Activity by 2,2-diphenyl-1-picrylhydrazyl (DPPH) Assay

ABTS decolorization assay

MTT assay

Antiviral assay

Anti-SARS-CoV-2 activity and cytotoxicity determination in Calu-3 cells

Virus yield reduction assay

In vivo studies

Abbreviations

Declarations

References

Additional Declarations

Supplementary Files

Status:

Version 1

Synthesis, H2S releasing properties, antiviral and antioxidant activities and acute cardiac effects of nucleoside 5’-dithioacetates

Status:

Version 1

Abstract

Figures

Introduction

Results and discussion

Synthesis

Evaluation of H2S releasing profile of the compounds

Antioxidant assays

Cell viability

Antivirals results

Results of in vivo experiments

Conclusions

Experimental methods

General informations

Synthesis of the compounds

Detection of H2S release of 5’-dithioacetyl nucleosides

Antioxidant assays

Determination of Antioxidant Activity by 2,2-diphenyl-1-picrylhydrazyl (DPPH) Assay

ABTS decolorization assay

MTT assay

Antiviral assay

Anti-SARS-CoV-2 activity and cytotoxicity determination in Calu-3 cells

Virus yield reduction assay

In vivo studies

Abbreviations

Declarations

References

Additional Declarations

Supplementary Files

Status:

Version 1

Evaluation of H₂S releasing profile of the compounds

Detection of H₂S release of 5’-dithioacetyl nucleosides