Synthesis and antiviral activities of spacer-linked 1-thioglucuronide analogues of glycyrrhizin

  1. 1,§ ,
  2. 2,§ ,
  3. 1 ,
  4. 1 ,
  5. 3 ,
  6. 2 and
  7. 1
1Department of Chemistry, University of Natural Resources and Life Sciences-Vienna, Muthgasse 18, A-1190 Vienna, Austria
2Savira Pharmaceuticals GmbH, Veterinärplatz 1, A-1210 Vienna, Austria
3Institute of Applied Synthetic Chemistry, Vienna University of Technology, Getreidemarkt 9, A-1060 Vienna, Austria
  1. Corresponding author email
§ These authors contributed equally to this work
Guest Editor: T. K. Lindhorst
Beilstein J. Org. Chem. 2012, 8, 705–711. https://doi.org/10.3762/bjoc.8.79
Received 09 Mar 2012, Accepted 12 Apr 2012, Published 08 May 2012
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Abstract

The influenza virus infection remains a significant threat to public health and the increase of antiviral resistance to available drugs generates an urgent need for new antiviral compounds. Starting from the natural, antivirally active compound glycyrrhizin, spacer-bridged derivatives were generated with improved antiviral activity against the influenza A virus infection. Simplified analogues of the triterpene saponin glycyrrhizin containing 1-thio-β-D-glucuronic acid residues have been prepared in good yields by alkylation of 3-amino and 3-thio derivatives of glycyrrhetinic acid with a 2-iodoethyl 1-thio-β-D-glucopyranosiduronate derivative. The spacer-connected 3-amino derivatives were further transformed into N-acetylated and N-succinylated derivatives. The deprotected compounds containing these carboxylic acid appendices mimic the glycon part of glycyrrhizin as well as the hemisuccinate derivative of glycyrrhetinic acid, carbenoxolone. Antiviral activities of the compounds were determined in a biological test based on influenza A virus-infected cells, wherein the 3-(2-thioethyl)-N-acetylamino- and 3-(2-thioethyl)-thio-linked glucuronide derivatives were effective inhibitors with IC50 values as low as 54 µM.

Introduction

The triterpene saponin glycyrrhizin (GL) and its aglycon glycyrrhetinic acid (GA) are the main triterpene components of licorice roots and harbor various pharmacological activities, including antitumor, anti-inflammatory, antioxidant and antiviral properties [1,2]. The antiviral activities have been reported to be directed against a broad spectrum of viruses comprising herpes-, corona-, alpha-, and flaviviruses, HIV, Epstein–Barr virus, influenza A virus (IAV), vaccinia and polio type I viruses as examples [3-8]. In particular anti-influenza virus activities have been described, although the underlying mechanisms of action are diverse [9-12]. In order to evaluate the potential antiviral properties of glycyrrhizin derivatives, we set out to modify the chemical environment in the vicinity of ring A of glycyrrhetinic acid. The envisaged modifications should assess the impact of acidic groups, which reside at the glucuronic acid residues in the β-(1→2)-linked disaccharide unit of GL, with respect to antiviral properties (Figure 1).

[1860-5397-8-79-1]

Figure 1: Structure of glycyrrhizin (GL), carbenoxolone (CBX), and spacer analogues.

Previously, ring A modified derivatives of glycyrrhetinic acid were prepared containing 3-amino, 3-thio and 1-thio groups, allowing for an extension of the oleanolic acid unit with spacer groups as well as facile covalent attachment of carboxyalkyl groups by alkylation or acylation reactions [13,14]. For the compounds included in this investigation, the size of the spacer group was selected to closely match the formal distances between the A-ring and the carboxylic acid function present in the glucopyranosiduronic residues of the parent compound glycyrrhizin (GL) and in the hemisuccinate moiety of the glycyrrhetinic acid derivative carbenoxolone (CBX) [15] (Figure 1). For the sake of clarity, the nomenclature and numbering for the triterpene system as used throughout this report is illustrated in Figure 1. In order to enhance resistance against enzymatic cleavage by glucuronidases, the glucuronic acid residue was introduced through a stable thioglycosidic linkage.

Results and Discussion

Synthesis of 3-amino derivatives

Commercially available methyl (2,3,4-tri-O-acetyl-D-glucopyranosyl)uronate bromide (1) was first reacted with potassium thioacetate in DMF to furnish the known 1-thioacetyl derivative 2 in 82% yield [16]. Subsequent treatment of 2 with sodium methoxide, under controlled conditions at low temperature (−60 °C → −45 °C), provided the corresponding glucuronyl 1-thiol 3 in 89% yield [17,18]. Reaction of 3 with an excess of 1,2-dibromoethane (3–4 equiv) in DMF in the presence of sodium hydride, with the strict exclusion of oxygen, afforded the 2-bromoethyl 1-thioglycoside 4 in 80% yield. Under these conditions formation of the bis-substitution product 5 (3%) and the disulfide oxidation product of 1-thiol 3 was observed in only very minor quanities. The corresponding 2-iodoethyl derivative 6 was prepared by a Finkelstein reaction from the bromoethyl 1-thioglycoside 4 in 95% yield (Scheme 1).

[1860-5397-8-79-i1]

Scheme 1: Synthesis of methyl 2-haloethyl 1-thio-glucuronide derivatives: (a) 1 M NaOMe, MeOH, −60 °C to −45 °C, 89% ; (b) Br(CH2)2Br, NaH, DMF, −5 °C (80% for 4, 3% for 5); (c) NaI, acetone, 4 °C, 16 h, 95%.

The previously reported 3β-amino derivative of the diphenylmethyl ester of glycyrrhetinic acid 7 [19] was then used for the introduction of the spacer-extended 1-thio-glucopyranosiduronate residue. Coupling of the 3β-amino derivative 7 with two equivalents of the 2-iodoethyl glycoside 6 in DMF in the presence of Hünig base proceeded smoothly to provide the alkylated amine 8 in 79% yield without the formation of a bis-alkylated product (Scheme 2), whereas the use of the corresponding bromide 4 resulted in a significantly slower reaction. At elevated temperature, elimination leading to the corresponding hexenuronic acid derivative was observed (structure not shown). The secondary amino group in compound 8 was subjected to further derivatization by N-acetylation (triethylamine, acetic anhydride), which gave compound 9 in 96% yield. Deprotection of the ethyl 1-thio-glucuronide derivatives 8 and 9 was achieved by acid-catalyzed cleavage of the diphenylmethyl ester group with TFA/anisole (as carbocation scavenger), giving the monoacid derivatives 10 and 11 in 75% and 89% yield, respectively. Subsequent transesterification of 10 and 11 with methanolic NaOMe afforded the deacetylated methyl ester glucuronide derivatives 12 and 14, respectively, which were finally fully deprotected by hydrolysis of the methyl ester group with 0.2 M methanolic NaOH to furnish the diacid derivatives 13 and 15, in high overall yield.

[1860-5397-8-79-i2]

Scheme 2: Synthesis of thioalkylglucuronide GA derivatives: (a) DMF, DIPEA, 45–50 °C, 16 h, 79%; (b) TEA, Ac2O, DCM, 0 °C, 2 h, 96%; (c) anisole, TFA, DCM, rt, 3 h (75% for 10, 89% for 11); (d) 0.1 M NaOMe, MeOH, 0 °C (89% for 12, 97% for 14, 99% for 18); (e) 0.2 M NaOH, MeOH, rt, 3 h (91% for 13, ~quant. for 15, 99% for 19); (f) MeO2C(CH2)2COCl in DCM, DIPEA, 0 °C to rt, 90 min, then anisole, TFA, DCM, 0 °C, 3 h, 83% for two steps.

A second series of compounds was designed as glucuronide-extended amide derivatives of the previously reported carbenoxolone analogue 16 [20,21]. Reaction of the 3-amino group of 8 with the monomethyl ester of succinic acid chloride in dichloromethane in the presence of Hünig base was followed by deblocking of the diphenylmethyl ester group to afford 17 in a combined yield of 83%. The acetyl groups of 17 were removed under Zemplén conditions to afford the dimethyl ester 18. Alkaline hydrolysis of the ester groups eventually gave the triacid derivative 19 in good yield. In contrast to the straightforward chemical transformations, analysis of the NMR spectra of this series of compounds was challenging and the N-acylated derivatives 9, 11, 14, 15 and 1719 revealed complex spectra. Whereas the secondary amides of 3β-amino-glycyrrhetinic acid derivatives displayed coherent NMR signals [22,23], the tertiary amides frequently exist as mixtures of cis/trans rotamers leading to the duplication of signals [24,25]. The steric congestion at position 3 exerted by the two adjacent methyl groups may additionally contribute to the restricted rotation of the amide linkage. Thus, in the 1H NMR spectra of the N-acetyl- and N-succinyl derivatives, recorded at room temperature, two sets of signals in an approximate 6:4 ratio were observed. Reversible coalescence of these signal groups was observed upon heating a solution of the N-acetyl derivative 11 up to 100 °C in DMSO-d6 and subsequent cooling to room temperature (Figure 2), supporting the assignment of two signal data sets for two rotamers. The orientation of the amide carbonyl group in the rotamers also had a pronounced effect on the NMR chemical shifts of carbon and proton signals in ring A, which led to a shift of H-3 to lower field (δ 4.47) and to a shielding of C-3 (δ 59.9) for the minor isomer, whereas the inverse effects were seen for the major rotamer (δ for H-3 at 3.36 and δ for C-3 at 66.7). Similar, but less-pronounced effects were observed for the respective 1H and 13C signals at position 5 of ring A (see Supporting Information File 1).

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Figure 2: 400 MHz 1H NMR expansion plots of the carbohydrate region of compound 11, recorded at various temperatures.

Synthesis of 3-thio derivatives

Complementing the series of the 3β-amino series, related 3-thio derivatives were employed for the spacer elongation [14]. The previously reported 1,2-dehydro-3-thiol derivative 20 was subjected to alkylation with the 2-iodoethyl 1-thioglucuronide compound 6 in the presence of K2CO3 to furnish the thioether-bridged glucuronide triterpene 21 in 60% yield. Deprotection of 21 was performed in two steps as described for 10, which furnished the methyl ester derivative 22 and the glucuronic acid compound 23, respectively, in good yields (Scheme 3).

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Scheme 3: Synthesis of 3-thioether-bridged glucuronide derivatives: (a) K2CO3, acetone, 60%; (b) 0.8 M NaOMe, MeOH, 71%; (c) 0.2 M NaOH, MeOH, 95% .

Antiviral activities

For biological testing the compounds were dissolved in DMSO and diluted in cell culture medium to a maximum final DMSO concentration of 1%. For determination of the cytotoxicity of the compounds, MDCK cells were treated with compound concentrations ranging from 3.1 µM to 250 µM for 48 h and then cell viability was determined as a surrogate endpoint for cytotoxicity. Except for the aglycons of GL, namely glycyrrhetinic acid (GA) and the hemisuccinate carbenoxolone (CBX), which showed CC50 values (half-maximal cytotoxic concentration) of 7.4 µM and 17.8 µM, respectively, none of the compounds tested were toxic at concentrations up to 250 µM. GL was not toxic at 2500 µM (Table 1). The antiviral activity of the compounds was determined by infecting MDCK cells with influenza A H3N2 virus and treating them with different concentrations of compounds at the same time. Most compounds prevented virus-induced cytopathicity and restored cell viability compared to virus-infected control cells. The antiviral activity of glycyrrhizin (GL) against influenza and other viruses reported in the literature was confirmed in this study resulting in an IC50 of 1026 µM (Table 1). GA and CBX did not show any antiviral activity at nontoxic concentrations. Compounds 12, 13, 14, 15, 18 and 19, which possess a (1-thio-β-D-glucopyranosyluronic acid)ethylamino substituent at position 3 of GA did not show toxicity at concentrations up to 250 µM, but showed enhanced antiviral activity compared to GL. Good activities were found for compounds 12 and 18 with IC50 values of 220.4 μM and 125 µM, respectively, being between 4.7-fold to 8-fold more active compared to the lead compound GL. The methyl ester 14 containing the N-acetylated spacer group was approximately 14-fold more active compared to GL, reflected by an IC50 value of 72.1 µM. The free acid 15 displayed an IC50 value in the same range as the methyl ester 14. Replacement of the N-acetyl group of 14 with a methylsuccinyl group (18) did not improve the activity; however, the compound was still active with an IC50 value of 125 µM. The cleavage of both methyl ester groups of this compound resulted in compound 19 and led to the loss of antiviral activity up to the highest concentration tested (250 µM). Compound 16 containing only the N-succinyl substituent is a close analogue to CBX bearing an amide instead of the ester group. Unlike CBX, which is toxic at low concentrations, 16 was not toxic but inactive, indicating that the glucuronic acid moiety is associated with the antiviral properties. This was further supported by the data obtained with compound 23 containing a 1-thioethyl-linked glucuronic acid residue at position 3 of 1,2-dehydro-glycyrrhetinic acid. Compound 23 showed good activity with an even lower IC50 value of 54 µM compared to 15, and exhibited also no cytotoxicity at the concentrations tested.

Table 1: Cytotoxic concentration 50% (CC50) of compound-treated uninfected cells and antiviral activities, shown as half-maximal inhibitory concentration (IC50) values of glycyrrhizin (GL) analogues.

Compound Substructure CC50 [µM] IC50 [µM]
GL [Graphic 1] >2500 1026 ± 181
GA [Graphic 2] 7.4 ± 0.05 nda
CBX [Graphic 3] 17.8 ± 2.3 nda
12 [Graphic 4] >250 220.4 ± 41
13 [Graphic 5] >250 nd (>250)b
14 [Graphic 6] >75 72.1 ± 19.1c
15 [Graphic 7] >250 87 ± 7.9
16 [Graphic 8] >250 nd (>250)b
18 [Graphic 9] >250 125 ± 15.9
19 [Graphic 10] >250 nd (>250)b
23 [Graphic 11] >250 54 ± 13

and not determined due to cytotoxicity; bnd (>250) no detectable antiviral activity up to 250 µM; capproximate value, since the compound precipitates at concentrations >75 μM.

Conclusion

3-Amino and 3-thio derivatives of glycyrrhetinic acid served as versatile scaffolds for the attachment of glycosyl extensions through high-yielding alkylation reactions. The glucuronide derivatives linked via a thioethyl spacer group to the oleanolic acid unit exhibited no toxicity at concentrations up to 250 μM and significantly enhanced the anti-influenza virus activity of the natural triterpene glycoside glycyrrhizin.

Supporting Information

Supporting Information File 1: Experimental details for the preparation of compounds 219 and 2123 as well as the biological assays.
Format: PDF Size: 304.2 KB Download

Acknowledgements

The work was supported by the ZIT Zentrum für Innovation und Technologie GmbH (Vienna Spot of Excellence: 182081). We thank Michaela Mutzl, Barbara Butzendobler and Eva Zingler for the performance of antiviral activity assays and David Baum and Karin Hofbauer for technical assistance in the organic syntheses of precursors.

References

  1. Baltina, L. A. Curr. Med. Chem. 2003, 10, 155–171.
    Return to citation in text: [1]
  2. Schwarz, S.; Csuk, R. Bioorg. Med. Chem. 2010, 18, 7458–7474. doi:10.1016/j.bmc.2010.08.054
    Return to citation in text: [1]
  3. Lampis, G.; Deidda, D.; Pinza, M.; Pompei, R. Antiviral Chem. Chemother. 2001, 12, 125–131.
    Return to citation in text: [1]
  4. Cinatl, J.; Morgenstern, B.; Bauer, G.; Chandra, P.; Rabenau, H.; Doerr, H. W. Lancet 2003, 361, 2045–2046. doi:10.1016/S0140-6736(03)13615-X
    Return to citation in text: [1]
  5. Crance, J. M.; Scaramozzino, N.; Jouan, A.; Garin, D. Antiviral Res. 2003, 58, 73–79. doi:10.1016/S0166-3542(02)00185-7
    Return to citation in text: [1]
  6. Hattori, T.; Ikematsu, S.; Koito, A.; Matsushita, S.; Maeda, Y.; Hada, M.; Fujimaki, M.; Takatsuki, K. Antiviral Res. 1989, 11, 255–261. doi:10.1016/0166-3542(89)90035-1
    Return to citation in text: [1]
  7. Harada, S. Biochem. J. 2005, 392, 191–199. doi:10.1042/BJ20051069
    Return to citation in text: [1]
  8. Lin, J.-C. Antiviral Res. 2003, 59, 41–47. doi:10.1016/S0166-3542(03)00030-5
    Return to citation in text: [1]
  9. Pompei, R.; Paghi, L.; Ingianni, A.; Uccheddu, P. Microbiologica 1983, 6, 247–250.
    Return to citation in text: [1]
  10. Utsunomiya, T.; Kobayashi, M.; Pollard, R. B.; Suzuki, F. Antimicrob. Agents Chemother. 1997, 41, 551–556.
    Return to citation in text: [1]
  11. Wolkerstorfer, A.; Kurz, H.; Bachhofner, N.; Szolar, O. Antiviral Res. 2009, 83, 171–178. doi:10.1016/j.antiviral.2009.04.012
    Return to citation in text: [1]
  12. Michaelis, M.; Geiler, J.; Naczk, P.; Sithisarn, P.; Leutz, A.; Doerr, H. W.; Cinatl, J., Jr. PLoS One 2011, 6, e19705. doi:10.1371/journal.pone.0019705
    Return to citation in text: [1]
  13. Claßen-Houben, D.; Kueenburg, B.; Kosma, P.; Jordis, U.; Stanetty, C.; Szolar, O.; Wolkerstorfer, A. Antiviral Triterpene Derivatives. EP 2 258 713 A1, Dec 8, 2010.
    Return to citation in text: [1]
  14. Amer, H.; Mereiter, K.; Stanetty, C.; Hofinger, A.; Czollner, L.; Beseda, I.; Jordis, U.; Kueenburg, B.; Claßen-Houben, D.; Kosma, P. Tetrahedron 2010, 66, 4390–4402. doi:10.1016/j.tet.2010.03.098
    Return to citation in text: [1] [2]
  15. Jellinck, P. H.; Monder, C.; McEwen, B. S.; Sakai, R. R. J. Steroid Biochem. Mol. Biol. 1993, 46, 209–213. doi:10.1016/0960-0760(93)90296-9
    Return to citation in text: [1]
  16. Florio, P.; Thomson, R. J.; von Itzstein, M. Carbohydr. Res. 2000, 328, 445–448. doi:10.1016/S0008-6215(00)00228-7
    Return to citation in text: [1]
  17. MacDougall, J. M.; Zhang, X.-D.; Polgar, W. E.; Khroyan, T. V.; Toll, L.; Cashman, J. R. J. Med. Chem. 2004, 47, 5809–5815. doi:10.1021/jm049554t
    Return to citation in text: [1]
  18. Cao, H.; Yu, B. Tetrahedron Lett. 2005, 46, 4337–4340. doi:10.1016/j.tetlet.2005.04.088
    Return to citation in text: [1]
  19. Beseda, I.; Czollner, L.; Shah, P. S.; Khunt, R.; Gaware, R.; Kosma, P.; Stanetty, C.; del Ruiz-Ruiz, M. C.; Amer, H.; Mereiter, K.; Da Cunha, T.; Odermatt, A.; Claßen-Houben, D.; Jordis, U. Bioorg. Med. Chem. 2010, 18, 433–454. doi:10.1016/j.bmc.2009.10.036
    Return to citation in text: [1]
  20. Ijichi, S.; Tamagaki, S. Chem. Lett. 2005, 34, 356–357. doi:10.1246/cl.2005.356
    Return to citation in text: [1]
  21. Brieskorn, C. H.; Eschelbach, H. Arch. Pharm. 1979, 312, 752–762. doi:10.1002/ardp.19793120907
    Return to citation in text: [1]
  22. Stanetty, C.; Czollner, L.; Koller, I.; Shah, P.; Gaware, R.; Da Cunha, T.; Odermatt, A.; Jordis, U.; Kosma, P.; Claßen-Houben, D. Bioorg. Med. Chem. 2010, 18, 7522–7541. doi:10.1016/j.bmc.2010.08.046
    Return to citation in text: [1]
  23. Csuk, R.; Schwarz, S.; Siewert, B.; Kluge, R.; Ströhl, D. Eur. J. Med. Chem. 2011, 46, 5356–5369. doi:10.1016/j.ejmech.2011.08.038
    Return to citation in text: [1]
  24. Zhou, C. C.; Stewart, K. D.; Dhaon, M. K. Magn. Reson. Chem. 2005, 43, 41–46. doi:10.1002/mrc.1501
    Return to citation in text: [1]
  25. Stewart, W. E.; Siddall, T. H., III. Chem. Rev. 1970, 70, 517–551. doi:10.1021/cr60267a001
    Return to citation in text: [1]
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