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5-(4-alkyl-1,2,3-triazol-1-yl)methyl derivatives of 2′-deoxyuridine as inhibitors of viral and bacterial growth

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Abstract

A series of 5-(4-alkyl-1,2,3-triazol-1-yl)methyl derivatives of 2′-deoxyuridine have been synthesized by the interaction of 3′,5′-diacetyl-5-azidomethyl-2′-deoxyuridine with the corresponding 1-alkynes in a biphasic methylene chloride—water system catalyzed by Cu(I) followed by the deblocking with a water-alcohol ammonia solution. A low cytotoxicity of the compounds in Vero, Jurkat, and A549 cell cultures has been shown. The 2′-deoxyuridine derivatives exhibited an antiherpetic activity in vitro toward two laboratory strains of human herpes simplex virus type 1 (HSV-1): acyclovir-sensitive (HSV-1/L2) and acyclovir-resistant (HSV-1/L2RACV). They also inhibited the growth of some bacteria (Mycobacterium smegmatis, Staphylococcus aureus, Micrococcus luteus, and Leuconostoc mesenteroides) and yeasts Saccharomyces cerevisiae in vitro.

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Abbreviations

CD50 :

the concentration of a compound that causes the death of 50% of uninfected cells

CPE:

the cytopathic effect

ED50 :

the concentration of preparations that induce a 50% inhibition of the CPE

HSV-1:

human herpes simplex virus type 1

SI:

the chemotherapeutic index, which is calculated as the CD50/ED50 ratio

PFU:

plaque-forming unit

MOI:

multiplicity of infection

ACV:

acyclovir

References

  1. World Health Organization, Global Tuberculosis Report 2016. http://www.who.int/tb/publications/ global_report/en/. Cited October 17, 2016.

  2. De Clercq, E, Curr. Opin. Virol., 2012, vol. 2, pp. 572–579.

    Article  PubMed  Google Scholar 

  3. Skorobogatyi, M.V., Ustinov, A.V., Stepanova, I.A., Pchelintseva, A.A., Petrunina, A.L., Andronova, V.L., Galegov, G.A., Malakhov, A.D., and Korshun, V.A, Org. Biomol. Chem., 2006, vol. 4, pp. 1091–1096.

    Article  CAS  PubMed  Google Scholar 

  4. Ivanov, A.V., Simonyan, A.R., Belanov, E.F., and Aleksandrova, L.A, Russ. J. Bioorg. Chem., 2005, vol. 31, pp. 556–562.

    Article  CAS  Google Scholar 

  5. Shmalenyuk, E.R., Kochetkov, S.N., and Alexandrova, L.A, Usp. Khim., 2013, vol. 82, pp. 896–915.

    Article  Google Scholar 

  6. Rai, D., Johar, M., Manning, T., Agrawal, B., Kunimoto, D.Y., and Kumar, R., J. Med. Chem., 2005, vol. 48, pp. 7012–7017.

    Article  CAS  PubMed  Google Scholar 

  7. Matyugina, E., Khandazhinskaya, A., Chernousova, L., Andreevskaya, S., Smirnova, T., Chizhov, A., Karpenko, I., Kochetkov, S., and Alexandrova, L, Bioorg. Med. Chem., 2012, vol. 20, pp. 6680–6686.

    Article  CAS  PubMed  Google Scholar 

  8. Shmalenyuk, E.R., Chernousova, L.N., Karpenko, I.L., Kochetkov, S.N., Smirnova, T.G., Andreevskaya, S.N., Efremenkova, O.V., and Alexandrova, L.A, Bioorg. Med. Chem., 2013, vol. 21, pp. 4874–4884.

    Article  CAS  PubMed  Google Scholar 

  9. Alexandrova, L.A., Shmalenyuk, E.R., Kochetkov, S.N., Erokhin, V.V., Smirnova, T.G., Andreevskaia, S.N., and Chernousova, L.N, Acta Naturae, 2010, vol. 2, pp. 84–86.

    Google Scholar 

  10. Alexandrova, L.A., Chekhov, V.O., Shmalenyuk, E.R., Kochetkov, S.N, Abu El-Asrar, R., and Herdewijn, P, Bioorg. Med. Chem., 2015, vol. 23, pp. 7131–7137.

    Article  CAS  PubMed  Google Scholar 

  11. Shmalenyuk, E.R., Karpenko, I.L., Chernousova, L.N., Chizhov, A.O., Smirnova, T.G., Andreevskaya, S.N., and Alexandrova, L.A, Izv. Akad. Nauk, Ser. Khim., 2014, vol. 63, pp. 1197–1200.

    CAS  Google Scholar 

  12. Ustinov, A.V., Stepanova, I.A., Dubniakova, V.V., Zatsepin, T.S., Nozhevnikova, E.V., and Korshun, V.A, Russ. J. Bioorg. Chem., 2010, vol. 36, pp. 401–445.

    Article  CAS  Google Scholar 

  13. Lee, B.-Y., Park, S.R., Jeon, H.B., and Kim, R.S, Tetrahedron Lett., 2006, vol. 47, pp. 5105–5109.

    Article  CAS  Google Scholar 

  14. Levina, A.S., Tabatadse, D.R., Khalimskaya, L.M., Prichodko, T.A., Shishkin, G.V., Alexandrova, L.A., and Zarytova, V.P, Bioconjugate Chem., 1993, vol. 4, pp. 319–325.

    Article  CAS  Google Scholar 

  15. Zarytova, V.F., Komarova, N.I., Levina, A.S., Lokhov, S.G., Tabatadze, D.R., Khalimskaya, L.M., and Alexandrova, L.A, Russ. J. Bioorg. Chem., 1991, vol. 17, pp. 1059–1065.

    CAS  Google Scholar 

  16. Niks, M. and Otto, M., J. Immunol. Methods, 1990, vol. 130, pp. 149–151.

    Article  CAS  PubMed  Google Scholar 

  17. Gus’kova, A.A., Skoblov, M.Yu., Korovina, A.N., Yasko, M.V., Karpenko, I.L., Kukhanova, M.K., Andronova, V.L., Galegov, G.A., and Skoblov, Yu.S, Chem. Biol. Drug Des., 2009, vol. 74, pp. 382–389.

    Article  PubMed  Google Scholar 

  18. Korovina, A.N., Gus’kova, A.A., Skoblov, M.Yu., Andronova, V.L., Galegov, G.A., Kochetkov, S.N., Kukhanova, M.K., and Skoblov, Yu.S, Mol. Biol. (Moscow), 2010, vol. 44, pp. 431–438.

    Article  CAS  Google Scholar 

  19. Malanicheva, I.A., Kozlov, D.G., Sumarukova, I.G., Efremenkova, O.V., Zenkova, V.A., Katrukha, G.S., Reznikova, M.I., Tarasova, O.D., Sineokii, S.P., and El’-Registan, G.I, Microbiology (Moscow), 2012, vol. 81, pp. 178–185.

    Article  CAS  Google Scholar 

  20. Levine, D.P, Clin. Infect. Dis., 2006, vol. 42 (suppl. 1), pp. 40–50.

    Google Scholar 

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Correspondence to L. A. Alexandrova.

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Dedicated to the memory of the Academician A. S. Khokhlov

Original Russian Text © L.A. Alexandrova, O.V. Efremenkova, V.L. Andronova, G.A. Galegov, P.N. Solyev, I.L. Karpenko, S.N. Kochetkov, 2016, published in Bioorganicheskaya Khimiya, 2016, Vol. 42, No. 6, pp. 746–754.

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Alexandrova, L.A., Efremenkova, O.V., Andronova, V.L. et al. 5-(4-alkyl-1,2,3-triazol-1-yl)methyl derivatives of 2′-deoxyuridine as inhibitors of viral and bacterial growth. Russ J Bioorg Chem 42, 677–684 (2016). https://doi.org/10.1134/S1068162016050022

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  • DOI: https://doi.org/10.1134/S1068162016050022

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