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Synthesis and antioxidant properties of some N- and O-containing 2-isobornyl-6-methylphenol derivatives

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Abstract

A series of 2-isobornyl-6-methylphenol derivatives bearing either hydroxymethyl, aminomethyl, or N-acetylaminomethyl group at the para-position with respect to the hydroxy group of phenol moiety was synthesized. Antioxidant properties of the obtained derivatives were comparatively evaluated using in vitro models.

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References

  1. M. Cirri, P. Mura, P. Corvi Mora, Int. J. Pharm., 2007, 340, 84.

    Article  CAS  PubMed  Google Scholar 

  2. O. I. Kiselev, Khimiopreparaty i Khimioterapiya Grippa [Chemotherapeutic Agents and Chemotherapy of Influenza], Rostok, St. Petersburg, 2012, p. 272 (in Russian).

    Google Scholar 

  3. E. V. Buravlev, I. Yu. Chukicheva, O. G. Schevchenko, K. Yu. Suponitskii, A. V. Kutchin, Russ. Chem. Bull., 2017, 66, 91.

    Article  CAS  Google Scholar 

  4. O. G. Shevchenko, S. N. Plyusnina, E. V. Buravlev, I. Yu. Chukicheva, I. V. Fedorova, O. V. Shchukina, A. V. Kutchin, Russ. Chem. Bull., 2017, 66, 1881.

    Article  CAS  Google Scholar 

  5. E. V. Buravlev, I. Yu. Chukicheva, O. G. Schevchenko, A. V. Kutchin, Russ. Chem. Bull., 2017, 66, 297.

    Article  CAS  Google Scholar 

  6. E. V. Buravlev, O. V. Shchukina, O. G. Shevchenko, I. Yu. Chukicheva, A. V. Kutchin, Russ. J. Org. Chem., 2017, 53, 1756.

    Article  CAS  Google Scholar 

  7. G. Roman, Eur. J. Med. Chem., 2015, 89, 743.

    Article  CAS  PubMed  Google Scholar 

  8. A.-Y. Shen, M.-H. Huang, L.-F. Liao, T.-S. Wang, Drug. Dev. Res., 2005, 64, 195.

    Article  CAS  Google Scholar 

  9. I. Yu. Chukicheva, E. V. Buravlev, I. V. Fedorova, M. F. Borisenkov, A. V. Kutchin, Russ. Chem. Bull., 2010, 59, 2276.

    Article  CAS  Google Scholar 

  10. E. V. Buravlev, I. Yu. Chukicheva, A. V. Churakov, A. V. Kutchin, Russ. J. Org. Chem., 2012, 48, 64.

    Article  CAS  Google Scholar 

  11. E. V. Buravlev, I. Yu. Chukicheva, K. Yu. Suponitskii, A. V. Kuchin, Russ. J. Gen. Chem., 2008, 78, 1411.

    Article  CAS  Google Scholar 

  12. V. K. Kolvolter, Russ. Chem. Bull., 2010, 59, 37.

    Article  CAS  Google Scholar 

  13. E. V. Buravlev, O. G. Shevchenko, Russ. Chem. Bull., 2019, 68, 79.

    Article  CAS  Google Scholar 

  14. S. A. Popova, O. G. Shevchenko, I. Y. Chukicheva, A. V. Kutchin, Chem. Biodiversity, 2019, 16, e18003.

    Article  CAS  Google Scholar 

  15. E. V. Buravlev, O. G. Shevchenko, I. Y. Chukicheva, A. V. Kutchin, Chem. Pap., 2018, 72, 201.

    Article  CAS  Google Scholar 

  16. E. V. Buravlev, O. G. Shevchenko, A. A. Anisimov, K. Yu. Suponitsky, Eur. J. Med. Chem., 2018, 152, 10.

    Article  CAS  PubMed  Google Scholar 

  17. D. Tamilvendan, S. Rajeswari, S. Ilavenil, K. Chakkaravarthy, G. Venkatesa Prabhu, Med. Chem. Res., 2012, 21, 4129.

    Article  CAS  Google Scholar 

  18. E. Bendary, R. R. Francis, H. M. G. Ali, M. I. Sarwat, S. El Hady, Ann. Agric. Sci., 2013, 58, 173.

    Article  Google Scholar 

  19. J. Wang, P. Cai, X.-L. Yang, F. Li, J.-J. Wu, L.-Y. Kong, X.-B. Wang, Eur. J. Med. Chem., 2017, 139, 68.

    Article  CAS  PubMed  Google Scholar 

  20. R. Bashary, G. L. Khatik, Bioorg. Chem., 2019, 82, 156.

    Article  CAS  PubMed  Google Scholar 

  21. K. Sevgi, B. Tepe, C. Sarikurkcu, Food Chem. Toxicol., 2015, 77, 12.

    Article  CAS  PubMed  Google Scholar 

  22. U. Sukatta, M. Takenaka, H. Ono, H. Okadome, I. Sotome, K. Nanayama, W. Thanapase, S. Isobe, Biosci. Biotechnol. Biochem., 2013, 77, 984.

    Article  CAS  PubMed  Google Scholar 

  23. J. Lin, Y. Gao, H. Li, L. Zhang, X. Li, Adv. Pharm. Bull., 2014, 4, 147.

    PubMed  Google Scholar 

  24. C. I. Acker, R. Brandao, A. R. Rosario, C. W. Nogueira, Environ. Toxicol. Pharmacol., 2009, 28, 280.

    Article  CAS  PubMed  Google Scholar 

  25. S. T. Stefanello, A. S. Prestes, T. Ogunmoyole, S. M. Salman, R. S. Schwab, C. R. Brender, L. Dornelles, J. B. T. Rocha, F. A. A. Soares, Toxicol. in Vitro, 2013, 27, 1433.

    Article  CAS  PubMed  Google Scholar 

  26. N. A. V. Belle, G. D. Dalmolin, G. Fonini, M. A. Rubim, J. B. T. Rocha, Brain Res., 2004, 1008, 245.

    Article  CAS  PubMed  Google Scholar 

  27. R. Chawla, R. Arora, R. Kumar, A. Sharma, J. Prasad, S. Singh, R. Sagar, P. Chaudhary, S. Shukla, G. Kaur, R. K. Sharma, S. C. Puri, K. L. Dhar, G. Handa, V. K. Gupta, G. N. Qazi, Mol. Cell. Biochem., 2005, 273, 193.

    Article  CAS  PubMed  Google Scholar 

  28. T. Asakawa, S. Matsushita, Lipids, 1980, 15, 137.

    Article  CAS  Google Scholar 

  29. J. Takebayashi, J. Chen, A. A. Tai, Methods Mol. Biol., 2010, 594, 287.

    Article  CAS  PubMed  Google Scholar 

  30. J. J. M. Van den Berg, J. A. F. Opden Kamp, B. H. Lubin, B. Roelofsen, F. A. Kuypers, Free Radical Biol. Med., 1992, 12, 487.

    Article  Google Scholar 

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Buravlev, E.V., Fedorova, I.V., Shevchenko, O.G. et al. Synthesis and antioxidant properties of some N- and O-containing 2-isobornyl-6-methylphenol derivatives. Russ Chem Bull 68, 1558–1564 (2019). https://doi.org/10.1007/s11172-019-2592-2

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  • DOI: https://doi.org/10.1007/s11172-019-2592-2

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