Skip to main content
Log in

Synthesis, Biological Activity, and Molecular Docking Assessment of Some New Sulfonylated Tetrazole Derivatives

  • Published:
Russian Journal of General Chemistry Aims and scope Submit manuscript

Abstract

The designed molecular structures have been subjected to computational analysis for calculating their physicochemical properties and drug likeness. The calculated data indicate that most of the compound possess the bioactivity score in the active zone. Synthetic approach to the target compounds is straightforward and easy to handle. Structures of the new compounds are supported by FT-IR, 1H, and 13C NMR, and mass spectra. Antimicrobial tests of the products against pathogens (S. aureus, S. epidermidis, E. coli, and P. mirabilis) indicate the products as active or highly active. Their cyto-toxicity is determined to be 92–98% at concentration of 3.125 µmol/L. The molecular docking analysis carried out for the target compounds against the receptor Glc-N-6P exhibits low binding energy and various binding sites of those.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Myznikov, L.V., Hrabalek, A., and Koldobskii, G.I., Chem. Heterocycl. Comp., 2007, vol. 43, p. 1. https://doi.org/10.1007/s10593-007-0001-5

    Article  CAS  Google Scholar 

  2. Soliman, H.A., Kalmouch, A., Awad, H.M., and Abdel Wahed, N.A.M., Russ. J. Gen. Chem., 2018, vol. 88, p. 1726. https://doi.org/10.1134/S1070363218080273

    Article  CAS  Google Scholar 

  3. Issell, B.F., Cancer Chemother. Pharmacol., 1982, vol. 7, p. 73. https://doi.org/10.1007/BF00254525

    CAS  PubMed  Google Scholar 

  4. Arshad, M., Bhat, A.R., Pokharel, S., Lee, E.J., Athar, F., and Choi, I., Eur. J. Med. Chem., 2014, vol. 71, p. 229. https://doi.org/10.1016/j.ejmech.2013.11.008

    Article  CAS  Google Scholar 

  5. Marc, A.I., Bernard, M., Stephanie, R., Andrea, S., Gheorghe, C., Valentin, C., and Claudiu, T.S., Bioorg. Med. Chem., 2004, vol. 12, p. 2717. https://doi.org/10.1016/j.bmc.2004.03.008

    Article  Google Scholar 

  6. Bhat, A.R., Arshad, M., Lee, E.J., Pokharel, S., Choi, I., and Athar, F., Chem. Biod., 2013, vol. 10, p. 2267. https://doi.org/10.1002/cbdv.201300009

    Article  CAS  Google Scholar 

  7. Molinspiration Cheminformatics. Nova ulica, SK-90026 Slovensky Grob, Slovak Republic. [Online] Available from: http://www.molinspiration.com [Accessed on 3rd July, 2012].

  8. Verma, A., Asian Pac. J. Trop. Biomed., 2012, vol. 2, p. S1735. https://doi.org/10.1016/S2221-1691(12)60486-9.

    Article  Google Scholar 

  9. Alodeani, E.A., Arshad, M., and Izhari, M.A., Eur. J. Pharm. Med. Res., 2017, vol. 4, p. 447. https://www.ejpmr.com/admin/assets/article_issue/1490961035.pdf.

    Google Scholar 

  10. Alodeani, E.A., Arshad, M., and Izhari, M.A., Eur. J. Pharm. Med. Res., 2015, vol. 2, p. 296. http://www.ejpmr.com/admin/assets/article_issue/1446625932.pdf

    Google Scholar 

  11. Arshad, M., Russ J Gen Chem., 2018, vol. 88, p. 1886. https://doi.org/10.1134/S1070363218090207

    Article  CAS  Google Scholar 

  12. Alodeani, E.A., Arshad, M., and Izhari, M.A., Asian Pac. J. Trop Biomed., 2015, vol. 5, p. 676. https://doi.org/10.1016/j.apjtb.2015.04.010

    Article  Google Scholar 

  13. Arshad, M., Bhat, A.R., Hoi, K.K., Choi, I., and Athar, F., Chin. Chem. Lett., 2017, vol. 28 p. 1559. https://doi.org/10.1016/j.cclet.2016.12.037

    Article  CAS  Google Scholar 

  14. Kareem, A., Laxmi, Arshad, M., and Nishat, N., J. Photochem. Photobiol. B, 2016, vol. 160, p. 163. https://doi.org/10.1016/j.jphotobiol.2016.03.030

    Article  CAS  Google Scholar 

  15. Iram, N., Khan, M.S., Jolly, R., Arshad, M., Alam, M., Alam, P., Khan, R.H., and Firdaus, F., J. Photochem. Photobiol. B, 2015, vol. 153, p. 20. https://doi.org/10.1016/j.jphotobiol.2015.09.001

    Article  CAS  Google Scholar 

  16. Nami, S.A.A., Arshad, M., Shakir, M., Khan, M.S., Alam, M., Lee, D.U., Park, S., and Sarikavakli, N., Polym. Adv. Technol., 2015, vol. 26, p. 1627. https://doi.org/10.1002/pat.3591

    Article  CAS  Google Scholar 

  17. Bushra, R., Shahadat, M., Khan, M.A., Adnan, R., Arshad, M., Rafatullah, M., and Naushad, M., Int. J. Env. Sci. Technol., 2015, vol. 12, p. 3635. https://doi.org/10.1007/s13762-014-0726-5

    Article  CAS  Google Scholar 

  18. Nami, S.A.A., Khan, M.S., Arshad, M., Raza, M.A., and Khan, I., Polym. Adv. Technol., 2017, vol. 28, p. 10. https://doi.org/10.1002/pat.3846

    Article  CAS  Google Scholar 

  19. Nayab, P.S., Arif, R., Arshad, M., and Rahisuddin, Heterocyc. Lett., 2015, vol. 5, p. 223. http://www.heteroletters.org/issue25/PDF/Paper-9.pdf.

    CAS  Google Scholar 

  20. Gupta, M.K., Neelakantan, TV., Sanghamitra, M., Tyagi, R.K., Dinda, A., Maulik, S., Mukhopadhyay, C.K., and Goswami, S.K., Antioxid. Redox Signal, 2006, vol. 8, p. 1081. https://doi.org/10.1089/ars.2006.8.1081

    Article  CAS  Google Scholar 

  21. Mosmann, T., J. Immunol. Methods, 1983, vol. 65, p. 55. https://doi.org/10.1016/0022-1759(83)90303-4.

    Article  CAS  Google Scholar 

  22. Morris, G.M., Goodsell, D.S., Halliday, R.S., Huey, R., Hart, W.E., Belew, R.K., Olson, A.J., J. Comput. Chem., 1998, vol. 19, p. 1639. https://doi.org/10.1002/(SICI)1096-987X(19981115)19:14%3C1639::AID-JCC10%3E3.0.CO;2-B.

    Article  CAS  Google Scholar 

  23. Mouilleron, S., Badet-Denisot, M.A., and Golinelli-Pimpaneau, B., J. Mol. Biol., 2008, vol. 377, no. 4, p. 1174. https://doi.org/10.1016/j.jmb.2008.01.077

    Article  CAS  Google Scholar 

  24. Trott, O. and Olson, A.J., J. Comput. Chem., 2010, vol. 31, p. 455. https://doi.org/10.1002/jcc.21334

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

The author Dr. Mohammad Arshad is highly thankful to Dr. Feras AlMarshad, the Dean College of Medicine Al-Dawadmi, Shaqra University Kingdom of Saudi Arabia for his kind cooperation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Arshad.

Ethics declarations

No conflict of interest was declared by the authors.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Arshad, M., Khan, M.S. & Nami, S.A.A. Synthesis, Biological Activity, and Molecular Docking Assessment of Some New Sulfonylated Tetrazole Derivatives. Russ J Gen Chem 89, 1851–1858 (2019). https://doi.org/10.1134/S1070363219090202

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070363219090202

Keywords

Navigation