Issue

Vol. 35 No. 5 (2023): Vol 35 Issue 5, 2023

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Chalcone-based Ferrocenyl-Derivatives as an Antimicrobial Drug; A Review

https://doi.org/10.14233/ajchem.2023.27795
A. Mondal
Department of Chemistry, Brahmananda Keshab Chandra College, 111/2, B. T. Road, Kolkata-700108, India
https://orcid.org/0009-0003-7355-3036

Corresponding Author(s) : A. Mondal

dhakuriamit@yahoo.com

Asian Journal of Chemistry, Vol. 35 No. 5 (2023): Vol 35 Issue 5, 2023

Abstract

The lack of development of new antibiotics is the major concern at the present scenario. One key factor contributing to the rise of antibiotic-resistant bacteria is the widespread movement of people throughout the world. The world has seen the consequences of the migration in the case of COVID-19 very recently. To tackle or cope with the situation, development of new antibiotics is very essential, which can be inhibited multidrug-resistant bacteria. In this framework, chalcone-based ferrocenyl containing compounds showed a diversity of pharmacological properties and its derivatives possess a high degree of structural diversity and it is helpful for the discovery of new therapeutic agents. Thus, there is a need for new antibacterial drug candidates with increased strength, new targets, low cost, superior pharmacokinetic properties and minimum side effects. The present review concluded and focuses on the recent developments in the area of medicinal chemistry to explore the diverse chemical structures of potent antibacterial agents and also describes its structure-activity relationship studies (SAR). This review will help to the researchers in the medical field to find out the future generation potential drug discovery and development.

Keywords

Chalcone-based ferrocenyl-derivatives Drug resistant bacteria Promising antibiotics
Mondal, A. (2023). Chalcone-based Ferrocenyl-Derivatives as an Antimicrobial Drug; A Review. Asian Journal of Chemistry, 35(5), 1063–1068. https://doi.org/10.14233/ajchem.2023.27795
Download Citation
Endnote/Zotero/Mendeley (RIS)
BibTeX
References
  1. B. Aslam, W. Wang, M.I. Arshad, M. Khurshid, S. Muzammil, M.H. Rasool, M.A. Nisar, R.F. Alvi, M.A. Aslam, M.U. Qamar, M. Salamat and Z. Baloch, Infect. Drug Resist., 11, 1645 (2018); https://doi.org/10.2147/IDR.S173867
  2. S.B. Levy and B. Marshall, Nat. Med., 10(S12), S122 (2004); https://doi.org/10.1038/nm1145
  3. C. Ghosh and J. Haldar, ChemMedChem, 10, 1606 (2015); https://doi.org/10.1002/cmdc.201500299
  4. C. Nathan, Nature, 431, 899 (2004); https://doi.org/10.1038/431899a
  5. J.M. Munita and C.A. Arias, Microbiol. Spectr., 4, 1 (2016); https://doi.org/10.1128/microbiolspec.VMBF-0016-2015
  6. M. Naeem, M. Adil, S.M. Naz, S.H. Abbas, M.Z.I. Khan, A. Khan and M.U. Khan, J. Postgrad. Med. Inst., 27, 42 (2012).
  7. H. Grundmann, M. Aires-de-Sousa, J. Boyce and E. Tiemersma, Lancet, 368, 874 (2006); https://doi.org/10.1016/S0140-6736(06)68853-3
  8. K.E. Dombrowski, W. Baldwin and J.E. Sheats, J. Organomet. Chem., 302, 281 (1986); https://doi.org/10.1016/0022-328X(86)80097-3
  9. M.F.R. Fouda, M.M. Abd-Elzaher, R.A. Abdelsamaia and A.A. Labib, Appl. Organomet. Chem., 21, 613 (2007); https://doi.org/10.1002/aoc.1202
  10. P. Meunier, I. Ouattara, B. Gautheron, J. Tirouflet, D. Camboli and J. Besançon, J. Med. Chem., 26, 351 (1991); https://doi.org/10.1016/0223-5234(91)90070-4
  11. S. Top, J. Tang, A. Vessieres, D. Carrez, C. Provot and G. Jaouen, Chem. Commun., 8, 955 (1996); https://doi.org/10.1039/CC9960000955
  12. A.S. Hassan, T.S. Hafez, S.A. Osman and M.M. Ali, Turk. J. Chem., 39, 1102 (2015); https://doi.org/10.3906/kim-1504-12
  13. A.S. ABD El-All, A.S. Hassan, S.A. Osman, H.A.A. Yosef, W.H. Abdel-Hady, M.A. El-Hashash, S.R. Atta-Allah, M.M. Ali and A.A. El Rashedy, Acta Pol. Pharm., 73, 79 (2016).
  14. P. Köpf-Maier and H. Köpf, Drugs Future, 11, 297 (1986).
  15. T.S. Hafez, S.A. Osman, H.A.A. Yosef, A.S. Abd El-All, A.S. Hassan, A.A. El-Sawy, M.M. Abdallah and M. Youns, Sci. Pharm., 81, 339 (2013); https://doi.org/10.3797/scipharm.1211-07
  16. B. Long, S. Liang, D. Xin, Y. Yang and J. Xiang, Eur. J. Med. Chem., 44, 2572 (2009); https://doi.org/10.1016/j.ejmech.2009.01.029
  17. C. Biot, N. Francois, L. Maciejewski, J. Brocard and D. Poulain, Bioorg. Med. Chem. Lett., 10, 839 (2000); https://doi.org/10.1016/S0960-894X(00)00120-7
  18. K. Kumar, B. Pradines, M. Madamet, R. Amalvict, N. Benoit and V. Kumar, Eur. J. Med. Chem., 87, 801 (2014); https://doi.org/10.1016/j.ejmech.2014.10.024
  19. T. Itoh, S. Shirakami, N. Ishida, Y. Yamashita, T. Yoshida, H.-S. Kim and Y. Wataya, Bioorg. Med. Chem. Lett., 10, 1657 (2000); https://doi.org/10.1016/S0960-894X(00)00313-9
  20. Y.Y. Dou, Y.F. Xie and L.F. Tang, Appl. Organomet. Chem., 22, 25 (2008); https://doi.org/10.1002/aoc.1345
  21. R.A. Hussain, A. Badshash, M. Sohail, B. Lal and A.A. Altaf, Inorg. Chem. Acta, 402, 133 (2013); https://doi.org/10.1016/j.ica.2013.04.003
  22. W. Liu, Y. Tang, Y. Guo, B. Sun, H. Zhu, Y. Xiao, D. Dong and C. Yang, Appl. Organomet. Chem., 26, 189 (2012); https://doi.org/10.1002/aoc.2837
  23. M.M. Abd-Elzaher and I.A.I. Ali, Appl. Organomet. Chem., 20, 107 (2006); https://doi.org/10.1002/aoc.1016
  24. A.Z. Al-Rubaie, S.A.S. Al-Jadaan, S.K. Muslim, E.A. Saeed, E.T. Ali, A.K.J. Al-Hasani, H.N.K. Al-Salman and S.A.M. Al-Fadal, J. Organomet. Chem., 774, 43 (2014); https://doi.org/10.1016/j.jorganchem.2014.10.007
  25. D.R. van Staveren and N. Metzler-Nolte, Chem. Rev., 104, 5931 (2004); https://doi.org/10.1021/cr0101510
  26. A.D. Sai Krishna, G. Panda and A.K. Kondapi, Arch. Biochem. Biophys., 438, 206 (2005); https://doi.org/10.1016/j.abb.2005.04.014
  27. R.H. Fish and G. Jaouen, Organometallics, 22, 2166 (2003); https://doi.org/10.1021/om0300777
  28. G. Di Carlo, N. Mascolo, A.A. Izzo and F. Capasso, Life Sci., 65, 337 (1999); https://doi.org/10.1016/S0024-3205(99)00120-4
  29. N.K. Sahu, S.S. Balbhadra, J. Choudhary and D.V. Kohli, Curr. Med. Chem., 19, 209 (2012); https://doi.org/10.2174/092986712803414132
  30. J. Muskinja, A. Burmudzija, Z. Ratkovic, B. Rankovic, M. Kosanic, G.A. Bogdanovic and S.B. Novakovic, Med. Chem. Res., 25, 1744 (2016); https://doi.org/10.1007/s00044-016-1609-8
  31. S. Moodley, N.A. Koorbanally, T. Moodley, D. Ramjugernath and M. Pillay, J. Microbiol. Methods, 104, 72 (2014); https://doi.org/10.1016/j.mimet.2014.06.014
  32. N. Ahmed, N.K. Konduru and M. Owais, Arab. J. Chem., 12, 1879 (2019); https://doi.org/10.1016/j.arabjc.2014.12.008
  33. J.R. Zgoda and J.R. Porter, Pharm. Biol., 39, 221 (2001); https://doi.org/10.1076/phbi.39.3.221.5934
  34. A.R. Twinkle, D.R. Leenaraj, Z. Ratkovic, B.S. Arunsasi, K.C. Bright and R. Reshma, J. Mol. Struct., 1210, 128049 (2020); https://doi.org/10.1016/j.molstruc.2020.128049
  35. L.L.E. Crouch, The Synthesis of Organometallic Chalcones, Preston, Lancashire, UK: University of Central Lancashire (2014).
  36. E.J. Henry, S.J. Bird, P. Gowland, M. Collins and J.P. Cassella, J. Antibiot., 73, 299 (2020); https://doi.org/10.1038/s41429-020-0280-y
  37. J.M. Andrews, J. Antimicrob. Chemother., 48(suppl_1), 5 (2001); https://doi.org/10.1093/jac/48.suppl_1.5
  38. A. Burmudzija, Z. Ratkovic, J. Muskinja, N. Jankovic, B. Rankovic, M. Kosanic and S. Dordevic, RSC Adv., 6, 91420 (2016); https://doi.org/10.1039/C6RA18977F
  39. Y.T. Liu, G.D. Lian, D.W. Yin and B.J. Su, Res. Chem. Intermed., 38, 1043 (2012); https://doi.org/10.1007/s11164-011-0440-6
Read More
Author biographies is not available.
Download
AJC-35-5-2
Statistic
Read Counter : 2 Download : 1