Skip to main content

Advertisement

Log in

Benzimidazole Ring System as a Privileged Template for Anticancer Agents

  • Published:
Pharmaceutical Chemistry Journal Aims and scope

Cancer still remains a continued threat for human race in the 21st century. It is the major cause of human casualties globally and is thus, a hot topic of research in medicinal laboratories. Scientists are striving to find selective anticancer agents having low toxicity for normal human cells. Heterocyclic ring systems play key role as templates/pharmacophores for various drugs, and benzimidazole ring is especially important for its anticancer derivatives. In this review article, we have focused on the structural features of anticancer derivatives based on benzimidazole ring system. It highlights various benzimidazole-based anticancer compounds which have been developed in recent years.

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.

Institutional subscriptions

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5.
Fig. 6.
Fig. 7.
Fig. 8.
Fig. 9.
Fig. 10.
Fig. 11.
Fig. 12.
Fig. 13.

Similar content being viewed by others

References

  1. S. Sarno, H. Reddy, F. Meggio, et al., FEBS Lett., 1, 44 – 48 (2001).

    Article  Google Scholar 

  2. D. Hao, J. D. Rizzo, S. Stringer, et al., Invest. New Drugs., 3, 261 – 70 (2002).

    Article  Google Scholar 

  3. R. L. Fenichel, H. E. Alburn, P. A. Schreck, et al., J. Immunopharmacol., 4, 491 – 508 (1980).

    Article  Google Scholar 

  4. M. A. Shaabana, A. M. Kamala, and H. E. Tebab. J. Chem. Res., 40, 228 – 234 (2016).

    Article  Google Scholar 

  5. M. Hranjec, M. Kralj, L. Piantanida, et al., J. Med. Chem., 50, 5696 – 5711 (2007).

    Article  CAS  PubMed  Google Scholar 

  6. A. K. Piskin, Z. Ates-Alagoz, F. B. Atac, et al., Turk. J. Bioch., 1, 39 – 43 (2009).

    Google Scholar 

  7. S. Bansal, D. Sinhal, M. Singh, et al., J. Antimicrob. Chemother., 67, 2882 – 2891 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. S. Sarno, H. Reddy, F. Meggio, et al., FEBS. Lett., 1, 44 – 48 (2001).

    Article  Google Scholar 

  9. X. J. Wang, M. Y. Xi, J. H. Fu, et al., Chin. Chem. Lett., 23, 707 – 710 (2012).

    Article  CAS  Google Scholar 

  10. S. Yadav, D. Sinha, S. K. Singh, et al., Chem. Biol. Drug. Des., 80, 625 – 630 (2012).

    Article  CAS  PubMed  Google Scholar 

  11. A. Noor, N. G. Oazi, H. Nadeem, et al., Chem. Centr. J. (2017); https: //doi.org/https://doi.org/10.1186/s13065–017–0314–0

  12. N. Kumar, C. S. Sharma, M. S. Ranawat, et al., J. Pharm. Investig, 45, 65 – 71 (2015).

    Article  CAS  Google Scholar 

  13. P. A. Datar and S. A. Limaye. Antiinflamm. Antiallergy. Agents. Med. Chem., 14, 35 – 46 (2015).

    Article  CAS  PubMed  Google Scholar 

  14. G. Ayhan-Kilcigil, C. Kus, T. Coban, et al., J. Enzyme. Inhib. Med. Chem., 19, 129 – 35 (2004).

    Article  CAS  PubMed  Google Scholar 

  15. A. M. Monforte, S. Ferro, L. D. Luca, et al., Bioorg. Med. Chem., 22, 14590 – 1467 (2014).

    Article  Google Scholar 

  16. Y. He, J. Yang, B. Wu, et al., Bioorg. Med. Chem. Lett., 14, 1217 – 1220 (2004).

    Article  CAS  PubMed  Google Scholar 

  17. A. S. G. Alp, H. Goker, M. Alp, et al., Arch. Pharm. Res., 38, 650 – 658 (2014).

    PubMed  Google Scholar 

  18. T. S. Reddy, H. Kulhari, V. G. Reddy, et al., Eur. J. Med. Chem., 101, 790 – 805 (2015).

    Article  CAS  PubMed  Google Scholar 

  19. M. A. Abdelgawad, R. B. Baki, and A. Omar. Bioorg. Med. Chem., 74, 82 – 90 (2017).

    Article  CAS  Google Scholar 

  20. M. Rashid, A. Husain, and R. Mishra. Eur. J. Med. Chem., 54, 855 – 866 (2012).

    Article  CAS  PubMed  Google Scholar 

  21. Y. Ozkay, Z. Incesu, N. I. Onder, et al., Med. Chem. Res., 22, 211 – 218 (2013).

    Article  CAS  Google Scholar 

  22. Salahuddin, M. Shaharyar, A. Mazumder, et al., Arab. J. Chem., 7, 418 – 424 (2014).

  23. H. Varshney, A. Ahmad, A. Rauf et al, Med. Chem. Res., 24, 944 – 953 (2015).

    Article  CAS  Google Scholar 

  24. M. J. Akhtar, A. A. Siddique, A. A. Khan, et al., Eur. J. Med. Chem., 126, 853 – 869 (2017).

    Article  CAS  PubMed  Google Scholar 

  25. A. Husain, M. Rashid, M. Shaharyar, et al., Eur. J. Med. Chem., 62, 785 – 798 (2013).

    Article  CAS  PubMed  Google Scholar 

  26. G. N. Masoud, A. M. Youssef, M. M. A. Khalek, et al., Med. Chem. Res., 22, 707 – 725 (2013).

    Article  CAS  Google Scholar 

  27. K. J. Harkala, L. Eppakayala, and T. C. Maringanti. Org. Med. Chem. Lett., 4, 14 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  28. M. Rashid, A. Husain, R. Mishra, et al., Arab. J. Chem. (2015); dx.doi.org/https://doi.org/10.1016/j.arabjc.2015.08.019

  29. P. Sharma, T. S. Reddy, N. P. Kumar, et al., Eur. J. Med. Chem., 138, 234 – 245 (2017).

    Article  CAS  PubMed  Google Scholar 

  30. A. Nowicka, H. Liszkiewicz,W. P. Nawrocka, et al., Centr. Eur. J. Chem., 12, 1047 – 1055 (2014).

    Article  CAS  Google Scholar 

  31. B. Mathew, J. Suresh, and D. Vinod. Med. Chem. Res., 22, 3911 – 3917 (2013).

    Article  CAS  Google Scholar 

  32. K. P. Shao, X. Y. Zhang, P. J. Chen, et al., Bioorg. Med. Chem. Lett., 24, 3877 – 3881 (2014).

    Article  CAS  PubMed  Google Scholar 

  33. A. S. A. E. All, A. A. M. Din, F. A. F. Ragab, et al., Arch. Pharm. Chem. Life. Sci., 348, 1 – 12 (2015).

    Article  Google Scholar 

  34. V. A. Risley, S. Henry, M. V. Kosyrikhina, et al., Chem. Heterocycl. Compd., 50, 209 – 218 (2014).

    Article  Google Scholar 

  35. H. Qiang, F. U. Qiangqiang, L. I. U. Yajing, et al., Chem. Res. Chin. Univ., 30, 257 – 265 (2014).

    Article  Google Scholar 

  36. Q. W. Huang, S. G. Liu, G. B. Li, et al., J. Struct. Chem., 56, 458 – 462 (2015).

    Article  CAS  Google Scholar 

  37. G. J. Kumar, S. N. Kumar, D. Thummuri, et al., Med. Chem. Res., 24, 3991 – 4001 (2015).

    Article  CAS  Google Scholar 

  38. P. Singla, V. Luxami, and K. Paul. Bioorg. Med. Chem., 23, 1691 – 1700 (2015).

    Article  CAS  PubMed  Google Scholar 

  39. B. Soni, M. S. Ranawat, A. Bhandari, et al., Int. J. Drug Res. Technol., 2, 479 – 485 (2012).

    Google Scholar 

  40. Z. Li, S. Zhang, L. Deng, et al., Med. Chem. Res., 23, 4050 – 4059 (2014).

    Article  CAS  Google Scholar 

  41. S. D. Gupta, R. Revathi, G. I. Mazaira, et al., Bioorg. Chem., 59, 97 – 105 (2015).

    Article  Google Scholar 

  42. R. A. Haque, M. A. Iqbal, P. Asekunowo, et al., Med. Chem. Res., 22, 4663 – 4676 (2013).

    Article  CAS  Google Scholar 

  43. M. A. Iqbal, R. A. Haque, S. F. Nasri, et al., Chem. Cent. J., 7, 27 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  44. S. Utku, A. B. Ozcelik, F. Gumus, et al., J. Pharm. Pharmacol., 66, 1593 – 1605 (2014).

    Article  CAS  PubMed  Google Scholar 

  45. L. B. Wu, W. Y. Su, Y. M. He, et al., Synth. React. Inorg., Metalorg. Nanometal Chem., 45, 1401 – 1406 (2015).

    Article  CAS  Google Scholar 

  46. V. Certal, F. Halley, A. V. Oddos, et al., J. Med. Chem., 55, 4788 – 4805 (2012).

    Article  CAS  PubMed  Google Scholar 

  47. H. M. Refaat. Med. Chem. Res., 21, 1253 – 1260 (2012).

    Article  CAS  Google Scholar 

  48. K. Bacharaju, S. R. Jambula, S. Sivan, et al., Bioorg. Med. Chem. Lett., 22, 3274 – 3277 (2012).

    Article  CAS  PubMed  Google Scholar 

  49. K. Paul, S. Bindal, and V. Luxami. Bioorg. Med. Chem. Lett., 23, 3667 – 3672 (2013).

    Article  CAS  PubMed  Google Scholar 

  50. P. N. K. Babu, B. Ramadevi, Y. Poornachandra, et al., Med. Chem. Res., 23, 3970 – 3978 (2014).

    Article  Google Scholar 

  51. A. Kamal, V. Seinivasulu, M. Sathish, et al., Asian. J. Org. Chem., 3, 68 – 76 (2014).

    Article  CAS  Google Scholar 

  52. S. Madabhushi, K. K. R. Mallu, V. S. Vangipuram, et al., Bioorg. Med. Chem. Lett., 24, 4822 – 4825 (2014).

    Article  CAS  PubMed  Google Scholar 

  53. M. Azam, A. A. Khan, S. I. Al-Resayes, et al., Spectrochim. Acta. Mol. Biomol. Spectrosc., 142, 286 – 291 (2015).

    Article  CAS  Google Scholar 

  54. D. Farmanzadeh and M. Najafi. J. Theor. Comput. Chem., 14, 1550018 (1 – 12) (2015).

  55. N. S. El-Gohary and M. I. Shaaban. Eur. J. Med. Chem., 137, 439 – 449 (2017).

    Article  CAS  PubMed  Google Scholar 

  56. S. Yadav, D. Sinha, S. K. Singh, et al., Chem. Biol. Drug. Des., 80, 625 – 630 (2012).

    Article  CAS  PubMed  Google Scholar 

  57. Z. Hu, L. Ou, S. Li, et al., Med. Chem. Res., 23, 3029 – 3038 (2014).

    Article  CAS  Google Scholar 

  58. S. Demirayak and L. Yurttas. J. Enzyme Inhib. Med. Chem., 29, 811 – 822 (2014).

    Article  CAS  PubMed  Google Scholar 

  59. Y. K. Yoon, M. A. Ali, A. C. Wei, et al., Eur. J. Med. Chem., 83, 448 – 454 (2014).

    Article  CAS  PubMed  Google Scholar 

  60. B. Banerji and S. K. Pramanik. J. Chem. Biol., 8, 73 – 78 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  61. S. Akkoc, V. Kayser, I. O. Ilhan, et al., J. Organometallic Chem., 839, 98 – 107 (2017).

    Article  CAS  Google Scholar 

  62. M. Verma, V. Luxami, and K. Paul. Eur. J. Med. Chem., 68, 352 – 360 (2013).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

Some authors (A. K. and M. A.) greatly acknowledge the Higher Education Commission of Pakistan for financial support through research project No. 20-3715/NRPU/R&D/HEC/14/162.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Matloob Ahmad.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kanwal, A., Saddique, F.A., Aslam, S. et al. Benzimidazole Ring System as a Privileged Template for Anticancer Agents. Pharm Chem J 51, 1068–1077 (2018). https://doi.org/10.1007/s11094-018-1742-4

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11094-018-1742-4

Keywords

Navigation