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.
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S. Sarno, H. Reddy, F. Meggio, et al., FEBS Lett., 1, 44 – 48 (2001).
D. Hao, J. D. Rizzo, S. Stringer, et al., Invest. New Drugs., 3, 261 – 70 (2002).
R. L. Fenichel, H. E. Alburn, P. A. Schreck, et al., J. Immunopharmacol., 4, 491 – 508 (1980).
M. A. Shaabana, A. M. Kamala, and H. E. Tebab. J. Chem. Res., 40, 228 – 234 (2016).
M. Hranjec, M. Kralj, L. Piantanida, et al., J. Med. Chem., 50, 5696 – 5711 (2007).
A. K. Piskin, Z. Ates-Alagoz, F. B. Atac, et al., Turk. J. Bioch., 1, 39 – 43 (2009).
S. Bansal, D. Sinhal, M. Singh, et al., J. Antimicrob. Chemother., 67, 2882 – 2891 (2012).
S. Sarno, H. Reddy, F. Meggio, et al., FEBS. Lett., 1, 44 – 48 (2001).
X. J. Wang, M. Y. Xi, J. H. Fu, et al., Chin. Chem. Lett., 23, 707 – 710 (2012).
S. Yadav, D. Sinha, S. K. Singh, et al., Chem. Biol. Drug. Des., 80, 625 – 630 (2012).
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
N. Kumar, C. S. Sharma, M. S. Ranawat, et al., J. Pharm. Investig, 45, 65 – 71 (2015).
P. A. Datar and S. A. Limaye. Antiinflamm. Antiallergy. Agents. Med. Chem., 14, 35 – 46 (2015).
G. Ayhan-Kilcigil, C. Kus, T. Coban, et al., J. Enzyme. Inhib. Med. Chem., 19, 129 – 35 (2004).
A. M. Monforte, S. Ferro, L. D. Luca, et al., Bioorg. Med. Chem., 22, 14590 – 1467 (2014).
Y. He, J. Yang, B. Wu, et al., Bioorg. Med. Chem. Lett., 14, 1217 – 1220 (2004).
A. S. G. Alp, H. Goker, M. Alp, et al., Arch. Pharm. Res., 38, 650 – 658 (2014).
T. S. Reddy, H. Kulhari, V. G. Reddy, et al., Eur. J. Med. Chem., 101, 790 – 805 (2015).
M. A. Abdelgawad, R. B. Baki, and A. Omar. Bioorg. Med. Chem., 74, 82 – 90 (2017).
M. Rashid, A. Husain, and R. Mishra. Eur. J. Med. Chem., 54, 855 – 866 (2012).
Y. Ozkay, Z. Incesu, N. I. Onder, et al., Med. Chem. Res., 22, 211 – 218 (2013).
Salahuddin, M. Shaharyar, A. Mazumder, et al., Arab. J. Chem., 7, 418 – 424 (2014).
H. Varshney, A. Ahmad, A. Rauf et al, Med. Chem. Res., 24, 944 – 953 (2015).
M. J. Akhtar, A. A. Siddique, A. A. Khan, et al., Eur. J. Med. Chem., 126, 853 – 869 (2017).
A. Husain, M. Rashid, M. Shaharyar, et al., Eur. J. Med. Chem., 62, 785 – 798 (2013).
G. N. Masoud, A. M. Youssef, M. M. A. Khalek, et al., Med. Chem. Res., 22, 707 – 725 (2013).
K. J. Harkala, L. Eppakayala, and T. C. Maringanti. Org. Med. Chem. Lett., 4, 14 (2014).
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
P. Sharma, T. S. Reddy, N. P. Kumar, et al., Eur. J. Med. Chem., 138, 234 – 245 (2017).
A. Nowicka, H. Liszkiewicz,W. P. Nawrocka, et al., Centr. Eur. J. Chem., 12, 1047 – 1055 (2014).
B. Mathew, J. Suresh, and D. Vinod. Med. Chem. Res., 22, 3911 – 3917 (2013).
K. P. Shao, X. Y. Zhang, P. J. Chen, et al., Bioorg. Med. Chem. Lett., 24, 3877 – 3881 (2014).
A. S. A. E. All, A. A. M. Din, F. A. F. Ragab, et al., Arch. Pharm. Chem. Life. Sci., 348, 1 – 12 (2015).
V. A. Risley, S. Henry, M. V. Kosyrikhina, et al., Chem. Heterocycl. Compd., 50, 209 – 218 (2014).
H. Qiang, F. U. Qiangqiang, L. I. U. Yajing, et al., Chem. Res. Chin. Univ., 30, 257 – 265 (2014).
Q. W. Huang, S. G. Liu, G. B. Li, et al., J. Struct. Chem., 56, 458 – 462 (2015).
G. J. Kumar, S. N. Kumar, D. Thummuri, et al., Med. Chem. Res., 24, 3991 – 4001 (2015).
P. Singla, V. Luxami, and K. Paul. Bioorg. Med. Chem., 23, 1691 – 1700 (2015).
B. Soni, M. S. Ranawat, A. Bhandari, et al., Int. J. Drug Res. Technol., 2, 479 – 485 (2012).
Z. Li, S. Zhang, L. Deng, et al., Med. Chem. Res., 23, 4050 – 4059 (2014).
S. D. Gupta, R. Revathi, G. I. Mazaira, et al., Bioorg. Chem., 59, 97 – 105 (2015).
R. A. Haque, M. A. Iqbal, P. Asekunowo, et al., Med. Chem. Res., 22, 4663 – 4676 (2013).
M. A. Iqbal, R. A. Haque, S. F. Nasri, et al., Chem. Cent. J., 7, 27 (2013).
S. Utku, A. B. Ozcelik, F. Gumus, et al., J. Pharm. Pharmacol., 66, 1593 – 1605 (2014).
L. B. Wu, W. Y. Su, Y. M. He, et al., Synth. React. Inorg., Metalorg. Nanometal Chem., 45, 1401 – 1406 (2015).
V. Certal, F. Halley, A. V. Oddos, et al., J. Med. Chem., 55, 4788 – 4805 (2012).
H. M. Refaat. Med. Chem. Res., 21, 1253 – 1260 (2012).
K. Bacharaju, S. R. Jambula, S. Sivan, et al., Bioorg. Med. Chem. Lett., 22, 3274 – 3277 (2012).
K. Paul, S. Bindal, and V. Luxami. Bioorg. Med. Chem. Lett., 23, 3667 – 3672 (2013).
P. N. K. Babu, B. Ramadevi, Y. Poornachandra, et al., Med. Chem. Res., 23, 3970 – 3978 (2014).
A. Kamal, V. Seinivasulu, M. Sathish, et al., Asian. J. Org. Chem., 3, 68 – 76 (2014).
S. Madabhushi, K. K. R. Mallu, V. S. Vangipuram, et al., Bioorg. Med. Chem. Lett., 24, 4822 – 4825 (2014).
M. Azam, A. A. Khan, S. I. Al-Resayes, et al., Spectrochim. Acta. Mol. Biomol. Spectrosc., 142, 286 – 291 (2015).
D. Farmanzadeh and M. Najafi. J. Theor. Comput. Chem., 14, 1550018 (1 – 12) (2015).
N. S. El-Gohary and M. I. Shaaban. Eur. J. Med. Chem., 137, 439 – 449 (2017).
S. Yadav, D. Sinha, S. K. Singh, et al., Chem. Biol. Drug. Des., 80, 625 – 630 (2012).
Z. Hu, L. Ou, S. Li, et al., Med. Chem. Res., 23, 3029 – 3038 (2014).
S. Demirayak and L. Yurttas. J. Enzyme Inhib. Med. Chem., 29, 811 – 822 (2014).
Y. K. Yoon, M. A. Ali, A. C. Wei, et al., Eur. J. Med. Chem., 83, 448 – 454 (2014).
B. Banerji and S. K. Pramanik. J. Chem. Biol., 8, 73 – 78 (2015).
S. Akkoc, V. Kayser, I. O. Ilhan, et al., J. Organometallic Chem., 839, 98 – 107 (2017).
M. Verma, V. Luxami, and K. Paul. Eur. J. Med. Chem., 68, 352 – 360 (2013).
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.
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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
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DOI: https://doi.org/10.1007/s11094-018-1742-4