Issue

Vol. 34 No. 10 (2022): Vol 34 Issue 10, 2022

Copyright (c) 2022 AJC

Creative Commons License

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

Amino Acid Based Schiff Bases and Their Metal Complexes as Biologically Potent Agents: A Review

https://doi.org/10.14233/ajchem.2022.23757
Suman Kumari
Department of Chemistry, University of Rajasthan, Jaipur-302004, India
Poonam Yadav
Department of Chemistry, University of Rajasthan, Jaipur-302004, India
Shobhana Sharma
Department of Chemistry, University of Rajasthan, Jaipur-302004, India
Mamta Ranka
Department of Chemistry, University of Rajasthan, Jaipur-302004, India

Corresponding Author(s) : Mamta Ranka

mmt31ran@gmail.com

Asian Journal of Chemistry, Vol. 34 No. 10 (2022): Vol 34 Issue 10, 2022

Abstract

Schiff bases derived from amino acids and their corresponding metal complexes have been widely studied in different ways and have increased attention of chemists in biological, pharmaceutical and biochemical fields due to their easy synthesis and broad spectrum of applications. In this review, we have focused on the synthesis and biological evaluation involving antifungal, antibacterial, anticancer, antioxidant and antidiabetic activities of some amino acid derived Schiff bases and their respective metal complexes.

Keywords

Amino acid Schiff base Metal complexes Biological evaluation
Kumari, S., Yadav, P., Sharma, S., & Ranka, M. (2022). Amino Acid Based Schiff Bases and Their Metal Complexes as Biologically Potent Agents: A Review. Asian Journal of Chemistry, 34(10), 2465–2477. https://doi.org/10.14233/ajchem.2022.23757
Download Citation
Endnote/Zotero/Mendeley (RIS)
BibTeX
References
  1. M. Shamsipur, A.R. Ghiasvand, H. Sharghi and H. Naeimi, Anal. Chim. Acta, 408, 271 (2000); https://doi.org/10.1016/S0003-2670(99)00873-9
  2. N. Davison, K. Zhou, P.G. Waddell, C. Wills, C. Dixon, S.-X. Hu and E. Lu, Inorg. Chem., 61, 3674 (2022); https://doi.org/10.1021/acs.inorgchem.1c03786
  3. M.A. Ali and M.T.H. Tarafdar, J. Inorg. Nucl. Chem., 39, 1785 (1977); https://doi.org/10.1016/0022-1902(77)80202-9
  4. S.S. Shah, D. Shah, I. Khan, S. Ahmad, U. Ali and A.U. Rahman, Biointerface Res. Appl. Chem., 10, 6936 (2020); https://doi.org/10.33263/BRIAC106.69366963
  5. H. Schiff, Justus Liebigs Ann. Chem., 131, 118 (1864); https://doi.org/10.1002/jlac.18641310113
  6. P. Souza, J.A. Garcia-Vazquez and J.R. Masaguer, Transition Met. Chem., 10, 410 (1985); https://doi.org/10.1007/BF01096746
  7. M.I.E. Khalil, E.H. Ismail, G.G. Mohamed, E.M. Zayed and A. Badr, Open J. Inorg. Chem., 2, 13 (2012); https://doi.org/10.4236/ojic.2012.22003
  8. W. Qin, S. Long, M. Panunzio and S. Biondi, Molecules, 18, 12264 (2013); https://doi.org/10.3390/molecules181012264
  9. E. Bulatov, R. Sayarova, R. Mingaleeva, R. Miftakhova, M. Gomzikova, Y. Ignatyev, A. Petukhov, P. Davidovich, A. Rizvanov and N.A. Barlev, Cell Death Discov., 4, 103 (2018); https://doi.org/10.1038/s41420-018-0120-z
  10. G. Cerchiaro, K. Aquilano, G. Filomeni, G. Rotilio, M.R. Ciriolo and A.M.D.C. Ferreira, J. Inorg. Biochem., 99, 1433 (2005); https://doi.org/10.1016/j.jinorgbio.2005.03.013
  11. A.S. Smirnov, D.N. Nikolaev, V.V. Gurzhiy, S.N. Smirnov, V.S. Suslonov, A.V. Garabadzhiu and P.B. Davidovich, RSC Adv., 7, 10070 (2017); https://doi.org/10.1039/C6RA26779C
  12. T. Aboul-Fadl, F.A.-H. Mohammed and E.A.-S. Hassan, Arch. Pharm. Res., 26, 778 (2003); https://doi.org/10.1007/BF02980020
  13. R. Miri, N. Razzaghi-asl and M.K. Mohammadi, J. Mol. Model., 19, 727 (2013); https://doi.org/10.1007/s00894-012-1586-x
  14. G. Cerchiaro and A.M.C. Ferreira, J. Braz. Chem. Soc., 17, 1473 (2006); https://doi.org/10.1590/S0103-50532006000800003
  15. V.K. Sharma, A. Srivastava and S. Srivastava, J. Serb. Chem. Soc., 71, 917 (2006); https://doi.org/10.2298/JSC0609917S
  16. P.G. Avaji, C.H. Vinod Kumar, S.A. Patil, K.N. Shivananda and C. Nagaraju, Eur. J. Med. Chem., 44, 3552 (2009); https://doi.org/10.1016/j.ejmech.2009.03.032
  17. K.N. Venugopala and B.S. Jayashree, Indian J. Heterocycl. Chem., 12, 307 (2003).
  18. P. Zhang, C. Bi, S.M. Schmitt, X. Li, Y. Fan, N. Zhang and Q.P. Dou, Int. J. Mol. Med., 34, 870 (2014); https://doi.org/10.3892/ijmm.2014.1838
  19. P. Tyagi, S. Chandra, B.S. Saraswat and D. Yadav, Spectrochim. Acta A Mol. Biomol. Spectrosc., 145, 155 (2015); https://doi.org/10.1016/j.saa.2015.03.034
  20. M. Sobiesiak, M. Cieslak, K. Krolewska, J. Kazmierczak-Baranska, B. Pasternak and E. Budzisz, New J. Chem., 40, 9761 (2016); https://doi.org/10.1039/C6NJ02899C
  21. G. Matela, Anticancer Agents Med Chem., 20, 1908 (2020); https://doi.org/10.2174/1871520620666200507091207
  22. E.M. Osoro, S.O. Wandiga, D.A. Abongo, V.O. Madadi and J.W. Macharia, IOSR J. Appl. Chem., 9, 56 (2016); https://doi.org/10.9790/5736-0909025663
  23. B.S. Sathe, E. Jaychandran, V.A. Jagtap and G.M. Sreenivasa, Int. J. Pharm. Res. Dev., 3, 164 (2011).
  24. S.M. Sondhi, N. Singh, A. Kumar, O. Lozach and L. Meijer, Bioorg. Med. Chem., 14, 3758 (2006); https://doi.org/10.1016/j.bmc.2006.01.054
  25. A. Pandey, D. Dewangan, S. Verma, A. Mishra and R.D. Dubey, Int. J. ChemTech Res., 3, 178 (2011).
  26. C. Chandramouli, M.R. Shivanand, T.B. Nayanbhai and B. Bheemachari, J. Chem. Pharm. Res., 4, 1151 (2012).
  27. R.P. Chinnasamy, R. Sundararajan and S. Govindaraj, J. Adv. Pharm. Technol. Res., 1, 342 (2010); https://doi.org/10.4103/0110-5558.72428
  28. M.M. Ali Shaikh, A. M. AbulKalam, M. Jesmin, S. Ahsan, M.M. Rahman, J.A. Khanam, M.N. Islam, S.M.S. Shahriar, Asian Pac. J. Trop. Biomed., 2, 438 (2012).
  29. S.N. Pandeya, A.S. Raja and J.P. Stables, J. Pharm. Pharm. Sci., 5, 266 (2002).
  30. T.R. Bal, B. Anand, P. Yogeeswari and D. Sriram, Bioorg. Med. Chem. Lett., 15, 4451 (2005); https://doi.org/10.1016/j.bmcl.2005.07.046
  31. S.N. Pandeya, D. Sriram, G. Nath and E. de Clercq, Arzneimittelforschung, 50, 55 (2000); https://doi.org/10.1055/s-0031-1300164
  32. M.F. AlAjmi, A. Hussain, A. Alsalme and R.A. Khan, RSC Adv., 6, 19475 (2016); https://doi.org/10.1039/C5RA25071D
  33. R. Fulwood, H. Schmidt and D. Rehder, J. Chem. Soc. Chem. Commun., 1443 (1995); https://doi.org/10.1039/c39950001443
  34. Á. García-Raso, J.J. Fiol, A. López-Zafra, A. Cabrero, I. Mata and E. Molins, Polyhedron, 18, 871 (1999); https://doi.org/10.1016/S0277-5387(98)00373-8
  35. J.C. Pessoa, I. Cavaco, I. Correia, I. Tomaz, T. Duarte and P.M. Matias, Inorg. Biochem., 80, 35 (2000); https://doi.org/10.1016/S0162-0134(00)00037-4
  36. J.C. Pessoa, M.J. Calhorda, V. Felix, S. Gama, I. Correia, M.T. Duarte, S. Marcao, M.F.M. Piedade and I. Tomaz, J. Inorg. Biochem., 86, 188 (2001).
  37. B. Baruah, S. Das and A. Chakravorty, Inorg. Chem., 41, 4502 (2002); https://doi.org/10.1021/ic020259d
  38. D. Voet and J. Voet, Biochemistry, John Wiley & Sons: New York, pp. 59 (1993).
  39. K.H. Zimmermann, An Introduction to Protein Informatics, Kluwer Academic Publishers: London (2003).
  40. N.C.V. Marbel, M. Stenberg, R. Oste, G. Markovarga, L. Gorton, H. Lingeman and U.A. Brinkman, Theor. J. Chromatogr., 141, 6 (2005).
  41. C.T. Yang, B. Moubaraki, K.S. Murray, J.D. Ranford and J.J. Vittal, Inorg. Chem., 40, 5934 (2001); https://doi.org/10.1021/ic010479b
  42. W.L. Liu, Y. Zou, C.L. Ni, Z.P. Ni, Y.Z. Li, Y.G. Yao and Q.J. Meng, Polyhedron, 23, 849 (2004); https://doi.org/10.1016/j.poly.2003.11.049
  43. C.T. Yang, B. Moubaraki, K.S. Murray and J.J. Vittal, J. Chem. Soc., Dalton Trans., 5, 880 (2003); https://doi.org/10.1039/b211496h
  44. N.M. Hosny and F.I. El-Dossoki, J. Chem. Eng. Data, 53, 2567 (2008); https://doi.org/10.1021/je800415n
  45. M M. Yousaf, M. Pervaiz, A.F. Zahoor, A.I. Hussain, M.K.K. Khosa, S. Ashraf, M. Sagir, Ashar-uz-Zaman and K. Shehzad, Asian J. Chem., 25, 521 (2013); https://doi.org/10.14233/ajchem.2013.13412
  46. E.J. Waheed, M.Sc. Thesis, Synthesis and Characterization of Complexes with Some Amino Acid Derivatives of the Glycine with Some Metal Salts, University of Baghdad, College of Education for Pure Sciences, Ibn Al Haitham, Iraq (2008).
  47. M.R. Shehata, Arab. J. Chem., 12, 1395 (2019); https://doi.org/10.1016/j.arabjc.2014.11.017
  48. N.S. Buttrus, Res. J. Chem. Sci., 4, 41 (2014).
  49. L.J. Ming, Med. Res. Rev., 23, 697 (2003); https://doi.org/10.1002/med.10052
  50. S. Krishnaraj, M. Muthukumar, P. Viswanathamurthi and S. Sivakumar, Transition Met. Chem., 33, 643 (2008); https://doi.org/10.1007/s11243-008-9091-x
  51. M. Shamsi, S. Yadav and F. Arjmand, J. Photochem. Photobiol. B, 136, 1 (2014); https://doi.org/10.1016/j.jphotobiol.2014.04.009
  52. M.A. Neelakantan, S.S. Marriappan, J. Dharmaraja, T. Jeyakumar and K. Muthukumaran, Spectrochim. Acta A Mol. Biomol. Spectrosc., 71, 628 (2008); https://doi.org/10.1016/j.saa.2008.01.023
  53. B.E. Ziegler, R.A. Marta, M.B. Burt and T.B. McMahon, Inorg. Chem., 53, 2349 (2014); https://doi.org/10.1021/ic402755q
  54. M.S. Nair, S.S. Kumari and M.A. Neelakantan, J. Coord. Chem., 60, 1291 (2007); https://doi.org/10.1080/00958970601053776
  55. X. Qiao, Z.Y. Ma, C.Z. Xie, F. Xue, Y.W. Zhang, J.Y. Xu, Z.Y. Qiang, J.S. Lou, G.J. Chen and S.P. Yan, J. Inorg. Biochem., 105, 728 (2011); https://doi.org/10.1016/j.jinorgbio.2011.01.004
  56. H.L. Singh and J. Singh, Int. J. Inorg. Chem., 2013, 847071 (2013); https://doi.org/10.1155/2013/847071
  57. H.L. Singh and J. Singh, Res. Chem. Intermed., 39, 1997 (2013); https://doi.org/10.1007/s11164-012-0732-5
  58. J. Al-Shaheen, A. Amira Al-M, Miaa, Res. J.. Chem. Sci., 4, 25 (2014).
  59. S. Islam, A.K.M.N.A. Siddiki, S. Begum and M.A. Salam, Open J. Inorg. Chem., 8, 55 (2018); https://doi.org/10.4236/ojic.2018.82005
  60. L.H. Abdel-Rahman, R.M. El-Khatib, L.A.E. Nassr, A.M. Abu-Dief and F.E.-D. Lashin, J. Mol. Struct., 111, 266 (2013); https://doi.org/10.1016/j.saa.2013.03.061
  61. M.N. Islam, S.M.S. Shahriar, M.K. Islam, M. Jesmin, M.M. Ali and J.A. Khanam, Int. Lett. Chem. Phys. Astron., 10, 12 (2013); https://doi.org/10.18052/www.scipress.com/ILCPA.10.12
  62. S. Alghool, M.S. Zoromba and H.F.A. El-Halim, J. Rare Earths, 31, 715 (2013); https://doi.org/10.1016/S1002-0721(12)60347-0
  63. F.H. Al-Jeboori, T.A.M. Al-Shimiesawi and A.O. Mithal, J. Chem. Pharm. Res., 6, 44 (2014).
  64. H. Sachdeva, R. Saroj, S. Khaturia, D. Dwivedi and O.P. Chauhan, J. Chem., 2014, 1 (2014); https://doi.org/10.1155/2014/848543
  65. H.L. Singh and J. Singh, Bioinorg. Chem. Appl., 2014, 1 (2014); https://doi.org/10.1155/2014/716578
  66. A.K. Abbas, Iraqi J. Sci., 56(4C), 3297 (2015).
  67. F. Ciolan, L. Patron, L. Marutescu and M.C. Chifiriuc, Farmacia, 63, 86 (2015).
  68. G.E. Iniama, I.T. Iorkpiligh and S.O. Olanrele, Int. J. Sci. Res., 4, 979 (2015).
  69. K. Saranya, S.S. Lakshmi, P. Mahadevi and G. Logesh, J. Chem. Pharm. Res., 7, 851 (2015).
  70. J. Saranya and S.S. Lakshmi, J. Chem. Pharm. Res., 7, 180 (2015).
  71. A. Abbas and R.S. Kadhim, J. Appl. Chem., 9, 20 (2016); https://doi.org/10.9790/5736-0908022031
  72. A. Antony, F. Fasna F, P.A. Ajil and J.T. Varkey, Rev. J. Chem., 5, 37 (2016).
  73. J.A. Shampa, M.R. Islam, M.S. Hossain, G.T. Rahman, C.M. Zakaria and M. Kudrat-E, Am. J. Heterocycl. Chem., 3, 37 (2017); https://doi.org/10.11648/j.ajhc.20170304.11
  74. M.M. Salama, S.G. Ahmed and S.S. Hassan, Adv. Biol. Chem., 7, 182 (2017); https://doi.org/10.4236/abc.2017.75013
  75. B.K. Al-Salami, R.A. Gata and K.A. Asker, Adv. Appl. Sci. Res., 8, 4 (2017).
  76. G.E. Iniama, B.P. Essien and I.T. Iorkpiligh, Int. J. Adv. Sci. Res. Eng. Trends, 3, 17 (2018).
  77. M. Pervaiz, I. Ahmad, M. Yousaf, S. Kirn, A. Munawar, Z. Saeed, A. Adnan, T. Gulzar, T. Kamal, A. Ahmad and A. Rashid, Spectrochim. Acta A Mol. Biomol. Spectrosc., 206, 642 (2019); https://doi.org/10.1016/j.saa.2018.05.057
  78. E.A. Nyawade, M.O. Onani, S. Meyer and P. Dube, Chem. Pap., 74, 3705 (2020); https://doi.org/10.1007/s11696-019-00986-5
  79. L.H. Abdel-Rahman, A.M. Abu-Dief, M. Ismael, M.A.A. Mohamed and N.A. Hashem, J. Mol. Struct., 1103, 232 (2016); https://doi.org/10.1016/j.molstruc.2015.09.039
  80. L. Subha, C. Balakrishnan, S. Thalamuthu and M.A. Neelakantan, J. Coord. Chem., 68, 1021 (2015); https://doi.org/10.1080/00958972.2015.1008466
  81. M. Theetharappan, L. Subha, C. Balakrishnan and M.A. Neelakantan, Appl. Organomet. Chem., 31, e3713 (2017); https://doi.org/10.1002/aoc.3713
  82. S. Zehra, T. Roisnel and F. Arjmand, ACS Omega, 4, 7691 (2019); https://doi.org/10.1021/acsomega.9b00131
  83. S.S. Lakshmi, K. Geetha, M. Gayathri and G. Shanmugam, J. Chem. Sci., 128, 1095 (2016); https://doi.org/10.1007/s12039-016-1099-8
  84. S.S. Wazalwar and N.S. Bhave, Synth. React. Inorg. Met.-Org. NanoMet. Chem., 42, 1098 (2012); https://doi.org/10.1080/15533174.2012.680100
  85. S.S. Lakshmi and K. Geetha, J. Chem. Pharm. Res., 8, 668 (2016).
  86. N.K. Kubra, A. Suganya, J. Saranya and S.S. Lakshmi, World J. Pharm. Res., 7, 411 (2018); https://doi.org/10.20959/wjpr20188-11037
  87. H.L. Salem, Acta Sci. Microbiol., 2, 7 (2019).
  88. N.A. Tas, A. Senocak and A. Aydin, J. Turkish Chem. Soc., 5, 585 (2018); https://doi.org/10.18596/jotcsa.373904
  89. C. Camacho-Camacho, I. Rojas-Oviedo, A. Garza-Ortiz, R.A. Toscano, L. Sánchez-Sánchez, J. Cardenas and H. López-Muñoz, Appl. Organomet. Chem., 30, 199 (2016); https://doi.org/10.1002/aoc.3417
  90. Y. Wang, W. Gu, Y. Shan, F. Liu, X. Xu, Y. Yang, Q. Zhang, Y. Zhang, H. Kuang, Z. Wang and S. Wang, Bioorg. Med. Chem. Lett., 27, 2360 (2017); https://doi.org/10.1016/j.bmcl.2017.04.024
  91. M. Arockia doss, S. Savithiri, G. Rajarajan, V. Thanikachalam and H. Saleem, Spectrochim. Acta A Mol. Biomol. Spectrosc., 148, 189 (2015); https://doi.org/10.1016/j.saa.2015.03.117
  92. F.A. Beckford and K.R. Webb, Spectrochim. Acta A Mol. Biomol. Spectrosc., 183, 158 (2017); https://doi.org/10.1016/j.saa.2017.04.057
  93. T.A. Yousef, O.K. Alduaij, S.F. Ahmed, G.M. Abu El-Reash and O.A. El-Gammal, J. Mol. Struct., 1125, 788 (2016); https://doi.org/10.1016/j.molstruc.2016.07.045
  94. M.A. Hussein, M.A. Iqbal, M.I. Umar, R.A. Haque and T.S. Guan, Arab. J. Chem., 12, 3183 (2015); https://doi.org/10.1016/j.arabjc.2015.08.013
  95. S. Farhadi, F. Mahmoudi and J. Simpson, J. Mol. Struct., 1108, 583 (2016); https://doi.org/10.1016/j.molstruc.2015.12.038
  96. M. Kawahara, Y. Sadakane, H. Koyama, K. Konoha and S. Ohkawara, Metallomics, 5, 453 (2013); https://doi.org/10.1039/c3mt20264j
  97. B.M. Sarhan, E.J. Waheed and B.Z. Naema, Ibn Al- Haitham J. Pure Appl. Sci., 24, 144 (2011).
  98. L. Antolini, L.P. Battaglia, A. Bonamartini Corradi, G. Marcotrigiano, L. Menabue, G.C. Pellacani and M. Saladini, Inorg. Chem., 21, 1391 (1982); https://doi.org/10.1021/ic00134a024
  99. V.N. Vandyshev and S.F. Ledenkov, Russ. J. Phys. Chem., 83, 2177 (2009); https://doi.org/10.1134/S0036024409120310
  100. P.R. Reddy, A. Shilpa, N. Raju and P. Raghavaiah, J. Inorg. Biochem., 105, 1603 (2011); https://doi.org/10.1016/j.jinorgbio.2011.08.022
  101. O.E. Offiong, E. Nfor, A.A. Ayi and S. Martelli, Transition Met. Chem., 25, 369 (2000); https://doi.org/10.1023/A:1007055304150
Read More
Author biographies is not available.
Download
PDF
Statistic
Read Counter : 2 Download : 1