Research Article
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Year 2025, Volume: 53 Issue: 1, 19 - 30
https://doi.org/10.15671/hjbc.1495468

Abstract

References

  • Reference1. Z. Hussain, M. Khalaf, H. Adil, D. Zageer, F. Hassan, S. Mohammed, E. Yousif, Metal complexes of Schiff's bases containing sulfonamides nucleus: A review, Res. J. Pharm. Biol. Chem. Sci., 7(2016) 1008-1025.
  • Reference2. S. Zehra, T. Roisnel, F. Arjmand, Enantiomeric amino acid Schiff base copper(II) complexes as a new class of RNA-targeted metallo-intercalators: single X-ray crystal structural details, comparative in vitro DNA/RNA binding profile, cleavage, and cytotoxicity, ACS Omega 4 (2019) 7691-7705.
  • Reference3. T. Hermann, Strategies for the design of drugs targeting RNA and RNA-protein complexes, Angew. Chem. Int. Ed. Engl., 39 (2000) 1890-1905.
  • Reference4. K.A. Meadows, F. Liu, J. Sou, B.P. Hudson, D.R. McMillin, Spectroscopic and photophysical studies of the binding interactions between copper phenanthroline complexes and RNA, Inorg. Chem., 32 (1993) 2919-2923.
  • Reference5. M. Asif, An overview on synthesis and medicinal chemistry potentials of biologically active antimicrobial Schiff’s bases and its complexes: a review, Mor. J. Chem., 3(3) (2015) 627-652.
  • Reference6. L. Kafi-Ahmadi, A. P. Marjani, M. Pakdaman-Azari, S. Afr, Synthesis, characterization and antibacterial properties of N,N'-Bis(4-dimethylaminobenzylidene)benzene-1,3-diamine as new Schiff Base ligand and its binuclear Zn(II), Cd(II) complexes. J. Chem. Eng., (71) (2018) 155-159.
  • Reference7. S. S. Hassan, E. A. Bedir, A. E.-R. M. Hamza, A. M. Ahmed, N. M. Ibrahim, M. S. Abd El-Ghany, N. N. Khattab, B. M. Emeira, M. M. Salama, E. F. Mohamed, D. B. Fayed, The dual therapeutic effect of metformin nuclei-based drugs modified with one of Tulbaghia violacea extract compounds, Appl. Organomet. Chem. 36(9) (2022) e6804.
  • Reference8. T. H.Al-Noor, N. S. Al-barki, A. A. Maihub, M. M. El-ajaily, Synthesis and Spectroscopic Characterization of some Mixed Schiff Base Complexes, International Journal of Science and Research (IJSR), 6(3) (2017) 2421-2426.
  • Reference9. A. A. Ahmed, H. N. Aliyu, Synthesis, Structural Characterization and Antimicrobial Potency of Anthranilic Acid Based Mn(II) Schiff Base Complex, Chemistry Research Journal, 4(5) (2019) 54-61.
  • Reference10. Y. Zhang, B. Zou, Z. Chen, Y. Pan, H. Wang, H. Liang and X. Yi, Synthesis and antioxidant activities of novel 4-Schiff base-7-benzyloxycoumarin derivatives, Bioorg. Med. Chem. Lett., (21) (2011) 6811-6815.
  • Reference11. W. A. Zoubi, A. A. S. Al-Hamdani, M. Kaseem, Synthesis and antioxidant activities of Schiff bases and their complexes: a review, Appl. Organometal. Chem., 30 (2016) 810-817.
  • Reference12. K. J. Barnham, C. L. Masters, A. I. Bush, Neurodegenerative diseases and oxidative stress, Nat. Rev. Drug Discov., 3(3) (2004) 205-214.
  • Reference13. B. Uttara, A. V. Singh, P. Zamboni, R. T. Mahajan, Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options, Curr. Neuropharm., 7(1) (2009) 65-74.
  • Reference14. D. Inci, R. Aydın, Y. Zorlu, NOO-type tridentate Schiff base ligand and its one-dimensional Cu(II) coordination polymer: synthesis, crystal structure, biomacromolecular interactions and radical scavenging activities, Inorg. Chim. Acta 514 (2021) 119994.
  • Reference15. D. Inci, A new ternary Cu (II) complex with 4,7-dimethyl-1,10-phenanthroline and NOO-type tridentate Schiff base ligand: synthesis, crystal structure, biomacromolecular interactions, and radical scavenging activities, Appl. Organomet. Chem. 34 (2020) e6016.
  • Reference16. B. Gültekin, D. İ. Özbağcı, İ. Aydın, R. Aydın, F. Arı, Y. Zorlu, New copper(II) complexes containing tryptophan based Schiff bases as promising antiproliferative agents on breast cancer cells, J. Mol. Struct., 1301 (2024) 137273.
  • Reference17. D. İ. Özbağcı, B. Gültekin, İ. Aydın, R. Aydın, F. Arı, Y. Zorlu, New copper (II) complexes bearing tryptophan-based Schiff bases and 2,2′-bipyridine: Crystal structures, DNA/BSA interactions and antiproliferative activities, Appl. Organomet. Chem., 38(4) (2024) e7369.
  • Reference18. J. R. Lakowicz, G. Weber, Quenching of fluorescence by oxygen. A probe for structural fluctuations in macromolecules, Biochemistry, 12 (21) (1973) 4161-4170.
  • Reference19. K. D. Karlin, B. I. Cohen, J. C. Hayes, A. Farooq, J. Zubieta, Models for methemocyanin derivatives: structural and spectroscopic comparisons of related azido-coordinated (N3-) mono- and dinuclear copper(II) complexes, Inorg. Chem. 26 (1) (1987) 147-153.
  • Reference20. M. Lee, A. L. Rhodes, M.D. Wyatt, S. Forrow, J.A. Hartley, GC base sequence recognition by oligo(imidazolecarboxamide) and C-terminus-modified analogues of distamycin deduced from circular dichroism, proton nuclear magnetic resonance, and methidium propylethylenediaminetetraacetate-iron(II) footprinting studies, Biochemistry, 32 (16) (1993) 4237-4245.
  • Reference21. L. N. Zhang, F. Y. Wu, A. H. Liu, Study of the interaction between 2,5-di-[2- (4-hydroxy-phenyl)ethylene]-terephthalonitril and bovine serum albumin by fluorescence spectroscopy. Spectrochim. Acta A Mol. Biomol. Spectrosc., 79 (2011) 97-103.
  • Reference22. X. X. Cheng, Y. Lui, B. Zhou, X. H. Xiao, Y. Liu, Probing the binding sites and the effect of berbamine on the structure of bovine serum albumin, Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 72 (2009) 922-928.
  • Reference23. S. Prasanth, D. R. Raj, T. V. Vineeshkumar, R. K. Thomas, C. Sudarsanakumar, Exploring the interaction of L-cysteine capped CuS nanoparticles with bovine serum albumin (BSA): a spectroscopic study, RSC Adv., 6 (2016) 58288-28295.
  • Reference24. T. Göktürk, T. Zengin, T. Hökelek, C. G. Topkaya, R. Güp, Synthesis, Crystal Structure, Hirshfeld Surface Analysis, DNA/BSA Interaction and Molecular Docking Studies of 2-(6-(4-chlorophenyl)-1,2,4-triazin-3-yl)quinoline, J. Mol. Struct., 1292 (2023) 136128.
  • Reference25. K. Preetha, E. Seena, P. K. Maniyampara, E. Manoj, M. P. Kurup, Synthesis, crystal structure, Hirshfeld surface analysis, DFT, molecular docking and in vitro antitumor studies of (2E)-2-[4-(diethylamino)benzylidene]-N-ethylhydrazinecarbothioamide, J. Mol. Struct., 1295 (2024) 136700.
  • Reference26. S. K. Tarai, S. Mandal, A. Tarai, I. Som, A. Pan, A. Bagchi, A. Biswas, S. C. Moi, Biophysical study on DNA and BSA binding activity of Cu(II) complex: Synthesis, molecular docking, cytotoxic activity, and theoretical approach, Appl. Organomet. Chem,. 37(8) (2023) e7164.
  • Reference27. S. K. Tarai, A. Tarai, S. Mandal, B. Nath, I. Som, R. Bhaduri, A. Bagchi, S. Sarkar, A. Biswas, S. Ch. Moi, Cytotoxic behavior and DNA/BSA binding activity of thiosemicarbazone based Ni(II) complex: bio-physical, molecular docking and DFT study, J. Mol. Liq., 383 (2023) 121921.
  • Reference28. T. Tantimongcolwat, S. Prachayasittikul, V. Prachayasittikul, Unravelling the interaction mechanism between clioquinol and bovine serum albumin by multi-spectroscopic and molecular docking approaches, Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 216 (2019) 25-34.
  • Reference29. T. Kroetz, P. A. Nogara, F. da Silveira Santos, L. C. da Luz, V. S. Câmara, J. B. T. da Rocha, A. Gonçalves Dal-Bó, F. S. Rodembusch, Interaction Study between ESIPT Fluorescent Lipophile-Based Benzazoles and BSA, Molecules, 26(21) (2021) 6728.
  • Reference30. W. Widowati, A. P. Rani, R. A. Hamzah, S. Arumwardana, E. Afifah, H. S. W. Kusuma, D. D. Rihibiha, H. Nufus, A. Amalia, Antioxidant and Antiaging Assays of Hibiscus sabdariffa Extract and Its Compounds, Nat. Prod. Sci., 23(3) (2017) 192-200.

5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity

Year 2025, Volume: 53 Issue: 1, 19 - 30
https://doi.org/10.15671/hjbc.1495468

Abstract

A novel 5ClAA-Schiff base (Schiff base derived from the condensation of 5-chloroanthranilic acid and 4-(dimethylamino)benzaldehyde) has been synthesized. The structure of the 5ClAA-Schiff base was clarified by CHN analysis, FTIR, electronic absorption spectroscopy, ESI-MS and X-ray single crystal diffraction methods. In biological activity studies, the interactions of the 5ClAA-Schiff base with calf thymus DNA (CT-DNA) were examined using fluorescence spectroscopy. The interactions of the 5ClAA-Schiff base with bovine serum albumin (BSA) were investigated using electronic absorption and fluorescence spectroscopy techniques and the BSA quenching mechanism was found. The molecular docking simulation was investigated to explore the interactions between the 5ClAA-Schiff base and biomolecules such as DNA and BSA using in silico techniques. Results confirmed that the 5ClAA-Schiff base was inserted into DNA via a minor groove and into BSA with subdomain IIA. The antioxidant activity of the 5ClAA-Schiff base was also investigated in comparison with the compounds used as standard.

Thanks

The author would like to thank Prof. Dr. Rahmiye Aydın for allowing me to use the facilities at the Inorganic Chemistry Laboratory to conduct in this study. The author also would like to acknowledge Prof. Dr. Yunus Zorlu for the discussion about the single-crystal X-ray diffraction data analysis and Assist. Prof. Dr. Sevinç İlkar Erdağı for the discussion about the molecular docking data analysis.

References

  • Reference1. Z. Hussain, M. Khalaf, H. Adil, D. Zageer, F. Hassan, S. Mohammed, E. Yousif, Metal complexes of Schiff's bases containing sulfonamides nucleus: A review, Res. J. Pharm. Biol. Chem. Sci., 7(2016) 1008-1025.
  • Reference2. S. Zehra, T. Roisnel, F. Arjmand, Enantiomeric amino acid Schiff base copper(II) complexes as a new class of RNA-targeted metallo-intercalators: single X-ray crystal structural details, comparative in vitro DNA/RNA binding profile, cleavage, and cytotoxicity, ACS Omega 4 (2019) 7691-7705.
  • Reference3. T. Hermann, Strategies for the design of drugs targeting RNA and RNA-protein complexes, Angew. Chem. Int. Ed. Engl., 39 (2000) 1890-1905.
  • Reference4. K.A. Meadows, F. Liu, J. Sou, B.P. Hudson, D.R. McMillin, Spectroscopic and photophysical studies of the binding interactions between copper phenanthroline complexes and RNA, Inorg. Chem., 32 (1993) 2919-2923.
  • Reference5. M. Asif, An overview on synthesis and medicinal chemistry potentials of biologically active antimicrobial Schiff’s bases and its complexes: a review, Mor. J. Chem., 3(3) (2015) 627-652.
  • Reference6. L. Kafi-Ahmadi, A. P. Marjani, M. Pakdaman-Azari, S. Afr, Synthesis, characterization and antibacterial properties of N,N'-Bis(4-dimethylaminobenzylidene)benzene-1,3-diamine as new Schiff Base ligand and its binuclear Zn(II), Cd(II) complexes. J. Chem. Eng., (71) (2018) 155-159.
  • Reference7. S. S. Hassan, E. A. Bedir, A. E.-R. M. Hamza, A. M. Ahmed, N. M. Ibrahim, M. S. Abd El-Ghany, N. N. Khattab, B. M. Emeira, M. M. Salama, E. F. Mohamed, D. B. Fayed, The dual therapeutic effect of metformin nuclei-based drugs modified with one of Tulbaghia violacea extract compounds, Appl. Organomet. Chem. 36(9) (2022) e6804.
  • Reference8. T. H.Al-Noor, N. S. Al-barki, A. A. Maihub, M. M. El-ajaily, Synthesis and Spectroscopic Characterization of some Mixed Schiff Base Complexes, International Journal of Science and Research (IJSR), 6(3) (2017) 2421-2426.
  • Reference9. A. A. Ahmed, H. N. Aliyu, Synthesis, Structural Characterization and Antimicrobial Potency of Anthranilic Acid Based Mn(II) Schiff Base Complex, Chemistry Research Journal, 4(5) (2019) 54-61.
  • Reference10. Y. Zhang, B. Zou, Z. Chen, Y. Pan, H. Wang, H. Liang and X. Yi, Synthesis and antioxidant activities of novel 4-Schiff base-7-benzyloxycoumarin derivatives, Bioorg. Med. Chem. Lett., (21) (2011) 6811-6815.
  • Reference11. W. A. Zoubi, A. A. S. Al-Hamdani, M. Kaseem, Synthesis and antioxidant activities of Schiff bases and their complexes: a review, Appl. Organometal. Chem., 30 (2016) 810-817.
  • Reference12. K. J. Barnham, C. L. Masters, A. I. Bush, Neurodegenerative diseases and oxidative stress, Nat. Rev. Drug Discov., 3(3) (2004) 205-214.
  • Reference13. B. Uttara, A. V. Singh, P. Zamboni, R. T. Mahajan, Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options, Curr. Neuropharm., 7(1) (2009) 65-74.
  • Reference14. D. Inci, R. Aydın, Y. Zorlu, NOO-type tridentate Schiff base ligand and its one-dimensional Cu(II) coordination polymer: synthesis, crystal structure, biomacromolecular interactions and radical scavenging activities, Inorg. Chim. Acta 514 (2021) 119994.
  • Reference15. D. Inci, A new ternary Cu (II) complex with 4,7-dimethyl-1,10-phenanthroline and NOO-type tridentate Schiff base ligand: synthesis, crystal structure, biomacromolecular interactions, and radical scavenging activities, Appl. Organomet. Chem. 34 (2020) e6016.
  • Reference16. B. Gültekin, D. İ. Özbağcı, İ. Aydın, R. Aydın, F. Arı, Y. Zorlu, New copper(II) complexes containing tryptophan based Schiff bases as promising antiproliferative agents on breast cancer cells, J. Mol. Struct., 1301 (2024) 137273.
  • Reference17. D. İ. Özbağcı, B. Gültekin, İ. Aydın, R. Aydın, F. Arı, Y. Zorlu, New copper (II) complexes bearing tryptophan-based Schiff bases and 2,2′-bipyridine: Crystal structures, DNA/BSA interactions and antiproliferative activities, Appl. Organomet. Chem., 38(4) (2024) e7369.
  • Reference18. J. R. Lakowicz, G. Weber, Quenching of fluorescence by oxygen. A probe for structural fluctuations in macromolecules, Biochemistry, 12 (21) (1973) 4161-4170.
  • Reference19. K. D. Karlin, B. I. Cohen, J. C. Hayes, A. Farooq, J. Zubieta, Models for methemocyanin derivatives: structural and spectroscopic comparisons of related azido-coordinated (N3-) mono- and dinuclear copper(II) complexes, Inorg. Chem. 26 (1) (1987) 147-153.
  • Reference20. M. Lee, A. L. Rhodes, M.D. Wyatt, S. Forrow, J.A. Hartley, GC base sequence recognition by oligo(imidazolecarboxamide) and C-terminus-modified analogues of distamycin deduced from circular dichroism, proton nuclear magnetic resonance, and methidium propylethylenediaminetetraacetate-iron(II) footprinting studies, Biochemistry, 32 (16) (1993) 4237-4245.
  • Reference21. L. N. Zhang, F. Y. Wu, A. H. Liu, Study of the interaction between 2,5-di-[2- (4-hydroxy-phenyl)ethylene]-terephthalonitril and bovine serum albumin by fluorescence spectroscopy. Spectrochim. Acta A Mol. Biomol. Spectrosc., 79 (2011) 97-103.
  • Reference22. X. X. Cheng, Y. Lui, B. Zhou, X. H. Xiao, Y. Liu, Probing the binding sites and the effect of berbamine on the structure of bovine serum albumin, Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 72 (2009) 922-928.
  • Reference23. S. Prasanth, D. R. Raj, T. V. Vineeshkumar, R. K. Thomas, C. Sudarsanakumar, Exploring the interaction of L-cysteine capped CuS nanoparticles with bovine serum albumin (BSA): a spectroscopic study, RSC Adv., 6 (2016) 58288-28295.
  • Reference24. T. Göktürk, T. Zengin, T. Hökelek, C. G. Topkaya, R. Güp, Synthesis, Crystal Structure, Hirshfeld Surface Analysis, DNA/BSA Interaction and Molecular Docking Studies of 2-(6-(4-chlorophenyl)-1,2,4-triazin-3-yl)quinoline, J. Mol. Struct., 1292 (2023) 136128.
  • Reference25. K. Preetha, E. Seena, P. K. Maniyampara, E. Manoj, M. P. Kurup, Synthesis, crystal structure, Hirshfeld surface analysis, DFT, molecular docking and in vitro antitumor studies of (2E)-2-[4-(diethylamino)benzylidene]-N-ethylhydrazinecarbothioamide, J. Mol. Struct., 1295 (2024) 136700.
  • Reference26. S. K. Tarai, S. Mandal, A. Tarai, I. Som, A. Pan, A. Bagchi, A. Biswas, S. C. Moi, Biophysical study on DNA and BSA binding activity of Cu(II) complex: Synthesis, molecular docking, cytotoxic activity, and theoretical approach, Appl. Organomet. Chem,. 37(8) (2023) e7164.
  • Reference27. S. K. Tarai, A. Tarai, S. Mandal, B. Nath, I. Som, R. Bhaduri, A. Bagchi, S. Sarkar, A. Biswas, S. Ch. Moi, Cytotoxic behavior and DNA/BSA binding activity of thiosemicarbazone based Ni(II) complex: bio-physical, molecular docking and DFT study, J. Mol. Liq., 383 (2023) 121921.
  • Reference28. T. Tantimongcolwat, S. Prachayasittikul, V. Prachayasittikul, Unravelling the interaction mechanism between clioquinol and bovine serum albumin by multi-spectroscopic and molecular docking approaches, Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 216 (2019) 25-34.
  • Reference29. T. Kroetz, P. A. Nogara, F. da Silveira Santos, L. C. da Luz, V. S. Câmara, J. B. T. da Rocha, A. Gonçalves Dal-Bó, F. S. Rodembusch, Interaction Study between ESIPT Fluorescent Lipophile-Based Benzazoles and BSA, Molecules, 26(21) (2021) 6728.
  • Reference30. W. Widowati, A. P. Rani, R. A. Hamzah, S. Arumwardana, E. Afifah, H. S. W. Kusuma, D. D. Rihibiha, H. Nufus, A. Amalia, Antioxidant and Antiaging Assays of Hibiscus sabdariffa Extract and Its Compounds, Nat. Prod. Sci., 23(3) (2017) 192-200.
There are 30 citations in total.

Details

Primary Language English
Subjects Bioinorganic Chemistry, Inorganic Chemistry (Other)
Journal Section Research Article
Authors

Duygu İnci Özbağcı 0000-0002-0483-9642

Publication Date
Submission Date June 4, 2024
Acceptance Date August 26, 2024
Published in Issue Year 2025 Volume: 53 Issue: 1

Cite

APA İnci Özbağcı, D. (n.d.). 5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity. Hacettepe Journal of Biology and Chemistry, 53(1), 19-30. https://doi.org/10.15671/hjbc.1495468
AMA İnci Özbağcı D. 5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity. HJBC. 53(1):19-30. doi:10.15671/hjbc.1495468
Chicago İnci Özbağcı, Duygu. “5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity”. Hacettepe Journal of Biology and Chemistry 53, no. 1 n.d.: 19-30. https://doi.org/10.15671/hjbc.1495468.
EndNote İnci Özbağcı D 5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity. Hacettepe Journal of Biology and Chemistry 53 1 19–30.
IEEE D. İnci Özbağcı, “5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity”, HJBC, vol. 53, no. 1, pp. 19–30, doi: 10.15671/hjbc.1495468.
ISNAD İnci Özbağcı, Duygu. “5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity”. Hacettepe Journal of Biology and Chemistry 53/1 (n.d.), 19-30. https://doi.org/10.15671/hjbc.1495468.
JAMA İnci Özbağcı D. 5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity. HJBC.;53:19–30.
MLA İnci Özbağcı, Duygu. “5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity”. Hacettepe Journal of Biology and Chemistry, vol. 53, no. 1, pp. 19-30, doi:10.15671/hjbc.1495468.
Vancouver İnci Özbağcı D. 5-Chloroanthranilic Acid Schiff Base: Crystal Structure, DNA/BSA Interactions, Molecular Docking and Antioxidant Activity. HJBC. 53(1):19-30.

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