Skip to main content
Log in

Synthesis, structure, Hirshfeld surface analysis, and molecular docking studies of the Cu(II) complex with 3-nitro-4-aminobenzoic acid

  • Research
  • Published:
Structural Chemistry Aims and scope Submit manuscript

Abstract

The first representative of 3-nitro-4-aminobenzoic acid (3N-4ABA) monoligand metal complexes has been obtained on an example of the Cu(II) complex. The structure of the compound was studied using element analysis, IR- and UV-spectroscopy, and Hirshfeld surface analysis while bioactivity is assessed by molecular docking. Cu(II) ions coordinate two 3N-4ABA molecules bidentately through the oxygen atoms of the carboxylate group, and there are water molecules in the other two positions of the coordination sphere, i.e., all coordinated atoms are only oxygen ones which leads to the formation of the essentially distorted octahedron due to the Janh-Teller effect. Moreover, there is one water molecule in the outer sphere, making this compound a crystal hydrate with the formula of [Cu(3N-4ABA)2(H2O)2]·H2O. The complicated system of the intermolecular H-bonds and π···π staking interactions incorporate complex molecules into the 3D network. In silico studies of the 3N-4ABA ligand and Cu-complex attested that antimicrobial and antitumor activities indicate a higher affinity of the complex for some key binding sites especially relatively to S. aureus and KDM4 with binding energies of − 9.6 and − 9.2 kcal/mol, respectively.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

Data availability

No datasets were generated or analyzed during the current study.

References

  1. Maki T, Kazuo T (2000) Benzoic acid and derivatives. Ullmann’s encyclopedia of industrial chemistry. First published. https://doi.org/10.1002/14356007.a03_555

  2. Del Olmo A, Calzada J, Nuñez M (2017) Benzoic acid and its derivatives as naturally occurring compounds in foods and as additives: uses, exposure, and controversy. Crit Rev Food Sci Nutr 57(14):3084–3103. https://doi.org/10.1080/10408398.2015.1087964

    Article  CAS  PubMed  Google Scholar 

  3. Krátký M, Konečná K, Janoušek J, Brablíková M, Janďourek O, Trejtnar F, Vinšová J (2019) 4-Aminobenzoic acid derivatives: converting folate precursor to antimicrobial and cytotoxic agents. Biomolecules 10(1):9. https://doi.org/10.3390/biom10010009

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Oufqir Y, Fortin L, Girouard J, Cloutier F, Cloutier M, Leclerc MF, Reyes-Moreno C (2022) Synthesis of new para-aminobenzoic acid derivatives, in vitro biological evaluation and preclinical validation of DAB-2-28 as a therapeutic option for the treatment of bladder cancer. Eur J Med Chem Rep 6:100069. https://doi.org/10.1016/j.ejmcr.2022.100069

    Article  CAS  Google Scholar 

  5. Bérubé G, Reyes-Moreno C (2020) Aminobenzoic acid derivatives for use as anti-inflammatory agents, anti-metastatic agents and/or anticancer agents US patent no. 10,759,754.4.

  6. Rohini M, Sachdeva S, Jain A, Chaudhary J (2013) A comprehensive review on biological activities of p-hydroxy benzoic acid and its derivatives. Int J Pharm Sci Rev Res 22(2):109–115.

    Google Scholar 

  7. Correa-Basurto J, Alcántara IV, Espinoza-Fonseca LM, Trujillo-Ferrara JG (2005) p–Aminobenzoic acid derivatives as acetylcholinesterase inhibitors. Eur J Med Chem 40(7):732–735.

    Article  CAS  PubMed  Google Scholar 

  8. Bruze M, Gruvberger B, Thulin I (1990) PABA, benzocaine, and other PABA esters in sunscreens and after-sun products. Photodermatol Photoimmunol Photomed 7(3):106–108.

    CAS  PubMed  Google Scholar 

  9. Chowdhury FT, Sarker M, Islam MS, Nur HP, Islam MR, Khan H (2022) Investigation of antimicrobial activity and identification of bioactive volatile metabolites of jute endophytic fungus Aspergillus flavus. Bioresearch Communications - (BRC), 4(1):476–482. https://www.bioresearchcommunications.com/index.php/brc/article/view/95

  10. Sharma B, Shukla S, Rattan R, Fatima M, Goel M, Bhat M, Dutta S, Ranjan RK, Sharma M (2022) Antimicrobial agents based on metal complexes: present situation and future prospects. Int J Biomater 6819080. https://doi.org/10.1155/2022/6819080

  11. Ibragimov AB, Ashurov ZM, Ibragimov AB, Tashpulatov ZZ (2017) Synthesis, structure, and fungicidal activity of mono- and binuclear mixed-ligand copper complex with p-nitrobenzoic acid and monoethanolamine. Russ J Coord Chem 43:380–388. https://doi.org/10.1134/S1070328417060021

    Article  CAS  Google Scholar 

  12. Ibragimov AB, Ashurov JM, Ibragimov AB, Eshimbetov AG (2021) Synthesis of the three mixed-ligand metal complexes and one organic salt of 3,5-dinitrobenzoic acid for biopharmaceutical optimization through monoethanolamine: structures and DFT studies of complexes. J Chem Cryst 51(3):405–417.

    Article  CAS  Google Scholar 

  13. Ibragimov AB, Ashurov JM, Zakirov BS (2016) X-Ray Structures of three polymeric and two mononuclear metal complexes on the base of p-aminobenzoic acid. J Chem Crystallogr 46:352–363.https://doi.org/10.1007/s10870-016-0665-8

    Article  CAS  Google Scholar 

  14. Ibragimov AB, Ashurov ZM, Ibragimov AB, Zakirov BS (2017) Two supramolecular complexes based on 4-hydroxybenzoic acid and triethanolamine: synthesis and structure. Russ J Inorg Chem 62:439–445. https://doi.org/10.1134/S0036023617040064

    Article  CAS  Google Scholar 

  15. Rigaku OD, CrysAlis PRO (2020) Rigaku Oxford Diffraction, Yarnton, England

  16. Sheldrick GM (2015) SHELXT - integrated space-group and crystal-structure determination. Acta Crystallogr A Found Adv 71:3–8. https://doi.org/10.1107/S2053273314026370

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Sheldrick GM (2015) Crystal structure refinement with SHELXL. Acta Crystallogr C Struct Chem 71:3–8. https://doi.org/10.1107/S2053229614024218

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Macrae CF, Sovago I, Cottrell SJ, Galek PT, McCabe P, Pidcock E, Platings M, Shields GP, Stevens JS, Towler M, Wood PA (2020) Mercury 4.0: from visualization to analysis, design and prediction. J Appl Crystallogr 53:226–235. https://doi.org/10.1107/S1600576719014092

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Ibragimov AB, Ashurov ZM, Zakirov BS (2017) Molecular and crystal structure of a mixed-ligand cadmium complex with p-hydroxybenzoic acid and monoethanolamine. J Str Chemi 58:588–590. https://doi.org/10.1134/s0022476617030209

    Article  CAS  Google Scholar 

  20. Ibragimov AB, Ashurov JM, Ibragimov BT, Zakirov BS (2017) Preparation, structures and antimicrobial activity of four different type metal complexes on the base of diethanolamine and o-nitrobenzoic acid. J Mol Str 1128:307–316. https://doi.org/10.1016/j.molstruc.2016.08.079

    Article  CAS  Google Scholar 

  21. Seaton CC, Chadwick K, Sadiq G, Guo K, Davey RJ (2010) Designing acid/acid co-crystals through the application of Hammett substituent constants. Cryst Growth Des 10(2):726–733. https://doi.org/10.1021/cg9011235

    Article  CAS  Google Scholar 

  22. Win YF, Choong CS, Teoh SG, Goh JH, Fun HK (2010) Bis([mu]2-4-amino-3-nitro­benzoato)bis­(4-amino-3-nitro­benzoato)octa­butyldi-[mu]3-oxido-tetra­tin(IV). Acta Cryst E66:m1406-1407. https://doi.org/10.1107/S1600536810040146

    Article  CAS  Google Scholar 

  23. Liu Y, Yang X, Gan J, Chen S, Xiao ZX, Cao Y (2022) CB-Dock 2: Improved protein–ligand blind docking by integrating cavity detection, docking and homologous template fitting. Nucleic acids research 50(W1):W159–W164. https://doi.org/10.1093/nar/gkac394

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Liu JS, Fang WK, Yang SM, Wu MC, Chen TJ, Chen CM, Lin TY, Liu KL, Wu CM, Chen YC, Chuu CP, Wang LY, Hsieh HP, Kung HJ, Wang WC (2022) Natural product myricetin is a pan-KDM4 inhibitor which with poly lactic-co-glycolic acid formulation effectively targets castration-resistant prostate cancer. J Biomed Sci 29:29. https://doi.org/10.1186/s12929-022-00812-3

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Berry WL, Janknecht R (2013) KDM4/JMJD2 histone demethylases: epigenetic regulators in cancer cells. Can Res 73(10):2936–2942. https://doi.org/10.1158/0008-5472.CAN-12-4300

    Article  CAS  Google Scholar 

  26. Labbé RM, Holowatyj A, Yang ZQ (2014) Histone lysine demethylase (KDM) subfamily 4: structures, functions and therapeutic potential. American journal of translational research 6(1):1–15.

    Google Scholar 

  27. BIOVIA DS (2021) Discovery Studio Visualizer; v21. 1.0. 20298 Dassault Systèmes: San Diego. CA, USA

  28. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE (2000) The protein data bank. Nucleic Acids Res 28(1):235–242.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Ibragimov AB, Ashurov JM, Ibragimov BT, Eshimbetov AG, Azimova SS, Tilyakov Z G, Dusmatov AF. (2023) Synthesis, structure, Hirshfeld surface analysis of the new copper complex of 3, 5-dinitrobenzoic acid and docking study of its metal complexes bioactivity. J Mol Struct 136105. https://doi.org/10.1016/j.molstruc.2023.136105

  30. Kouser S, Joythi M, Begum AB, Asha MS, Al-Ostoot FH, Lakshmeesha DP, Khanum SA (2023) Molecular docking, synthesis and antimicrobial evaluation of metal complexes with Schiff base. Results in Chemistry 5:100650.

    Article  Google Scholar 

Download references

Acknowledgements

Authors gratefully acknowledge Ministry of Higher Education, Science and Innovation for the financial support (project number F3-20200929348).

Funding

Financial support from Ministry of Higher Education, Science and Innovation (project number F3-20200929348).

Author information

Authors and Affiliations

Authors

Contributions

All authors have contributed equally to writing and reviewing the manuscript.

Corresponding author

Correspondence to A. B. Ibragimov.

Ethics declarations

Ethical approval

Not applicable.

Informed consent

Not applicable.

Competing interest

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 125 KB)

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Narmanova, F.S., Turaev, K.K., Kasimov, S.A. et al. Synthesis, structure, Hirshfeld surface analysis, and molecular docking studies of the Cu(II) complex with 3-nitro-4-aminobenzoic acid. Struct Chem (2024). https://doi.org/10.1007/s11224-024-02320-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s11224-024-02320-6

Keywords

Navigation