120
Views
0
CrossRef citations to date
0
Altmetric
Research Articles

Fabricate, advancement, molecular docking and DNA reactivity of preferred divalent metal(II) complexes attributing (E)-N’-((6-hydroxybenzo[d]oxazol-5-yl) methylene)isonicotinohydrazide

, , , ORCID Icon, &
Pages 824-840 | Received 09 Feb 2022, Accepted 20 May 2022, Published online: 30 May 2022

References

  • Ndagi, U.; Mhlongo, N.; Soliman, M. E. Metal Complexes in Cancer Therapy - An Update from Drug Design Perspective. Drug Des. Devel. Ther. 2017, 11, 599–616. DOI: 10.2147/DDDT.S119488.
  • Neuvonen, P. J. Interactions with the Absorption of Tetracyclines. Drugs 1976, 11, 45–54. DOI: 10.2165/00003495-197611010-00004.
  • Abu-Dief, A. M.; Mohamed, I. M. A. A Review on Versatile Applications of Transition Metal Complexes Incorporating Schiff Bases. Beni Suef Univ. J. Basic Appl. Sci. 2015, 4, 119–133. DOI: 10.1016/j.bjbas.2015.05.004.
  • Abdel-Rhman, M. H.; Motawea, R.; Belal, A.; Hosny, N. M. Spectral, Structural and Cytotoxicity Studies on the Newly Synthesized n’1,n’3-Diisonicotinoylmalonohydrazide and Some of Its Bivalent Metal Complexes. J. Mol. Struct. 2022, 1251, 131960. DOI: 10.1016/j.molstruc.2021.131960.
  • Hosny, N. M.; Hassan, N. Y.; Mahmoud, H. M.; Abdel-Rhman, M. H. Synthesis, Characterization and Cytotoxicity of New 2-isonicotinoyl-N-Phenylhydrazine-1-Carbothioamide and Its Metal Complexes. Appl. Organomet. Chem. 2019, 33, e4998. DOI: 10.1002/aoc.4998.
  • Abdel-Rhman, M. H.; Hussien, M. A.; Mahmoud, H. M.; Hosny, N. M. Synthesis, Characterization, Molecular Docking and Cytotoxicity Studies on N-Benzyl-2-Isonicotinoylhydrazine-1-Carbothioamide and Its Metal Complexes. J. Mol. Struct. 2019, 1196, 417–428. DOI: 10.1016/j.molstruc.2019.06.092.
  • Hosny, N. M.; Hassan, N. Y.; Mahmoud, H. M.; Abdel-Rhman, M. H. Spectral, Optical and Cytotoxicity Studies on 2-isonicotinoyl-N-Phenylhydrazine-1-Carboxamide(H3L) and Some of Its Metal Complexes. J. Mol. Struct. 2018, 1156, 602–611. DOI: 10.1016/j.molstruc.2017.11.114.
  • Hosny, N. M.; Hassan, N. Y.; Mahmoud, H. M.; Abdel-Rhman, M. H. Spectral, Optical, and Cytotoxicity Studies on N-(2-Isonicotinoylhydrazine-Carbonothioyl)Benzamide and Its Metal Complexes. Heteroatom Chem. 2018, 29, e21415. DOI: 10.1002/hc.21415.
  • Aldossary, S. A. Review on Pharmacology of Cisplatin: Clinical Use, Toxicity and Mechanism of Resistance of Cisplatin. Biomed Pharmacol J. 2019, 12. DOI: 10.13005/bpj/1608.
  • Aguiar, I.; Tavares, A.; Roveda, A. C.; Jr.da Silva, A. C.; Marino, L. B.; Lopes, É. O.; Pavan, F. R.; Lopes, L. G.; Franco, D. W. Antitubercular Activity of Ru (II) Isoniazid Complexes. Eur. J. Pharm. Sci. 2015, 70, 45–54. DOI: 10.1016/j.ejps.2015.01.008.
  • Kaur, A.; Pathak, D. P.; Sharma, V.; Wakode, S. Synthesis, Biological Evaluation and Docking Study of a New Series of di-Substituted Benzoxazole Derivatives as Selective COX-2 Inhibitors and anti-Inflammatory Agents. Bioorg. Med. Chem. 2018, 26, 891–902. DOI: 10.1016/j.bmc.2018.01.007.
  • Patil, M. L.; Gaikwad, S. S.; Gaikwad, N. J. Anti-Nociceptive and anti-Inflammatory Activity of Synthesized Novel Benzoxazole Derivatives. Antiinflamm. Antiallergy Agents Med. Chem. 2021, 20, 333–343. DOI: 10.2174/1871523020666210203103433.
  • Tariq, S.; Kamboj, P.; Alam, O.; Amir, M. 1,2,4-Triazole-Based Benzothiazole/Benzoxazole Derivatives: Design, Synthesis, p38α MAP Kinase Inhibition, anti-Inflammatory Activity and Molecular Docking Studies. Bioorg. Chem. 2018, 81, 630–641. DOI: 10.1016/j.bioorg.2018.09.015.
  • Trott, O.; Olson, A. J. AutoDock Vina: improving the Speed and Accuracy of Docking with a New Scoring Function, Efficient Optimization, and Multithreading. J. Comput. Chem. 2010, 31, 455–461. DOI: 10.1002/jcc.21334.
  • Zainab, M. A.; Al-Onazi, W. A.; Asma, A. A.; Al-Mohaimeed, A. M.; Al-Farraj, E. S. Synthesis, DNA Binding, and Molecular Docking Studies of Dimethylaminoben- Zaldehyde Based Bioactive Schiff Bases. J. Chem. 2019, 2019, 1–14. DOI: 10.1155/2019/8152721.
  • Mayuri, B.; Kavitha, P.; Shweta, R.; Prakash, S.; Durgaiah, G.; Narsimha, R. Y.; Laxma, R. K. Novel Schiff Base Metal Complexes: synthesis, Characterization, DNA Binding, DNA Cleavage and Molecular Docking Studies. J. Iran Chem. Soc. 2018, 15, 1377–1389. DOI: 10.1007/s13738-018-1338-7.
  • Vidyavathi, G. T.; Vinay Kumar, B.; Raghu, A. V.; Aravinda, T.; Hani, U.; Ananda Murthy, H. C.; Shridhar, A. H. Punica Granatum Pericarp Extract Catalyzed Green Chemistry Approach for Synthesizing Novel Ligand and Its Metal(II) Complexes: Molecular Docking/DNA Interactions. J. Mol. Struct. 2022, 1249, 131656. DOI: 10.1016/j.molstruc.2021.131656.
  • Vidyavathi, G. T.; Vinay Kumar, B.; Aravinda, T.; Hani, U. Cashew Nutshell Liquid Catalyzed Green Chemistry Approach for Synthesis of a Schiff Base and Its Divalent Metal Complexes: molecular Docking and DNA Reactivity. Nucleosides Nucleotides Nucleic Acids 2021, 40, 264–287. DOI: 10.1080/15257770.2020.1868502.
  • El-Sayed, Y.; Gaber, M.; El-Wakeil, N.; El-Nagar, A. Metal Complexes of Azo Mesalamine Drug: Synthesis, Characterization, and Their Application as an Inhibitor of Pathogenic Fungi. Appl. Organomet. Chem. 2021, 35, e6290.
  • Geary, W. J. The Use of Conductivity Measurements in Organic Solvents for the Characterisation of Coordination Compounds. Coord. Chem. Rev. 1971, 7, 81–122. DOI: 10.1016/S0010-8545(00)80009-0.
  • Kirthan, B. R.; Prabhakara, M. C.; Bhojyanaik, H. S.; Amith Nayak, P. H.; Viswanath, R.; Teja.; H. B.; Ereshanaik. Optoelectronic, Photocatalytic, and DNA Interaction Studies of Synthesized Cu(II), Co(II), and Ni(II) Complexes Containing Schiff Base Ligand. Inorg. Chem. Commun. 2022, 135, 109109. DOI: 10.1016/j.inoche.2021.109109.
  • Gaber, M.; El-Ghamry, H. A.; Fathalla, S. K. Synthesis, Structural Identification, DNA Interaction and Biological Studies of Divalent Mn, Co and Ni Chelates of 3-Amino-5-Mercapto-1,2,4-Triazole Azo Ligand. Appl. Organomet. Chem. 2020, 34, e5678.
  • Vinay Kumar, B.; Ananda Murthy, H. C.; Aravinda, T.; Harish, K. N.; Bhojya Naik, H. S. Advancement in Specific Strand Scission of DNA and Evaluation of in-Vitro Biological Assessment by Pharmacologically Significant Tetraaza Macrocyclic Metal Complexes Constrained by Triazole. Nucleosides Nucleotides Nucleic Acids 2021, 40, 896–913. DOI: 10.1080/15257770.2021.1962536.
  • Hussien, M. A.; Nawar, N.; Radwan, F. M.; Hosny, N. M. Spectral Characterization, Optical Band Gap Calculations and DNA Binding of Some Binuclear Schiff-Base Metal Complexes Derived from 2-Amino-Ethanoic Acid and Acetylacetone. J. Mol. Struct. 2015, 1080, 162–168. DOI: 10.1016/j.molstruc.2014.09.071.
  • Mendu, P.; Kumari, C. G.; Ragi, R. Synthesis, Characterization, DNA Binding, DNA Cleavage and Antimicrobial Studies of Schiff Base Ligand and Its Metal Complexes. J. Fluoresc. 2015, 25, 369–378. DOI: 10.1007/s10895-015-1520-6.
  • Abdel Aziz, A. A.; Seda, S. H. Synthesis, Spectral Characterization, SEM, Antimicrobial, Antioxidative Activity Evaluation, DNA Binding and DNA Cleavage Investigation of Transition Metal(II) Complexes Derived from a Tetradentate Schiff Base Bearing Thiophene Moiety. J. Fluoresc. 2017, 27, 1051–1066. DOI: 10.1007/s10895-017-2039-9.
  • Naik, S.; Naik, P. P.; Krishnamurthy, G.; Venugopal, N.; Naik, N.; Naik, T. R. R. Synthesis, Characterization, DFT Studies and Biological Activity of Ru(III), La(III) and Ce(III) Triphenylphosphine Complexes Containing 2-Aminothiazole and 2-Aminotriazole. J Inorg Organomet Polym 2020, 30, 3332–3356. DOI: 10.1007/s10904-020-01492-y.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.