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Year 2024, Volume: 28 Issue: 5, 1070 - 1085, 25.10.2024

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References

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  • R. Kataria, D. Vashisht, P. Rani, J. Sindhu, S. Kumar, S. Sharma, S. C. Sahoo, V. Kumar, S. Kumar Mehta, "Experimental and Computational Validation of Structural Features and BSA Binding Tendency of 5-Hydroxy5trifluoromethyl3arylpyrazolines," Chemistry Select, vol. 6, no. 38, pp. 10324-10335, 2021.
  • N. Dege, M. A. Raza, O. E. Doğan, T. Ağar, M. W. Mumtaz, "Theoretical and experimental approaches of new Schiff bases: efficient synthesis, X-ray structures, DFT, molecular modeling and ADMET studies," Journal of the Iranian Chemical Society, vol. 18, no. 9, pp. 2345-2368, 09/01/ 2021.
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  • S. Zolezzi, E. Spodine, A. Decinti, "Electrochemical studies of copper(II) complexes with Schiff-base ligands," Polyhedron, vol. 21, no. 1, pp. 55-59, 01/15/ 2002.
  • P. G. Cozzi, "Metal–Salen Schiff base complexes in catalysis: practical aspects," Chemical Society Reviews, vol. 33, no. 7, pp. 410-421, 2004.
  • H. Zafar, A. Ahmad, A. U. Khan, T. A. Khan, "Synthesis, characterization and antimicrobial studies of Schiff base complexes," Journal of Molecular Structure, vol. 1097, pp. 129-135, 10/05/ 2015.
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  • Raza, M. A., Farwa, U., Danish, M., Ozturk, S., Aagar, A. A., Dege, N., Rehman, S. U., Al-Sehemi, A. G., "Computational modeling of imines based anti-oxidant and anti-esterases compounds: Synthesis, single crystal and In-vitro assessment," Computational Biology and Chemistry, vol. 104, p. 107880, 06/01/ 2023.
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  • M. A. Raza, K. Fatima, Z. Saqib, J. K. Maurin, A. Budzianowski, "Designing of diamino based esterases inhibitors; synthesis, characterization, density functional theory and molecular modeling," Journal of Molecular Structure, vol. 1195, pp. 712-722, 2019.
  • Z. H. Chohan, M. Hanif, "Design, synthesis, and biological properties of triazole derived compounds and their transition metal complexes," Journal of Enzyme Inhibition and Medicinal Chemistry, vol. 25, no. 5, pp. 737-749, 10/01/2010.
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  • A. U. Hassan, S. H. Sumrra, M. A. Raza, M. Zubair, M. N. Zafar, E. U. Mughal, M. F. Nazar, A. Irfan, M. Imran, M.A. Assiri, "Design, facile synthesis, spectroscopic characterization, and medicinal probing of metal-based new sulfonamide drugs: A theoretical and spectral study," Applied Organometallic Chemistry, vol. 35, no. 1, p. e6054, 2021.
  • R. Ilmi, S. Kansız, N. K. Al-Rasbi, N. Dege, P. R. Raithby, M. S. Khan, "Towards white light emission from a hybrid thin film of a self-assembled ternary samarium (III) complex," New Journal of Chemistry, vol. 44, no. 15, pp. 5673-5683, 2020.
  • A. Bashir, I. Siraj, "Synthesis, Characterization and Antimicrobial Studies of Schiff Base Derived from the Reaction of 2-Thiophenecarboxaldehyde and Ethylenediamine and its Metal (II) Complexes," ChemSearch Journal, vol. 12, no. 1, pp. 143-148, 2021.
  • E. Ermiş, K. Durmuş, "Novel thiophene-benzothiazole derivative azomethine and amine compounds: Microwave assisted synthesis, spectroscopic characterization, solvent effects on UV–Vis absorption and DFT studies," Journal of Molecular Structure, vol. 1217, p. 128354, 2020.
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Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine

Year 2024, Volume: 28 Issue: 5, 1070 - 1085, 25.10.2024

Abstract

The current research was conducted to assess the in silico and in vitro potential of the heterocyclic Schiff base compound (E)-1-(5-nitrothiophen-2-yl)-N-(2-(trifluoromethyl)phenyl)methanimine(N2TPM). This Schiff base was synthesized according to the reported method using ethanol as solvent, and the reaction was monitored on TLC till completion of the reaction. The compound structure was elucidated using spectroscopic techniques such as UV/Vis, FT-IR, 1H-NMR, and 13C-NMR. Molecular structure was determined using a single XRD, which revealed that the compound was triclinic. Analysis of intermolecular interactions in crystalline compounds was performed using Hirshfeld surface analysis and 2D fingerprint plots. The structure of the compound was optimized using the B3LYP hybrid functional with the basis set 6-31G(d,p). The compound’s theoretical and experimental parameters (bond length, bond angle, molecular orbital energies, electronic transitions, and vibration frequencies) were compared with each other which are in close agreement. R² values were found to be 0.9914 for bond lengths and 0.9859 for bond angles. In vitro, esterase potential of the synthesized compound was checked using a spectrophotometric model, while in silico molecular docking studies were performed with Auto-dock against two enzymes of the esterase family. The docking studies and in vitro assessment predicted that such molecules could be used as enzyme inhibitors against tested enzymes; acetylcholine esterase (AChE) and butyrylcholine esterase (BChE). the compound showed a binding score of -10.4159, a binding energy of -10.2743 with AChE, a binding score of -10.3378 and a binding energy of -9.8889 with BChE.

Thanks

Dr. Taşkın Basılı

References

  • M. A. Raza, N. Dege, O. E. Dogan, T. Agar, S. H. Sumrra, "Synthesis of two new Schiff bases; crystal structure, Hirshfeld surface analysis, density functional theory and molecular docking," Journal of Molecular Structure, vol. 1226, p. 129330, 02/15/ 2021.
  • R. Kataria, D. Vashisht, P. Rani, J. Sindhu, S. Kumar, S. Sharma, S. C. Sahoo, V. Kumar, S. Kumar Mehta, "Experimental and Computational Validation of Structural Features and BSA Binding Tendency of 5-Hydroxy5trifluoromethyl3arylpyrazolines," Chemistry Select, vol. 6, no. 38, pp. 10324-10335, 2021.
  • N. Dege, M. A. Raza, O. E. Doğan, T. Ağar, M. W. Mumtaz, "Theoretical and experimental approaches of new Schiff bases: efficient synthesis, X-ray structures, DFT, molecular modeling and ADMET studies," Journal of the Iranian Chemical Society, vol. 18, no. 9, pp. 2345-2368, 09/01/ 2021.
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  • S. Zolezzi, E. Spodine, A. Decinti, "Electrochemical studies of copper(II) complexes with Schiff-base ligands," Polyhedron, vol. 21, no. 1, pp. 55-59, 01/15/ 2002.
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  • Raza, M. A., Farwa, U., Danish, M., Ozturk, S., Aagar, A. A., Dege, N., Rehman, S. U., Al-Sehemi, A. G., "Computational modeling of imines based anti-oxidant and anti-esterases compounds: Synthesis, single crystal and In-vitro assessment," Computational Biology and Chemistry, vol. 104, p. 107880, 06/01/ 2023.
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  • S. Wolff, D. Grimwood, J. McKinnon, M. Turner, D. Jayatilaka, M. Spackman, "Crystal explorer," ed: University of Western Australia Perth, 2012.
  • K. Azouzi, B. Hamdi, R. Zouari, A. b. Salah, "Synthesis, structure and Hirshfeld surface analysis, vibrational and DFT investigation of (4-pyridine carboxylic acid) tetrachlorocuprate (II) monohydrate," Bulletin of Materials Science, vol. 40, pp. 289-299, 2017.
  • M. A. Raza, K. Fatima, Z. Saqib, J. K. Maurin, A. Budzianowski, "Designing of diamino based esterases inhibitors; synthesis, characterization, density functional theory and molecular modeling," Journal of Molecular Structure, vol. 1195, pp. 712-722, 2019.
  • Z. H. Chohan, M. Hanif, "Design, synthesis, and biological properties of triazole derived compounds and their transition metal complexes," Journal of Enzyme Inhibition and Medicinal Chemistry, vol. 25, no. 5, pp. 737-749, 10/01/2010.
  • É. Tozzo, S. Romera, M. P. dos Santos, M. Muraro, R. H. de A. Santos, L.M. Lião, L. Vizotto, E. R. Dockal, "Synthesis, spectral studies and X-ray crystal structure of N,N′-(±)-trans-1,2-cyclohexylenebis(3-ethoxysalicylideneamine) H2(t-3-EtOsalchxn)," Journal of Molecular Structure, vol. 876, no. 1, pp. 110-120, 03/30/2008.
  • A. Bartyzel, "Synthesis, thermal study and some properties of N2O4—donor Schiff base and its Mn(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes," Journal of Thermal Analysis and Calorimetry, vol. 127, pp. 2133-2147, 2017.
  • A. U. Hassan, S. H. Sumrra, M. A. Raza, M. Zubair, M. N. Zafar, E. U. Mughal, M. F. Nazar, A. Irfan, M. Imran, M.A. Assiri, "Design, facile synthesis, spectroscopic characterization, and medicinal probing of metal-based new sulfonamide drugs: A theoretical and spectral study," Applied Organometallic Chemistry, vol. 35, no. 1, p. e6054, 2021.
  • R. Ilmi, S. Kansız, N. K. Al-Rasbi, N. Dege, P. R. Raithby, M. S. Khan, "Towards white light emission from a hybrid thin film of a self-assembled ternary samarium (III) complex," New Journal of Chemistry, vol. 44, no. 15, pp. 5673-5683, 2020.
  • A. Bashir, I. Siraj, "Synthesis, Characterization and Antimicrobial Studies of Schiff Base Derived from the Reaction of 2-Thiophenecarboxaldehyde and Ethylenediamine and its Metal (II) Complexes," ChemSearch Journal, vol. 12, no. 1, pp. 143-148, 2021.
  • E. Ermiş, K. Durmuş, "Novel thiophene-benzothiazole derivative azomethine and amine compounds: Microwave assisted synthesis, spectroscopic characterization, solvent effects on UV–Vis absorption and DFT studies," Journal of Molecular Structure, vol. 1217, p. 128354, 2020.
  • M. I. Jaafar, R. K. Ahmed, A.J. M. Al-Karawi, Al. Bariz OmarAli, S.Kansız, Y. Sert, N. Dege, "Synthesis, structural studies, Hirshfeld surface analysis, and molecular docking studies of a thiophene-based Schiff base compound," Journal of Molecular Structure, vol. 1265, p. 133477, 2022.
  • M. Shakir, A. Abbasi, M. Azam, A. U. Khan, "Synthesis, spectroscopic studies and crystal structure of the Schiff base ligand L derived from condensation of 2-thiophenecarboxaldehyde and 3, 3′-diaminobenzidine and its complexes with Co (II), Ni (II), Cu (II), Cd (II) and Hg (II): Comparative DNA binding studies of L and its Co (II), Ni (II) and Cu (II) complexes," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 79, no. 5, pp. 1866-1875, 2011.
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There are 50 citations in total.

Details

Primary Language English
Subjects Physical Chemistry (Other), Inorganic Chemistry (Other), Organic Chemistry (Other)
Journal Section Research Articles
Authors

Seyhan Öztürk 0000-0003-4638-5578

Early Pub Date October 18, 2024
Publication Date October 25, 2024
Submission Date August 14, 2024
Acceptance Date October 1, 2024
Published in Issue Year 2024 Volume: 28 Issue: 5

Cite

APA Öztürk, S. (2024). Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine. Sakarya University Journal of Science, 28(5), 1070-1085.
AMA Öztürk S. Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine. SAUJS. October 2024;28(5):1070-1085.
Chicago Öztürk, Seyhan. “Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-Yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine”. Sakarya University Journal of Science 28, no. 5 (October 2024): 1070-85.
EndNote Öztürk S (October 1, 2024) Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine. Sakarya University Journal of Science 28 5 1070–1085.
IEEE S. Öztürk, “Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine”, SAUJS, vol. 28, no. 5, pp. 1070–1085, 2024.
ISNAD Öztürk, Seyhan. “Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-Yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine”. Sakarya University Journal of Science 28/5 (October 2024), 1070-1085.
JAMA Öztürk S. Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine. SAUJS. 2024;28:1070–1085.
MLA Öztürk, Seyhan. “Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-Yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine”. Sakarya University Journal of Science, vol. 28, no. 5, 2024, pp. 1070-85.
Vancouver Öztürk S. Experimental and Theoretical Characterization, In Silico and In Vitro Studies of (E)-1-(5-Nitrothiophen-2-yl)-N-(2-(Trifluoromethyl)Phenyl)Methanimine. SAUJS. 2024;28(5):1070-85.