Araştırma Makalesi
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Yıl 2024, Cilt: 28 Sayı: 5, 1070 - 1085, 25.10.2024

Öz

Kaynakça

  • 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.
  • M. Shakir, N. Shahid, N. Sami, M. Azam, A. U. Khan, "Synthesis, spectroscopic characterization and comparative DNA binding studies of Schiff base complexes derived from L-leucine and glyoxal," (in eng), Spectrochim Acta A Mol Biomol Spectrosc, vol. 82, no. 1, pp. 31-36, 2011.
  • 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.
  • P. Arora, V. Arora, H. Lamba, D. Wadhwa, "Importance of heterocyclic chemistry: A review," International Journal of Pharmaceutical Sciences and Research, vol. 3, no. 9, p. 2947, 2012.
  • T. Kunied, H. Mutsanga, "The chemistry of heterocyclic compounds," Palmer (B), vol. 175, 2002.
  • M. S. Saini, A. Kumar, J. Dwivedi, R. Singh, "A review: biological significances of heterocyclic compounds," International Journal of Pharma Sciences and Research, vol. 4, no. 3, pp. 66-77, 2013.
  • J. Zhang, W. Liu, Q. Xue, "The effect of molecular structure of heterocyclic compounds containing N, O and S on their tribological performance," Wear, vol. 231, no. 1, pp. 65-70, 1999.
  • A. W. Czarnik, "Guest Editorial," Accounts of Chemical Research, vol. 29, no. 3, pp. 112-113, 03/13/1996.
  • B. J. McConkey, V. Sobolev, M. Edelman, "The performance of current methods in ligand-protein docking," Current Science, vol. 83, pp. 845-856, 2002.
  • N. K. Sharma, K. Jha, "Molecular docking: an overview," Journal of Advanced Scientific Research, vol. 1, no. 1, pp. 67-72, 2010.
  • A. Vijesh, A. M. Isloor, S. Telkar, T. Arulmoli, H.-K. Fun, "Molecular docking studies of some new imidazole derivatives for antimicrobial properties," Arabian Journal of Chemistry, vol. 6, no. 2, pp. 197-204, 2013.
  • 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.
  • C. Stoe, "X-area (version 1.18) and X-red32 (version 1.04)," Stoe & Cie, Darmstadt, Germany, 2002.
  • G. M. Sheldrick, "SHELXT–Integrated space-group and crystal-structure determination," Acta Crystallographica Section A: Foundations and Advances, vol. 71, no. 1, pp. 3-8, 2015.
  • G. M. Sheldrick, "Crystal structure refinement with SHELXL," Acta Crystallographica Section C: Structural Chemistry, vol. 71, no. 1, pp. 3-8, 2015.
  • L. J. Farrugia, "WinGX suite for small-molecule single-crystal crystallography," journal of Applied Crystallography, vol. 32, no. 4, pp. 837-838, 1999.
  • A. D. Becke, "Density-functional exchange-energy approximation with correct asymptotic behavior," Physical review A, vol. 38, no. 6, p. 3098, 1988.
  • C. Lee, W. Yang, R. G. Parr, "Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density," Physical review B, vol. 37, no. 2, p. 785, 1988.
  • R. Dennington, T. Keith, J. Millam, "GaussView, Version 4.1. 2," Semichem Inc., Shawnee Mission, KS, 2007.
  • N. M. O'boyle, A. L. Tenderholt, K. M. Langner, "Cclib: a library for package‐independent computational chemistry algorithms," Journal of computational chemistry, vol. 29, no. 5, pp. 839-845, 2008.
  • M. P. Andersson, P. Uvdal, "New scale factors for harmonic vibrational frequencies using the B3LYP density functional method with the triple-ζ basis set 6-311+ G (d, p)," The Journal of Physical Chemistry A, vol. 109, no. 12, pp. 2937-2941, 2005.
  • M. H. Jamróz, "Vibrational energy distribution analysis (VEDA): scopes and limitations," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 114, pp. 220-230, 2013.
  • A. D. Becke, "Density‐functional thermochemistry. I. The effect of the exchange‐only gradient correction," The Journal of chemical physics, vol. 96, no. 3, pp. 2155-2160, 1992.
  • M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, Ö. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski, D. J. Fox, Gaussian 09 (Gaussian, Inc., Wallingford CT, 2009)., vol. 121, pp. 150-166, 2009.
  • M. Danish, A. Bibi, K. Gilani, M. Asam Raza, M. Ashfaq, M. Nadeem Arshad, A. M. Asiri, K. Ayub, "Antiradical, antimicrobial and enzyme inhibition evaluation of sulfonamide derived esters; synthesis, X-Ray analysis and DFT studies," Journal of Molecular Structure, vol. 1175, pp. 379-388, 2019.
  • 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.
  • M. N. Uddin, D. A. Chowdhury, M. M. Rony, M. E. Halim, "Metal complexes of Schiff bases derived from 2-thiophenecarboxaldehyde and mono/diamine as the antibacterial agents," Modern Chemistry, vol. 2, no. 2, pp. 6-14, 2014.
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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

Yıl 2024, Cilt: 28 Sayı: 5, 1070 - 1085, 25.10.2024

Öz

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.

Teşekkür

Dr. Taşkın Basılı

Kaynakça

  • 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.
  • M. Shakir, N. Shahid, N. Sami, M. Azam, A. U. Khan, "Synthesis, spectroscopic characterization and comparative DNA binding studies of Schiff base complexes derived from L-leucine and glyoxal," (in eng), Spectrochim Acta A Mol Biomol Spectrosc, vol. 82, no. 1, pp. 31-36, 2011.
  • 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.
  • P. Arora, V. Arora, H. Lamba, D. Wadhwa, "Importance of heterocyclic chemistry: A review," International Journal of Pharmaceutical Sciences and Research, vol. 3, no. 9, p. 2947, 2012.
  • T. Kunied, H. Mutsanga, "The chemistry of heterocyclic compounds," Palmer (B), vol. 175, 2002.
  • M. S. Saini, A. Kumar, J. Dwivedi, R. Singh, "A review: biological significances of heterocyclic compounds," International Journal of Pharma Sciences and Research, vol. 4, no. 3, pp. 66-77, 2013.
  • J. Zhang, W. Liu, Q. Xue, "The effect of molecular structure of heterocyclic compounds containing N, O and S on their tribological performance," Wear, vol. 231, no. 1, pp. 65-70, 1999.
  • A. W. Czarnik, "Guest Editorial," Accounts of Chemical Research, vol. 29, no. 3, pp. 112-113, 03/13/1996.
  • B. J. McConkey, V. Sobolev, M. Edelman, "The performance of current methods in ligand-protein docking," Current Science, vol. 83, pp. 845-856, 2002.
  • N. K. Sharma, K. Jha, "Molecular docking: an overview," Journal of Advanced Scientific Research, vol. 1, no. 1, pp. 67-72, 2010.
  • A. Vijesh, A. M. Isloor, S. Telkar, T. Arulmoli, H.-K. Fun, "Molecular docking studies of some new imidazole derivatives for antimicrobial properties," Arabian Journal of Chemistry, vol. 6, no. 2, pp. 197-204, 2013.
  • 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.
  • C. Stoe, "X-area (version 1.18) and X-red32 (version 1.04)," Stoe & Cie, Darmstadt, Germany, 2002.
  • G. M. Sheldrick, "SHELXT–Integrated space-group and crystal-structure determination," Acta Crystallographica Section A: Foundations and Advances, vol. 71, no. 1, pp. 3-8, 2015.
  • G. M. Sheldrick, "Crystal structure refinement with SHELXL," Acta Crystallographica Section C: Structural Chemistry, vol. 71, no. 1, pp. 3-8, 2015.
  • L. J. Farrugia, "WinGX suite for small-molecule single-crystal crystallography," journal of Applied Crystallography, vol. 32, no. 4, pp. 837-838, 1999.
  • A. D. Becke, "Density-functional exchange-energy approximation with correct asymptotic behavior," Physical review A, vol. 38, no. 6, p. 3098, 1988.
  • C. Lee, W. Yang, R. G. Parr, "Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density," Physical review B, vol. 37, no. 2, p. 785, 1988.
  • R. Dennington, T. Keith, J. Millam, "GaussView, Version 4.1. 2," Semichem Inc., Shawnee Mission, KS, 2007.
  • N. M. O'boyle, A. L. Tenderholt, K. M. Langner, "Cclib: a library for package‐independent computational chemistry algorithms," Journal of computational chemistry, vol. 29, no. 5, pp. 839-845, 2008.
  • M. P. Andersson, P. Uvdal, "New scale factors for harmonic vibrational frequencies using the B3LYP density functional method with the triple-ζ basis set 6-311+ G (d, p)," The Journal of Physical Chemistry A, vol. 109, no. 12, pp. 2937-2941, 2005.
  • M. H. Jamróz, "Vibrational energy distribution analysis (VEDA): scopes and limitations," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 114, pp. 220-230, 2013.
  • A. D. Becke, "Density‐functional thermochemistry. I. The effect of the exchange‐only gradient correction," The Journal of chemical physics, vol. 96, no. 3, pp. 2155-2160, 1992.
  • M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, Ö. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski, D. J. Fox, Gaussian 09 (Gaussian, Inc., Wallingford CT, 2009)., vol. 121, pp. 150-166, 2009.
  • M. Danish, A. Bibi, K. Gilani, M. Asam Raza, M. Ashfaq, M. Nadeem Arshad, A. M. Asiri, K. Ayub, "Antiradical, antimicrobial and enzyme inhibition evaluation of sulfonamide derived esters; synthesis, X-Ray analysis and DFT studies," Journal of Molecular Structure, vol. 1175, pp. 379-388, 2019.
  • 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.
  • M. N. Uddin, D. A. Chowdhury, M. M. Rony, M. E. Halim, "Metal complexes of Schiff bases derived from 2-thiophenecarboxaldehyde and mono/diamine as the antibacterial agents," Modern Chemistry, vol. 2, no. 2, pp. 6-14, 2014.
  • C. N. R. Rao, "Chemical applications of infrared spectroscopy," in Chemical applications of infrared spectroscopy, 1963, pp. 681-681.
  • S.-J. Koyambo-Konzapa, R. Premkumar, R. V. Berthelot Saïd Duvalier, M. K. Gilbert Yvon, M. Nsangou, A. M. F. Benial, "Electronic, spectroscopic, molecular docking and molecular dynamics studies of neutral and zwitterionic forms of 3, 4-dihydroxy-l-phenylalanine: A novel lung cancer drug," Journal of Molecular Structure, vol. 1260, p. 132844, 07/15/2022.
  • [45] V. K. Rastogi, M. A. Palafox, R. P. Tanwar, L. Mittal, "3,5-Difluorobenzonitrile: ab initio calculations, FTIR and Raman spectra," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 58, no. 9, pp. 1987-2004, 07/01/2002.
  • D. G. Iraiyadian, S. J. Vedhagiri, M. Govindarajan, K. Parimala, "Molecular Dynamic Simulation Studies of 4-(Trifluoromethyl) phenylacetonitrile," Bulgarian Journal of Physics, vol. 48, no. 4, 2021.
  • D. Li Ping, F. H. Zhang, Y. S. Zhu, C. Lu, X. Yu Kuang, J. LvPeng Shao, "Understanding the structural transformation, stability of medium-sized neutral and charged silicon clusters," (in eng), Scientific Reports, vol. 5, p. 15951, Nov 3 2015.
  • T. Hökelek, S. Özkaya, H. Necefoğlu, "Crystal structure and Hirshfeld surface analysis of aqua-bis-(nicotinamide-κN(1))bis-(2,4,6-tri-methyl-benzoato-κ(2)O,O')cadmium(II)," (in eng), Acta Crystallogr E Crystallogr Commun, vol. 74, no. Pt 2, pp. 246-251, Feb 1 2018.
  • R. Thomsen, M. H. Christensen, "MolDock:  A New Technique for High-Accuracy Molecular Docking," Journal of Medicinal Chemistry, vol. 49, no. 11, pp. 3315-3321, 06/01/2006.
  • D. S. Goodsell, A. J. Olson, "Automated docking of substrates to proteins by simulated annealing," (in eng), Proteins, vol. 8, no. 3, pp. 195-202, 1990.
Toplam 50 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Fiziksel Kimya (Diğer), İnorganik Kimya (Diğer), Organik Kimya (Diğer)
Bölüm Araştırma Makalesi
Yazarlar

Seyhan Öztürk 0000-0003-4638-5578

Erken Görünüm Tarihi 18 Ekim 2024
Yayımlanma Tarihi 25 Ekim 2024
Gönderilme Tarihi 14 Ağustos 2024
Kabul Tarihi 1 Ekim 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 28 Sayı: 5

Kaynak Göster

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. Ekim 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, sy. 5 (Ekim 2024): 1070-85.
EndNote Öztürk S (01 Ekim 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, c. 28, sy. 5, ss. 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 (Ekim 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, c. 28, sy. 5, 2024, ss. 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.

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