Synthesis, Characterization, Biological Activity, and Molecular Docking Study of Some New Sulfamethoxazole Derivatives.

Authors

  • Athra G. Sager Department of Chemistry, College of Science, University of Waist, Waist, Iraq. https://orcid.org/0000-0002-7792-5365
  • Jawad Kadhim Abaies Department of Chemistry, College of Science, University of Waist, Waist, Iraq.
  • Rusul Abdulridah Issa Department of Biology, College of Science, University of Waist, Waist, Iraq.

DOI:

https://doi.org/10.21123/bsj.2024.9047

Keywords:

Bacteria, Insilico, Mannich bases, Molecular docking, Sulfamethoxazole.

Abstract

In this paper, new Sulfamethoxazole derivatives were studied in order to improve the treatment efficiency of this medicinal compound. Six compounds of Schiff bases were prepared via an intermediate reaction of Mannich bases. Two derivatives of thiadiazine heterocyclic compound were prepared as well. Characterization and the stereo conformations of the synthesized compounds were determined using 1H-NMR, 13C-NMR, and FT-IR techniques, in addition to elemental analysis and melting point measurements. The biological activity of the produced compounds against five types of bacteria including (Staphylococcus aureus Escherichia coli, Klebsiella pneumonia Salmonella, and Proteus) was investigated. The obtained results showed that biological activities against bacteria vary from high activity to not active. Moreover, (PyRx) software was utilized for the calculation of the binding affinity (kcal/mol) for the prepared compounds with proteins FYV (S. aureus), 4H2M (E. coli), 6P4T (Salmonella). The highest linking values with proteins were found to be (-9.4) with 4H2M   and (-7.8) with 6P4T, whereas the lowest values were found (-5.3) with FYV. On the other hand, the results revealed that amino acids located around the prepared compound, which were linked through hydrogen bonding or charged and (aryne-aryne) hydrophobic interactions were also determined.  In addition, the three dimensions’ shape, which explains the linkage way between proteins and the synthesized compounds, was stated.  By recognizing the characteristic features of amino acids, which surround these compounds, the electronic densities of the compounds were also reported.

References

Escala N, Pineda LM, Ng M G, Coronado LM, Spadafora C, Olmo E D. Antiplasmodial activity, structure–activity relationship and studies on the action of novel benzimidazole derivatives. Sci Rep. 2023; 2023 Jan 6;13(1):285-298. https://doi.org/10.1038/s41598-022-27351-z.

Alsahib S A. Characterization and Biological Activity of Some New Derivatives Derived from Sulfamethoxazole Compound., Baghdad Sci J. 2020; 17(2): 471-480. https://dx.doi.org/10.21123/bsj.2020.17.2.047.

Lee Y T, Tan Y J, On C E. Benzimidazole and its derivatives as cancer therapeutics: The potential role from traditional to precision medicine. Acta Pharm Sin B. 2023; 13(2): 478-497. https://doi.org/10.1016/j.apsb.2022.09.010.

Al-Mudhafar M M J, Omeer T N-A, Abdul Hadi S L. Bis-Schiff Bases of Isatin Derivatives Synthesis, and their Biological Activities: A Review, Al Must J Pharm Sci. 2022; 22(1): 23-48. https://doi.org/10.32947/ajps.v22i1.827.

Li Q, Guan X, Wu P, Wang X, Zhou L, Tong Y, Ren R, at el. Early transmission dynamics in Wuhan, China, of novel coronavirus-infected pneumonia. N Engl. J Med. 2020; 382(13); 1199-1207. https://doi.org/10.1056/NEJMoa2001316.

Olyaei A, Sadeghpour M, Khalaj M. Mannich bases derived from lawsone and their metal complexes: synthetic strategies and biological properties, RSC Adv. 2020; 10: 30265-30281. https://doi.org/10.1039/D0RA05717G.

Deepak M N, Shelke U S. Synthesis of N-Mannich bases from 3, 4-dihydropyridine-2 (1H)-ones by using nanostructured Cobalt Chloride Doped Polyaniline Composite as Catalyst (PANI-Co). J Phys.: Conf Ser. IOP Publishing. 2020; 1644: 012018. https://doi.org/10.1088/1742-6596/1644/1/012018.

Hayun H, Gavrila I, Silviana S, Siahaan A E K, Vonnan R F, Latifah M I. Synthesis and antioxidant activity study of new Mannich bases derived from vanillic. Rasayan J Chem. 2020; 13(1): 131-138. https://dx.doi.org/10.31788/RJC.2020.1315300.

Raoof S S, Sadiq A S. Mannich Bases: Synthesis, Pharmacological Activity, and Applications: A Review. Iraq J. Sci. 2022: 63( 12): 5086-5105. https://dx.doi.org/10.24996/ijs.2022.63.12.1.

Mizushima Y, Kobayashi M. Interaction of anti-inflammatory drugs with serum proteins, especially with some biologically active proteins. J Pharm Pharmacol. 1968; 20: 169–173. https://dx.doi.org/10.1111/j.2042-7158.1968.tb09718.x.

Ahmed F S, Mohammed K M. Hameed A S. Three-component one-pot synthesis of some Mannich base from morpholine and primary amines. Kirkuk Uni. J Sci Stud. 2017; 12(1): 186-201. http://dx.doi.org/10.32894/kujss.2017.124970.

Abdelgawad M A, Bukhari S NA, Musa A, Elmowafy M, Elkomy M H, Nayl A A, et. al. New Sulfamethoxazole Derivatives as Selective Carbonic Anhydrase IX and XII Inhibitors: Design, Synthesis, Cytotoxic Activity and Molecular Modeling. Pharmaceuticals. 2022; 15(9):1134. https://doi.org/10.3390/ph15091134.

Xu S, Uddin M J, Banerjee S, Duggan K, Musee J, Kiefer J R. et al. Fluorescent indomethacin dansyl conjugates utilize the membrane-binding domain of cyclooxygenase-2 to block the opening to the active site. J Biol Chem. 2019; 294(22): 8690–8698. https://doi.org/10.1074/jbc.RA119.007405.

Elshihawy M M S, Abdel Aziz Y M , Elgawish MS, Elewa M, Elshihawy HA, Said MM. Pharmacophore modeling, 3D-QSAR, synthesis, and anti-lung cancer evaluation of novel thieno [2,3-d][1,2,3] triazines targeting EGFR. Arch Pharm. 2020; 353: 1900108. https://doi.org/10.1002/ardp.201900108.

Alkhaldi A A M, Al-Sanea M M, Nocentini A, Bonardi A, Lasheen D S, Elrazaz E Z, et al. 3-Methylthiazolo[3,2-a]benzimidazole-benzene sulfonamide conjugates as novel carbonic anhydrase inhibitors endowed with anticancer activity: design, synthesis, biological and molecular modeling studies. Eur J Med Chem. 2020; 207: 112745. https://doi.org/10.1016/j.ejmech.2020.112745.

Eldeeb A H, Abo-Ashour MF, Angeli A, Bonardi A, Lasheen D S, Elrazaz EZ, et al. Novel benzene sulfonamides aryl and aryl sulfone conjugates adopting tail/dual tail approaches: synthesis, carbonic anhydrase inhibitory activity and molecular modeling studies. Eur J Med Chem. 2021; 221: 113486. https://doi.org/10.1016/j.ejmech.2021.113486.

Yamali C, Sakagami H, Uesawa Y, Kurosaki K, Satoh K , Masuda Y, et al. Comprehensive study on potent and selective carbonic anhydrase inhibitors: Synthesis, bioactivities and molecular modelling studies of 4-(3-(2-arylidenehydrazine-1-carbonyl)-5-(thiophen-2-yl)-1H-pyrazole-1-yl)benzenes sulfonamides. Eur J Med Chem 217. 2021: 113351. https://doi.org/10.1016/j.ejmech.2021.113351.

Sager G S, Salah A S, Mekky A H. Microwave Synthesis, Characterization of Some Novel Curcumin Compound and its Metal Complexes with Antimicrobial, Antioxidant Studies. Int J Med Pharm Res. 2020; 12(1): 429-448. https://doi.org/10.31838/ijpr/2020.12.01.200.

Kamoon R A, Al-Mudhafar M M J, Omar T N-A. Synthesis, Characterization and Antimicrobial Evaluation New Azo Compounds Derived from Sulfonamides and Isatin Schiff Base, Int. J Drug Deliv. Technol. 2020; 10(1): 150-155.

Akili S, Hadda D B, Bitar Y, Balash A, Chehna MF. Design, Synthesis and Characterization of Novel Sulfonamides Derivatives as Anticancer Agent Targeting EGFR TK, and Development of New Methods of Synthesis by Microwave Irradiation. Int J Org Chem. 2021; 11(4): 119-123. https://doi.org/10.4236/ijoc.2021.114014.

Sangande F, Julianti E, Tjahjono D H. Ligand-Based Pharmacophore Modeling, Molecular Docking, and Molecular Dynamic Studies of Dual Tyrosine Kinase Inhibitor of EGFR. Int J Cell Sci Mol Biol. 2020; 21(20): 7779. https://doi.org/10.3390/ijms21207779.

Ibraheem I H, Mubder N S, Abdullah M A, Al-Neshmi H. Synthesis, characterization and bioactivity Study from azo –ligand derived frommethyl-2-amino benzoate with some metal ions. Baghdad Sci J. 2023; 20(1): 114-120. https://dx.doi.org/10.21123/bsj.2022.6584.

Rasheed A M, Al-Bayati S M M, Al-Hasani R A M, Shaker M A. Synthesizing Structure and Characterizing Bioactivities of Cr (III), La(III) and Ce(III)Complexes with Nitrogen ,Oxygen and Sulphur donor bidentate Schiff base ligands. Baghdad Sci. J. 2021;b18(4): 1547. https://doi.org/10.21123/bsj.2021.18.4(Suppl.).1545.

Abdul Kareem H M, Al-Tameemi M, Ibraheem I H, Sameer M. Surfactant Cloud Point Extraction as a Procedure of Preconcentrating for Metoclopramide Determination Using Spectro Analytical Technique. Baghdad Sci J . 2020; 17(1): 57-65. https://dx.doi.org/10.21123/bsj.2020.17.1.0057.

Brito T O, Abreu L O, Gomes K M, Lourenço M C S, Pereira P M L, Yamada-Ogatta S F, at.el. Benzoyl thioureas: design, synthesis and antimyco bacterial evaluation, Med. Chem,2020; 16:93-103, https://doi.org/10.2174/1573406415666181208110753.

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Synthesis, Characterization, Biological Activity, and Molecular Docking Study of Some New Sulfamethoxazole Derivatives. Baghdad Sci.J [Internet]. [cited 2024 May 3];21(11). Available from: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/9047