New Schiff Base Derived Organotin (IV) Complexes: Synthesis, Characterization, In vitro and In silico Biological Studies

  • Авторы: Kumar M.1,2, Siwach P.2, Sharma H.1, Tuli H.3, Varol M.4, Rani A.5, Aggarwal P.6
  • Учреждения:
    1. Department of Chemistry, Maharishi Markandeshwar Engineering College, Maharishi Markandeshwar (Deemed to be) University, Mullana, Ambala, 133207, India
    2. Department of Chemistry, Maharishi Markandeshwar University, Sadopur, 134007, India
    3. Department of Biotechnology, Maharishi Markandeshwar Engineering College, Maharishi Markandeshwar (Deemed to be) University, Mullana, Ambala, 133207, India
    4. Department of Molecular Biology and Genetics, Faculty of Science, Kotekli Campus, Mugla Sitki Kocman University, Mugla TR-48000, Turkey
    5. Department of Chemistry, IEC University, Baddi, Himachal Pardesh, 174103, India
    6. Department of Chemistry, Govt. College Karnal, Haryana, 132001, India
  • Выпуск: Том 22, № 5 (2024)
  • Раздел: Medicine
  • URL: https://ter-arkhiv.ru/2211-3525/article/view/642332
  • DOI: https://doi.org/10.2174/0122113525305623240409075331
  • ID: 642332

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Аннотация

Aims:The creation and testing of new Schiff base-based antibacterial organotin (IV) complexes were the objectives of this investigation.

Background:Due to developed resistance, antibiotics that were once often used to treat microor-ganisms are no longer effective against them. It is thought that organotin compounds synthesized from Schiff bases have significant pharmacological effectiveness and work well as antibacterial agents.

Methods:Thiocarbohydrazide and dehydroacetic acid were condensed to create the Schiff base, followed by processing with dialkyltin(IV)dichloride to synthesize the final product. Modern an-alytical techniques were used to clarify the compounds' probable structural details. The crystalline nature of the produced compounds was tested using PXRD.

Results:All of the compounds were thermally stable up to 300°C. All of the synthesized com-plexes showed potent antibacterial activity in the range of 250 to 400 µg/ml. Furthermore, the computational biology research showed that, in contrast to ligands, which had a binding energy of -7.3 to -7.4 kcal/mol, complexes interacted well with dihydropteroate synthase and DNA gy-rase.

Conclusion:The current study offered a unique technique for synthesizing diorganotin(IV) de-rivatives of N-substituted Schiff bases that are physiologically active. The results show that the chemicals created are promising antibacterial mediators against diseases that affect humans in the modern world. It might also open the door to future studies on drug-resistant microorganisms that could have biological uses.

Об авторах

Manoj Kumar

Department of Chemistry, Maharishi Markandeshwar Engineering College, Maharishi Markandeshwar (Deemed to be)
University, Mullana, Ambala, 133207, India; Department of Chemistry, Maharishi Markandeshwar University,
Sadopur, 134007, India

Автор, ответственный за переписку.
Email: info@benthamscience.net

Priyanka Siwach

Department of Chemistry, Maharishi Markandeshwar University,
Sadopur, 134007, India

Email: info@benthamscience.net

Harish Sharma

Department of Chemistry, Maharishi Markandeshwar Engineering College, Maharishi Markandeshwar (Deemed to be)
University, Mullana, Ambala, 133207, India

Email: info@benthamscience.net

Hardeep Tuli

Department of Biotechnology, Maharishi Markandeshwar Engineering College, Maharishi
Markandeshwar (Deemed to be) University, Mullana, Ambala, 133207, India

Email: info@benthamscience.net

Mehmet Varol

Department of Molecular Biology and
Genetics, Faculty of Science, Kotekli Campus, Mugla Sitki Kocman University, Mugla TR-48000, Turkey

Email: info@benthamscience.net

Anita Rani

Department of
Chemistry, IEC University, Baddi, Himachal Pardesh, 174103, India

Email: info@benthamscience.net

Pallvi Aggarwal

Department of Chemistry, Govt. College Karnal,
Haryana, 132001, India

Email: info@benthamscience.net

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