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Synthesis and molecular docking studies of some 4-phthalimidobenzenesulfonamide derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors

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  • معلومة اضافية
    • Contributors:
      Ege Üniversitesi
    • بيانات النشر:
      Taylor & Francis Ltd
    • الموضوع:
      2017
    • Collection:
      Ege University Institutional Repository
    • نبذة مختصرة :
      WOS: 000392591100005 ; PubMed ID: 27766908 ; A series of 4-phthalimidobenzenesulfonamide derivatives were designed, synthesized and evaluated for the inhibitory activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). Structures of the title compounds were confirmed by spectral and elemental analyses. The cholinesterase (ChE) inhibitory activity studies were carried out using Ellman's colorimetric method. The biological activity results revealed that all of the title compounds (except for compound 8) displayed high selectivity against AChE. Among the tested compounds, compound 7 was found to be the most potent against AChE (IC50 = 1.35 +/- 0.08 mu M), while compound 3 exhibited the highest inhibition against BuChE (IC50 = 13.41 +/- 0.62 mu M). Molecular docking studies of the most active compound 7 in AChE showed that this compound can interact with both the catalytic active site (CAS) and the peripheral anionic site (PAS) of AChE. ; Ege UniversityEge University [12/Ecz/016] ; This study was supported by research grants from Ege University (Project Number: 12/Ecz/016).
    • ISSN:
      1475-6366
      1475-6374
    • Relation:
      Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Journal of Enzyme Inhibition and Medicinal Chemistry; https://doi.org/10.1080/14756366.2016.1226298; https://hdl.handle.net/11454/33093; 32; 13; 19
    • الرقم المعرف:
      10.1080/14756366.2016.1226298
    • الدخول الالكتروني :
      https://hdl.handle.net/11454/33093
      https://doi.org/10.1080/14756366.2016.1226298
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.E4ECD4CF