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Phthalimide-tethered imidazolium salts: Synthesis, characterization,

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dc.contributor.author Yigit, M
dc.contributor.author Demir, Y
dc.contributor.author Celepci, DB
dc.contributor.author Taskin-Tok, T
dc.contributor.author Arinc, A
dc.contributor.author Yigit, B
dc.contributor.author Aygun, M
dc.contributor.author Ozdemir, I
dc.contributor.author Gulcin, I
dc.date.accessioned 2022-10-05T13:18:06Z
dc.date.available 2022-10-05T13:18:06Z
dc.identifier.uri http://hdl.handle.net/11616/62624
dc.description.abstract A series of new imidazolium salts were prepared in good yield by the reaction between 1-alkylimidazole and a variety of alkyl halides. The structures of the compounds were identified by FT-IR, H-1 NMR, and C-13 NMR spectroscopy, elemental analysis, and mass spectrometry. The crystal structure of 1b was determined by the single-crystal X-ray diffraction method. The phthalimide-tethered imidazolium salts exhibited inhibition abilities toward acetylcholinesterase (AChE) and human carbonic anhydrases (hCAs) I and II, with K-i values in the range of 24.63 +/- 3.45 to 305.51 +/- 35.98 nM for AChE, 33.56 +/- 3.71 to 218.01 +/- 25.21 nM for hCA I and 17.75 +/- 0.96 to 308.67 +/- 13.73 nM for hCA II. The results showed that the new imidazolium salts can play a key role in the treatment of Alzheimer's disease, epilepsy, glaucoma, and leukemia, which is related to their inhibition abilities of hCA I, hCA II, and AChE. Molecular docking and in silico absorption, distribution, metabolism, excretion and toxicity studies were used to look into how the imidazolium salts interacted with the specific protein targets. To better visualize and understand the binding positions and the influence of the imidazolium salts on hCA I, hCA II, and AChE conformations, each one was subjected to molecular docking simulations.
dc.description.abstract C1 [Yigit, Murat] Adiyaman Univ, Vocat Sch Tech Sci, Dept Chem & Chem Proc Technol, TR-02040 Adiyaman, Turkey.
dc.description.abstract [Demir, Yeliz] Ardahan Univ, Nihat Delibalta Gole Vocat High Sch, Dept Pharm Serv, Ardahan, Turkey.
dc.description.abstract [Celepci, Duygu Barut; Aygun, Muhittin] Dokuz Eylul Univ, Fac Sci, Dept Phys, Izmir, Turkey.
dc.description.abstract [Taskin-Tok, Tugba] Gaziantep Univ, Fac Arts & Sci, Dept Chem, Gaziantep, Turkey.
dc.description.abstract [Taskin-Tok, Tugba] Gaziantep Univ, Inst Hlth Sci, Dept Bioinformat & Computat Biol, Gaziantep, Turkey.
dc.description.abstract [Arinc, Ali; Yigit, Beyhan] Adiyaman Univ, Fac Sci & Art, Dept Chem, Adiyaman, Turkey.
dc.description.abstract [Ozdemir, Ismail] Inonu Univ, Fac Sci & Art, Dept Chem, Malatya, Turkey.
dc.description.abstract [Gulcin, Ilhami] Ataturk Univ, Fac Sci, Dept Chem, Erzurum, Turkey.
dc.source ARCHIV DER PHARMAZIE
dc.title Phthalimide-tethered imidazolium salts: Synthesis, characterization,
dc.title enzyme inhibitory properties, and in silico studies


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