dc.contributor.author | Behçet, Ayten | |
dc.contributor.author | Çağlılar, Tuba | |
dc.contributor.author | Celepci, DuyguBarut | |
dc.contributor.author | Aktaş, Aydın | |
dc.contributor.author | Taslimi, Parham | |
dc.contributor.author | Gök, Yetkin | |
dc.contributor.author | Aygün, Muhittin | |
dc.contributor.author | Kaya, Ruya | |
dc.contributor.author | Gülçin, İlhami | |
dc.date.accessioned | 2019-05-06T13:22:39Z | |
dc.date.available | 2019-05-06T13:22:39Z | |
dc.date.issued | 2018-10-15 | |
dc.identifier.uri | http://hdl.handle.net/11772/1154 | |
dc.description.abstract | This paper reports the synthesis of 2-(4-hydroxyphenyl)ethyl and 2-(4-nitrophenyl)ethyl substituted benzimidazolium salts. The benzimidazolium salts were synthesized by N-substituted benzimidazolium and aryl halides. The 2-(4-hydroxyphenyl)ethyl and 2-(4-nitrophenyl)ethyl substituted benzimidazolium salts were characterized by using H-1 NMR, C-13 NMR, FT-IR spectroscopy and elemental analysis techniques. Molecular and crystal structure of the complex 2d and 3d were obtained by single-crystal X-ray diffraction method. Additionally, The enzyme inhibition activities of the benzimidazolium salts were investigated. These 2-(4-hydroxyphenyl)ethyl and 2-(4-nitrophenyl)ethyl substituted benzimidazolium salts (1, 2a-g, and 3a-f) showed good inhibitory action against acetylcholinesterase (AChE), and human (h) carbonic anhydrase (CA) isoforms I, and II. Ki values for AChE were in range of 5.97 +/- 0.56 -23.15 +/- 3.98 nM. On the other hand, the hCA I, and II isoenzymes were effectively inhibited by these compounds, with K-i values in the range of 17.33 +/- 4.55-99.23 +/- 44.91 nM for hCA I, and 33.98 +/- 3.43 -113.23 +/- 39.31 nM for hCA II, respectively. (C) 2018 Elsevier B.V. All rights reserved. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | 10.1016/j.molstruc.2018.05.077 | en_US |
dc.rights | info:eu-repo/semantics/restrictedAccess | en_US |
dc.subject | N-heterocyclic carbenes precursors | en_US |
dc.subject | Benzimidazole | en_US |
dc.subject | Single-crystal X-ray diffraction | en_US |
dc.subject | Carbonic anhydrase | en_US |
dc.subject | Acetylcholinesterase | en_US |
dc.subject | Enzyme inhibition | en_US |
dc.title | Synthesis, characterization and crystal structure of 2-(4-hydroxyphenyl)ethyl and 2-(4-nitrophenyl)ethyl Substituted Benzimidazole Bromide Salts: Their inhibitory properties against carbonic anhydrase and acetylcholinesterase | en_US |
dc.type | article | en_US |
dc.relation.journal | Journal of Molecular Structure | en_US |
dc.contributor.department | Bartın Üniversitesi, Fen Fakültesi, Biyoteknoloji Bölümü | en_US |
dc.identifier.volume | 1170 | en_US |
dc.identifier.startpage | 160 | en_US |
dc.identifier.endpage | 169 | en_US |