Discovery of potent carbonic anhydrase, acetylcholinesterase, and butyrylcholinesterase enzymes inhibitors: The new amides and thiazolidine-4-ones synthesized on an acetophenone base

dc.contributor.authorParham, Taslimi
dc.contributor.authorSabiya, Osmanova
dc.contributor.authorGülçin, İlhami
dc.contributor.authorSabira, Sardarova
dc.contributor.authorVagif, Farzaliyev
dc.contributor.authorAfsun, Sujayev
dc.contributor.authorRuya, Kaya
dc.contributor.authorFatma, Koc
dc.contributor.authorSukru, Beydemir
dc.contributor.authorSaleh H., Alwasel
dc.contributor.authorOmer Irfan, Kufrevioglu
dc.date.accessioned2019-05-17T08:13:25Z
dc.date.available2019-05-17T08:13:25Z
dc.date.created2017
dc.date.issued2017
dc.date.issuedyyyymmdd2017-09
dc.departmentFakülteler, Fen Fakültesi, Biyoteknoloji Bölümü
dc.description.abstractCompounds containing nitrogen and sulfur atoms can be widely used in various fields, including industry, medicine, biotechnology, and chemical technology. Among them, amides of acids and heterocyclic compounds have an important place. These amides and thiazolidine-4-ones showed good inhibitory action against butyrylcholinesterase (BChE), acetylcholinesterase (AChE), and human carbonic anhydrase isoforms. AChE exists at high concentrations in the brain and red blood cells. BChE is an important enzyme that is plentiful in the liver, and it is released into the blood in a soluble form. They were demonstrated to have effective inhibition profiles with K-i values of 23.76-102.75nM against hCA I, 58.92-136.64nM against hCA II, 1.40-12.86nM against AChE, and 9.82-52.77nM against BChE. On the other hand, acetazolamide showed K-i value of 482.63 +/- 56.20nM against hCA I, and 1019.60 +/- 163.70nM against hCA II. Additionally, Tacrine inhibited AChE and BChE, showing K-i values of 397.03 +/- 31.66 and 210.21 +/- 15.98nM, respectively.
dc.identifier.doi10.1002/jbt.21931
dc.identifier.issue9
dc.identifier.startpagee21931
dc.identifier.urihttps://hdl.handle.net/11772/1195
dc.identifier.volume31
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofJournal of Biochemical and Molecular Toxicology
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectAcetophenone
dc.subjectAcetylcholinesterase
dc.subjectButyrylcholinesterase
dc.subjectCarbonic anhydrase
dc.subjectEnzyme inhibition
dc.titleDiscovery of potent carbonic anhydrase, acetylcholinesterase, and butyrylcholinesterase enzymes inhibitors: The new amides and thiazolidine-4-ones synthesized on an acetophenone base
dc.typeArticle
dspace.entity.typePublication

Dosyalar

Lisans paketi

Listeleniyor 1 - 1 / 1
Yükleniyor...
Küçük Resim
İsim:
license.txt
Boyut:
1.71 KB
Biçim:
Item-specific license agreed upon to submission
Açıklama: