Investigation of inhibitory properties of some hydrazone compounds on hCA I, hCA II and AChE enzymes

dc.contributor.authorKucukoglu, Kaan
dc.contributor.authorGul, Halise Inci
dc.contributor.authorTaslimi, Parham
dc.contributor.authorGülçin, İlhami
dc.contributor.authorSupuran, Claudiu T.
dc.contributor.authorTaslimi, Parham
dc.date.accessioned2019-04-29T07:33:46Z
dc.date.available2019-04-29T07:33:46Z
dc.date.created2019
dc.date.issued2019
dc.date.issuedyyyymmdd2019-02-04
dc.departmentFakülteler, Fen Fakültesi, Biyoteknoloji Bölümü
dc.description.abstractRecently, inhibition of carbonic anhydrase (hCA) and acetylcholinesterase (AChE) have appeared as a promising approach for pharmacological intervention in a variety of disorders such as glaucoma, epilepsy, obesity, cancer, and Alzheimer’s disease. Keeping this in mind, N,N?-bis[(1-aryl-3-heteroaryl)propylidene]hydrazine dihydrochlorides, N1-N11, P1, P4-P8, and R1-R6, were synthesized to investigate their inhibitory activity against hCA I, hCA II, and AChE enzymes. All compounds in N, P, and R-series inhibited hCAs (I and II) and AChE more efficiently than the reference compounds acetazolamide (AZA), and tacrine. According to the activity results, the most effective inhibitory compounds were in R-series with the Ki values of 203?±?55–473?±?67?nM and 200?±?34–419?±?94?nM on hCA I, and hCA II, respectively. N,N?-Bis[1-(4-fluorophenyl)-3-(morpholine-4-yl)propylidene]hydrazine dihydrochlorides, N8, in N-series, N,N?-Bis[1-(4-hydroxyphenyl)-3-(piperidine-1-yl)propylidene]hydrazine dihydrochlorides, P4, in P-series, and N,N?-bis[1-(4-chlorophenyl)-3-(pyrrolidine-1-yl)propylidene]hydrazine dihydrochlorides, R5, in R-series were the most powerful compounds against hCA I with the Ki values of 438?±?65?nM, 344?±?64?nM, and 203?±?55?nM, respectively. Similarly, N8, P4, and R5 efficiently inhibited hCA II isoenzyme with the Ki values of 405?±?60?nM, 327?±?80?nM, and 200?±?34?nM, respectively. On the other hand, P-series compounds had notable inhibitory effect against AChE than the reference compound tacrine and the Ki values were between 66?±?20?nM and 128?±?36?nM. N,N?-Bis[1-(4-fluorophenyl)-3-(piperidine-1-yl)propylidene]hydrazine dihydrochlorides, P7, was the most potent compound on AChE with the Ki value of 66?±?20?nM. The other most promising compounds, N,N?-bis[1-(4-hydroxyphenyl)-3-(morpholine-4-yl)propylidene]hydrazine dihydrochlorides, N4 in N-series and N,N?-bis[1-(4-hydroxyphenyl)-3-(pyrrolidine-1-yl)propylidene]hydrazine dihydrochlorides, R4 in R-series were againts AChE with the Ki values of 119?±?20?nM, 88?±?14?nM, respectively.
dc.identifier.doi10.1016/j.bioorg.2019.02.008
dc.identifier.endpage321
dc.identifier.startpage316
dc.identifier.urihttps://hdl.handle.net/11772/1118
dc.identifier.volume86
dc.language.isoen
dc.publisherBioorganic Chemistry
dc.relation.ispartofBioorganic Chemistry
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectHydrazone
dc.subjectMannich base
dc.subjectCarbonic anhydrase
dc.subjectAcetylcholinesterase
dc.subjectEnzyme inhibition
dc.titleInvestigation of inhibitory properties of some hydrazone compounds on hCA I, hCA II and AChE enzymes
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationdadfa319-65b8-4543-92b4-bea49e0139e9
relation.isAuthorOfPublication.latestForDiscoverydadfa319-65b8-4543-92b4-bea49e0139e9

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