Investigation of inhibitory properties of some hydrazone compounds on hCA I, hCA II and AChE enzymes
| dc.contributor.author | Kucukoglu, Kaan | |
| dc.contributor.author | Gul, Halise Inci | |
| dc.contributor.author | Taslimi, Parham | |
| dc.contributor.author | Gülçin, İlhami | |
| dc.contributor.author | Supuran, Claudiu T. | |
| dc.contributor.author | Taslimi, Parham | |
| dc.date.accessioned | 2019-04-29T07:33:46Z | |
| dc.date.available | 2019-04-29T07:33:46Z | |
| dc.date.created | 2019 | |
| dc.date.issued | 2019 | |
| dc.date.issuedyyyymmdd | 2019-02-04 | |
| dc.department | Fakülteler, Fen Fakültesi, Biyoteknoloji Bölümü | |
| dc.description.abstract | Recently, 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.doi | 10.1016/j.bioorg.2019.02.008 | |
| dc.identifier.endpage | 321 | |
| dc.identifier.startpage | 316 | |
| dc.identifier.uri | https://hdl.handle.net/11772/1118 | |
| dc.identifier.volume | 86 | |
| dc.language.iso | en | |
| dc.publisher | Bioorganic Chemistry | |
| dc.relation.ispartof | Bioorganic Chemistry | |
| dc.rights | info:eu-repo/semantics/restrictedAccess | |
| dc.subject | Hydrazone | |
| dc.subject | Mannich base | |
| dc.subject | Carbonic anhydrase | |
| dc.subject | Acetylcholinesterase | |
| dc.subject | Enzyme inhibition | |
| dc.title | Investigation of inhibitory properties of some hydrazone compounds on hCA I, hCA II and AChE enzymes | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | dadfa319-65b8-4543-92b4-bea49e0139e9 | |
| relation.isAuthorOfPublication.latestForDiscovery | dadfa319-65b8-4543-92b4-bea49e0139e9 |
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