dc.contributor.author | Taslimi, Parham | |
dc.contributor.author | Akıncıoğlu, Hülya | |
dc.contributor.author | İlhami, Gülçin | |
dc.date.accessioned | 2019-05-17T08:25:32Z | |
dc.date.available | 2019-05-17T08:25:32Z | |
dc.date.issued | 2017-11 | |
dc.identifier.uri | http://hdl.handle.net/11772/1199 | |
dc.description.abstract | In this paper, synephrine and phenylephrine compounds showed excellent inhibitory effects against human carbonic anhydrase (hCA) isoforms I and II, -amylase, -glycosidase, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE). Synephrine and phenylephrine had K-i values of 199.02 +/- 16.01 and 65.01 +/- 5.00M against hCA I and 336.02 +/- 74.01 and 92.04 +/- 18.03M against hCA II, respectively. On the other hand, their K-i values were found to be 169.10 +/- 80.03 and 88.03 +/- 5.01nM against AChE and 177.06 +/- 6.01 and 78.03 +/- 3.05nM against BChE, respectively. -Amylase and -glycosidase enzymes were easily inhibited by these compounds. -Glycosidase inhibitors, generally defined to as starch blockers, are anti-diabetic drugs that help to decrease post comestible blood glucose levels. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Wiley | en_US |
dc.relation.isversionof | 10.1002/jbt.21973 | en_US |
dc.rights | info:eu-repo/semantics/restrictedAccess | en_US |
dc.subject | Alpha-amylase | en_US |
dc.subject | Alpha-glycosidase | en_US |
dc.subject | Carbonic anhydrase | en_US |
dc.subject | Phenylephrine | en_US |
dc.subject | Synephrine | en_US |
dc.title | Synephrine and phenylephrine act as -amylase, -glycosidase, acetylcholinesterase, butyrylcholinesterase, and carbonic anhydrase enzymes inhibitors | en_US |
dc.type | article | en_US |
dc.relation.journal | Journal of Biochemical and Molecular Toxicology | en_US |
dc.contributor.department | Bartın Üniversitesi, Fen Fakültesi, Biyoteknoloji Bölümü | en_US |
dc.identifier.volume | 31 | en_US |
dc.identifier.issue | 11 | en_US |
dc.identifier.startpage | e21973 | en_US |