Synthesis, characterization, carbonic anhydrase inhibitor activity, and docking studies of phenylthiazol-2 (3h)-ylidene-isoquinoline-5-amine Derivatives
dc.authorid | Gencer, Nahit/0000-0001-7092-8857 | |
dc.authorid | SAHUTOGLU, Arif Sercan/0000-0003-1183-3553 | |
dc.authorid | Berber, Nurcan/0000-0002-1595-585X | |
dc.contributor.author | Berber, Nurcan | |
dc.contributor.author | Sahutoglu, Arif Sercan | |
dc.contributor.author | Gokce, Basak | |
dc.contributor.author | Cikrikci, Kuebra | |
dc.contributor.author | Gencer, Nahit | |
dc.date.accessioned | 2025-01-27T20:54:07Z | |
dc.date.available | 2025-01-27T20:54:07Z | |
dc.date.issued | 2023 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | Phenylthiazol-2(3h)-ylidene-isoquinoline-5-amine derivatives(5a-r) were easily prepared from 5-aminoisoquinoline, thioisocyanate, and phenacyl bromide derivatives in the presence of triethylamine in tetrahydrofuran (THF), and dimethyl formamide (DMF) in two steps. In the first step, thiourea was synthesized in THF reflux, 24 h and then in the second step, the formation of thiazole ring was ensured in EtOH-DMF (5:5 v/v), reflux, 24 h. The newly synthesized compounds were characterized using 1H NMR, 13C NMR, IR, and elemental analysis. The inhibitory effects of 18 newly synthesized compounds (5a-r) on hydratase and esterase activities of carbonic anhydrase isoenzymes (hCA I, II, IX, and X) were studied in vitro. | |
dc.description.sponsorship | Research Fund of the anakkale Onsekiz Mart University [FBA-2020-3128] | |
dc.description.sponsorship | This work was supported by the Research Fund of the Canakkale Onsekiz Mart University. Project Number: FBA-2020-3128. | |
dc.identifier.doi | 10.1016/j.molstruc.2023.136061 | |
dc.identifier.issn | 0022-2860 | |
dc.identifier.issn | 1872-8014 | |
dc.identifier.scopus | 2-s2.0-85163542622 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.uri | https://doi.org/10.1016/j.molstruc.2023.136061 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/25982 | |
dc.identifier.volume | 1291 | |
dc.identifier.wos | WOS:001036378700001 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.relation.ispartof | Journal of Molecular Structure | |
dc.relation.publicationcategory | info:eu-repo/semantics/openAccess | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.snmz | KA_WoS_20250125 | |
dc.subject | Isoquinoline | |
dc.subject | Thiazole | |
dc.subject | Thiourea | |
dc.subject | Carbonic anhydrase | |
dc.subject | Enzyme inhibitor | |
dc.title | Synthesis, characterization, carbonic anhydrase inhibitor activity, and docking studies of phenylthiazol-2 (3h)-ylidene-isoquinoline-5-amine Derivatives | |
dc.type | Article |