Synthesis and Inhibitor Effect Novel Alkoxymethyl Derivatives of Dihetero Cycloalkanes on Carbonic Anhydrase and Acetylcholinesterase

dc.contributor.author Farzaliyev, Vagif
dc.contributor.author Erturk, Adem
dc.contributor.author Abbasova, Malahat
dc.contributor.author Nabiyev, Oruj
dc.contributor.author Demir, Yeliz
dc.contributor.author Kiziltas, Hatice
dc.contributor.author Gulcin, Ilhami
dc.date.accessioned 2025-05-10T17:22:59Z
dc.date.available 2025-05-10T17:22:59Z
dc.date.issued 2024
dc.description Farzaliyev, Vagif/0009-0004-4301-475X; Demir, Yeliz/0000-0003-3216-1098; Sucayev, Afsun/0000-0002-4135-9568 en_US
dc.description.abstract 1,3-Diheterocycloalkanes derivatives are important starting materials in fine organic synthesis. These compounds can be widely used in various fields such as industry, medicine, biotechnology and chemical technology. The paper is focused on synthesis and study of alkoxymethyl derivatives of diheterocycloalkanes (M1-M15) and inhibition effect on carbonic anhydrase and acetylcholinesterase. The structures of compounds were confirmed by 1H and 13C NMR spectroscopy. Also, in this study alkoxymethyl derivatives of diheterocycloalkanes were assessed for their influence on various metabolic enzymes, including acetylcholinesterase (AChE) and human carbonic anhydrase isoenzymes (hCA I and hCA II). The results demonstrated that all these compounds exhibited potent inhibitory effects on all the target enzymes, surpassing the standard inhibitors, as evidenced by their IC50 and Ki values. The Ki values for the compounds concerning AChE, hCA I, and hCA II enzymes were in the ranges of 1.02 +/- 0.17-8.38 +/- 1.02, 15.30 +/- 3.15-58.14 +/- 5.17 and 24.05 +/- 3.70-312.94 +/- 27.24 nM, respectively. image en_US
dc.identifier.doi 10.1002/cbdv.202400296
dc.identifier.issn 1612-1872
dc.identifier.issn 1612-1880
dc.identifier.scopus 2-s2.0-85191950879
dc.identifier.uri https://doi.org/10.1002/cbdv.202400296
dc.identifier.uri https://hdl.handle.net/20.500.14720/10744
dc.language.iso en en_US
dc.publisher Wiley-v C H verlag Gmbh en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject 1,3-Oxazine en_US
dc.subject 1,3-Oxazolidine en_US
dc.subject 1,3-Imidazolidine en_US
dc.subject Benzothiazol-2-Thione en_US
dc.subject Enzyme Inhibition en_US
dc.subject Acetylcholinesterase en_US
dc.subject Carbonic Anhydrase en_US
dc.title Synthesis and Inhibitor Effect Novel Alkoxymethyl Derivatives of Dihetero Cycloalkanes on Carbonic Anhydrase and Acetylcholinesterase en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Farzaliyev, Vagif/0009-0004-4301-475X
gdc.author.id Demir, Yeliz/0000-0003-3216-1098
gdc.author.id Sucayev, Afsun/0000-0002-4135-9568
gdc.author.scopusid 6506451719
gdc.author.scopusid 57703431700
gdc.author.scopusid 57217231809
gdc.author.scopusid 57201726629
gdc.author.scopusid 57208078744
gdc.author.scopusid 24066867300
gdc.author.scopusid 57188551333
gdc.author.wosid Farzaliyev, Vagif/Mck-4253-2025
gdc.author.wosid Malahat, Abbasova/Lpp-4706-2024
gdc.author.wosid Kızıltaş, Hatice/Gxf-8734-2022
gdc.author.wosid Gulcin, Ilhami/F-1428-2014
gdc.author.wosid Demir, Yeliz/Abi-5719-2020
gdc.author.wosid Ertürk, Adem/Acs-5808-2022
gdc.author.wosid Sucayev, Afsun/Glu-9292-2022
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Farzaliyev, Vagif; Abbasova, Malahat; Nabiyev, Oruj; Sujayev, Afsun] Minist Sci & Educ Republ Azerbaijan, Inst Chem Addit, Baku 1029, Azerbaijan; [Farzaliyev, Vagif] Baku State Univ, Z Khalilov Str 23, AZ-1148 Baku, Azerbaijan; [Erturk, Adem; Gulcin, Ilhami] Ataturk Univ, Fac Sci, Dept Chem, TR-25240 Erzurum, Turkiye; [Demir, Yeliz] Ardahan Univ, Nihat Delibalta Gole Vocat High Sch, Dept Pharm Serv, TR-75700 Ardahan, Turkiye; [Kiziltas, Hatice] Van Yuzuncu Yil Univ, Van Vocat Sch Hlth Serv, TR-65080 Van, Turkiye en_US
gdc.description.issue 6 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.volume 21 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q3
gdc.identifier.pmid 38575390
gdc.identifier.wos WOS:001217116100001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

Files