2-Amino-3-cyanopyridine derivatives as carbonic anhydrase inhibitors

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Özet

Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous enzymes that catalyze the hydration of CO2 to bicarbonate and protons. Inhibition of CAs has been clinically exploited for the treatment of various classes of diseases for decades, but investigating new classes of inhibitors continues to be important. We have synthesized a series of 2-amino-3-cyano-4-heteroaryl (5a-l) compounds and characterized the structures by NMR, IR and elemental analyses. We tested the ability of these compounds to inhibit two metalloenzyme human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, hCA I and hCA II. Compounds 5d and 5b showed the best inhibition activity against hCA I (IC50: 33 and 34 μM, respectively), and compound 5d showed the best activity against hCA II (IC50: 56 μM). © 2013 Informa UK, Ltd.

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Tam Kayıt
AlanDeğerDil
dc.contributor.authorAyvaz, Selçuk
dc.contributor.authorÇankaya, Murat
dc.contributor.authorAtasever, Ali
dc.contributor.authorAltuntas, Aliye
dc.date.accessioned2026-10-18T20:30:36.679039549Z
dc.date.available2026-10-18T20:30:36.679039549Z
dc.date.issued2013
dc.description.abstractCarbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous enzymes that catalyze the hydration of CO2 to bicarbonate and protons. Inhibition of CAs has been clinically exploited for the treatment of various classes of diseases for decades, but investigating new classes of inhibitors continues to be important. We have synthesized a series of 2-amino-3-cyano-4-heteroaryl (5a-l) compounds and characterized the structures by NMR, IR and elemental analyses. We tested the ability of these compounds to inhibit two metalloenzyme human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, hCA I and hCA II. Compounds 5d and 5b showed the best inhibition activity against hCA I (IC50: 33 and 34 μM, respectively), and compound 5d showed the best activity against hCA II (IC50: 56 μM). © 2013 Informa UK, Ltd.
dc.description.sponsorshipThe authors thank the Gazi University Scientific Research Fund (Project number: 05/2008-47) for financial support.
dc.identifier.doi10.3109/14756366.2011.639016
dc.identifier.eissn1475-6374
dc.identifier.endpage310
dc.identifier.issn1475-6366
dc.identifier.issue2
dc.identifier.pmid22141460
dc.identifier.scopus2-s2.0-84891403878
dc.identifier.startpage305
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15766
dc.identifier.volume28
dc.identifier.wosWOS:000314531000010
dc.language.isoen
dc.publisherInforma Healthcare
dc.relation.ispartofJournal of Enzyme Inhibition and Medicinal Chemistry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject2-amino-3-cyanopyridines
dc.subject4-furyl
dc.subject4-thienyl
dc.subjectCarbonic anhydrase
dc.subjectEnzyme inhibition
dc.subjectAminopyridines
dc.subjectCarbonic Anhydrase Inhibitors
dc.subjectCarbonic Anhydrases
dc.subjectDose-Response Relationship, Drug
dc.subjectErythrocytes
dc.subjectHumans
dc.subjectMolecular Structure
dc.subjectNitriles
dc.subjectProtein Isoforms
dc.subjectStructure-Activity Relationship
dc.subjectaminopyridine derivative
dc.subjectcarbonate dehydratase
dc.subjectcarbonate dehydratase inhibitor
dc.subjectisoprotein
dc.subjectnitrile
dc.subjectantagonists and inhibitors
dc.subjectchemical structure
dc.subjectchemistry
dc.subjectdose response
dc.subjectenzymology
dc.subjecterythrocyte
dc.subjecthuman
dc.subjectisolation and purification
dc.subjectmetabolism
dc.subjectstructure activity relation
dc.title2-Amino-3-cyanopyridine derivatives as carbonic anhydrase inhibitors
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus25
rdl.citation.wos24
rdl.oa.statusgreen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)