2-Amino-3-cyanopyridine derivatives as carbonic anhydrase inhibitors
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.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Ayvaz, Selçuk | |
| dc.contributor.author | Çankaya, Murat | |
| dc.contributor.author | Atasever, Ali | |
| dc.contributor.author | Altuntas, Aliye | |
| dc.date.accessioned | 2026-10-18T20:30:36.679039549Z | |
| dc.date.available | 2026-10-18T20:30:36.679039549Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | The authors thank the Gazi University Scientific Research Fund (Project number: 05/2008-47) for financial support. | |
| dc.identifier.doi | 10.3109/14756366.2011.639016 | |
| dc.identifier.eissn | 1475-6374 | |
| dc.identifier.endpage | 310 | |
| dc.identifier.issn | 1475-6366 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 22141460 | |
| dc.identifier.scopus | 2-s2.0-84891403878 | |
| dc.identifier.startpage | 305 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/15766 | |
| dc.identifier.volume | 28 | |
| dc.identifier.wos | WOS:000314531000010 | |
| dc.language.iso | en | |
| dc.publisher | Informa Healthcare | |
| dc.relation.ispartof | Journal of Enzyme Inhibition and Medicinal Chemistry | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | 2-amino-3-cyanopyridines | |
| dc.subject | 4-furyl | |
| dc.subject | 4-thienyl | |
| dc.subject | Carbonic anhydrase | |
| dc.subject | Enzyme inhibition | |
| dc.subject | Aminopyridines | |
| dc.subject | Carbonic Anhydrase Inhibitors | |
| dc.subject | Carbonic Anhydrases | |
| dc.subject | Dose-Response Relationship, Drug | |
| dc.subject | Erythrocytes | |
| dc.subject | Humans | |
| dc.subject | Molecular Structure | |
| dc.subject | Nitriles | |
| dc.subject | Protein Isoforms | |
| dc.subject | Structure-Activity Relationship | |
| dc.subject | aminopyridine derivative | |
| dc.subject | carbonate dehydratase | |
| dc.subject | carbonate dehydratase inhibitor | |
| dc.subject | isoprotein | |
| dc.subject | nitrile | |
| dc.subject | antagonists and inhibitors | |
| dc.subject | chemical structure | |
| dc.subject | chemistry | |
| dc.subject | dose response | |
| dc.subject | enzymology | |
| dc.subject | erythrocyte | |
| dc.subject | human | |
| dc.subject | isolation and purification | |
| dc.subject | metabolism | |
| dc.subject | structure activity relation | |
| dc.title | 2-Amino-3-cyanopyridine derivatives as carbonic anhydrase inhibitors | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 25 | |
| rdl.citation.wos | 24 | |
| rdl.oa.status | green | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
