Synthesis of some natural sulphonamide derivatives as carbonic anhydrase inhibitors

MakaleAçık ErişimScopus SJRQ4
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

Carbonic anhydrase inhibitor; sulphonamides; p-hydroxybenzoic acid; 3,4,5-trihydroxybenzoic acid (gallic acid).Carbonic anhydrase inhibitors are both in clinical use as antiglaucoma, diuretics, antiepileptics and management of altitude sickness, and under investigation as anticancer, anticonvulsant and antiobesity agents. Sulphonamides have been known for decades as carbonic anhydrase inhibitors and are in clinical use. Sulphonamide derivatives of p-hydroxybenzoic acid and 3,4,5-trihydroxybenzoic acid (gallic acid) were synthesized and their inhibition values over hCA I and hCA II isozymes, purified from human erythrocyte cells by Sepharose-4B-L-tyrosine-sulphanilamide, were determined. Compounds synthesized showed efficient carbonic anhydrase inhibition activity at low nM levels.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/10306Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.25135/acg.oc.4.16.05.418Yayıncı resmi DOI adresi
Atıflar
Scopus
27
WoS
24
OpenAlex
27
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorGokcen, Taner
dc.contributor.authorAl, Melike
dc.contributor.authorTopal, Meryem
dc.contributor.authorGulcin, Ilhami
dc.contributor.authorOzturk, Turan
dc.contributor.authorGoren, Ahmet C.
dc.date.accessioned2026-10-22T09:22:53.631660582Z
dc.date.available2026-10-22T09:22:53.631660582Z
dc.date.issued2017-01
dc.description.abstractCarbonic anhydrase inhibitor; sulphonamides; p-hydroxybenzoic acid; 3,4,5-trihydroxybenzoic acid (gallic acid).Carbonic anhydrase inhibitors are both in clinical use as antiglaucoma, diuretics, antiepileptics and management of altitude sickness, and under investigation as anticancer, anticonvulsant and antiobesity agents. Sulphonamides have been known for decades as carbonic anhydrase inhibitors and are in clinical use. Sulphonamide derivatives of p-hydroxybenzoic acid and 3,4,5-trihydroxybenzoic acid (gallic acid) were synthesized and their inhibition values over hCA I and hCA II isozymes, purified from human erythrocyte cells by Sepharose-4B-L-tyrosine-sulphanilamide, were determined. Compounds synthesized showed efficient carbonic anhydrase inhibition activity at low nM levels.
dc.description.sponsorshipTUBITAK UME
dc.identifier.doi10.25135/acg.oc.4.16.05.418
dc.identifier.endpage23
dc.identifier.issn1307-6175
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85011290464
dc.identifier.startpage15
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/10306
dc.identifier.volume10
dc.identifier.wosWOS:000411598300005
dc.language.isoen
dc.publisherACG PUBLICATIONS
dc.relation.ispartofORGANIC COMMUNICATIONS
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCarbonic anhydrase inhibitor
dc.subjectsulphonamides
dc.subjectp-hydroxybenzoic acid
dc.subject3,4,5-trihydroxybenzoic acid (gallic acid)
dc.subject.classificationChemistry, Organic
dc.subject.classificationChemistry
dc.subject.otherISOENZYMES INHIBITORS
dc.subject.otherGALLIC ACID
dc.subject.otherIN-VITRO
dc.subject.otherLIQUID-CHROMATOGRAPHY
dc.subject.otherPHENOLIC-COMPOUNDS
dc.subject.otherMASS-SPECTROMETRY
dc.subject.otherISOZYMES I
dc.subject.otherPOLYPHENOLS
dc.subject.otherISOFORMS
dc.subject.otherEXTRACTION
dc.titleSynthesis of some natural sulphonamide derivatives as carbonic anhydrase inhibitors
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex27
rdl.citation.scopus27
rdl.citation.wos24
rdl.oa.statusgold
rdl.oa.urlhttps://doi.org/10.25135/acg.oc.4.16.05.418
rdl.scopus.quartileQ4
rdl.sdgSDG03
rdl.source.indexWOS
rdl.source.indexSCOPUS
rdl.wos.indexEmerging Sources Citation Index (ESCI)