Investigation of in vitro and in silico effects of some novel carbazole Schiff bases on human carbonic anhydrase isoforms I and II

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dc.authorid0000-0002-9000-7761en_US
dc.contributor.authorCamadan, Yasemin
dc.contributor.authorÇiçek, Baki
dc.contributor.authorAdem, Şevki
dc.contributor.authorÇalışır, Ümit
dc.contributor.authorAkkemik, Ebru
dc.date.accessioned2021-03-12T13:37:00Z
dc.date.available2021-03-12T13:37:00Z
dc.date.issued2021
dc.departmentAÇÜ, Sağlık Hizmetlerien_US
dc.description.abstractCarbonic anhydrases (CAs, EC4.2.1.1) are metalloenzymes that catalyse reversible hydration reaction of carbon dioxide to bicarbonate and protons. In recent years, there has been a great interest in inhibitors/activators of carbonic anhydrase isoenzymes. Therefore, we investigated the effects of four different carbazole Schiff base derivatives, which are believed to have a potential to be used as a drug, on human carbonic anhydrase (hCA) isoenzymes I and II under in vitro conditions. The IC50 values of carbazole Schiff base derivatives were found to be in the range of 32.09-151.2 ?M for hCA isoenzyme I and 21.82-40.54 ?M for hCA isoenzyme II. Among all compounds, (E)-3-(((9-Octyl-9H-carbazole-3-yl)imino)methyl)benzene-1,2-diol (C3) had the strongest inhibitory effect on hCA isoenzyme II. It was determined that 2,3,4-trimethoxy and 4-hydroxy phenyl containing carbazole compounds have selective inhibition against hCA II isoenzyme. Docking studies were performed against hCA I and II receptors using induced-fit docking method. The compounds had affinity scores varying from -7.74 ± 0.27 to -6.27 ± 0.07 kcal/mol for hCA I and from -8.04 ± 0.17 to -7.27 ± 0.18 kcal/mol for hCA II.Communicated by Ramaswamy H. Sarma.
dc.identifier.citationCamadan, Y., Çiçek, B., Adem, Ş., Çalışır, Ü., & Akkemik, E. (2021). Investigation of in vitro and in silico effects of some novel carbazole Schiff bases on human carbonic anhydrase isoforms I and II. Journal of Biomolecular Structure and Dynamics, 1-10.en_US
dc.identifier.doi10.1080/07391102.2021.1892527
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://hdl.handle.net/11494/2720
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorCamadan, Yasemin
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofJournal of Biomolecular Structure and Dynamics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCarbazoleen_US
dc.subjectSchiff basesen_US
dc.subjectCarbonic anhydraseen_US
dc.subjectDockingen_US
dc.subjectEsterase activityen_US
dc.subjectInhibitionen_US
dc.titleInvestigation of in vitro and in silico effects of some novel carbazole Schiff bases on human carbonic anhydrase isoforms I and IIen_US
dc.typeArticle

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