Oxidation of cyanobenzocycloheptatrienes: Synthesis, photooxygenation reaction and carbonic anhydrase isoenzymes inhibition properties of some new benzotropone derivatives

MakaleAçık Erişim

Özet

The oxidation of some cyanocycloheptatrienes with CrO3 and pyridine was investigated and a few new nitrile functionalised benzotropone derivatives were obtained. Photooxygenation reaction of these products was also studied. The structures of the formed products were determined on the basis of NMR spectroscopy and the formation mechanism of unusual products was discussed. Human carbonic anhydrase isoenzymes I, and II (hCA I and hCA II) inhibition properties of nitrile functionalized new benzotropone derivatives were also studied. Both CA isozymes were inhibited in the low micromolar range by these nitrile functionalized benzotropone analogues. The newly synthesized benzotropone derivatives showed inhibition constants in the sub-micromolar range (2.51-4.06 mu M). The best hCA I inhibition was observed in 5H-benzocycloheptene-7-carbonitrile (K-1: 2.88 +/- 0.86 mu M). On the other hand, 5-oxo-5H-benzocycloheptatriene-7-carbonitrile showed the powerful inhibitory effect against hCA II (K-i: 2.51 +/- 0.34 mu M). (C) 2014 Elsevier Ltd. All rights reserved.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/10328Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1016/j.bmc.2014.04.007Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorGüney, Murat
dc.contributor.authorCoskun, Ahmet
dc.contributor.authorTopal, Fevzi
dc.contributor.authorDastan, Arif
dc.contributor.authorGülçin, Ilhami
dc.contributor.authorSupuran, Claudiu T.
dc.date.accessioned2026-10-22T09:22:54.475953443Z
dc.date.available2026-10-22T09:22:54.475953443Z
dc.date.issued2014-07
dc.description.abstractThe oxidation of some cyanocycloheptatrienes with CrO3 and pyridine was investigated and a few new nitrile functionalised benzotropone derivatives were obtained. Photooxygenation reaction of these products was also studied. The structures of the formed products were determined on the basis of NMR spectroscopy and the formation mechanism of unusual products was discussed. Human carbonic anhydrase isoenzymes I, and II (hCA I and hCA II) inhibition properties of nitrile functionalized new benzotropone derivatives were also studied. Both CA isozymes were inhibited in the low micromolar range by these nitrile functionalized benzotropone analogues. The newly synthesized benzotropone derivatives showed inhibition constants in the sub-micromolar range (2.51-4.06 mu M). The best hCA I inhibition was observed in 5H-benzocycloheptene-7-carbonitrile (K-1: 2.88 +/- 0.86 mu M). On the other hand, 5-oxo-5H-benzocycloheptatriene-7-carbonitrile showed the powerful inhibitory effect against hCA II (K-i: 2.51 +/- 0.34 mu M). (C) 2014 Elsevier Ltd. All rights reserved.
dc.description.sponsorshipTUBITAK [104T401]
dc.description.sponsorshipAtaturk University
dc.identifier.doi10.1016/j.bmc.2014.04.007
dc.identifier.eissn1464-3391
dc.identifier.endpage3543
dc.identifier.issn0968-0896
dc.identifier.issue13
dc.identifier.pmid24856184
dc.identifier.scopus2-s2.0-84901938556
dc.identifier.startpage3537
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/10328
dc.identifier.volume22
dc.identifier.wosWOS:000337215900035
dc.language.isoen
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relation.ispartofBIOORGANIC & MEDICINAL CHEMISTRY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBenzocycloheptatriene
dc.subjectBenzotropone
dc.subjectOxidation
dc.subjectRearrangement
dc.subjectNitrile-substituted drugs
dc.subjectCarbonic anhydrase inhibition
dc.subject.classificationBiochemistry & Molecular Biology
dc.subject.classificationChemistry, Medicinal
dc.subject.classificationChemistry, Organic
dc.subject.classificationPharmacology & Pharmacy
dc.subject.classificationChemistry
dc.subject.otherERYTHROCYTE ISOZYMES I
dc.subject.otherSINGLET OXYGEN
dc.subject.otherISOFORMS I
dc.subject.otherSULFONAMIDE DERIVATIVES
dc.subject.otherCYCLOADDITION REACTIONS
dc.subject.otherBICYCLIC ENDOPEROXIDES
dc.subject.otherANTITUMOR AGENTS
dc.subject.otherESTER ANALOGS
dc.subject.otherVITRO
dc.subject.otherANTIOXIDANT
dc.titleOxidation of cyanobenzocycloheptatrienes: Synthesis, photooxygenation reaction and carbonic anhydrase isoenzymes inhibition properties of some new benzotropone derivatives
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex127
rdl.citation.scopus128
rdl.citation.wos132
rdl.departmentAtatürk University, Faculty of Science, Department of Chemistry, 25240 Erzurum, Turkey
rdl.departmentGumushane University, Vocational School of Health Services, Department of Medical Services and Techniques, 29100 Gumushane, Turkey
rdl.oa.statuspreprint
rdl.oa.statusgreen
rdl.oa.urlhttps://hdl.handle.net/20.500.12501/1086
rdl.source.indexWOS
rdl.source.indexSCOPUS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)
rdl.wos.indexIndex Chemicus (IC)