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dc.contributor.authorGeorgiades, Savvas N.en
dc.contributor.authorClardy, J.en
dc.creatorGeorgiades, Savvas N.en
dc.creatorClardy, J.en
dc.date.accessioned2019-11-21T06:19:06Z
dc.date.available2019-11-21T06:19:06Z
dc.date.issued2005
dc.identifier.issn1523-7060
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55494
dc.description.abstract(Chemical Equation Presented) Two inhibitors of FOXO1a-mediated nuclear export, psammaplysenes A and B, have been synthesized by a flexible and efficient route. A common starting material, 4-iodophenol, was used to prepare both halves of these pseudosymmetric dibromotyrosine-derived metabolites. © 2005 American Chemical Society.en
dc.sourceOrganic lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-25444454350&doi=10.1021%2fol0513286&partnerID=40&md5=43c089e5515cb82e2249e7a4337a626f
dc.subjectarticleen
dc.subjectdrug derivativeen
dc.subjectmetabolismen
dc.subjectchemistryen
dc.subjectdrug antagonismen
dc.subjectsynthesisen
dc.subjectchemical structureen
dc.subjectMolecular Structureen
dc.subjectforkhead transcription factoren
dc.subjectForkhead Transcription Factorsen
dc.subjecttyrosineen
dc.subjectActive Transport, Cell Nucleusen
dc.subjectpsammaplysene Aen
dc.subjectpsammaplysenes Ben
dc.subjectactive transporten
dc.titleTotal synthesis of psammaplysenes A and B, naturally occurring inhibitors of FOXO1a nuclear exporten
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1021/ol0513286
dc.description.volume7
dc.description.issue19
dc.description.startingpage4091
dc.description.endingpage4094
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :21</p>en
dc.source.abbreviationOrg.Lett.en
dc.contributor.orcidGeorgiades, Savvas N. [0000-0002-6106-9904]
dc.gnosis.orcid0000-0002-6106-9904


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