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Dipeptide vinyl sultams

dc.contributor.authorValente, Claudia
dc.contributor.authorGuedes, Rita C.
dc.contributor.authorMoreira, Rui
dc.contributor.authorIley, Jim
dc.contributor.authorGut, Jiri
dc.contributor.authorRosenthal, Philip J.
dc.date.accessioned2015-12-30T10:18:16Z
dc.date.available2015-12-30T10:18:16Z
dc.date.issued2006
dc.description.abstractThe synthesis of phosphonate derivatives of N-phenyl- and N-benzyl-gamma and delta-sultams, and their application in the Wittig-Horner reaction with N-BOC-L-phenylalanine aldehyde to afford E- and Z-isomers, are described. These compounds were further processed to provide five dipeptide vinyl sultams, which were found to be inactive against papain at concentrations up to 50 mu M. In contrast, vinyl sultams demonstrated weak activity against recombinant falcipain-2 and Plasmodium falciparum W2. (c) 2006 Elsevier Ltd. All rights reserved.
dc.formatapplication/pdf
dc.identifier.citationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS. - Vol. 16, n. 15 (AUG 1 2006), p. 4115-4119
dc.identifier.doihttp://dx.doi.org/10.1016/j.bmcl.2006.04.079
dc.identifier.issn0960-894X
dc.identifier.urihttp://hdl.handle.net/10451/21501
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.subjectChemistry, Medicinal
dc.subjectChemistry, Organic
dc.titleDipeptide vinyl sultams
dc.titleSynthesis via the Wittig-Horner reaction and activity against papain, falcipain-2 and Plasmodium falciparum
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage4119por
oaire.citation.startPage4115por
oaire.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERSpor
oaire.citation.volumeVol. 16por
rcaap.rightsrestrictedAccess
rcaap.typearticle

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