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Cyclotides as templates in drug design

dc.contributor.authorHenriques, Sónia Troeira
dc.contributor.authorCraik, David J.
dc.date.accessioned2013-01-31T18:00:45Z
dc.date.available2013-01-31T18:00:45Z
dc.date.issued2010
dc.description© 2009 Elsevier Ltd. All rights reservedeng
dc.description.abstractCyclotides are remarkably stable proteins from plants that have a range of pharmaceutical and agricultural applications based on both their various bioactivities and their potential for use as stable protein-engineering templates. This article discusses literature on pharmaceutically relevant activities of cyclotides, including anti-HIV, antimicrobial and cytotoxic activities, and evaluates their potential therapeutic applications. Their applications as templates for the design of antiangiogenic agents for the treatment of cancer and as anti-infective agents are also described. Toxic effects of cyclotides, whose native function is as insecticidal agents, can be removed by simple mutagenesis, thus rationalizing the apparent conundrum of proposing insecticidal agents as leads for human therapeutics.eng
dc.description.sponsorshipStudies in our laboratory on cyclotides are supported by grants from the Australian Research Council (DP0880105) and the National Health and Medical Research Council (NHMRC). D.J.C. is an NHMRC Professorial Fellow. S.T.H. is a Marie Curie Postdoctoral Fellowawarded by EuropeanCommission (PIOF-GA-2008-220318).eng
dc.identifier.citationDrug Discovery Today . Volume 15, Numbers 1/2 ∙ January 2010eng
dc.identifier.issn1359-6446
dc.identifier.urihttp://dx.doi.org/10.1016/j.drudis.2009.10.007
dc.identifier.urihttp://hdl.handle.net/10451/7619
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relation.publisherversionThe definitive version is available at http://www.elsevier.com/eng
dc.titleCyclotides as templates in drug designeng
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage64por
oaire.citation.startPage57por
oaire.citation.titleDrug Discovery Todayeng
oaire.citation.volume15por
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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