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dc.creatorGauna, Adriana
dc.creatorSánches-Hoyos, Fredys
dc.creatorHuerta, Maycol
dc.creatorKogan, Marcelo
dc.creatorAraya, Eyleen
dc.date2024-10-06
dc.date.accessioned2024-11-19T14:36:03Z
dc.date.available2024-11-19T14:36:03Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/2639
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/246297
dc.descriptionRGD-containing peptides (linear and cyclic) have been developed to target some types of cancer cells through interaction with the αvβ3 Integrin. Due to their reduced conformational freedom, cyclic peptides exhibit improved metabolic stability and binding affinity/specificity to their molecular targets. However, macrocyclization is considered a significant synthetic challenge that is affected by the ring size, peptide sequence, and reaction conditions, making tetra- and pentapeptides more difficult to cyclize. In this work, we report some optimized cyclization conditions for the obtention of a cyclic RGDfK peptide that combine the use of low reaction temperature and the addition of LiCl, a combination not yet reported that resulted in a reduction of the formation of oligomers and an improvement of the cyclization efficiency.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/2639/641
dc.rightsCopyright (c) 2024 SChQen-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 69 No 1 (2024): JCChemS; 6038-6041en-US
dc.source0717-9707
dc.source0717-9324
dc.subjectCyclic(RGDfK)en-US
dc.subjecthead-to-tail cyclizationen-US
dc.subjectIntegrinsen-US
dc.subjectpeptide cyclization conditionsen-US
dc.subjectTargetingen-US
dc.titleImprovement of Head-to-Tail RGD peptide Cyclization Efficiency Combining Low Temperature and Lithium Chlorideen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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