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A Chemical Strategy for the Preparation of Multimodified Peptide Imaging Probes

Title: A Chemical Strategy for the Preparation of Multimodified Peptide Imaging Probes
Authors: De Rosa L.; Hawala I.; Di Stasi R.; Stefania R.; Capozza M.; Nava D.; D'Andrea L. D.
Contributors: De Rosa, L.; Hawala, I.; Di Stasi, R.; Stefania, R.; Capozza, M.; Nava, D.; D'Andrea, L. D.
Publication Year: 2023
Collection: Università degli Studi del Piemonte Orientale: CINECA IRIS
Description: Multimodality probes appear of great interest for innovative imaging applications in disease diagnosis. Herein, we present a chemical strategy enabling site-specific doublemodification and cyclization of a peptide probe exploiting native chemical ligation (NCL) and thiol-maleimide addition. The synthetic strategy is straightforward and of general applicability for the development of double-labeled peptide multimodality probes.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/36988421; info:eu-repo/semantics/altIdentifier/wos/WOS:000962162800001; volume:88; issue:7; firstpage:4546; lastpage:4553; numberofpages:8; journal:JOURNAL OF ORGANIC CHEMISTRY; https://hdl.handle.net/11579/153360
DOI: 10.1021/acs.joc.3c00014
Availability: https://hdl.handle.net/11579/153360; https://doi.org/10.1021/acs.joc.3c00014
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.8134ACF
Database: BASE