ArticleChemMedChem2026
Sugar Amino Acid Linkers for the Design of [
Article in ChemMedChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
6 authors.
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Abstract
The pronounced lipophilicity of tert-butyl-substituted silicon-fluoride-acceptor (SiFA) scaffolds represents a major limitation in radiotracer development, often resulting in elevated nonspecific uptake and reduced tumor-to-background ratios. To address this challenge, we designed and synthesized a series of prostate-specific membrane antigen (PSMA)-targeted radioligands incorporating furanose- and pyranose-based sugar amino acid (SAA) linkers to evaluate physicochemical properties while maintaining efficient
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