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Updated: May 3, 2026

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
Published on: March 6, 2019
Synthesis of triazole-functionalized 2-DOS analogues and their evaluation as A-site binders
Panoula Anastasopoulou1, Georgia Kythreoti1, Tilemachos Cosmidis1
1Chemical Biology Laboratories, National Center for Scientific Research 'Demokritos', Agia Paraskevi Attikis, GR 15310, Greece.
Abstract:
Aminoglycoside-antibiotics represent important tools for studying the biological functions of RNA. An orthogonal protection strategy applied on 2-deoxystreptamine (2-DOS) revealed a series of key intermediates that enable its regioselective functionalization. Our approach allowed the construction of selected representatives of triazole-containing analogues with diverse molecular frameworks for biological evaluation regarding their binding and antibacterial potencies.
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