Synthesis of novel 3’,3’‐cyclic dinucleotide analogues targeting STING protein - Institut de Chimie Organique et Analytique Access content directly
Journal Articles Asian Journal of Organic Chemistry Year : 2022

Synthesis of novel 3’,3’‐cyclic dinucleotide analogues targeting STING protein

Abstract

The Stimulator of Interferon Genes (STING) plays an important role in innate immunity by inducing type I interferons in response to sensing viral or bacterial cytosolic DNA. Cyclic dinucleotides (CDNs) are known to activate STING. Here, we describe the synthesis and biological evaluation of two new 3’,3’-CDN, in which the internucleotide linkages were replaced, respectively, by a 1,2,3-triazole moiety (as more stable isosteres of phosphate linkers) and an unsaturated carbon chain (as flexibility can led to crucial binding affinity and specificity). Thus, CuAAC and macrocyclization by RCM are the two key steps
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Dates and versions

hal-03859427 , version 1 (21-11-2022)

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Jérémy Magand, Vincent Roy, Hervé Meudal, Stéphanie Rose, Valérie Quesniaux, et al.. Synthesis of novel 3’,3’‐cyclic dinucleotide analogues targeting STING protein. Asian Journal of Organic Chemistry, 2022, 2022, pp.e202200597. ⟨10.1002/ajoc.202200597⟩. ⟨hal-03859427⟩
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