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Publication — IRIC

Squaramide Formation for DNA-Encoded Library Synthesis.

DNA-encoded libraries (DELs) can be considered as one of the most powerful tools for the discovery of small molecules of biological interest. However, the ability to access large DELs is contingent upon having chemical transformations that work in aqueous phase and generate minimal DNA alterations and the availability of building blocks compatible with on-DNA chemistry. In addition, accessing scaffolds of interest to medicinal chemists can be challenging in a DEL setting because of inherent limitations of DNA-supported chemistry. In this context, a squaramide formation reaction was developed by using a two-step process. The mild and high-yielding reaction tolerates a wide array of functional groups and was shown to be safe for DNA, thereby making this methodology ideal for DELs.

Date de publication
14 juin 2024
Chercheur(euse)s
Douchez A, Poupart J, Yang G, Vaillancourt L, Marinier A
Référence PubMed
Bioconjug Chem 2024
ID PubMed
38874002
Affiliation
Drug Discovery Unit, Institute of Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec H3C 3J7, Canada.