Abstract
For the last 15 years, kinetic target-guided syntheses, including in situ click chemistry, have been used as alternative methods to find ligands to therapeutically relevant proteins. In this review, a comprehensive survey of biological targets used in kinetic target-guided synthesis covers historical and recent examples. The chemical reactions employed and practical aspects, including controls, library sizes and product detection, are presented. A particular focus is on the reagents and warhead selection and design with a critical overview of the challenges encountered. As protein supply remains a key success factor, it appears that increased efforts should be taken toward miniaturization in order to expand the scope of this strategy and qualify it as a fully fledged drug discovery tool.
Cite
CITATION STYLE
Bosc, D., Jakhlal, J., Deprez, B., & Deprez-Poulain, R. (2016, March 1). Kinetic target-guided synthesis in drug discovery and chemical biology: A comprehensive facts and figures survey. Future Medicinal Chemistry. Future Science. https://doi.org/10.4155/fmc-2015-0007
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.