Kinetic target-guided synthesis in drug discovery and chemical biology: A comprehensive facts and figures survey

36Citations
Citations of this article
63Readers
Mendeley users who have this article in their library.

This article is free to access.

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

APA

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.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free