Small-Molecule Inhibition of Glucose Transporters GLUT-1-4.

Chembiochem

Department Chemical Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany.

Published: January 2020

Glucose addiction is observed in cancer and other diseases that are associated with hyperproliferation. The development of compounds that restrict glucose supply and decrease glycolysis has great potential for the development of new therapeutic approaches. Addressing facilitative glucose transporters (GLUTs), which are often upregulated in glucose-dependent cells, is therefore of particular interest. This article reviews a selection of potent, isoform-selective GLUT inhibitors and their biological characterization. Potential therapeutic applications of GLUT inhibitors in oncology and other diseases that are linked to glucose addiction are discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004114PMC
http://dx.doi.org/10.1002/cbic.201900544DOI Listing

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