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pubmed-article:16555088pubmed:abstractTextSince 2-deoxy-D-glucose (2-DG) is currently in phase I clinical trials to selectively target slow-growing hypoxic tumor cells, 2-halogenated D-glucose analogs were synthesized for improved activity. Given the fact that 2-DG competes with D-glucose for binding to hexokinase, in silico modeling of molecular interactions between hexokinase I and these new analogs was used to determine whether binding energies correlate with biological effects, i.e. inhibition of glycolysis and subsequent toxicity in hypoxic tumor cells.lld:pubmed
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pubmed-article:16555088pubmed:articleTitleEfficacy of 2-halogen substituted D-glucose analogs in blocking glycolysis and killing "hypoxic tumor cells".lld:pubmed
pubmed-article:16555088pubmed:affiliationSchool of Medicine and Sylvester Cancer Center, The University of Miami, Miami, FL, USA.lld:pubmed
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