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Dimethyloxaloylglycine (DMOG) is a cell-permeable, competitive inhibitor of hypoxia-inducible factor (HIF) prolyl hydroxylases (HIF-PH) and prolyl 4-hydroxylase (P4H). By mimicking hypoxia, DMOG prevents the hydroxylation of proline residues on HIF-1α and HIF-2α, thereby preventing their recognition by the von Hippel-Lindau (VHL) E3 ubiquitin ligase and subsequent proteasomal degradation. This leads to the stabilization and accumulation of HIF-1α, promoting the transcription of downstream target genes involved in angiogenesis, glycolysis, and cell survival, such as vascular endothelial growth factor (VEGF) and erythropoietin (EPO). DMOG is widely utilized as a research tool to investigate cellular responses to hypoxia, ischemic injury, and tissue regeneration in preclinical models.
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