LTURM34, soluble in DMSO and ethanol and insoluble in water, impairs the non-homologous end joining (NHEJ) pathway of DNA repair, thereby sensitizing cancer cells to treatments that induce DNA double-strand breaks. It targets DNA-PK, PI3Kβ, and PI4Kδ.
LTURM34 can be used to study its selective inhibition of specific signaling pathways involved in cancer progression.
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