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Review Open access Sep 2026

ALKBH5 inhibitors for cancer therapy: molecular docking, challenges and future prospects

N 6 -Methyladenosine (m 6 A), the most abundant internal modification of eukaryotic mRNA, is dynamically reversed by the Fe II /α-ketoglutarate-dependent dioxygenase ALKBH5, a key m 6 A “eraser” that regulates target mRNA fate through demethylation. ALKBH5 is aberrantly overexpressed in acute myeloid leukemia...

Chen Deng, Hai Xu, Jian Pu et al. · 0 citations

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