Drug intelligence / Profile preview

idarubicin

Development stage
Approved
Lead developer
Pfizer
Modality
Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

Idarubicin is an anthracycline antineoplastic agent primarily used in combination chemotherapy for the treatment of acute myeloid leukemia (AML) in adults. It works by intercalating into DNA and inhibiting the enzyme topoisomerase II, which leads to DNA strand breaks and inhibition of nucleic acid synthesis, ultimately resulting in cell death. The absence of a methoxy group at position 4 increases its lipophilicity compared to other anthracyclines, enhancing cellular uptake and potency. Idarubicin is considered more potent than daunorubicin and may have reduced cardiac toxicity relative to other drugs in its class.

Brand names
IdamycinIdamycin PFS
Other names
4-demethoxydaunorubicin
02

Targets

DNATOP2B (DNA topoisomerase II beta)TOP2A (DNA topoisomerase II)

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