Chemical Name: 1,4-Dihydroxy-5,8-bis[[2-[(2-hydroxyethyl)amino]ethyl]amino]-9,10-anthracenedione dihydrochloride
Biological ActivityMitoxantrone dihydrochloride is a type II DNA topoisomerase inhibitor. Disrupts DNA synthesis and repair and induces damage by DNA cross-linking. Also inhibits PIM1 kinase (IC50 = 51 nM). Immunomodulatory, antineoplastic and chemotherapeutic agent. Also USP11 inhibitor (IC50= 3.15 μM). Induces cell death of pancreatic cancer cell lines expressing wild-type BRCA2.
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Tocris products are intended for laboratory research use only, unless stated otherwise.
Mitoxantrone targets human ubiquitin-specific peptidase 11 (USP11) and is a potent inhibitor of pancreatic cancer cell survival.
Burkhart et al.
Mol.Cancer Res., 2013;11:901
Mitoxantrone: a review of its uses in multiple sclerosis.
Scott and Figgit
CNS Drugs., 2004;18:379
Mitoxantrone affects topoisomerase activities in human breast cancer cells.
Crespi et al.
A new target for an old drug: identifying mitoxan. as a nanomolar inhibitor of PIM1 kinase via kinome-wide selectivity modeling.
Wan et al.
Citations for Mitoxantrone dihydrochloride
The citations listed below are publications that use Tocris products. Selected citations for Mitoxantrone dihydrochloride include:
2 Citations: Showing 1 - 2
The BTK Inhibitor, Ibrutinib (PCI-32765) Overcomes PacT. Resistance in ABCB1 and ABCC10 Overexpressing Cells and Tumors.
Mol Cancer Ther 2017;16(6):1021
The small molecule tyrosine kinase inhibitor NVP-BHG712 antagonizes ABCC10-mediated PacT. resistance: a preclinical and pharmacokinetic study.
Authors: Kathawala Et al.
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