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Deferoxamine mesylate (CAS 138-14-7) is an iron-specific chelating agent used primarily to manage acute iron poisoning It binds iron ions to form a water-soluble complex ferrioxamine thus preventing iron from participating in harmful oxidative reactions and facilitating renal excretion In rat mammary adenocarcinoma models deferoxamine mesylate treatment particularly combined with low-iron diet reduces tumor growth Additionally preoperative administration attenuates oxidative stress markers and pancreatic tissue damage by inducing HIF-1 expression in rat liver transplantation studies highlighting its utility in anticancer and cytoprotective research
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Also available in 1 mL, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Deferoxamine Mesylate (DFOM) is an iron chelator and ferroptosis inhibitor. Deferoxamine Mesylate binds free iron into a stable complex and reduces iron accumulation. Deferoxamine Mesylate up-regulates HIF-1alpha levels and induces apoptosis. Purity 99.8%
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PBT434 mesylate (PBT434 methanesulfonate, ATH434) is a brain-penetrant, orally active small molecule inhibitor of α-synuclein aggregation with iron-chelating activity, supplied for research use in studies of synucleinopathies and neurodegeneration.
Inhibits α-synuclein aggregation and reduces iron-mediated aggregation.
Acts as an iron chelator and modulates iron trafficking.
Brain-penetrant and orally active, suitable for in vivo studies.
High purity appropriate for biochemical and cellular assays.
Solid, white to off-white appearance; store sealed at 4°C.
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PBT434 mesylate is the methanesulfonate salt of PBT434, a brain-penetrant, orally active small molecule inhibitor of α-synuclein aggregation used in preclinical Parkinson's disease research.
Acts as an iron chelator and modulates transcellular iron trafficking.
Inhibits iron-mediated redox activity and α-synuclein aggregation.
Orally active and crosses the blood-brain barrier.
Supplied as a mesylate salt, solid, white to off-white.
High purity suitable for research (99.9%).
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PBT434 mesylate is the methanesulfonate salt of a small-molecule inhibitor of α-synuclein aggregation that demonstrates oral activity and crosses the blood-brain barrier, supplied for preclinical research. It also exhibits iron-modulating properties and is provided as a high-purity solid with defined storage conditions.
High purity: 99.9%.
Molecular weight 398.26 g·mol⁻1.
Chemical formula C13H17Cl2N3O5S.
Available in small pack sizes including 50 MG.
Store sealed at 4°C; in solvent keep at -80°C up to 6 months, or -20°C up to 1 month.
Intended for preclinical studies of protein aggregation and iron modulation; follow appropriate safety guidance.
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Deferoxamine mesylate is the mesylate salt of Deferoxamine which forms iron complexes and is used as a chelating agent Deferoxamine is a ferroptosis inhibitor that stabilizes HIF-1 expression and improves HIF-1 transactivity in hypoxic and hyperglycemic states in vitro Deferoxamine decreases beta-amyloid (A ) deposition and induces autophagy Please do not prepare stock solutions with normal saline or PBS as precipitation may occur
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Deferoxamine mesylate is the mesylate salt of Deferoxamine which forms iron complexes and is used as a chelating agent Deferoxamine is a ferroptosis inhibitor that stabilizes HIF-1 expression and improves HIF-1 transactivity in hypoxic and hyperglycemic states in vitro Deferoxamine decreases beta-amyloid (A ) deposition and induces autophagy Please do not prepare stock solutions with normal saline or PBS as precipitation may occur
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PBT434 mesylate is the methanesulfonate salt of PBT434, an orally active, blood-brain barrier-penetrant small molecule that inhibits α-synuclein aggregation and modulates iron-mediated redox activity for preclinical neurodegeneration research.
Orally active α-synuclein aggregation inhibitor.
Crosses the blood-brain barrier.
High purity suitable for research use.
Soluble in DMSO at approximately 100 mg/mL; ultrasonic agitation recommended.
Store solid at 4°C sealed; stock solutions tolerate -80°C for long-term storage.
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