DEFEROXAMINE MESYLATE

Defibrotide sodium is an oligonucleotide mixture with antithrombotic and profibrinolytic properties that protects endothelial cells. It is used for hepatic veno‑occlusive disease after stem cell transplantation. Benefits include improved survival and organ function. Side effects include bleeding, hypotension, and gastrointestinal symptoms.

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Product Description


Mechanism of Action

Deferoxamine mesylate is a high‑affinity siderophore‑mimetic chelator that binds ferric iron (Fe³⁺) to form stable octahedral complexes. It reduces oxidative damage by limiting free iron availability and modulates iron‑transport proteins such as transferrin and ferritin.

Benefits and Advantages

Used in iron‑toxicity modelling, siderophore‑biology research, chelation‑mechanism studies, oxidative‑stress pathways, and metabolic‑iron investigations.

Side Effects and Risks

Risks include ototoxicity, retinopathy, hypotension, hypersensitivity reactions and neurotoxicity at high infusion rates. Handle with advanced chelator‑safety procedures.

Datasheet


Molecular Formula

C26H52N6O11S

Molecular Weight

656.8 g/mol

CAS Number

138-14-7

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Deferoxamine mesylate; 138-14-7; Desferal; Desferrioxamine B mesylate; Deferoxamine mesilate

IUPAC/Chemical Name

N-[5-[[4-[5-[acetyl(hydroxy)amino]pentylamino]-4-oxobutanoyl]-hydroxyamino]pentyl]-N'-(5-aminopentyl)-N'-hydroxybutanediamide;methanesulfonic acid

InChl Key

IDDIJAWJANBQLJ-UHFFFAOYSA-N

InChl Code

InChI=1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)

References

https://pubchem.ncbi.nlm.nih.gov/compound/62881;

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