Deferoxamine Mesylate
The mesylate salt form of deferoxamine used parenterally to treat iron toxicity and chronic transfusional iron overload. The mesylate salt form is the standard pharmaceutical preparation for subcutaneous, intramuscular, or intravenous administration.
Peso Molecular
656,8000 g/mol
TPSA
269,00 Ų
Áreas Terapêuticas
Mecanismo de Ação
Forms stable, water-soluble chelate complexes with specific metal ions, facilitating their excretion from the body through the kidneys. This reduces toxic metal burden in affected tissues.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Forms stable, water-soluble chelate complexes with specific metal ions, facilitating their excretion from the body through the kidneys. This reduces toxic metal burden in affected tissues.
Estrutura 2D
Cite this structure
Embed this structure
SMILES
CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN.CS(=O)(=O)O
InChI
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)
Molecular Formula
C26H52N6O11S
HBD / HBA
7 / 12
Ligações Rotacionáveis
23
Átomos Pesados
44
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
The mesylate salt form of deferoxamine used parenterally to treat iron toxicity and chronic transfusional iron overload. The mesylate salt form is the standard pharmaceutical preparation for subcutaneous, intramuscular, or intravenous administration.
Forms stable, water-soluble chelate complexes with specific metal ions, facilitating their excretion from the body through the kidneys. This reduces toxic metal burden in affected tissues.
Yes, Deferoxamine Mesylate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1234. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 62881. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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