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Home > Encyclopedia > Deferoxamine mesylate

Deferoxamine mesylate

pharmaceutical raw materials
Deferoxamine mesylate structure

Deferoxamine mesylate 

structure
  • CAS No:

    138-14-7

  • Formula:

    C25H48N6O8.CH4O3S

  • Chemical Name:

    Deferoxamine mesylate

  • Synonyms:

    Butanediamide,N4-[5-[[4-[[5-(acetylhydroxyamino)pentyl]amino]-1,4-dioxobutyl]hydroxyamino]pentyl]-N1-(5-aminopentyl)-N1-hydroxy-,methanesulfonate (1:1);Propionohydroxamic acid,N-[5-[3-[(5-aminopentyl)hydroxycarbamoyl]propionamido]pentyl]-3-[[5-(N-hydroxyacetamido)pentyl]carbamoyl]-,monomethanesulfonate (salt);Butanediamide,N′-[5-[[4-[[5-(acetylhydroxyamino)pentyl]amino]-1,4-dioxobutyl]hydroxyamino]pentyl]-N-(5-aminopentyl)-N-hydroxy-,monomethanesulfonate (salt);Propionohydroxamic acid,N-[5-[3-[(5-aminopentyl)hydroxycarbamoyl]propionamido]pentyl]-3-[[5-(N-hydroxyacetamido)pentyl]carbamoyl]-,methanesulfonate;Desferrioxamine methanesulfonate;Desferrioxamine B mesylate;Desferrioxamine B methanesulfonate;Deferoxamine B mesylate;Deferrioxamine methanesulfonate;Desferrioxamine mesylate;Desferal mesylate;Desferal;Deferrioxamine B methanesulfonate;Deferoxamine mesylate;Deferoxamine methanesulfonate;DFOM;Ba 33112;NSC 644468;DFX mesylate;Desferrioxamine mesilate;17688-38-9;35908-62-4

  • Categories:

    Active Pharmaceutical Ingredients  >  Specialty Drugs

Description

Deferoxamine mesylate is an iron chelator that binds free iron in a stable complex, preventing it from engaging in chemical reactions.


Deferoxamine is a parenterally administered iron chelating agent used to treat transfusion related chronic iron overload. Deferoxamine rarely causes serum aminotransferase elevations during therapy and has not been convincingly linked to instances of clinically apparent liver injury.|Deferoxamine Mesylate is the mesylate salt of an iron-chelating agent that binds free iron in a stable complex, preventing it from engaging in chemical reactions. Deferoxamine chelates iron from intra-lysosomal ferritin and ferrioxamine, a water-soluble complex excreted by the kidneys and in the feces via the bile. This agent does not readily chelate iron bound to transferrin, hemoglobin, myoglobin or cytochrome.|Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.

Deferoxamine mesylate Basic Attributes

656.79

752.329590

205-314-3

V9TKO7EO6K

756718|644468

DTXSID6037649

C417

Characteristics

269

white to off-white powder

148-149 °C

1061.9°C at 760 mmHg

538.5ºC

H2O: 50 mg/mL

−20°C

221.4 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

Safety Information

NONH for all modes of transport

2

22-24/25

UG5310000

RECONSTITUTED SOLN ARE STABLE FOR 2 WK @ ROOM TEMP /MESYLATE/

P201, P202, P261, P264, P271, P272, P280, P281, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P308+P313, P312, P321, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P403+P233, P405, P501

H315

|Danger|H315 (80%): Causes skin irritation [Warning Skin corrosion/irritation]|P201, P202, P261, P264, P271, P272, P280, P281, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P308+P313, P312, P321, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 9 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

In large clinical trials, elevations in serum aminotransferase levels were rare in patients receiving deferoxamine and instances of acute, clinically apparent liver injury were not reported. Patients with transfusion related iron overload often have concurrent chronic hepatitis B or C, and elevations of serum aminotransferase levels during chelation therapy may be due to natural fluctuations in the underlying chronic liver disease activity. Nevertheless, elevations in serum aminotransferase levels and “hepatic dysfunction” are listed as potential adverse events in product labels for deferoxamine. After an early report of hepatitis occurring in patient on hemodialysis receiving deferoxamine to reduce aluminum levels, there have been no further published instances of clinically apparent liver injury that have been convincingly linked to deferoxamine therapy.

Drug Information

Deferoxamine is a parenterally administered iron chelating agent used to treat transfusion related chronic iron overload. Deferoxamine rarely causes serum aminotransferase elevations during therapy and has not been convincingly linked to instances of clinically apparent liver injury.

Hematological Agents

Low-molecular-weight compounds produced by microorganisms that aid in the transport and sequestration of ferric iron. (The Encyclopedia of Molecular Biology, 1994) (See all compounds classified as Siderophores.)

Deferoxamine

Deferoxamine mesylate Use and Manufacturing

Uses

chelating agent (Fe & Al)

Human drugs -> Rare disease (orphan)|Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:656.8
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:23
Exact Mass:656.34147767
Monoisotopic Mass:656.34147767
Topological Polar Surface Area:269
Heavy Atom Count:44
Complexity:832
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Extract from the above information

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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