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Merck

D9533

Deferoxamine mesylate salt

≥92.5% (TLC), powder, iron-chelating agent

Sinónimos:

DFX mesylate, DFOM, Deferoxamine methanesulfonate salt, Desferrioxamine mesylate salt

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Fórmula empírica (notación de Hill):
C25H48N6O8 · CH4O3S
Número CAS:
Peso molecular:
656.79
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
205-314-3
MDL number:
Assay:
≥92.5% (TLC)
Form:
powder
Servicio técnico
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Nombre del producto

Deferoxamine mesylate salt, ≥92.5% (TLC), powder

Quality Segment

assay

≥92.5% (TLC)

form

powder

color

white to off-white

solubility

H2O: 50 mg/mL

storage temp.

−20°C

SMILES string

CS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN

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)

InChI key

IDDIJAWJANBQLJ-UHFFFAOYSA-N

Application

Deferoxamine mesylate salt has been used



  • for cell pretreatment to assess its influenceon cell viability and its interactions with other compounds ()
  • to study the effect on Lipocalin 2(Lcn2) production triggered by amyloid-β(Aβ). ()
  • used to induce iron starvation in bacterial cultures.()

Biochem/physiol Actions

An iron chelator used often in the studies of cell proliferation and apoptosis. Also reported to induce p53.
An iron chelator used often in the studies of cell proliferation and apoptosis. Has been shown to have anti-proliferative effects on vascular smooth muscle cells in vitro and in vivo and to arrest cells in the G1 phase. Also reported to induce p53. Induces apoptosis in HL-60 cells by chelating iron. After 48 hrs treatment with 1μM deferoxamine, DNA fragmentation was apparent. Cells treated with 0.1 μM deferoxamine for as little as 24 hours were committed to apoptosis; by 48 hrs nuclear collapse was observed. In some studies it has been shown to have antioxidant properties and to protect cells against H2O2-induced damage.
Deferoxamine is used as a hypoxia-mimetic agent to stabilize Hypoxia Inducible Factor 1 (HIF-1). Deferoxamine stabilizes HIF-1 through the inhibition of Prolyl Hydroxylases (PHDs) which target HIF-1 through degradation. The mechanism of deferoxamine inhibition is likely through the chelation of Fe2+ bound to the active site of PHD which is required for enzymatic activity.


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Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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