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BP987

Desferrioxamine mesilate

British Pharmacopoeia (BP) Reference Standard

Synonim(y):

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

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Do Państwa/SKUDostępnośćCena netto
30 mg
Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności
1010,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C25H48N6O8 · CH4O3S
Numer CAS:
Masa cząsteczkowa:
656.79
UNSPSC Code:
41116107
NACRES:
NA.24
MDL number:

1010,00 zł


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grade

pharmaceutical primary standard

agency

BP

API family

desferrioxamine

form

solid

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

BP

application(s)

pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

2-8°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

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Desferrioxamine mesilate BP Reference standard, intended for use in laboratory tests only as specifically prescribed in the British Pharmacopoeia.

Also used in monographs such as:
  • Desferrioxamine Injection
  • 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.

    Packaging

    Unit quantity: 30 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia

    Other Notes

    Sales restrictions may apply.
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    manufacturer/tradename

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    grade

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    grade

    pharmaceutical primary standard

    grade

    pharmaceutical primary standard

    grade

    -

    form

    solid

    form

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    form

    -

    form

    powder

    application(s)

    pharmaceutical
    pharmaceutical small molecule

    application(s)

    pharmaceutical (small molecule)

    application(s)

    pharmaceutical (small molecule)

    application(s)

    -

    format

    neat

    format

    neat

    format

    neat

    format

    -

    shelf life

    limited shelf life, expiry date on the label

    shelf life

    -

    shelf life

    -

    shelf life

    -


    Klasa składowania

    11 - Combustible Solids

    wgk

    WGK 2

    flash_point_f

    Not applicable

    flash_point_c

    Not applicable



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