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Merck

567565

Sodium Stibogluconate

A pentavalent antimony compound that irreversibly inhibits protein tyrosine phosphatase (PTPase) activity, including Src homology PTPase-1 (SHP-1) (99% inhibition at ~11 µM) by forming a stable complex.

Sinónimos:

Sodium Stibogluconate, SSG, Antimony Sodium Gluconate, NaSbv, PTP Inhibitor XXIV, SHP1 Inhibitor IV

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Fórmula empírica (notación de Hill):
C12H17O17Sb2 · 3Na · 9H2O
Número CAS:
Peso molecular:
907.88
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥90% dry basis (≥30% Sb content, titration)
Form:
solid
Storage condition:
OK to freeze, desiccated, protect from light
Servicio técnico
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Quality Segment

description

Merck USA index - 14, 701

assay

≥90% dry basis (≥30% Sb content, titration)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, desiccated, protect from light

color

white

solubility

water: 1 mg/mL

shipped in

ambient

storage temp.

2-8°C

SMILES string

[Sb]2(=O)(O[C@@H]([C@@H]([C@@H](O2)C(=O)[O-])O)[C@H](O)CO)O[Sb]1(=O)O[C@@H]([C@@H]([C@@H](O1)C(=O)[O-])O)[C@H](O)CO.[Na+].[Na+].[Na+].O.O.O.O.O.O.O.O.O

InChI

1S/2C6H10O7.3Na.9H2O.3O.2Sb/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;;;;;;;;;;;;;;;;;/h2*2-5,7-8,10H,1H2,(H,12,13);;;;9*1H2;;;;;/q2*-2;3*+1;;;;;;;;;;;;;2*+2/p-2/t2*2-,3-,4+,5-;;;;;;;;;;;;;;;;;/m11................./s1

InChI key

CUEDNFKBTFCOSV-UZVLBLASSA-L

General description

A pentavalent antimony compound that forms a stable complex with and irreversibly inhibits Src homology protein tyrosine phosphatase (SHP-1) (99% inhibition at 11 µM). Also inhibits SHP-2 and PTP1B at an ~10-fold higher concentration (~110 µM). Does not inhibit the dual specificity protein tyrosine phosphatase (PTPase) or mitogen-activated protein kinase phosphatase-1 (MKP-1). Reported to induce general protein tyrosine phosphorylation and enhance IL-3-induced protein tyrosine phosphorylation of Jak2 and Stat5 in Baf3 cells. Also reported to augment IL-3-induced proliferation in Baf3 cells (ECmax = 44 µM) and GM-CSF-induced proliferation in TF-1 cells (ECmax = 55 µM). Exhibits anti-leishmanial effects.
A pentavalent antimony compound that irreversibly inhibits protein tyrosine phosphatase (PTPase) activity, including Src homology PTPase-1 (SHP-1) (99% inhibition at ~11 µM) by forming a stable complex. At higher concentrations (~110 µM), it inhibits SHP-2 and PTP1B activities.

Biochem/physiol Actions

Cell permeable: no
Primary Target
PTPase activity, including Src homology PTPase-1 (SHP-1)
Product does not compete with ATP.
Reversible: yes
Target IC50: ~11 µM causing 99% inhibition of protein tyrosine phosphatase (PTPase) activity, including Src homology PTPase-1 (SHP-1)

Packaging

Packaged under inert gas

Preparation Note

Heating to 75°C with constant stirring or constant stirring overnight at room temperature may be required for complete solubilization.
Unstable in solution; reconstitute just prior to use.

Other Notes

Wortmann, G., et al. 2002. Clin. Infect. Dis.35, 261.
Pathak, M.K. and Yi, T. 2001. J. Immunol.167, 3391.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)


Pictogramas

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Warning

Códigos de peligro

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2

Clase de almacenamiento

11 - Combustible Solids

¿Qué está pasando?

WGK 3

Punto de inflamación (°F)

Not applicable

Punto de inflamación (°C)

Not applicable



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