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Merck

D1159

Sigma-Aldrich

Dexamethasone 21-phosphate disodium salt

≥98%

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100 MG
114,00 €
500 MG
344,00 €
1 G
573,00 €
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2300,00 €

114,00 €


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100 MG
114,00 €
500 MG
344,00 €
1 G
573,00 €
5 G
2300,00 €

About This Item

Fórmula empírica (notación de Hill):
C22H28FNa2O8P
Número de CAS:
Peso molecular:
516.40
Beilstein:
6473066
Número CE:
Número MDL:
Código UNSPSC:
51422340
ID de la sustancia en PubChem:
NACRES:
NA.25

114,00 €


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Ensayo

≥98%

Formulario

powder

impurezas

≤1% ethanol

color

white to off-white

temp. de almacenamiento

2-8°C

cadena SMILES

[Na+].[Na+].[H][C@@]12CCC3=CC(=O)C=C[C@]3(C)[C@@]1(F)[C@@H](O)C[C@@]4(C)[C@@]2([H])C[C@@H](C)[C@]4(O)C(=O)COP([O-])([O-])=O

InChI

1S/C22H30FO8P.2Na/c1-12-8-16-15-5-4-13-9-14(24)6-7-19(13,2)21(15,23)17(25)10-20(16,3)22(12,27)18(26)11-31-32(28,29)30;;/h6-7,9,12,15-17,25,27H,4-5,8,10-11H2,1-3H3,(H2,28,29,30);;/q;2*+1/p-2/t12-,15+,16+,17+,19+,20+,21+,22+;;/m1../s1

Clave InChI

PLCQGRYPOISRTQ-FCJDYXGNSA-L

Información sobre el gen

human ... NR3C1(2908)

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Aplicación

Dexamethasone 21-phosphate disodium salt has been used:
  • as a positive control to study its effects on ocular shedding of herpes simplex virus type 1 (HSV-1) in the induced reactivation (IR) and spontaneous shedding (SS) rabbit models[1]
  • as a receptor analog to study its effects on glucocorticoid receptor activation in suprachiasmatic nuclei (SCN)-lesioned mice[2]
  • to study its protective effects against cisplatin-induced ototoxicity in the inner ear of guinea pigs[3]

Acciones bioquímicas o fisiológicas

Dexamethasone 21-phosphate (Dex 21-P) is a pro-drug[4] that can undergo dephosphorylation to form dexamethasone with the help of intra-erythrocyte enzymes.[5] It exhibits therapeutic effects against cystic fibrosis[4] and postoperative cataract.[6] Dex 21-P disodium salt is a synthetic adrenal corticosteroid and possesses anti-inflammatory activity.[6]

Pictogramas

Health hazardExclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Acute Tox. 4 Oral - Repr. 2

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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Morena B Sant'Anna et al.
Scientific reports, 6, 26955-26955 (2016-05-28)
Peripheral neuropathic pain is a consequence of an injury/disease of the peripheral nerves. The mechanisms involved in its pathophysiology are not entirely understood. To better understand the mechanisms involved in the development of peripheral nerve injury-induced neuropathic pain, more experimental
Kang Ho Kim et al.
Molecular endocrinology (Baltimore, Md.), 30(8), 905-916 (2016-06-30)
Liver fibrosis is a reversible wound-healing process that is protective in the short term, but prolonged fibrotic responses lead to excessive accumulation of extracellular matrix components that suppresses hepatocyte regeneration, resulting in permanent liver damage. Upon liver damage, nonparenchymal cells
Parawee Rattanakit et al.
International journal of pharmaceutics, 422(1-2), 254-263 (2011-11-22)
A novel extrusion printing system was used to create drug delivery structures wherein dexamethasone-21-phosphate disodium salt (Dex21P) was encapsulated within a biodegradable polymer (PLGA) and water soluble poly(vinyl alcohol) (PVA) configurations. The ability to control the drug release profile through
Andrew M McMillan et al.
BMJ (Clinical research ed.), 344, e3260-e3260 (2012-05-24)
To investigate the effectiveness of ultrasound guided corticosteroid injection in the treatment of plantar fasciitis. Randomised, investigator and participant blinded, placebo controlled trial. University clinic in Melbourne, Australia. 82 people with a clinical and ultrasound diagnosis of plantar fasciitis unrelated
Amy E Cohen et al.
Ophthalmology, 119(1), 66-73 (2011-11-26)
Determine safe, effective, iontophoretic dose(s) of EGP-437 (dexamethasone phosphate formulated for iontophoresis) in patients with noninfectious anterior uveitis; evaluate systemic drug exposures. Prospective, phase I/II, multicenter, double-masked, parallel group, randomized clinical trial. Forty outpatients with anterior uveitis. Forty of 42

Preguntas

  1. We planned to dissolve it into saline and use to to inject as prenatal stressor to Sprague-Dawley rats via IP way. What is the solubility? I want to dissolve 100µg and 200µg into 10ml of saline. After dissolving what is the shelf life of that solution?

    1 respuesta
    1. The solubility of this produst is tested in water at 50 mg/mL The solubility in saline has not been tested, however rates are expected to be similar. The solution stability has not been determined. Other sources state that solutions are stable for up to 1 month when stored in aliquots at -20°C.

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