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.
D1159
Dexamethasone 21-phosphate disodium salt
≥98%, Glucocorticoid , powder
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Wybierz wielkość
100 MG
316,00 zł
500 MG
980,00 zł
1 G
1394,00 zł
5 G
5390,00 zł
316,00 zł
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C22H28FNa2O8P
Numer CAS:
Masa cząsteczkowa:
516.40
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
51422340
EC Number:
219-243-0
MDL number:
Beilstein/REAXYS Number:
6473066
Przejdź do
Pomoc techniczna
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Pozwól nam pomócNazwa produktu
Dexamethasone 21-phosphate disodium salt, ≥98%
InChI key
PLCQGRYPOISRTQ-FCJDYXGNSA-L
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
SMILES string
[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
assay
≥98%
form
powder
impurities
≤1% ethanol
color
white to off-white
storage temp.
2-8°C
Quality Level
Gene Information
human ... NR3C1(2908)
Powiązane kategorie
1 of 4
Ta pozycja | |||
|---|---|---|---|
| assay ≥98% | assay ≥99% | assay ≥97% | assay ≥98% (HPLC) |
| form powder | form powder | form powder | form powder |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. room temp | storage temp. 2-8°C |
| color white to off-white | color - | color - | color off-white |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 200 |
| impurities ≤1% ethanol | impurities - | impurities - | impurities - |
Application
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]
Biochem/physiol Actions
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]
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Repr. 2
Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Bouledjouidja A, et al.
Journal of Supercritical Fluids, 130, 63-75 (2017)
Donal T Skelly et al.
Molecular psychiatry, 24(10), 1533-1548 (2018-06-08)
Systemic inflammation can impair cognition with relevance to dementia, delirium and post-operative cognitive dysfunction. Episodes of delirium also contribute to rates of long-term cognitive decline, implying that these acute events induce injury. Whether systemic inflammation-induced acute dysfunction and acute brain
Marieke Veurink et al.
Pharmaceutical research, 30(4), 1176-1187 (2013-02-16)
To investigate the mechanism behind the aggregation breaking properties of dexamethasone phosphate and related corticosteroids on the IgG1 antibody bevacizumab (Avastin®). An in silico 3D dimer model is developed to identify the bevacizumab-bevacizumab interface, and different corticosteroids are docked onto
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
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
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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?
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