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Dexamethasone Phosphate disodium

CAS No. 2392-39-4

Dexamethasone Phosphate disodium ( EGP-437; EGP 437; EGP437. Dex-Phos )

Catalog No. M26007 CAS No. 2392-39-4

Dexamethasone disodium phosphate is a water-soluble form of the synthetic glucocorticoid dexamethasone.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Dexamethasone Phosphate disodium
  • Note
    Research use only, not for human use.
  • Brief Description
    Dexamethasone disodium phosphate is a water-soluble form of the synthetic glucocorticoid dexamethasone.
  • Description
    Dexamethasone disodium phosphate is a water-soluble form of the synthetic glucocorticoid dexamethasone.(In Vitro):Dexamethasone regulates several transcription factors, including activator protein-1, nuclear factor-AT, and nuclear factor-kB, leading to the activation and repression of key genes involved in the inflammatory response. Dexamethasone potently inhibits granulocyte-macrophage colony stimulating factor (GM-CSF) release from A549 cells with EC50 of 2.2 nM. Dexamethasone (EC50=36 nM) induces transcription of the β2-receptor is found to correlate with glucocorticoid receptor (GR) DNA binding and occurred at 10-100 fold higher concentrations than the inhibition of GM-CSF release. Dexamethasone (IC50=0.5 nM) inhibits a 3×κB (NF-κB, IκBα, and I-κBβ), which is associated with inhibition of GM-CSF release.(In Vivo):Treatment with Dexamethasone at a dose of 2×5 mg/kg efficiently inhibits lipopolysaccharide (LPS)-induced inflammation. In our experimental system, treatment with a single dose of Dexamethasone 10 mg/kg (i.p.) significantly decreases recruitment of granulocytes as well as spontaneous production of oxygen radicals compared with animals expose to LPS and injected with solvent alone (saline). The effects are statistically significant when administered both 1 h before and 1 h after inhalation of LPS. The number of granulocytes in BALF decreased to levels comparable to healthy animals (given an aerosol of water). Rats treated with Dexamethasone consume less food and weighed less than control rats. Treated rats also weigh less than pair-fed animals though their food intake is similar. Five days of Dexamethasone injection result in a significant increase in both the liver mass (+42%) and the liver to body weight ratio (+65%). The wet weight of gastrocnemius muscle decreases 20% after 5 days of treatment, but it remains unaffected relative to body weight (g/100 g body weight), indicating that muscle weight loss paralleled body weight loss.
  • Synonyms
    EGP-437; EGP 437; EGP437. Dex-Phos
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    MRGPRX1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2392-39-4
  • Formula Weight
    516.4
  • Molecular Formula
    C22H28FNa2O8P
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    [Na+].[Na+].C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)COP([O-])([O-])=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Prchalová E, et al. Discovery of Benzamidine- and 1-Aminoisoquinoline-Based Human MAS-Related G-Protein-Coupled Receptor X1 (MRGPRX1) Agonists. J Med Chem. 2019 Sep 26;62(18):8631-8641.
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