Dexamethasone Phosphate disodium NEW
| Price | $30 | $41 |
| Package | 50mg | 100mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2024-11-19 |
Product Details
| Product Name: Dexamethasone Phosphate disodium | CAS No.: 2392-39-4 |
| Purity: 99.88% | Supply Ability: 10g |
| Release date: 2024/11/19 |
Product Introduction
Bioactivity
| Name | Dexamethasone Phosphate disodium |
| Description | Dexamethasone Phosphate disodium (EGP437. Dex-Phos) is a water-soluble form of the synthetic glucocorticoid dexamethasone. |
| In vitro | Dexamethasone regulates multiple transcription factors, including activator protein-1, nuclear factor-AT, and nuclear factor-kB, resulting in the activation and repression of key genes involved in the inflammatory response[1]. 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 | Administering Dexamethasone at 2×5 mg/kg effectively reduces lipopolysaccharide (LPS)-induced inflammation. This treatment, particularly a single 10 mg/kg dose (i.p.), significantly lessens granulocyte mobilization and the spontaneous production of oxygen radicals in comparison to animals exposed to LPS and treated with saline. These benefits are pronounced when Dexamethasone is given both 1 hour before and after LPS inhalation, with granulocyte numbers in BALF dropping to those seen in healthy animals (exposed to an aerosol of water)[3]. However, rats receiving Dexamethasone show reduced food consumption and weight compared to control rats, and exhibit lower weights even compared to pair-fed rats with similar food intakes. Continuous Dexamethasone treatment for five days results in notable liver enlargement (+42%) and an increased liver-to-body weight ratio (+65%), while the gastrocnemius muscle's wet weight diminishes by 20% without affecting the muscle to body weight ratio (g/100 g body weight), suggesting muscle weight reduction aligns with overall body weight loss. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility Information | H2O : 100 mg/mL (193.65 mM) DMSO : 1 mg/mL (1.94 mM), Sonication and heating to 80℃ are recommended. |
| Keywords | Dexamethasone Phosphate disodium | Dexamethasone Phosphate | Glucocorticoid Receptor | 55203-24-2 | inhibit | Inhibitor | Dexamethasone 21-phosphate disodium | EGP437 |
| Inhibitors Related | Hydrocortisone | Mifepristone | Corticosterone |
| Related Compound Libraries | Bioactive Compound Library | EMA Approved Drug Library | Drug Repurposing Compound Library | FDA-Approved Drug Library | Anti-Cancer Approved Drug Library | Bioactive Compounds Library Max |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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