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Dexamethasone acetate
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Dexamethasone acetate
CAS No. : 1177-87-3
MCE 站:Dexamethasone acetate
产品活性:Dexamethasone acetate (Dexamethasone 21-acetate) 是糖皮质素类甾体化合物,有抗炎和免疫抑制活性。Dexamethasone acetate 可用于眼部感染的研究。
研究领域:GPCR/G Protein | Autophagy | Anti-infection
作用靶点:Glucocorticoid Receptor | Autophagy | Mitophagy | Bacterial
In Vitro: Dexamethasone acetate (Dexamethasone 21-acetate) 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: It has previously been reported that treatment with Dexamethasone acetate (Dexamethasone 21-acetate) 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.
相关产品:Drug Repurposing Compound Library Plus | FDA-Approved Drug Library Plus | FDA-Approved Drug Library Mini | Bioactive Compound Library Plus | Anti-Infection Compound Library | GPCR/G Protein Compound Library | Immunology/Inflammation Compound Library | FDA-Approved Drug Library | Anti-Cancer Compound Library | CNS-Penetrant Compound Library | Autophagy Compound Library | Anti-Aging Compound Library | Drug Repurposing Compound Library | Endocrinology Compound Library | Antibacterial Compound Library | NMPA-Approved Drug Library | Orally Active Compound Library | FDA Approved & Pharmacopeial Drug Library | 3-Methyladenine | Doxorubicin hydrochloride | Bafilomycin A1 | Puromycin dihydrochloride | SB 203580 | Deferoxamine mesylate | Staurosporine | Dexamethasone | Metformin hydrochloride | U0126-EtOH | Doxycycline (hyclate) | Actinomycin D | G-418 disulfate | 5-Azacytidine | Etoposide | Mitomycin C | CCCP | AICAR | Nigericin sodium salt | Hydrocortisone | Brefeldin A | Resveratrol | Quercetin | Melatonin | Tunicamycin | Hygromycin B | Tacrolimus | Ionomycin | Curcumin | Valproic acid
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