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Triamcinolone acetonide

SKU: orb1310263

Description

Triamcinolone acetonide (Azmacort) is a synthetic glucocorticoid that acts as a corticosteroid receptor agonist, primarily used for its potent anti-inflammatory effects. It is widely applied in research models of dermatological, allergic, and autoimmune conditions, both in vitro for receptor studies and in vivo for evaluating anti-inflammatory efficacy.

Research Area

Cardiovascular Research, Metabolism Research, Signal Transduction

Images & Validation

Key Properties

CAS Number76-25-5
MW434.50
Purity99.91%
FormulaC24H31FO6
SMILESC(CO)(=O)[C@]12[C@]3(C)[C@@](C[C@]1(OC(C)(C)O2)[H])([C@]4([C@](F)([C@@H](O)C3)[C@]5(C)C(CC4)=CC(=O)C=C5)[H])[H]
TargetFGFR,Glucocorticoid Receptor
SolubilityEthanol:13 mg/mL (29.92 mM);DMSO:50 mg/mL (115.07 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (4.6 mM)

Bioactivity

In Vivo
Triamcinolone Acetonide reduced polysaccharide synthesis and increased the glycosaminoglycan (GAG) content in the culture medium compared to the blank group and IL-1 group. It also augmented GAG degradation. This compound significantly decreased the paracellular permeability of ECV304 cells and downregulated ICAM-1 expression, corroborating with immunocytochemical observations. In rat retinas, Triamcinolone reversed Müller glial cell swelling, a phenomenon observed under various experimental conditions: in retinas isolated 3 days post-transient retinal ischemia, in control retinas with 1 mM Ba^2+, 10 μM arachidonic acid, 200 μM H2O2, or 30 nM prostaglandin E2, and in retinas with lipopolysaccharide-induced ocular inflammation.
In Vitro
In horses subjected to a second injection of lipopolysaccharide, Triamcinolone Acetonide reduced edema, lameness, and joint fluid protein concentration. In mice, Triamcinolone Acetonide, a synthetic glucocorticoid, induced cleft palate resulting from impaired palatal development. In the jaws of rat embryos, Triamcinolone Acetonide inhibited the proliferation of mesenchymal cells and affected the differentiation of MEE (Medial Edge Epithelium) cells into stratified squamous epithelial cells. Compared to methoxycarbonyl alone, Triamcinolone Acetonide increased both the white blood cell count and methoxycarbonyl concentration in the synovial fluid.

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

inhibit, Inhibitor, GlucocorticoidReceptor, Glucocorticoid Receptor, Azmacort, Aristoderm, Aristogel, Triamcinolone acetonide

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Key Properties

No computed properties available.

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Triamcinolone acetonide (orb1310263)

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Available Sizes

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50 mg
¥ 910.00
1 ml x 10 mM (in DMSO)
¥ 1,170.00
DispatchUsually dispatched within 3-5 working days
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