Triamcinolone Acetonide

Triamcinolone acetonide is a synthetic glucocorticoid, used in the symptomatic treatment of inflammation.

Triamcinolone Acetonide Chemical Structure

Triamcinolone Acetonide Chemical Structure

CAS: 76-25-5

Selleck's Triamcinolone Acetonide has been cited by 4 publications

Purity & Quality Control

Batch: Purity: 100%
100

Choose Selective Glucocorticoid Receptor Inhibitors

Biological Activity

Description Triamcinolone acetonide is a synthetic glucocorticoid, used in the symptomatic treatment of inflammation.
Targets
Glucocorticoid receptor [1]
In vitro
In vitro Triamcinolone Acetonide significantly decreases the paracellular permeability of ECV304 cells and down-regulated ICAM-1 expression, consistent with immunocytochemical observations. [1] Triamcinolone reverses the osmotic swelling of glial cells in retinas of the rat that is observed under various experimental conditions: in retinas isolated at 3 days after transient retinal ischemia, in retinas of eyes with lipopolysaccharide-induced ocular inflammation, and in control retinas in the presence of Ba2+ (1 mM), H2O2 (200 mM), arachidonic acid (10 mM), or prostaglandin E2 (30 nM). [2] Triamcinolone Acetonide reduces GAG synthesis compared to control and IL-1 alone. Triamcinolone Acetonide increases GAG degradation. Triamcinolone Acetonide increases media GAG content compared to control and IL-1 explants. [3]
In Vivo
In vivo Triamcinolone Acetonide (TAC), a synthetic glucocorticoid, induces cleft palate resulting from poor development of palatal shelves in mice. Triamcinolone Acetonide inhibits the proliferation of mesenchymal cells and affects the differentiation of MEE cells into stratified squamous epithelia in the palatal shelves of rat embryos. [4] Triamcinolone Acetonide reduces lameness, edema, and concentration of synovial fluid protein after the second LPS injection in horse. Triamcinolone Acetonide also induces higher WBC counts and mepivacaine concentrations in synovial fluid, compared with results for Mepivacaine alone. [5]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT04658836 Completed Vestibular Schwannoma Medical University of Vienna February 1 2020 Phase 1
NCT03378076 Completed Bilateral Knee Osteoarthritis Pacira Pharmaceuticals Inc December 6 2017 Phase 2
NCT03382262 Completed Osteoarthritis of the Shoulder|Osteoarthritis of the Hip Pacira Pharmaceuticals Inc December 18 2017 Phase 2

Chemical lnformation & Solubility

Molecular Weight 434.5 Formula

C24H31FO6

CAS No. 76-25-5 SDF Download Triamcinolone Acetonide SDF
Smiles CC1(OC2CC3C4CCC5=CC(=O)C=CC5(C4(C(CC3(C2(O1)C(=O)CO)C)O)F)C)C
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 87 mg/mL ( (200.23 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 13 mg/mL

Water : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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