Mometasone furoate

Catalog No.S1987 Synonyms: SCH-32088

Mometasone furoate Chemical Structure

Molecular Weight(MW): 521.43

Mometasone Furoate is a glucocorticoid receptor agonist, used topically to reduce inflammation of the skin or in the airways.

Size Price Stock Quantity  
In DMSO USD 90 In stock
USD 70 In stock
USD 170 In stock
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Biological Activity

Description Mometasone Furoate is a glucocorticoid receptor agonist, used topically to reduce inflammation of the skin or in the airways.
Targets
Glucocorticoid receptor [1]
In vitro

Mometasone furoate efficiently suppresses production of cytokines including interleukin (IL)-4, IL-5, and interferon-gamma in anti-CD3-stimulated human CD4+ T cells. Mometasone furoate effectively inhibits the activation of Th cells including type 2 Th (Th2) in the draining LN, thus leading to the suppression of the IgE response. [1]

In vivo Mometasone causes a decrease in the instances of nasal rubbing and an inhibition of this response is observed during the treatment period in rats. [2] Mometasone (3 mg/kg) inhibits the increased airway sensitivity to aerosolized methacholine at the highest dose tested in mice. Mometasone, given an hour after the last allergen challenge, dose-dependently inhibits the allergen-induced increase in Penh with about a 10-fold loss of potency when compared with the pre-challenge treatment schedule. [3] Mometasone furoate (0.02%) and fluticasone propionate (0.1%) significantly inhibits the increase of antigen-induced nasal rubbing even 6 hours after topical application, indicating that both drugs have a long-lasting effect. [4] Mometasone furoate dose-dependently inhibits the elevated eosinophil numbers in the bronchoalveolar lavage fluid and lung tissues of sensitized, ovalbumin challenged mice. Mometasone furoate (33 mg/kg) reduces the percentage of CD44+ T-helper cells (activated/memory cells) to the levels observed in non-sensitized, ovalbumin-challenged mice. [5]

Protocol

Solubility (25°C)

In vitro DMSO 6 mg/mL (11.5 mM)
Water Insoluble
Ethanol Insoluble

* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

Chemical Information

Molecular Weight 521.43
Formula

C27H30Cl2O6

CAS No. 83919-23-7
Storage powder
Synonyms SCH-32088

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Clinical Trial Information

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT02953379 Not yet recruiting Allergic Rhinitis EMS September 2017 Phase 3
NCT02953366 Not yet recruiting Allergic Rhinitis EMS September 2017 Phase 3
NCT02588326 Not yet recruiting Hypersensitivity University of Florida July 2017 Phase 1
NCT02967731 Not yet recruiting Chronic Sinusitis 480 Biomedical, Inc. January 2017 Phase 1
NCT03011632 Not yet recruiting Sinusitis|Asthma Medical Universtity of Lodz January 2017 Phase 4
NCT02912468 Recruiting Nasal Polyps Sanofi|Regeneron Pharmaceuticals December 2016 Phase 3

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Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID