Betamethasone

For research use only.

Catalog No.S1500 Synonyms: NSC-39470, SCH-4831

Betamethasone  Chemical Structure

CAS No. 378-44-9

Betamethasone (NSC-39470, SCH-4831) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties.

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10mM (1mL in DMSO) USD 130 In stock
USD 97 In stock
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Biological Activity

Description Betamethasone (NSC-39470, SCH-4831) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties.
Targets
Glucocorticoid receptor [1]
()
In vitro

Betamethasone has a specific affinity for type II glucocorticoid receptors which are present in most brain regions. [1]

In vivo Betamethasone has direct vasoconstrictor effects on peripheral femoral resistance vessels in late gestation fetal sheep. Betamethasone exposure decreases cerebral blood flow (CBF) in all brain regions measured except the hippocampus after 24 hours of infusion in sheep. [1] Betamethasone reduces the activation of NF-kappaB and elevation of TNFalpha and IL-1beta, and induces the expression of IL-10 in the brain, all of which correlate with the changes of pain thresholds in rats. [2] Betamethasone exposure reduces synaptophysin-LI in the frontal neocortex, caudate putamen and hippocampus by 46.9%, 41.0% and 55.4%, respectively, that is not accompanied by irreversible neuronal damage in the fetal sheep brain. [3] Betamethasone modestly increases cytidylyltransferase (CT) mRNA, but does not alter the levels of immunoreactive enzyme in adult rat lung. Betamethasone decreases the activities of the sphingomyelin hydrolases: acid sphingomyelinase by 33% and of alkaline ceramidase by 21%. [4] Betamethasone injected at the time of nerve injury partially inhibits the development of neuropathic hyperalgesia and reduces the subsequent elevated levels of pro-inflammatory cytokines in the brain of rats, while stimulating the expression of the anti-inflammatory cytokine IL-10. [5]

Protocol

Solubility (25°C)

In vitro DMSO 79 mg/mL (201.29 mM)
Water Insoluble
Ethanol '10 mg/mL

* 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 392.46
Formula

C22H29FO5

CAS No. 378-44-9
Storage powder
in solvent
Synonyms NSC-39470, SCH-4831
Smiles CC1CC2C3CCC4=CC(=O)C=CC4(C3(C(CC2(C1(C(=O)CO)O)C)O)F)C

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Clinical Trial Information

NCT Number Recruitment interventions Conditions Sponsor/Collaborators Start Date Phases
NCT04492072 Not yet recruiting Drug: Oxytocin|Drug: Misoprostol Cesarean Section|Misoprostol|Oxytocin|High Risk Pregnancy Thomas Jefferson University July 23 2020 Not Applicable
NCT04212312 Not yet recruiting -- Twin; Complicating Pregnancy Rambam Health Care Campus February 1 2020 --
NCT03979196 Recruiting Other: Inpatient Management|Other: Outpatient Management Preterm Birth|Pregnancy High Risk Sunnybrook Health Sciences Centre|North York General Hospital June 6 2019 Not Applicable
NCT03476746 Completed Drug: LEO 90100 foam|Drug: Dovobet® ointment Healthy LEO Pharma March 20 2018 Phase 1
NCT03462927 Completed Drug: MC2-01 Cream|Drug: CAL/BDP combination Psoriasis Vulgaris MC2 Therapeutics February 8 2018 Phase 2

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Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID