Prednisolone

Synonyms: NSC-9900

Prednisolone is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties.

Prednisolone Chemical Structure

Prednisolone Chemical Structure

CAS: 50-24-8

Selleck's Prednisolone has been cited by 14 Publications

2 Customer Reviews

Purity & Quality Control

Batch: Purity: 99.97%
99.97

Choose Selective Glucocorticoid Receptor Inhibitors

Biological Activity

Description Prednisolone is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties.
Targets
Glucocorticoid receptor [1]
In vitro
In vitro

Prednisolone (50 mg/kg, im) given 15 min before LPS-attenuated production of NO2- and NO3- by neutrophils and suppresses LPS-stimulated mRNA for NOS II in rat neutrophils. [1] Prednisolone reduces joint swelling through a mechanism associated with a reduction in IL-1beta and IL-6 protein and mRNA expression levels in SCW-induced arthritis rats. [2] Prednisolone's anti-inflammatory effects can be mediated by reducing cellular adhesion molecule (CAM) expression. Prednisolone (0.75 mg/kg) reduces macrophages (-59%, -57%), CD4(+) T-cells (-50%, -60%), CD8(+) T-cells (-58%, -48%), and eosinophils (-36%, -25%) in quadriceps and soleus muscles, respectively. Prednisolone-treated mice also exhibits decreased vascular P-selectin (-82%) and ICAM-1 (-52%) expression and fewer L-selectin (-79%) and ICAM-1 (-57%) expressing mononuclear cells in quadriceps. Prednisolone reduces sarcolemmal damage and degeneration as well in Dystrophin-deficient, mdx mice. [3]

In Vivo
In vivo

Prednisolone (5 mg/kg) causes alterations in diaphragmatic contractile properties and histological changes without fiber atrophy in rats. Prednisolone results in an increased number of diaphragmatic bundles in rats. [4] Prednisolone induces a significant decline of PL-pO2, while CoBF, CMs, CAPs, and ABRs revealed no change in guinea pigs. [5]

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06119529 Not yet recruiting Healthy|Atopic Dermatitis Eli Lilly and Company November 1 2023 Phase 1
NCT05986422 Recruiting Post-COVID-19 Syndrome Charite University Berlin Germany October 1 2023 Phase 2
NCT06066814 Not yet recruiting Acute on Chronic Liver Failure Institute of Liver and Biliary Sciences India October 7 2023 --
NCT05984381 Recruiting Bullous Pemphigoid All India Institute of Medical Sciences Bhubaneswar August 1 2023 Phase 4

Chemical lnformation & Solubility

Molecular Weight 360.44 Formula

C21H28O5

CAS No. 50-24-8 SDF Download Prednisolone SDF
Smiles CC12CC(C3C(C1CCC2(C(=O)CO)O)CCC4=CC(=O)C=CC34C)O
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 72 mg/mL ( (199.75 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 40 mg/mL

Water : Insoluble


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In vivo
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In vivo Formulation Calculator

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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.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, 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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