Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
grey literature
Title:
Methylprednisolone, Summary Report (2001)
Author:
European Medicines Agency (EMEA), The European Agency for the Evaluation of Medicinal Products, Veterinary Medicines Evaluation Unit, Committee for Veterinary Medicinal Products
Year:
2001
Bibliographic source:
HSDB data base; http://www.emea.europa.eu/pdfs/vet/mrls/079801en.pdf

Materials and methods

Principles of method if other than guideline:
Guideline not available
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Methylprednisolone
EC Number:
201-476-4
EC Name:
Methylprednisolone
Cas Number:
83-43-2
Molecular formula:
C22H30O5
IUPAC Name:
11,17,21-trihydroxy-6-methylpregna-1,4-diene-3,20-dione

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
not specified

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU