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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Developmental toxicity / teratogenicity

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Administrative data

Endpoint:
developmental toxicity
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: RTECS data are peer-reviewed.

Data source

Reference
Reference Type:
secondary source
Title:
Reproductive data (RTECS Number: KI7968000)
Author:
RTECS
Year:
1990
Bibliographic source:
http://ccinfoweb2.ccohs.ca/rtecs/Action.lasso?-database=rtecs&-layout=Display&-response=detail.html&-op=eq&RTECS+NUMBER=KI7968000&-search

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Mesna was administered to rats intravenously during days 7-17 of gestation. Lactating females were exposed 21 days post-birth. Effects on newborns and foetotoxicity effects were evaluated.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Mesna
EC Number:
243-285-9
EC Name:
Mesna
Cas Number:
19767-45-4
Molecular formula:
C2H6O3S2.Na
IUPAC Name:
sodium 2-sulfanylethanesulfonate

Test animals

Species:
rat

Results and discussion

Results: maternal animals

Effect levels (maternal animals)

Remarks on result:
not measured/tested

Results (fetuses)

Effect levels (fetuses)

Dose descriptor:
dose level: TDLo
Effect level:
10 400 mg/kg bw (total dose)
Basis for effect level:
other: fetotoxicity

Fetal abnormalities

Abnormalities:
not specified

Overall developmental toxicity

Developmental effects observed:
not specified

Applicant's summary and conclusion

Conclusions:
The lowest toxic dose (TDLo) of 10400 mg/kg bw (total dose) was reported for mesna.
Executive summary:

Mesna was administered to female rats intravenously during days 7-17 of gestation and effects on newborn rats and foetotoxicity were evaluated.

Mesna caused no deaths of foetuses. One stunted foetus was observed. Physical effects on newborns were reported (without details). The lowest toxic dose ((TDLo) of 10400 mg/kg bw (total dose) was reported.

Mesna is a suitable Read-Across substance for SPS as Dimesna and Mesna could be considered a metabolite of each other, which allows the conclusion that the same also applies for SPS and MPS, and their respective alkyl side chains differ only in one –CH2- group. This is in detail outlined in the read-across justification. Hence, it can be concluded that the derived results are applicable for SPS, too.