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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
sub-chronic toxicity: oral
Type of information:
(Q)SAR
Adequacy of study:
weight of evidence
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Overall, (Q)SAR approaches are currently not well validated for repeated dose toxicity. (Guidance on IR/CSA, Section R7.5.4.1).
Justification for type of information:
QSAR prediction: migrated from IUCLID 5.6

Data source

Reference
Reference Type:
other: Predicted data
Title:
Unnamed
Year:
2016

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: REACH guidance on QSARs R.6, May/July2008
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
/-/-1α-Ethyl-1,2,3,4,6,7,12,12b α-octahydro-indolo[2,3-a]-quinolizine-1β-yl-ethyl-pyruvate oxime
EC Number:
617-734-8
Cas Number:
85647-38-7
Molecular formula:
C22H29N3O3
IUPAC Name:
/-/-1α-Ethyl-1,2,3,4,6,7,12,12b α-octahydro-indolo[2,3-a]-quinolizine-1β-yl-ethyl-pyruvate oxime

Results and discussion

Effect levels

Dose descriptor:
NOEL
Effect level:
10.9 mg/kg bw/day (nominal)
Based on:
other: Database: Repeated Dose Toxicity (HESS)
Basis for effect level:
other: Oral: gavage, rat

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion

Conclusions:
According to (Q)SAR modells: QSAR Toolbox, the predicted value indicated that Hydroxy-imino-ethyl-ester causes several toxic effects (target organ toxicity). The result meets the requirement of STOT-RE Category 2.