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. Author manuscript; available in PMC: 2012 Feb 14.
Published in final edited form as: Environ Mol Mutagen. 2011 Apr 27;52(7):547–561. doi: 10.1002/em.20656

Table II.

Known Rodent Carcinogenicity and Genotoxicity of Compounds Selected for Additional Investigation1

Compound2 CASRN Purity Rodent Carcinogenicity In Vitro Mammalian Cell Genotoxicity3 Ames Test Mutagenicity3 Known DNA repair pathway (Reference)
Actinomycin D 50-76-0 98% Yes positive negative Nbs1 (Porcedda et al., 2006)
Adriamycin 25316-40-9 98% Yes positive positive NER, HR (Spencer et al., 2008)
Alachlor 15972-60-8 99.2% Yes positive - Excision repair (Surrallés et al., 1995)
Benzotrichloride 98-07-7 98% Yes positive negative4 none
Diglycidyl resorcinol ether 101-90-6 94% Yes positive positive none
Lovastatin 75330-75-5 ≥98% Yes negative negative none
Melphalan 148-82-3 95% Yes positive positive Fanconi anemia pathway (Nojima et al., 2005)
Trans-1,4-Dichloro-2-butene 110-57-6 98% Yes positive positive none
Tris(2,3-epoxypropyl)isocyanurate 2451-62-9 99.5 % Yes positive positive none
2-Aminothiamine 96-50-4 >90% Yes positive negative4 none
1

Abbreviations: CASRN = Chemical Abstracts Registry Service Number, ICL = interstrand cross-linking, Nbs1/p70 = Nijmegen breakage syndrome, NHEJ = non-homologous end joining.

2

Diglycidyl resorcinol ether was purchased from Alpha Aesar; the other compounds were purchased from Sigma-Aldrich, except that lovastatin was purchased from Sigma-Aldrich and then again from ENZO Life Science.

3

In vitro mammalian cell genotoxicity (e.g., tests for chromosomal aberrations, sister chromatid exchanges, or micronuclei in cultured Chinese hamster cells or mitogen-stimulated human lymphocytes, mutagenicity in mouse lymphoma cells) and Ames mutagenicity test results only in the absence of metabolic activation; test results were obtained from EPA ACToR and United States National Library of Medicine; TOXNET.

4

Positive in the presence of metabolic activation.