n-benzoyloxy-n-methyl-4-aminoazobenzene has been researched along with 2-acetylaminofluorene in 1 studies
*2-Acetylaminofluorene: A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines. [MeSH]
*2-Acetylaminofluorene: A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Miller, EC; Miller, JA; Tarpley, WG | 1 |
1 other study(ies) available for n-benzoyloxy-n-methyl-4-aminoazobenzene and 2-acetylaminofluorene
| Article | Year |
|---|---|
Rapid release of carcinogen-guanine adducts from DNA after reaction with N-acetoxy-2-acetylaminofluorene or N-benzoyloxy-N-methyl-4-aminoazobenzene.
Topics: 2-Acetylaminofluorene; Acetoxyacetylaminofluorene; Azo Compounds; Carbon Radioisotopes; Carcinogens; DNA; p-Aminoazobenzene | 1982 |