Weight | 223.275 g/mol |
---|---|
Formula | C15H13NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
4-Acetamidofluorene (28322-02-3)
4-acetylaminofluorene · 4-AAF
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- Mutations and Decreases in Density of Transforming DNA Produced by Derivatives of the Carcinogens 2-Acetylaminofluorene and N-Methyl-4-aminoazobenzene (Molecular Pharmacology, 1968)
- Protection by beverages, fruits, vegetables, herbs, and flavonoids against genotoxicity of 2-acetylaminofluorene and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in metabolically competent V79 cells. (Mutation Research-genetic Toxicology and Environmental Mutagenesis, 2002)
- Formation and removal of DNA adducts in rat liver treated with N-hydroxy derivatives of 2-acetylaminofluorene, 4-acetylaminobiphenyl, and, 2-acetylaminophenanthrene (Carcinogenesis, 1984)
- -Fetoprotein-containing cells in the early stages of liver carcinogenesis induced by 3-methyl-4-dimethyl-aminoazobenzene and 2-acetylaminofluorene (International Journal of Cancer, 1977)
- Molecular modelling of cytochrome CYP1A1: a putative access channel explains differences in induction potency between the isomers benzo(a)pyrene and benzo(e)pyrene, and 2- and 4-acetylaminofluorene (Toxicology Letters, 1994)
- Rapid release of carcinogen-guanine adducts from DNA after reaction with N-acetoxy-2-acetylaminofluorene or N-benzoyloxy-N-methyl-4-aminoazobenzene (Carcinogenesis, 1982)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-acetylaminofluorene
- 4-AAF
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SMILESCC(=O)NC1=CC=CC2=C1C3=CC=CC=C3C2
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InChIKeyPHPWISAFHNEMSR-UHFFFAOYSA-N
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