Weight | 183.214 g/mol |
---|---|
Formula | C11H9N3 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 3 |
Rotatable Bonds | 0 |
2-Amino-9H-pyrido[2,3-b]indole (26148-68-5)
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- Bioactivation of the heterocyclic aromatic amine 2-amino-3-methyl-9H-pyrido [2,3-b]indole (MeAC) in recombinant test systems expressing human xenobiotic-metabolizing enzymes (Carcinogenesis, 2003)
- Induction of aberrant crypt foci in C57BL/6N mice by 2-amino-9H-pyrido [2,3-b]indole (AC) and 2-amino-3,8-dimethylimidazo [4,5-f]quinoxaline (MeIQx) (Cancer Letters, 1997)
- Probiotic mixture decreases DNA adduct formation in colonic epithelium induced by the food mutagen 2-amino-9H-pyrido[2,3-b]indole in a human-flora associated mouse model. (European Journal of Cancer Prevention, 2003)
- Metabolic activation of 2-amino-9H-pyrido[2,3-b]indole by rat-liver microsomes (Mutation Research, 1982)
- Identification of the major hepatic DNA adduct formed by the food mutagen 2-amino-9H-pyrido[2,3-b]indole (A alpha C). (Chemical Research in Toxicology, 1997)
- Dose-dependent formation of preneoplastic foci and DNA adducts in rat Liver with 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeAC) and 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine (PhIP) (Carcinogenesis, 1992)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C3=C(N2)N=C(C=C3)N
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InChIKeyFJTNLJLPLJDTRM-UHFFFAOYSA-N
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