Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H11NO |
| Molecular Weight | 197.2325 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ONC1=CC=C2C(CC3=CC=CC=C23)=C1
InChI
InChIKey=JJCLXJPUTJMRTM-UHFFFAOYSA-N
InChI=1S/C13H11NO/c15-14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8,14-15H,7H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Aromatic amines in experimental cancer research: tissue-specific effects, an old problem and new solutions. | 2007-03 |
|
| Mass spectrometric investigation of the mechanism of inactivation of hamster arylamine N-acetyltransferase 1 by N-hydroxy-2-acetylaminofluorene. | 2004-03 |
|
| Preferential carcinogen-DNA adduct formation at codons 12 and 14 in the human K-ras gene and their possible mechanisms. | 2003-08-26 |
|
| Prostate expression of N-acetyltransferase 1 (NAT1) and 2 (NAT2) in rapid and slow acetylator congenic Syrian hamster. | 2003-03 |
|
| Effect of nucleotide substitutions in N-acetyltransferase-1 on N-acetylation (deactivation) and O-acetylation (activation) of arylamine carcinogens: implications for cancer predisposition. | 2002 |
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DTXSID50201045
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5895
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61M94X4V24
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2113
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53-94-1
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SUBSTANCE RECORD