Hydroxyacetylaminofluorene
Chemical compound
From Wikipedia, the free encyclopedia
Hydroxyacetylaminofluorene is a derivative of 2-acetylaminofluorene used as a biochemical tool in the study of carcinogenesis.
| Names | |
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| Preferred IUPAC name
N-(9H-Fluoren-2-yl)-N-hydroxyacetamide | |
| Other names
N-Hydroxy-2-acetamidofluorene; Hydroxyfluorenylacetamide | |
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| Properties | |
| C15H13NO2 | |
| Molar mass | 239.27 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Biochemistry
N-hydroxy-2-acetamidofluorene reductase is an enzyme that catalyzes the conversion of the carcinogen, hydroxyacetylaminofluorene to 2-acetylaminofluorene. It uses reduced nicotinamide adenine dinucleotide (NADH) as its cofactor.[1][2]

