Weight | 138.126 g/mol |
---|---|
Formula | C6H6N2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Nicotinamide N-oxide (1986-81-8)
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- Involvement of liver aldehyde oxidase in the reduction of nicotinamide N-oxide. (Biochemical and Biophysical Research Communications, 1984)
- Catalysis of the Direct Transfer of Oxygen from Nicotinamide N-Oxide to Xanthine by Xanthine Oxidase (Journal of Biological Chemistry, 1966)
- The Reduction of Nicotinamide N-Oxide by Xanthine Oxidase (Journal of Biological Chemistry, 1966)
- The metabolism of nicotinamide-N-oxide. (Biochimica et Biophysica Acta, 1959)
- Experimental thermochemical study of the enthalpies of formation and sublimation of isonicotinamide, picolinamide, nicotinamide, isonicotinamideN-oxide, and nicotinamideN-oxide. The dissociation enthalpies of the NO bonds (The Journal of Chemical Thermodynamics, 2001)
- Reduced nicotinamide adenine dinucleotide-dependent reduction of tertiary amine N-oxide by liver microsomal cytochrome P-450. (Biochemical Pharmacology, 1977)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C[N+](=C1)[O-])C(=O)N
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InChIKeyUSSFUVKEHXDAPM-UHFFFAOYSA-N
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