| Weight | 166.136 g/mol |
|---|---|
| Formula | C7H6N2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
3-Nitrobenzamide (645-09-0)
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- Potential chemotherapeutic activity of 4-iodo-3-nitrobenzamide. Metabolic reduction to the 3-nitroso derivative and induction of cell death in tumor cells in culture. (Biochemical Pharmacology, 1995)
- Anti-cancer action of 4-iodo-3-nitrobenzamide in combination with buthionine sulfoximine: inactivation of poly(ADP-ribose) polymerase and tumor glycolysis and the appearance of a poly(ADP-ribose) polymerase protease. (Biochemical Pharmacology, 2002)
- Bacterial cleavage of nitrogen to sulfone bonds in sulfamide and 1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide: formation of 2-nitrobenzamide by Gordonia sp. (Fems Microbiology Letters, 1999)
- Enzymatic mechanism of the tumoricidal action of 4-iodo-3-nitrobenzamide. (Molecular Medicine Reports, 2009)
- Regioselective and stereospecific synthesis, crystal structure and NMR assignments of N-[(Z)-1-oxo-1,3-diphenylprop-2-en-2-yl]-4-nitrobenzamide (Journal of Chemical Research-s, 2014)
- Photoreaction of N-butyl 3,4-dimethoxy-6-nitrobenzamide with butylamine. A model study for lysine-directed photoaffinity labelling (Collection of Czechoslovak Chemical Communications, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)[N+](=O)[O-])C(=O)N
-
InChIKeyKWAYEPXDGHYGRW-UHFFFAOYSA-N
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