| Weight | 166.136 g/mol |
|---|---|
| Formula | C7H6N2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-NITROBENZAMIDE (619-80-7)
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- A new cytotoxic, DNA interstrand crosslinking agent, 5-(aziridin-1-yl)-4-hydroxylamino-2-nitrobenzamide, is formed from 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB 1954) by a nitroreductase enzyme in Walker carcinoma cells. (Biochemical Pharmacology, 1988)
- The nitroreductase enzyme in walker cells that activates 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB 1954) to 5-(aziridin-1-YL)-4-hydroxylamino-2-nitrobenzamide is a form of NAD(P)H dehydrogenase (quinone) (EC 1.6.99.2) (Biochemical Pharmacology, 1988)
- 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)
- Synthesis, characterization and antibacterial activity of nickel (II) and copper (II) complexes of N-(alkyl(aryl)carbamothioyl)-4-nitrobenzamide (European Journal of Chemistry, 2010)
- Synthesis and reactions of N-(2,4-dichloro-6-oxo-2,4-cyclohexadien-1-ylidene)-4-nitrobenzamide with alkenes (Journal of Organic Chemistry, 1984)
- 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)
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SMILESC1=CC(=CC=C1C(=O)N)[N+](=O)[O-]
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InChIKeyZESWUEBPRPGMTP-UHFFFAOYSA-N
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4-NITROBENZAMIDE
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