| Weight | 174.159 g/mol |
|---|---|
| Formula | C9H6N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
5-Nitroisoquinoline (607-32-9)
5-nitroquinoline
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- Nitroxoline (8-hydroxy-5-nitroquinoline) is more a potent anti-cancer agent than clioquinol (5-chloro-7-iodo-8-quinoline). (Cancer Letters, 2011)
- The syntheses and structures of 3+2 and 2+2+1 oxorhenium mixed-ligand complexes employing 8-hydroxy-5-nitroquinoline as the bidentate N,O donor ligand (Inorganica Chimica Acta, 2000)
- The N2-guanine adduct but not the C8-guanine or N6-adenine adducts formed by 4-nitroquinoline 1-oxide blocks the 3'-5' exonuclease action of T4 DNA polymerase (Biochemistry, 1990)
- OXYGEN DEPENDENCE OF THE CYTOTOXICITY AND METABOLIC ACTIVATION OF 4-ALKYLAMINO-5-NITROQUINOLINE BIOREDUCTIVE DRUGS (British Journal of Cancer, 1994)
- KI-67 (MIB 5) IMMUNOSTAINING OF MOUSE LUNG TUMORS INDUCED BY 4-NITROQUINOLINE 1-OXIDE (Histochemistry and Cell Biology, 1998)
- NaH-Mediated One-Pot Cyclocondensation of 6-Nitroquinoline with Aromatic Hydrazones To Form [1.2.4]Triazino[6,5-f]quinolines and/or Pyrazolo[3,4-f]quinolines (Organic Letters, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-nitroquinoline
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SMILESC1=CC2=C(C=CN=C2)C(=C1)[N+](=O)[O-]
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InChIKeyPYGMPFQCCWBTJQ-UHFFFAOYSA-N
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