| Weight | 174.159 g/mol |
|---|---|
| Formula | C9H6N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
quinoxaline-5-carboxylic acid (6924-66-9)
6924-66-9
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- Metabolism of 2-amino-3,8-dimethylimidazo[4,5-f]-quinoxaline in human hepatocytes: 2-amino-3-methylimidazo[4,5-f]quinoxaline-8-carboxylic acid is a major detoxication pathway catalyzed by cytochrome P450 1A2 (Chemical Research in Toxicology, 2001)
- Synthesis and biological evaluation of analogues of 7-chloro-4,5-dihydro-4- oxo-8-(1,2,4-triazol-4-yl)-1,2,4-triazolo[1,5-a]quinoxaline-2-carboxylic acid (TQX-173) as novel selective AMPA receptor antagonists. (Journal of Medicinal Chemistry, 2004)
- Synthesis of 4,12-dihydro-4-oxoquino-[1,8a,8-a,b]quinoxaline-5-carboxylic acid derivatives (Journal of Heterocyclic Chemistry, 1988)
- Synthesis of novel quinoxaline-5-carboxylic acid derivatives (Journal of Heterocyclic Chemistry, 1999)
- Derivatives of 5-Oxy-pyrido(2,3-b)quinoxaline-9-carboxylic Acid: A Tricyclic System Useful for the Synthesis of Potential Intercalators (Journal of Heterocyclic Chemistry, 2002)
- Pyrimido[5,6-b]quinoxaline-4-(3H)-one-2-carboxylic acid compounds (1977)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 6924-66-9
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SMILESC1=CC(=C2C(=C1)N=CC=N2)C(=O)O
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InChIKeyQLZNISOPACYKOR-UHFFFAOYSA-N
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