| 2-Amino-3-carboxymuconic semialdehyde | |
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(Z)-2-Amino-3-[(Z)-3-oxoprop-1-enyl]but-2-enedioic acid
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| Identifiers | |
| CAS number | 16597-58-3 |
| PubChem | 5280673 |
| ChemSpider | 7822292 |
| ChEBI | CHEBI:994 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C7H7NO5 |
| Molar mass | 185.13 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
2-Amino-3-carboxymuconic semialdehyde is an intermediate in the metabolism of tryptophan in the tryptophan-niacin catabolic pathway. Quinolinate is a neurotoxin formed nonenzymatically from 2-amino-3-carboxymuconic semialdehyde in mammalian tissues. 2-Amino-3-carboxymuconic semialdehyde is enzymatically converted to 2-aminomuconate via 2-aminomuconic semialdehyde.
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