| Identification | Back Directory | [Name]
1,4-DIHYDRO-4-OXOQUINOLINE-2-CARBOXYLIC ACID | [CAS]
13593-94-7 | [Synonyms]
CCRIS 4428
Kynurenate
Transtorine
Kynuronic acid
Kinurenic acid
Quinaldic acid, 4-hydroxy-
Quinaldic acid, 4-hydroxy- (8CI)
4-oxo-1,4-dihydroquinoline-2-formate
4- oxy-1, 4-dihydroquinoline-2-formic acid
1,4-DIHYDRO-4-OXOQUINOLINE-2-CARBOXYLIC ACID
4-OXO-1,4-DIHYDROQUINOLINE-2-CARBOXYLIC ACID
2-Quinolinecarboxylicacid, 1,4-dihydro-4-oxo- | [Molecular Formula]
C10H7NO3 | [MDL Number]
MFCD03197717 | [MOL File]
13593-94-7.mol | [Molecular Weight]
189.17 |
| Chemical Properties | Back Directory | [Melting point ]
123 °C | [Boiling point ]
358.4±42.0 °C(Predicted) | [density ]
1.429±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Solid | [pka]
3.49±0.20(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
Transtorine is a quinoline alkaloid, found from Ephedra transitoria, with antibacterial activity[1]. | [Definition]
ChEBI: Kynurenic acid is a quinolinemonocarboxylic acid that is quinoline-2-carboxylic acid substituted by a hydroxy group at C-4. It has a role as a G-protein-coupled receptor agonist, a NMDA receptor antagonist, a nicotinic antagonist, a neuroprotective agent, a human metabolite and a Saccharomyces cerevisiae metabolite. It is a monohydroxyquinoline and a quinolinemonocarboxylic acid. It is a conjugate acid of a kynurenate. | [References]
[1] al-Khalil S, et al. Transtorine, a new quinoline alkaloid from Ephedra transitoria. J Nat Prod. 1998 Feb;61(2):262-3. DOI:10.1021/np9702998 |
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