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Submit ReviewThe first potent and selective inhibitor of kynurenine-3-hydroxylase. Increases the concentration of kynurenic acid in vivo.
M. Wt | 238.2 |
Storage | Store at RT |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Carpendo et al (1994) Inhibitors of kynurenine hydroxylase and kynureninase increase cerebral formation of kynurenate and have sedative and anticonvulsant activities. Neuroscience 61 237 PMID: 7969905
Chiarugi and Moroni (1999) Quinolinic acid formation in immune-activated mice: studies with (m-nitrobenzoyl)-alanine (mNBA) and 3,4-dimethoxy-[-N-4-(-3-nitrophenyl)thiazol-2yl]-benzenesulfonamide. Neuropharmacology 38 1225 PMID: 10462134
Pellicciari et al (1994) Modulation of the kynurenine pathway in search for new neuroprotective agents. Synthesis and preliminary evaluation of (m-nitrobenzoyl)alanine, a potent inhibitor of kynurenine-3-hydroxylase. J.Med.Chem. 37 647 PMID: 8126705
Keywords: (±)-3-(3-Nitrobenzoyl)alanine hydrochloride, (±)-3-(3-Nitrobenzoyl)alanine hydrochloride supplier, Non-selective, Ionotropic, Glutamate, 0799, Tocris Bioscience
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Epilepsy is a brain disease that affects 60 million people globally. More than 20 anti-seizure drugs are currently available, but these do not address the underlying causes of the condition. This poster summarizes current knowledge about the development of the condition and highlights some approaches that have disease-modifying effects in proof-of-concept studies.
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