Potent and selective glutamate uptake inhibitor.
Product Details
Formula: | C6H9NO4 |
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MW: | 159.1 |
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CAS: | 64769-66-0 |
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Purity: | ≥98% (HPLC) |
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Identity: | Determined by 1H-NMR and MS. |
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Appearance: | White solid. |
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Solubility: | Soluble in water (10 mg/ml). |
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Shipping: | Ambient Temperature |
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Long Term Storage: | Ambient |
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Regulatory Status: | RUO - Research Use Only |
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Product Literature References
Comparison of Na+-dependent glutamate transport activity in synaptosomes, C6 glioma, and Xenopus oocytes expressing excitatory amino acid carrier 1 (EAAC1): L. A. Dowd, et al.; Mol. Pharmacol.
49, 465 (1996),
Abstract;
Effects of L-trans-pyrrolidine-2,4-dicarboxylate and L-threo-3-hydroxyaspartate on the binding of [3H]L-aspartate, [3H]alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA), [3H]DL-(E)-2-amino-4-propyl-5-phosphono-3-pentenoate (CGP 39653), [3H]6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and [3H]kainate studied by autoradiography in rat forebrain: V. J. Balcar, et al.; Neurochem. Int.
26, 155 (1995),
Abstract;
L-trans-pyrrolidine-2,4-dicarboxylate and cis-1-aminocyclobutane-1,3-dicarboxylate behave as transportable, competitive inhibitors of the high-affinity glutamate transporters: R. Griffiths, et al.; Biochem. Pharmacol.
47, 267 (1994),
Abstract;
Regional differences in the inhibition of L-glutamate and L-aspartate sodium-dependent high affinity uptake systems in rat CNS synaptosomes by L-trans-pyrrolidine-2,4-dicarboxylate, threo-3-hydroxy-D-aspartate and D-aspartate: A. D. Mitrovic & G. A. Johnston; Neurochem. Int.
24, 583 (1994),
Abstract;
The neuronal and epithelial human high affinity glutamate transporter. Insights into structure and mechanism of transport: Y. Kanai, et al.; J. Biol. Chem.
269, 20599 (1994),
Abstract;
Full Text
Conformationally defined neurotransmitter analogues. Selective inhibition of glutamate uptake by one pyrrolidine-2,4-dicarboxylate diastereomer: R. J. Bridges, et al.; J. Med. Chem.
34, 717 (1991),
Abstract;