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γ-Carboxy-L-glutaminsäure
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About This Item
Empirische Formel (Hill-System):
C6H9NO6
CAS-Nummer:
Molekulargewicht:
191.14
Beilstein:
2417114
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
Lagertemp.
−20°C
SMILES String
N[C@@H](CC(C(O)=O)C(O)=O)C(O)=O
InChI
1S/C6H9NO6/c7-3(6(12)13)1-2(4(8)9)5(10)11/h2-3H,1,7H2,(H,8,9)(H,10,11)(H,12,13)/t3-/m0/s1
InChIKey
UHBYWPGGCSDKFX-VKHMYHEASA-N
Angaben zum Gen
rat ... Grm2(24415)
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Biochem./physiol. Wirkung
Gamma-carboxy-L-glutamic acid (GLA) is used as a metabotropic glutamate receptor (mGluR) subtype ligand wherein GLA is a group-II mGlu2 receptor and group-III mGlu7, mGlu8 antagonist and group-III mGlu4, mGlu6 agonist.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Randal X Moldrich et al.
European journal of pharmacology, 476(1-2), 3-16 (2003-09-13)
Metabotropic glutamate (mGlu) receptors have multiple actions on neuronal excitability through G-protein-linked modifications of enzymes and ion channels. They act presynaptically to modify glutamatergic and gamma-aminobutyric acid (GABA)-ergic transmission and can contribute to long-term changes in synaptic function. The recent
I Brabet et al.
Neuropharmacology, 37(8), 1043-1051 (1998-12-02)
In a previous study we reported that the addition of a carboxylic group to the mGlu receptor agonist aminocyclopentane-1,3-dicarboxylate (ACPD) changes its properties from agonist to antagonist at both mGlu1 and mGlu2 receptors, and resulted in an increase in affinity
G Gerber et al.
Neuroscience, 100(2), 393-406 (2000-09-29)
The effects of group II and group III metabotropic glutamate receptor agonists on synaptic responses evoked by primary afferent stimulation in the dorsal horn, but mostly substantia gelatinosa, neurons were studied in the spinal cord slice preparation using conventional intracellular
Hilde Lavreysen et al.
Current medicinal chemistry, 15(7), 671-684 (2008-03-14)
Metabotropic glutamate (mGlu) receptors have received much attention, driven by a strong belief in the potential of these modulatory glutamate receptors as drug targets. So far, major drug discovery programs have largely focused on group I (mGlu1 and 5) and
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