7-Chlorokynurenic acid，NMDA receptor glycine site拮抗剂
7-Chlorokynurenic acid, NMDA receptor glycine site antagonist
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(1 Publication)
MW 223.61 Da, Purity >99%. Potent NMDA receptor glycine site antagonist. Water-soluble form available - please see 7-Chlorokynurenic acid sodium salt (ab120255).
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15-PGDH, 15-hydroxyprostaglandin dehydrogenase [NAD+], AMPA 1, AMPA 2, AMPA 3, AMPA 4, AMPA-selective glutamate receptor 1, AMPA-selective glutamate receptor 2, AMPA-selective glutamate receptor 3, AMPA-selective glutamate receptor 4, AW490526, EIEE27, EPND, FESD, GLUH1, GLUK3, GLUR4C, GRIA1_HUMAN, GRIA2_HUMAN, GRIA3_HUMAN, GRIA4_HUMAN, GRIN 2A, GRIN 2B, GRIN3A, GRIN3B, GluA 4, GluA1, GluA2, GluA3, GluN1, GluN2A, GluN2C, GluR-1, GluR-2, GluR-3, GluR-4, GluR-A, GluR-B, GluR-C, GluR-D, GluR-K1, GluR-K2, GluR-K3, Glutamate Receptor Ionotropic N Methyl D Aspartate 2B, Glutamate Receptor Ionotropic N Methyl D Aspartate 2C, Glutamate Receptor Ionotropic N Methyl D Aspartate subunit 2B, Glutamate Receptor Ionotropic N methyl D aspartate 3A, Glutamate [NMDA] receptor subunit epsilon-1, Glutamate [NMDA] receptor subunit epsilon-2, Glutamate [NMDA] receptor subunit epsilon-3, Glutamate [NMDA] receptor subunit zeta-1, Glutamate ionotropic receptor AMPA type subunit 3, Glutamate receptor, Glutamate receptor 1, Glutamate receptor 2, Glutamate receptor 3, Glutamate receptor 4, Glutamate receptor C, Glutamate receptor ionotrophic AMPA 3, Glutamate receptor ionotrophic AMPA 4, Glutamate receptor ionotropic, Glutamate receptor ionotropic AMPA 1, Glutamate receptor ionotropic AMPA 2, Glutamate receptor ionotropic N methyl D aspartate 1, Glutamate receptor ionotropic N methyl D aspartate 2A, Glutamate receptor ionotropic N methyl D aspartate 3B, Glutamate receptor ionotropic NMDA2B, Glutamate receptor ionotropic, N-methyl-D aspartate, subunit 1, Glutamate receptor ionotropic, NMDA 2C, Glutamate receptor subunit 3, Glutamate receptor subunit epsilon 2, Glutamate receptor, ionotropic, AMPA 3, Glutamate receptor, ionotropic, NMDA2B (epsilon 2), Grin2c, HBGR1, HBGR2, Hpgd, Hydroxyprostaglandin dehydrogenase 15 (NAD), Ionotrophic Glutamate Receptor, Ionotropic Glutamate receptor 4, LKS, MGC133252, MGC142178, MGC142180, MRD6, MRD8, MRX94, N Methly D Aspartate Receptor Channel Subunit Epsilon 3, N methyl D asparate receptor channel subunit epsilon 2, N methyl D aspartate receptor channel subunit zeta 1, N methyl D aspartate receptor channel, subunit epsilon 1, N methyl D aspartate receptor subunit 2A, N methyl D aspartate receptor subunit 2B, N methyl D aspartate receptor subunit 2C, N-methyl D-aspartate receptor subtype 2A, N-methyl D-aspartate receptor subtype 2B, N-methyl D-aspartate receptor subtype 2C, N-methyl-D-aspartate receptor, N-methyl-D-aspartate receptor subunit 3, N-methyl-D-aspartate receptor subunit NR1, NAD+ dependent 15 hydroxyprostaglandin dehydrogenase, NMD-R1, NMDA 1, NMDA NR2B, NMDA receptor 1, NMDA receptor subtype 2A, NMDA receptor subunit 3A, NMDA receptor subunit 3B, NMDAR, NMDAR2C, NMDE1_HUMAN, NMDE2_HUMAN, NMDE3_HUMAN, NMDZ1_HUMAN, NR1, NR2A, NR2B, NR2C, NR3, OTTHUMP00000041930, OTTHUMP00000160135, OTTHUMP00000160643, OTTHUMP00000165781, OTTHUMP00000174531, OTTHUMP00000218960, OTTHUMP00000219016, OTTHUMP00000219018, OTTHUMP00000224241, OTTHUMP00000224242, OTTHUMP00000224243, PGDH1, PGDH_HUMAN, PHOAR1, Prostaglandin dehydrogenase 1, SDR36C1, Short chain dehydrogenase/reductase family 36C member 1, dJ1171F9.1, glutamate receptor ionotropic, NMDA 1, hNR 3, hNR2A
- FuncS
Unknown
Functional Studies - 7-Chlorokynurenic acid, NMDA receptor glycine site antagonist (AB120024)
ab12416 staining cGMP in SKNSH cells treated with 7-Chlorokynurenic acid (ab120024), by ICC/IF. Decrease in cGMP expression correlates with increased concentration of 7-Chlorokynurenic acid, as described in literature.
The cells were incubated at 37°C for 15 minutes in media containing different concentrations of ab120024 (7-Chlorokynurenic acid) in DMSO. Some samples where then further incubated with 15 µM NMDA (ab120052) for 5 minutes and all samples were fixed with 100% methanol for 5 minutes at -20°C and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab12416 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight® 488 anti-rabbit polyclonal antibody (ab96899) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.
- Chemical Structure
Lab
Chemical Structure - 7-Chlorokynurenic acid, NMDA receptor glycine site antagonist (AB120024)
2D chemical structure image of ab120024, 7-Chlorokynurenic acid, NMDA receptor glycine site antagonist
性能和储存信息
运输条件
推荐的短期储存条件
推荐的长期储存条件
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
These receptors integrate into complexes that facilitate excitatory postsynaptic potentials. They modulate neuron excitability and contribute to long-term potentiation—a cellular mechanism underlying learning and memory. NMDA receptors along with AMPA subtypes assemble at synaptic junctions allowing them to respond rapidly to neurotransmitter release. Their assembly and location permit precise control over neuronal communication. Across different tissues 15-Prostaglandin Dehydrogenase (15-PGDH) although not part of the glutamate receptor family may influence signals through its enzymatic activity affecting inflammatory processes.
Pathways
Glutamate receptors participate actively in the excitatory neurotransmission pathway and neuroplasticity-related signaling cascades. Their functionality connects closely to the calcium/calmodulin-dependent protein kinase (CaMK) pathway which amplifies synaptic transmission. These receptors also interact functionally with proteins like PSD-95 a postsynaptic density protein that organizes signaling molecules at synapses. Such protein-protein associations ensure that neuronal responses remain finely tuned enabling precise memory and learning processes.
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
Science advances 8:eabn3264 PubMed35275721
2022
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