GluR
Glutamate Receptor inhibitors are compounds that block the activity of glutamate receptors, which are the main excitatory neurotransmitter receptors in the brain. These receptors play a pivotal role in synaptic transmission, plasticity, learning, and memory. Dysregulation of glutamate signaling is associated with various neurological disorders, including epilepsy, stroke, and neurodegenerative diseases. GluR inhibitors are essential for investigating the mechanisms of excitotoxicity and developing neuroprotective strategies. At CymitQuimica, we offer a range of glutamate receptor inhibitors to support your research in synaptic function, neuroprotection, and cognitive disorders.
Found 265 products of "GluR"
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FP0429
CAS:FP0429 is an agonist of mGlu4.Formula:C10H12N2O7Purity:98%Color and Shape:SolidMolecular weight:272.21CVN636
CAS:CVN636, a potent and selective allosteric agonist for the mGluR7 receptor, exhibits oral activity and CNS permeability [1], with an EC50 of 7 nM for humanFormula:C19H20FNO4SColor and Shape:SolidMolecular weight:377.43mG2N001
CAS:mG2N001, a negative allosteric modulator (NAM) of the metabotropic glutamate receptor mGluR2, has an IC50 of 93 nM and binds to mGluR2 as an antagonist with a Ki of 63 nM. This compound is microparticle- and plasma-stable, and its radioisotope [11C] mG2N001 can be utilized in PET imaging. [11C] mG2N001 exhibits good brain heterogeneity and penetration, selectively accumulating in mGluR2-rich regions to produce high-contrast brain images [1].Formula:C18H19FN2O3Color and Shape:SolidMolecular weight:330.35LY3020371 hydrochloride
CAS:LY3020371 HCl: potent mGlu2/3 antagonist, antidepressant-like; Ki: 5.3/2.5 nM, IC50: 16.2 nM for cAMP inhibition.Formula:C15H16ClF2NO5SColor and Shape:SolidMolecular weight:395.81YM 202074
CAS:metabotropic glutamate receptor type 1 (mGlu1) antagonistFormula:C56H72N8O16S2Purity:98%Color and Shape:SolidMolecular weight:1177.34CPPG
CAS:CPPG: potent group II/III mGlu receptor antagonist, 20x more selective for group III (IC50: 2.2 nM) than II (46.2 nM) in rat cortex.Formula:C11H14NO5PColor and Shape:SolidMolecular weight:271.21LY2979165
CAS:LY2979165 (mGlu2 agonist) is an orthosteric agonist of mGluR2 and can be used in studies about serving as an anti-depressant.Formula:C13H22N6O6SPurity:98.41%Color and Shape:SolidMolecular weight:390.42YM-298198 hydrochloride
CAS:mGlu1 receptor antagonistFormula:C18H23ClN4OSPurity:98%Color and Shape:SolidMolecular weight:378.919Eglumegad
CAS:Eglumegad is a highly effective and selective agonist of group II (mGlu2/3) receptor (IC50s: 5 and 24 nM on transfected human mGlu2 and mGlu3 receptors, respectively).Formula:C8H11NO4Color and Shape:SolidMolecular weight:185.18(RS)-APICA
CAS:group II metabotropic glutamate receptor antagonistFormula:C10H12NO5PColor and Shape:SolidMolecular weight:257.18VU0080241
CAS:VU0080241 is a positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4).Formula:C19H23N5Color and Shape:SolidMolecular weight:321.42Eglumegad hydrochloride
Eglumegad (LY354740) hydrochloride is a potent, selective agonist for group II (mGlu2/3) receptors, showing IC50 values of 5 nM for mGlu2 and 24 nM for mGlu3 receptors in transfected human cells. This compound provides neuroprotection against NMDA-induced toxicity and exhibits anxiolytic- and antipsychotic-like properties [1].Formula:C8H12ClNO4Color and Shape:SolidMolecular weight:221.64YM 298198 Hydrochloride
CAS:YM 298198 HCl: non-competitive mGlu1 antagonist, Ki=19 nM. Inactive on mGlu2-7, stronger than CPCCOEt.Formula:C18H22N4OSColor and Shape:SolidMolecular weight:342.46CMPDA
CAS:CMPDA is a positive allosteric modulator of AMPA receptors [EC50s: 45.4 nM/63.4 nM for GluA2i/GluA2o receptor].Formula:C16H28N2O4S2Purity:98%Color and Shape:SolidMolecular weight:376.53UBP1112
CAS:group III mGlu receptor antagonistFormula:C10H14NO5PPurity:98%Color and Shape:SolidMolecular weight:259.2
