
GluR
Gli inibitori dei recettori del glutammato sono composti che bloccano l'attività dei recettori del glutammato, i principali recettori dei neurotrasmettitori eccitatori nel cervello. Questi recettori svolgono un ruolo cruciale nella trasmissione sinaptica, nella plasticità, nell'apprendimento e nella memoria. La disregolazione della segnalazione del glutammato è associata a vari disturbi neurologici, come l'epilessia, l'ictus e le malattie neurodegenerative. Gli inibitori dei recettori del glutammato sono essenziali per studiare i meccanismi dell'eccitotossicità e sviluppare strategie neuroprotettive. Presso CymitQuimica, offriamo una gamma di inibitori dei recettori del glutammato per supportare la vostra ricerca sulla funzione sinaptica, la neuroprotezione e i disturbi cognitivi.
Trovati 261 prodotti di "GluR"
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LY2794193
CAS:LY2794193, a potent and selective mGlu3 receptor agonist, reduces akathisia seizures and increases GAT1, GLAST and GLT-1 protein levels in rats.Formula:C16H18N2O6Purezza:98.15%Colore e forma:SolidPeso molecolare:334.32Azotomycin
CAS:Azotomycin is an antagonist of L-glutamine and may be used as an immunosuppressant.Formula:C17H23N7O8Purezza:98%Colore e forma:SolidPeso molecolare:453.41FP0429
CAS:FP0429 is an agonist of mGlu4.Formula:C10H12N2O7Purezza:98%Colore e forma:SolidPeso molecolare:272.21LY367385 hydrochloride
CAS:<p>LY367385 hydrochloride: selective mGluR1a antagonist, IC50 = 8.8 μM, neuroprotective, anticonvulsant, antiepileptic.</p>Formula:C10H12ClNO4Colore e forma:SolidPeso molecolare:245.66LY3020371 hydrochloride
CAS:LY3020371 HCl: potent mGlu2/3 antagonist, antidepressant-like; Ki: 5.3/2.5 nM, IC50: 16.2 nM for cAMP inhibition.Formula:C15H16ClF2NO5SColore e forma:SolidPeso molecolare:395.81CPPG
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:C11H14NO5PColore e forma:SolidPeso molecolare:271.21mG2N001
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:C18H19FN2O3Colore e forma:SolidPeso molecolare:330.35YM-202074
CAS:YM-202074: Selective mGlu1 antagonist, binds allosteric site (Ki=4.8 nM), inhibits mGlu1 (IC50=8.6 nM).Formula:C22H30N4O2SColore e forma:SolidPeso molecolare:414.56YM 202074
CAS:metabotropic glutamate receptor type 1 (mGlu1) antagonistFormula:C56H72N8O16S2Purezza:98%Colore e forma:SolidPeso molecolare:1177.34PF470
CAS:<p>PF470 (PF-06297470) is a negative allosteric modulator of the metabotropic glutamate receptor 5 (mGluR5), which demonstrated significant therapeutic effects in Parkinson's disease models. However, its clinical development was halted due to potential issues identified in toxicological studies.</p>Formula:C18H16N6OColore e forma:SolidPeso molecolare:332.36LY 541850
CAS:LY541850 is a selective orthosteric mGlu2 agonist and mGlu3 antagonist with IC50 values of 0.161 μM and 0.038 μM, respectively.LY 541850 is claimed from humanFormula:C9H13NO4Purezza:98%Colore e forma:SolidPeso molecolare:199.2CVN636
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:C19H20FNO4SColore e forma:SolidPeso molecolare:377.43LY2979165
CAS:LY2979165 (mGlu2 agonist) is an orthosteric agonist of mGluR2 and can be used in studies about serving as an anti-depressant.Formula:C13H22N6O6SPurezza:98.41%Colore e forma:SolidPeso molecolare:390.42Eglumegad
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:C8H11NO4Colore e forma:SolidPeso molecolare:185.18(RS)-APICA
CAS:group II metabotropic glutamate receptor antagonistFormula:C10H12NO5PColore e forma:SolidPeso molecolare:257.18YM-298198 hydrochloride
CAS:mGlu1 receptor antagonistFormula:C18H23ClN4OSPurezza:98%Colore e forma:SolidPeso molecolare:378.919Eglumegad hydrochloride
<p>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].</p>Formula:C8H12ClNO4Colore e forma:SolidPeso molecolare:221.64VU0080241
CAS:VU0080241 is a positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4).Formula:C19H23N5Colore e forma:SolidPeso molecolare:321.42CMPDA
CAS:CMPDA is a positive allosteric modulator of AMPA receptors [EC50s: 45.4 nM/63.4 nM for GluA2i/GluA2o receptor].Formula:C16H28N2O4S2Purezza:98%Colore e forma:SolidPeso molecolare:376.53YM 298198 Hydrochloride
CAS:YM 298198 HCl: non-competitive mGlu1 antagonist, Ki=19 nM. Inactive on mGlu2-7, stronger than CPCCOEt.Formula:C18H22N4OSColore e forma:SolidPeso molecolare:342.46Ref: TM-T71764
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