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Cat. No. Product Name Information
PC-49747

Mavoglurant

mGlu5 NAM

AFQ056 (Mavoglurant, AFQ-056) is a potent, subtype-selective and non-competitive inhibitor of mGluR5 with IC50 of 30 nM.
PC-49586

VU6046980

mGlu7 PAM

VU6046980 is a potent, selective and in vivo active mGlu7 positive allosteric modulator (PAM) with EC50 of 0.15 uM (rat mGlu7).
PC-49074

VU0360172

mGlu5 PAM

VU0360172 is a selective mGlu5 receptor positive allosteric modulator (PAM) with EC50 of 16 nM, Ki of 195 nM.
PC-49069

Dipraglurant

mGlu5 NAM

Dipraglurant (ADX-48621) is a negative allosteric modulator (NAM) of metabotropic glutamate 5 (mGlu5) receptor, shows potential for the treatment of Parkinson's disease levodopa-induced dyskinesia (PD-LID).
PC-73234

Decoglurant

mGluR2/3 NAM

Decoglurant (RO4995819) is a negative allosteric modulator of mGluR2 and mGluR3 with antidepressant effect.
PC-36001

VU6012962

mGlu7 modulator

VU6012962 (VU-6012962) is a potent, orally bioavailable and CNS penetrant mGlu7 negative allosteric modulator with IC50 of 0.35 uM.
PC-35962

BMS-984923

BMS-984923 (BMS-984923) is a potent silent allosteric modulator (SAM) of mGluR5 with competitive antagonism of MPEPy binding with Ki of 0.6 nM, but has no detectable agonist and antagonist activity at mGluR5 signaling.
PC-63197

VU0424238

VU0424238 (Auglurant) is a potent, selective, orally active mGlu5 negative allosteric modulator with Ki of 4.4 nM, displays >900-fold selectivity for mGlu5 versus the other mGlu receptors.
PC-63180

AZD8529

AZD8529 (AZD-8529) is a novel potent, selective mGluR2 positive allosteric modulator with EC50 of 195 nM, does not produce any positive allosteric modulator responses for mGluR1 and 3-8 subtypes.
PC-62984

DL-AP4 sodium salt

DL-AP4 sodium salt is a broad spectrum glutamate receptor antagonist..
PC-62983

LSP4-2022

LSP4-2022 is a novel potent, selective, brain-penetrant mGluR4 agonist with EC50 of 0.11 uM in cell-based assays.
PC-62957

VU0400195

mGluR4 modulator

VU0400195 (ML 182) is a potent, selective, brain penetrant and orally active positive allosteric modulator of mGluR4 with EC50 of 291 nM and 376 nM for human and rat mGluR4, respectively.

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