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Cat. No. Product Name Information
PC-42136

DFMTI

mGluR1 antagonist

DFMTI (MK5435) is a potent, selective, brain penetrant and orally active mGluR1 antagonist with 4.3 nM and 3.6 nM for huam and rat mGluR1, respectively.
PC-42134

CFMTI

mGluR1 antagonist

CFMTI is a potent, selective, allosteric and oral mGluR1 antaognist with IC50 of 2.6 and 2.3 nM for human and rat mGluR1, respectively.
PC-45423

JNJ-42153605

mGlu2 PAM

JNJ-42153605 is a potent, selective positive allosteric modulator of mGlu2 receptor with EC50 of 17 nM.
PC-42135

Ro 67-7476

p-ERK1/2 agonist, rat mGlu1R PAM

Ro 67-7476 is a potent, selective positive allosteric modulator (potentiator) of rat mGlu1R with pEC50 of 6.76 for the potentiation of 3 uM glutamate-induced Ca2+ int currents.
PC-42140

PHCCC

mGluR4 PAM

PHCCC is a potent, selective allosteric potentiator of mGluR4 with EC50 of 4.1 uM, also is a selective antagonist of group mGlu1 receptors.
PC-45568

LY354740

group 2 mGluR agonist

LY354740 (Eglumegad) is a potent and selective group 2 mGluRs agonist with EC50s of 55 ± 17 nM.
PC-45947

LY-341495

Group II mGluR antagonist

LY-341495 (LY341495) is a potent and selective antagonist of the group II mGluRs with IC50 of 21 nM and 14 nM for mGluR2 and mGluR3, respectively.
PC-42118

(RS)-MCPG

mGluR antagonist

(RS)-MCPG is a non-selective group I/group II metabotropic glutamate receptor (mGluR) antagonist.
PC-42119

E4CPG

mGluR antagonist

E4CPG is a non-selective group I/group II metabotropic glutamate receptor (mGluR) antagonist.
PC-45635

Trans-ACPD

mGluR agonist

Trans-ACPD is a equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD, selective agonist for metabotropic glutamate receptors.
PC-22952

FO-4-15

mGluR1 activator

FO-4-15 is a small molecule taregting mGluR1 with low cytotoxicity and anti-H2O2 effect, significantly reduces Aβ accumulation, Tau hyper-phosphorylation, and synaptic impairments in 3×Tg mice, activates mGluR1/CaMKIIα pathway.
PC-22950

LBG20304

GluK5 ligand

LBG20304 is a potent, selective ligand for homomeric GluK5 receptor with IC50 of 432 nM, >40-fold selective over GluK1-3 and >100-fold selectivity over native AMPA and NMDA receptors.

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