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Cat. No. Product Name Information
PC-62130

VU0155094

group III mGluR PAM

VU0155094 (ML397) is a potent, selective pan-Group III mGlu positive allosteric modulator with IC50 of 3.43/1.5/0.93 uM for mGlu8/7/4, respectively.
PC-62129

VU0422288

Group III mGluR modulator

VU0422288 is a potent, selective, CNS-penetrant pan-Group III mGlu positive allosteric modulator with IC50 of 110/146/130 nM for mGlu8/7/4, respectively, displays >30-fold selectivity over groups I and II mGlus (mGlu1/2/3/5/6).
PC-62120

ML353

mGlu5 modulator

ML353 (VU0478006) is a highly potent, selective, MPEP-site silent allosteric modulator of mGlu5 receptor with with sub-100 nM affinity.
PC-61613

Pomaglumetad Methionil

mGlu2/3 agonist

Pomaglumetad Methionil (LY2140023 monohydrate) is the methionine amide prodrug of the mGluR2/3 agonist LY-404039 with the potential oral treatment of schizophrenia.
PC-61612

LY-487379 hydrochloride

LY-487379 hydrochloride is a potent, selective positive allosteric modulator of mGluR2 (EC50=0.27 uM) without activity at mGluR3.
PC-61611

LY487379

mGlu2 PAM

LY487379 is a potent, selective positive allosteric modulator of mGluR2 (EC50=0.27 uM) without activity at mGluR3.
PC-61513

JNJ-40411813

mGlu2 PAM

JNJ-40411813 (ADX71149) is a novel potent positive allosteric modulator of mGlu2 with EC50 of 147 nM.
PC-61212

AMN 082 dihydrochloride

mGluR7 agonist

AMN 082 dihydrochloride (AMN082) is potent, selective, brain penetrant, orally acitve mGluR7 allosteric agonist, inhibits forskolin-stimulated cAMP accumulation in mGluR7b CHO cells with EC50 of 64 nM.
PC-61211

AMN 082

mGluR7 agonist

AMN 082 (AMN082) is a potent, selective mGluR7 allosteric agonist, inhibits forskolin-stimulated cAMP accumulation in mGluR7b CHO cells with EC50 of 64 nM.
PC-61070

BMS-955829

mGluR5 PAM

BMS-955829 is a potent, selective, low glutamate fold shift (2.4) mGluR5 positive allosteric modulator with EC50 of 2.6 nM, without inherent mGluR5 agonist activity (EC50>30 uM).
PC-61069

BMT-145027

mGluR5 PAM

BMT-145027 is a potent, selective, non-MPEP site mGluR5 positive allosteric modulator with EC50 of 47 nM, without inherent mGluR5 agonist activity (EC50>16 uM).
PC-61060

GRN-529

mGluR5 NAM

GRN-529 is a highly potent, selective, orally active mGluR5 negative allosteric modulator with Ki of 5.4 nM, IC50 of 3.1 nM.

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