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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T13318 | VU0650786 | GluR | |
VU0650786 is a selective and potent CNS penetrant negative allosteric modulator of metabotropic glutamate receptor subtype 3 (mGlu3 NAM) (IC50: 392 nM), with antidepressant and anxiolytic activity in rodents. | |||
T6022 | LY404039 | pomaglumetad | Glucocorticoid Receptor , GluR |
LY404039 (pomaglumetad) is an effective agonist of recombinant human mGlu2(Ki =149 nM)/mGlu3(Ki =92 nM). | |||
T23003 | ML337 | ML 337 | GluR |
ML337 is a negative allosteric modulator of mGlu3 with an IC50 of 593 nM. | |||
T3010 | Xanthurenic Acid | 8-Hydroxykynurenic acid,4,8-Dihydroxyquinaldic acid,xanthurenate | Apoptosis , Endogenous Metabolite , GluR |
Xanthurenic Acid (8-Hydroxykynurenic acid), a molecule arising from tryptophan metabolism by transamination of 3-hydroxykynurenine, activates mGlu2/3 Metabotropic glutamate receptors (mGlu2 and mGlu3). | |||
T23000 | ML289 | VU0463597,ML 289 | GluR |
ML289 (VU0463597) is a potent, selective, and CNS-penetrant negative allosteric modulator of mGlu3 (IC50=0.66 μM), demonstrating over 15-fold selectivity compared to mGlu2 and showing no activity against mGlu5. | |||
T22204 | LY 2389575 hydrochloride | Beta Amyloid , GluR | |
LY2389575 hydrochloride is an mGlu3 negative allosteric modulator (NAM) that is selective and non-competitive, with an IC50 value of 190 nM. LY2389575 hydrochloride induces an increase in the level of Mrc1, which amplifi... | |||
T6726 | VU0361737 | ML-128,VU 0361737 | GluR |
VU0361737 (ML-128) is a specific positive allosteric modulator (PAM) of mGlu4 receptor.The EC50 of VU 0361737 is 240 nM for the human receptors. The EC50 of VU 0361737 is110 nM for rat receptors.It exhibits weak activity... | |||
T38990 | MGS0274 | ||
MGS0274, an ester-based lipophilic prodrug of the metabotropic glutamate (mGlu)2 and mGlu3 receptor agonist MGS0008, demonstrates enhanced oral bioavailability and holds promise for schizophrenia research applications. | |||
T15807 | LY2794193 | SGLT | |
LY2794193 is a highly effective and selective agonist of the mGlu3 receptor (hmGlu3 Ki=0.927 nM,EC50=0.47 nM; hmGlu2 Ki=412 nM,EC50=47.5 nM). | |||
T15809 | LY2812223 | LIM Kinase | |
LY2812223 is a highly effective and functionally selective mGlu2 receptor agonist. It has a mGlu2 binding affinity for mGlu2 and mGlu3 (Ki=144 nM and 156 nM, respectively). | |||
T15817 | Eglumegad | Eglumetad,LY354740 | Others |
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). | |||
T61070 | VU6010572 | ||
VU6010572 is a highly potent and selective negative allosteric modulator of mGlu3, exhibiting an IC50 of 245 nM. Additionally, VU6010572 displays high central nervous system penetrance [1] [2]. | |||
T11906 | LY 541850 | GluR | |
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 human ionotropic and metabotropic glutamate (mGlu) receptors expres... | |||
T78094 | Eglumegad hydrochloride | LY354740 hydrochloride,Eglumetad hydrochloride | |
Eglumegad (LY354740) hydrochloride is a potent, selective agonist for group II (mGlu2/3) receptors, exhibiting IC50 values of 5 nM for mGlu2 and 24 nM for mGlu3 receptors when transfected into human cells. This compound ... | |||
T62756 | LY487379 | ||
LY487379 is a selective human mGluR2 positive allosteric modulator (PAM). lY487379 enhances glutamate-stimulated [35 S] GTPγS binding to mGlu2 receptors (EC50: 1.7 μM) and mGlu3 receptors (EC50>10 μM). lY487379 induces c... |