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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T22641 | CDPPB | GluR | |
CDPPB is a modulator of mGluR5 positive allosteric(with an EC50 of 27 nM in Chinese hamster ovary cells expressing human mGluR5). | |||
T3483 | FTIDC | GluR | |
FTIDC is a highly potent and selective allosteric antagonist of mGluR1 receptors and shows very weak potency against human and rat mGluR5 receptors. The inhibition of FTIDC for mGluR1 receptors is shown to be in noncompe... | |||
T6598 | MPEP | GluR | |
MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors. | |||
T3482 | CFMTI | GluR | |
CFMTI is a potent and selective metabotropic glutamate receptor (mGluR) 1 allosteric antagonist (IC50: 2.6 nM). The selectivity of CFMTI to mGluR1 is higher 2000-fold than mGluR5. | |||
T3477 | E4CPG | GluR | |
E4CPG is a novel group I/II metabotropic glutamate receptor antagonist, more potent than (RS)-MCPG. | |||
T21747 | VU0483605 | GluR | |
VU0483605 is an effective and selective positive allosteric modulator of mGluR1 with EC50s of 390 and 356 nM for human and rat, respectively. | |||
T2497 | MPEP hydrochloride | GluR | |
MPEP hydrochloride is an effective and highly specific non-competitive antagonist at the mGlu5 receptor subtype (IC50: 36 nM). | |||
T15275 | Fenobam | GluR | |
Fenobam shows inverse agonist activity which blocks the mGlu5 receptor basal activity(IC50: 84 nM). Fenobam has anxiolytic activity. Fenobam is a selective and non-competitive mGluR5 antagonist acting at an allosteric mo... | |||
T3464 | PHCCC | (-) PHCCC | GluR |
PHCCC ((-) PHCCC) is a Group I metabotropic glutamate receptor antagonist and a positive allosteric modulator of mGluR4. It also is a potent to antagonism for mGluR2 and mGluR8. | |||
T10573 | BMT-145027 | GluR | |
BMT-145027 is a positive allosteric modulator of mGluR5 without inherent agonist activity (EC50 = 47 nM). | |||
T13441 | (R)-ADX-47273 | GluR | |
(R)-ADX-47273 is a potent mGluR5 positive allosteric modulator(EC50 of 168 nM for potentiation ). | |||
T13321 | VU6005649 | GluR | |
VU6005649 is an agonist of CNS penetrant mGlu7/8 receptor (EC50s: 0.65 μM and 2.6 μM for mGlu7 receptor and mGlu8 receptor, respectively). | |||
T3451 | JNJ-42153605 | GluR | |
JNJ-42153605 is a mGlu2 receptor positive allosteric modulator (EC50: 17 nM). | |||
T4500 | ADX88178 | GluR | |
ADX88178 is a potent positive allosteric modulator for metabotropic glutamate receptor 4 (mGluR4) with EC50 of 4 nM for human mGluR4. | |||
T6725 | VU 0357121 | GluR | |
VU0357121, a positive allosteric modulator of mGlu5 (EC50: 33 nM), is inactive or very weakly antagonizing at other mGlu receptor subtypes. | |||
T6160 | VU 0364439 | GluR | |
VU 0364439 is a mGlu4 positive allosteric modulator (C50: 19.8 nM). | |||
T13323 | VU6012962 | GluR | |
VU6012962 is an orally bioavailable negative allosteric modulator of CNS-penetrant metabotropic glutamate receptor 7(mGlu7; IC50: 347 nM). | |||
T8862 | ML 254 | GluR | |
ML254 competitively interacts with the MPEP allosteric binding site. ML254 is highly selective for mGlu5 versus other mGlu receptors, has a clean ancillary Ricerca profile, and suitable dystrophia myotonica protein kinas... | |||
T6727 | VU0364770 | VU 0364770 | GluR |
VU0364770 (VU 0364770)(EC50=1.1 μM), a positive allosteric modulator(PAM) of mGlu4, shows insignificant activity at 68 other receptors, including other mGlu subtypes. | |||
T7494 | TCN238 | TCN 238 | GluR |
TCN238 is an orally bioavailable positive allosteric modulator of the metabotropic glutamate receptor 4 (mGluR4with an EC50 of 1 μM). |