mGluR

mGluR

mGluR related products

Structure Cat No. Product Name CAS No. Product Description
V4867 LY-341495 201943-63-7 LY 341495 is a novel, potent and selective orthosteric antagonist of the metabotropic glutamate receptors (mGluR) with IC50s of 2.9 nM, 10 nM, 170 nM for mGluR-2, mGluR-3, mGluR-8, respectively.
V70602 LY3020371 1377615-75-2 LY3020371 is a potent and specific glutamate receptor (mGluR2/3) antagonist (inhibitor) with Kis of 5.26 and 2.50 nM for hmGluR2 and hmGluR3, respectively.
V70604 LY3027788 1377615-76-3 LY3027788 is a diester analog of LY3020371, an antagonist of mGlu2/3 receptor, and a potent orally bioactive prodrug of LY3020371.
V70605 LY3027788 hydrochloride 1377615-55-8 LY3027788 HCl is a diester analog of LY3020371, an antagonist of mGlu2/3 receptor, and a potent orally bioactive prodrug of LY3020371.
V70593 LY367385 hydrochloride 2829282-00-8 LY367385 HCl is a highly efficient and selective mGluR1a antagonist, with IC50 of 8.8 μM for inhibiting quinquinoline-induced hydrolysis of phosphoinositide, while the IC50 for mGlu5a is greater than 100 μM.
V14550 LY487379 HCl 353229-59-1 LY-487379 is a novel, potent and selective PAM (positive allosteric modulator) for the metabotropic glutamate receptor group II subtype mGluR2.
V70624 MCPG sodium 1303994-09-3 MCPG is a carboxyphenylglycine.
V4662 MFZ 10-7 1224431-15-5 MFZ 10-7 is a selective mGluR5 negative allosteric modulator (NAM) with Ki of 0.67 nM for rat mGluR5.
V70600 mGluR2 antagonist 1 1432728-49-8 mGluR2 antagonist 1 is an orally bioactive, BBB (blood-brain barrier) permeable/penetrable, selective negative allosteric modulator (NAM) of mGluR2 (IC50 is 9 nM).
V70623 mGluR3 modulator-1 374548-18-2 mGluR3 modulator-1 (compound 3) is a modulator of mGluR3 with EC50 of 1-10 μM measured in the HEK293T-mGluR-Gqi5 calcium motility assay.
V70618 mGluR5 antagonist-1 2761424-76-2 mGluR5antagonist-1 is a high-affinity mGluR5 antagonist (inhibitor) with IC50 of 11.5 nM.
V70622 mGluR5 modulator 1 1261171-52-1 mGluR5 modulator 1 is a PAM (positive allosteric modulator) of mGluR5.
V70601 MGS0274 1501974-69-1 MGS0274 is a lipophilic precursor of the mGlu2 and mGlu3 receptor agonist MGS0008, which improves oral bioavailability (F).
V70631 MK-8768 1432729-22-0 MK-8768 is an orally bioactive, BBB (blood-brain barrier) permeable/penetrable, selective mGluR2 negative allosteric modulator (NAM) (IC50 of 9 nM).
V2285 ML 254 1428630-86-7 ML254 is a potent mGlu5 enhancer with EC50 and pEC50 of 9.3 nM for mouse mGlu5.
V76761 ML353 ML353 is a selective ligand for the mGlu5 silent allosteric modulator (SAM) with a Ki of 18.2 nM.
V70613 MMPIP hydrochloride 1215566-78-1 MMPIP HCl is an allosteric and selective metabotropic glutamate receptor 7 (mGluR7) antagonist (KB range 24-30 nM).
V3421 MPEP hydrochloride 219911-35-0 MPEP hydrochloride is a highly potent, selective, and non-competitive antagonist of mGlu5 receptor with IC50 of 36 nM, it exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.
V70611 MTEP 329205-68-7 MTEP is a potent, noncompetitive and selective mGluR5 antagonist.
V70621 NPEC-caged-LY379268 1315379-62-4 NPEC-caged-LY379268 is a Group II mGluR agonist.
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