mGluR
The mGluR (metabotropic glutamate receptor) is a group C GPCR and is active through an indirect metabotropic process.
Products Related to mGluR (123)
- GC50025Lamotrigine isethionateCAS: 113170-86-8Purity: >98%
Inhibits glutamate release. Water-soluble salt of lamotrigine
- GC50053LY 341495 disodium saltPurity: >98%
Potent and selective group II mGlu antagonist; disodium salt of LY 341495
- GC50144VU 0409106CAS: 1276617-62-9Purity: >98%
Potent and selective negative allosteric modulator of mGlu5 receptors
- GC50150TASP 0433864CAS: 1431980-60-7Purity: >98%
Selective positive allosteric modulator of mGlu2 receptors
- GC50154VU 0469650 hydrochlorideCAS: 1443748-47-7Purity: >98%
VU 0469650 hydrochloride is a potent, selective and CNS-penetrated negative allosteric modulator of mGlu1 receptor, with an IC50 of 99 nM.
- GC50245(+/-)-ADX 71743CAS: 1431641-29-0Purity: >98%
Negative allosteric modulator of mGlu7 receptors; brain penetrant
- GC50598VU 0424465CAS: 1428630-85-6Purity: >98%
Potent mGlu5 positive allosteric modulator and agonist; binds allosteric site with high affinity
- GC50612VU 6001966CAS: 2009052-76-8Purity: >98%
Potent and selective negative allosteric modulator of mGlu2 receptors
- GC60065AZD-8529 mesylateCAS: 1314217-69-0Purity: >99.00%
AZD-8529 mesylate is a potent, highly selective and orally bioavailable positive allosteric modulator of mGluR2, with an EC50 of 285 nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes.
- GC60614AZD 2066 hydratePurity: >99.00%
AZD 2066 hydrate is a selective, orally active and brain-penetrant antagonist of mGluR5.
- GC61537L-AP4 monohydrateCAS: 2247534-79-6Purity: >99.00%
L-AP4 (L-APB) monohydrate is a potent and specific agonist for the group III mGluRs, with EC50s of 0.13, 0.29, 1.0, 249 μM for mGlu4, mGlu8, mGlu6 and mGlu7 receptors, respectively.
- GC61816LY367385 hydrochlorideCAS: 2829282-00-8Purity: >99.00%
LY367385 hydrochloride is a highly selective and potent mGluR1a antagonist.
- GC63150Pomaglumetad methionil hydrochlorideCAS: 635318-26-2Purity: >98.00%
Pomaglumetad methionil hydrochloride (LY2140023 hydrochloride) is an orally active, methionine prodrug of the selective mGlu2/3 receptor agonist LY404039.
- GC63922AMN082 free baseCAS: 83027-13-8Purity: >98%
AMN082 free base, a selective, orally active, and brain penetrant mGluR7 agonist, directly activates receptor signaling via an allosteric site in the transmembrane domain.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC50025 | Lamotrigine isethionate | 113170-86-8 | >98% | |
Inhibits glutamate release. Water-soluble salt of lamotrigine | ||||
| GC50053 | LY 341495 disodium salt | - | >98% | |
Potent and selective group II mGlu antagonist; disodium salt of LY 341495 | ||||
| GC50087 | FTIDC | 873551-53-2 | >98% | |
Potent and selective negative allosteric modulator of mGlu1 receptors; also mGlu1 inverse agonist | ||||
| GC50125 | ABP 688 | 924298-51-1 | >98% | |
High affinity human mGlu5 antagonist | ||||
| GC50144 | VU 0409106 | 1276617-62-9 | >98% | |
Potent and selective negative allosteric modulator of mGlu5 receptors | ||||
| GC50150 | TASP 0433864 | 1431980-60-7 | >98% | |
Selective positive allosteric modulator of mGlu2 receptors | ||||
| GC50154 | VU 0469650 hydrochloride | 1443748-47-7 | >98% | |
VU 0469650 hydrochloride is a potent, selective and CNS-penetrated negative allosteric modulator of mGlu1 receptor, with an IC50 of 99 nM. | ||||
| GC50245 | (+/-)-ADX 71743 | 1431641-29-0 | >98% | |
Negative allosteric modulator of mGlu7 receptors; brain penetrant | ||||
| GC50497 | JF-NP-26 | 2341841-03-8 | >98% | |
Caged Raseglurant | ||||
| GC50598 | VU 0424465 | 1428630-85-6 | >98% | |
Potent mGlu5 positive allosteric modulator and agonist; binds allosteric site with high affinity | ||||
| GC50612 | VU 6001966 | 2009052-76-8 | >98% | |
Potent and selective negative allosteric modulator of mGlu2 receptors | ||||
| GC60065 | AZD-8529 mesylate | 1314217-69-0 | >99.00% | |
AZD-8529 mesylate is a potent, highly selective and orally bioavailable positive allosteric modulator of mGluR2, with an EC50 of 285 nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes. | ||||
| GC60614 | AZD 2066 hydrate | - | >99.00% | |
AZD 2066 hydrate is a selective, orally active and brain-penetrant antagonist of mGluR5. | ||||
| GC61537 | L-AP4 monohydrate | 2247534-79-6 | >99.00% | |
L-AP4 (L-APB) monohydrate is a potent and specific agonist for the group III mGluRs, with EC50s of 0.13, 0.29, 1.0, 249 μM for mGlu4, mGlu8, mGlu6 and mGlu7 receptors, respectively. | ||||
| GC61646 | (-)-Camphoric acid | 560-09-8 | >98.00% | |
| GC61816 | LY367385 hydrochloride | 2829282-00-8 | >99.00% | |
LY367385 hydrochloride is a highly selective and potent mGluR1a antagonist. | ||||
| GC63008 | HTL14242 | 1644645-32-8 | >98.00% | |
HTL14242 (HTL0014242) is an advanced and orally active mGlu5 NAM with a pKi?and a pIC50 of 9.3 and 9.2, respectively. | ||||
| GC63150 | Pomaglumetad methionil hydrochloride | 635318-26-2 | >98.00% | |
Pomaglumetad methionil hydrochloride (LY2140023 hydrochloride) is an orally active, methionine prodrug of the selective mGlu2/3 receptor agonist LY404039. | ||||
| GC63173 | RO0711401 | 714971-87-6 | >98.00% | |
RO0711401 is a selective and orally active positive allosteric modulator of mGlu1 receptor with an EC50 of 56 nM. | ||||
| GC63922 | AMN082 free base | 83027-13-8 | >98% | |
AMN082 free base, a selective, orally active, and brain penetrant mGluR7 agonist, directly activates receptor signaling via an allosteric site in the transmembrane domain. | ||||
| GC64218 | MMPIP | 479077-02-6 | >98% | |
MMPIP is an allosteric metabotropic glutamate receptor 7 (mGluR7) selective antagonist (KB values 24 -30 nM). | ||||
| GC64319 | LY487379 | 353231-17-1 | >98% | |
LY487379 is a selective human mGluR2 positive allosteric modulator (PAM). | ||||
| GC64513 | VU0360172 | 1310012-12-4 | >98.00% | |
VU0360172 is a potent and selective mGlu5 receptor positive allosteric modulator with an EC50 value of 16 nM and a Ki of 195 nM, respectively. | ||||
| GC65068 | L-Glutamine 15N | 80143-57-3 | >98.00% | |
