mGluR5: Products

Human metabotropic glutamate receptor 5 (mGluR5; also mGluR5b) is a 150 kDa, 7-transmembrane glycoprotein that belongs to group I of the C-family of G-protein coupled receptors. mGluR5 is constitutively expressed and regulates neuronal ion channel activity.

"mGluR5" has 36 results in Products.
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Human mGluR5 Antibody 

1 Image
CyTOF-ready, Flow, WB

MPEP hydrochloride 

Potent mGlu5 antagonist; also positive allosteric modulator of mGlu4 receptors

CHPG Sodium salt 

Selective mGlu5 agonist; sodium salt of CHPG (Cat. No. 1049)

Human/Mouse/Rat mGluR5/1a Antibody 

1 Image
IHC, WB

MTEP hydrochloride 

Potent and selective mGlu5 antagonist

Human mGluR5 Antibody 

IHC, WB

CHPG 

mGlu5 selective agonist

L-Quisqualic acid 

AMPA agonist; also group I mGlu agonist

PHCCC 

Potent group I mGlu antagonist

Fenobam 

Potent and selective mGlu5 negative allosteric modulator (NAM)

CDPPB 

Positive allosteric modulator of mGlu5 receptors

Topiramate 

GluK1 antagonist; inhibits carbonic anhydrase (CA) II and IV; also positive allosteric modulator of GABAA receptors

Licarbazepine 

Active metabolite of oxcarbazepine (Cat. No. 3864)

NPS 2390 

Group I mGlu antagonist

VU 0360172 hydrochloride 

Positive allosteric modulator of mGlu5 receptors

Ro 67-4853 

Positive allosteric modulator of group I mGlu receptors

ADX 10059 hydrochloride 

Negative allosteric modulator of mGlu5 receptors

CPPHA 

Positive allosteric modulator of mGlu1 and mGlu5 receptors

ABP 688 

High affinity human mGlu5 antagonist

LSN 2463359 

Potent and selective positive allosteric modulator of mGlu5 receptors

VU 0409106 

Potent and selective negative allosteric modulator of mGlu5 receptors

AZD 9272 

Potent and selective mGlu5 antagonist; brain penetrant

AZD 2066 

mGlu5 antagonist; orally bioavailable and brain penetrant

VU 0409551 

Selective positive allosteric modulator of mGlu5 receptors; brain penetrant and orally bioavailable

JF-NP-26 

Caged Raseglurant (Cat. No. 4416)

VU 0424465 

Potent mGlu5 positive allosteric modulator and agonist; binds allosteric site with high affinity
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