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 38 results in Products.
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CHPG Sodium salt 

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

Human mGluR5 Antibody 

1 Image
CyTOF-ready, Flow, WB

MTEP hydrochloride 

Potent and selective mGlu5 antagonist

Human/Mouse/Rat mGluR5/1a Antibody 

1 Image
IHC, WB

VU 0360172 hydrochloride 

Positive allosteric modulator of mGlu5 receptors

Human mGluR5 Antibody 

IHC, WB

CHPG 

mGlu5 selective agonist

CDPPB 

Positive allosteric modulator of mGlu5 receptors

SIB 1757 

Highly selective mGlu5 antagonist

DFB 

Positive allosteric modulator of mGlu5 receptors

DCB 

Allosteric modulator of mGlu5 receptors

DMeOB 

Negative allosteric modulator of mGlu5 receptors

ACDPP hydrochloride 

Selective mGlu5 antagonist

Fenobam 

Potent and selective mGlu5 negative allosteric modulator (NAM)

VU 1545 

Positive allosteric modulator of mGlu5 receptors

Ro 67-4853 

Positive allosteric modulator of group I mGlu receptors

VU 0285683 

Negative allosteric modulator of mGlu5 receptors

VU 0360223 

Negative allosteric modulator of mGlu5 receptors

ADX 10059 hydrochloride 

Negative allosteric modulator of mGlu5 receptors

VU 0357121 

Positive allosteric modulator of mGlu5 receptors

MFZ 10-7 

Negative allosteric modulator of mGlu5 receptors

VU 29 

Potent positive 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

AZD 2066 

mGlu5 antagonist; orally bioavailable and brain penetrant

VU 0409551 

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

VU 0424465 

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