GLPBio

MPEP

Catalog No.: GC10864Purity:>98.00%
MPEP is a noncompetitive, selective, potent, orally active and systemically active mGlu5 receptor antagonist, with an IC50 of 36nM for completely inhibiting quisqualate-stimulated phosphoinositide (PI) hydrolysis.

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MPEP
Cas No.: 96206-92-7
10mM (in 1mL DMSO)In Stock
$23.00
1
5mgIn Stock
$21.00
1
10mgIn Stock
$35.00
1
25mgIn Stock
$67.00
1
50mgIn Stock
$119.00
1
100mgIn Stock
$189.00
1

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Description

MPEP is a noncompetitive, selective, potent, orally active and systemically active mGlu5 receptor antagonist, with an IC50 of 36nM for completely inhibiting quisqualate-stimulated phosphoinositide (PI) hydrolysis[1]. MPEP has anxiolytic-or antidepressant-like effects[2] and is usually used in the study of neurological disorders, such as fragile X syndrome[3] and epilepsy[4] .

In vitro, pretreatment of MN9D cells with 10μM MPEP 30min prior to rotenone exposure reversed the increase in p-PERK and γ -H2AX expression levels and alleviated the decrease in tyrosine hydroxylase induced by rotenone treatment[5] .

In vivo, intraperitoneal injection of MPEP(30mg/kg; 3days) lowered alcohol consumption during Drinking in the Dark (DID) in male and female C57BL/6 mice without changes in Homer2/Erk2 expression[6] . Intraperitoneal injection of MPEP (3 mg/kg, 30min) facilitates amphetamine-induced effects independently on the behavior measured both in naïve and in dopamine lesioned mice[7].

References:
[1] Gasparini, F., Lingenhöhl, K., Stoehr, N., Flor, P. J., Heinrich, M., Vranesic, I., Biollaz, M., Allgeier, H., Heckendorn, R., Urwyler, S., Varney, M. A., Johnson, E. C., Hess, S. D., Rao, S. P., Sacaan, A. I., Santori, E. M., Veliçelebi, G., & Kuhn, R. (1999). 2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist. Neuropharmacology, 38(10), 1493–1503.
[2] Tatarczyńska, E., Klodzińska, A., Chojnacka-Wójcik, E., Palucha, A., Gasparini, F., Kuhn, R., & Pilc, A. (2001). Potential anxiolytic- and antidepressant-like effects of MPEP, a potent, selective and systemically active mGlu5 receptor antagonist. British journal of pharmacology, 132(7), 1423–1430.
[3] Castrén, M. L., & Castrén, E. (2014). BDNF in fragile X syndrome. Neuropharmacology, 76 Pt C, 729–736.
[4] Moldrich, R. X., Chapman, A. G., De Sarro, G., & Meldrum, B. S. (2003). Glutamate metabotropic receptors as targets for drug therapy in epilepsy. European journal of pharmacology, 476(1-2), 3–16.
[5] Gu, L., Luo, W. Y., Xia, N., Zhang, J. N., Fan, J. K., Yang, H. M., Wang, M. C., & Zhang, H. (2022). Upregulated mGluR5 induces ER stress and DNA damage by regulating the NMDA receptor subunit NR2B. Journal of biochemistry, 171(3), 349–359.
[6] Huang, G., Thompson, S. L., & Taylor, J. R. (2021). MPEP Lowers Binge Drinking in Male and Female C57BL/6 Mice: Relationship with mGlu5/Homer2/Erk2 Signaling. Alcoholism, clinical and experimental research, 45(4), 732–742.
[7] Managò, F., Lopez, S., Oliverio, A., Amalric, M., Mele, A., & De Leonibus, E. (2013). Interaction between the mGlu receptors 5 antagonist, MPEP, and amphetamine on memory and motor functions in mice. Psychopharmacology, 226(3), 541–550.

Protocol

Cell experiment [1]:

Cell lines

MN9D cells

Preparation Method

MN9D cells were pretreated with 10μM MPEP for 30min followed by different concentration of rotenone or (RS)-2-chloro-5- hydroxyphenylglycine (CHPG) treatment for indicated time. The expression levels of p-PERK, γ -H2AX and tyrosine hydroxylase were detected by Western blot.

Reaction Conditions

10μM; 30min

Applications

MPEP reversed the increase in p-PERK and γ -H2AX expression levels and alleviated the decrease in tyrosine hydroxylase induced by rotenone treatment.

Animal experiment [2]:

Animal models

C57BL/6NCrl mice

Preparation Method

The animals used in this study were male and female C57BL/6NCrl mice purchased from Charles River Laboratories (Strain Code #027) at seven weeks of age. Upon delivery, mice were singly housed with food ad libitum. Water was provided ad libitum via a water bottle except for during the Drinking in the Dark (DID) sessions.

A 20% ethanol drinking solution for the DID experiments was made with 200 proof ethanol diluted with tap water (v/v) and used within 24h. MPEP was dissolved in saline and injected i.p. at 10 ml/kg body weight. A range of doses from 0–30mg/kg MPEP were used in these studies. After the completion of the final MPEP dose the animals continued on DID for three days to test for blood ethanol concentrations.

Dosage form

0–30mg/kg for 3days; i.p.

Applications

30mg/kg MPEP lowered alcohol consumption during DID in male and female C57BL/6 mice without changes in Homer2/Erk2 expression.

References:
[1] Gu, L., Luo, W. Y., Xia, N., Zhang, J. N., Fan, J. K., Yang, H. M., Wang, M. C., & Zhang, H. (2022). Upregulated mGluR5 induces ER stress and DNA damage by regulating the NMDA receptor subunit NR2B. Journal of biochemistry, 171(3), 349–359.
[2] Huang, G., Thompson, S. L., & Taylor, J. R. (2021). MPEP Lowers Binge Drinking in Male and Female C57BL/6 Mice: Relationship with mGlu5/Homer2/Erk2 Signaling. Alcoholism, clinical and experimental research, 45(4), 732–742.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
96206-92-7
Chemical Name
2-methyl-6-(2-phenylethynyl)pyridine
SMILES
CC1=CC=CC(=N1)C#CC2=CC=CC=C2
Molecular Formula
C14H11N
Molecular Weight
193.24
Solubility
100mg/mL in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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