Methoxymethyl-MTEP
Methoxymethyl-MTEP is a selective, high-affinity mGluR5 antagonist. Methoxymethyl-MTEP can serve as a radiotracer ligand, readily entering the brain and providing mGluR5-specific signal in gray matter regions. Methoxymethyl-MTEP exhibits a Kd = 20 nM as measured by saturation binding assays in rat brain cell membranes, and an IC50 = 30 nM in competitive binding assays. Methoxymethyl-MTEP can be used for research on diseases related to the glutamatergic nervous system, such as excitotoxicity and schizophrenia.
For research use only. We do not sell to patients.
- CAS No.: 524924-75-2
- Formula: C13H12N2OS
- Molecular Weight:244.31
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
mGluR5 |
In Vitro
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
Methoxymethyl‑MTEP (radioligand; 50 μCi/kg; intravenous injection) exhibits only background levels of specific binding in the forebrain of mGlu5 knockout mice[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 524924-75-2
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Molecular Weight 244.31
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Formula C13H12N2OS
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SMILES
COCC1=CC(C#CC2=CSC(C)=N2)=CN=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- Methoxymethyl-MTEP
- 524924-75-2
- mGluR
- Drug Intermediate
- mGluR5
- glutamate-mediated calcium mobilization
- noncompetitive antagonist
- seven transmembrane domain
- negative allosteric modulator
- NMDA-evoked peak and steady-state currents
- phosphoinositide hydrolysis
- schizophrenia
- excitotoxicity
- MPEP site
- Inhibitor
- inhibitor
- inhibit