A selective mGluR1 PAM (EC50s = 0.39 and 0.36 μM for human and rat receptors

VU0483605 – 5 mg

Brand:
Cayman
CAS:
1623101-11-0
Storage:
-20
UN-No:
Non-Hazardous - /

Glutamate, the major excitatory neurotransmitter in the CNS, activates eight known subtypes of metabotropic glutamate receptors (mGluRs). Highly selective modulators designed to act at allosteric sites on certain mGluR subtypes are being developed to preferentially regulate subtype-specific, glutamate-induced receptor activation.{22053} VU0483605 is a selective positive allosteric modulator (PAM) of mGluR1, displaying EC50 values of 0.39 and 0.36 μM at human and rat receptors, respectively, and no activity as a mGlu4 PAM (EC50 >10 μM).{27299} It has been shown to potentiate a response to glutamate in wild-type cell lines stably expressing mGlu1 and to partially restore the reduction in glutamate-mediated calcium signaling in a mutant cell model of schizophrenia.{27299}  

 

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Description

A selective mGluR1 PAM (EC50s = 0.39 and 0.36 μM for human and rat receptors, respectively) with no activity as a mGlu4 PAM (EC50 >10 μM); potentiates a response to glutamate in wild-type cell lines stably expressing mGlu1 and partially restores the reduction in glutamate-mediated calcium signaling in a mutant cell model of schizophrenia

Formal name: 3-chloro-N-[3-chloro-4-(4-chloro-1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]-2-pyridinecarboxamide

Synonyms: 

Molecular weight: 446.7

CAS: 1623101-11-0

Purity: ≥98%

Formulation: A crystalline solid

Product Type|Biochemicals|Receptor Pharmacology|Allosteric Modulators||Research Area|Neuroscience|Behavioral Neuroscience|Schizophrenia & Psychosis

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