VU6053371 | VU6053371 : Positive Allosteric of GRM3
RATINGS:
Cellular Use: (0 reviews)

In Model Organisms: (0 reviews)
Control Compounds
Chemical Information
Vendors

Probe Summary

Targets Biochemical/Biophysical Potency Cellular Potency
GRM3
    • EC50:113 nM
    • EC50:90 nM
    up to 1 uM

    Selectivity

    In Vitro Selectivity Assessment
    Potency Assay Off-Target:
    Selectivity within targer family: selective versus the other mGlu receptors (EC50 > 10 μM) including ...
    In Vitro Selectivity Assessment
    Potency Assay Off-Target:
    In Eurofin SafetyScreen 44, the most significant displacement of radioligands was at the human dopam ...
    Selectivity Assessment Description:
    Follow-up radioligand binding assays for DAT produced a binding IC50 of 7.5 μM and a Ki of 6.0 μM (a ...

    Potency
    Cellular
    In Vitro

    GRM3

    Mode of Action: Positive Allosteric

    Structure-Activity-Relationship data available? No

    DOI Reference: 10.1021/acschemneuro.6c00325

    In Vivo Validations

    Rat
    Dose:
    Route of delivery: Intravenous
    Plasma half life: 2.6 h
    Systemic clearance: 10 mL/min/kg
    Volume of Distribution at Steady-State: 1.6 L/kg

    DOI Reference: 10.1021/acschemneuro.6c00325

    Dose:
    Route of delivery: Oral
    Cmax: 2.75 μM
    Tmax: 1 h
    Bioavailability: 82%

    DOI Reference: 10.1021/acschemneuro.6c00325

    Orthogonal Probes def

    VU6052959
    SMILES: CN1C2=CC=C(C=C2OC[C@@H]1C3=CC(=CC=C3)F)NC(=O)C4=NC=CC=N4

    Chemical Information

    Coming Soon...

    References

    Cross References

    Expert Reviews


    No SERP comments found for VU6053371

    Probe VU6053371 is in the process of SERP review.

    Please continue to check back for new reviews and commentary.