Chemical Structure : VU6033685
Catalog No.: PC-24064Not For Human Use, Lab Use Only.
VU6033685 (BI1752) is a potent, selective positive allosteric modulator (PAM) of metabotropic glutamate receptor subtype 1 (mGlu1) with EC50 of 39 nM, Emax=65% (human mGlu1), and EC50 of 107 nM, Emax=94%.
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VU6033685 (BI1752) is a potent, selective positive allosteric modulator (PAM) of metabotropic glutamate receptor subtype 1 (mGlu1) with EC50 of 39 nM, Emax=65% (human mGlu1), and EC50 of 107 nM, Emax=94%.
VU6033685 displays no activity against mGlu2/3/4, and mGlu6/6/8 receptors (Ec50>10 uM).
VU6033685 (1-10 mg/kg, p.o.) reverses amphetamine-induced hyperlocomotion (AHL) in rats.
VU6033685 (1-30 mg/kg) reverses MK-801-induced disruption of novel object recognition in rats.
M.Wt | 366.85 | |
Formula | C20H19ClN4O | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Reed CW, et al. ACS Chem Neurosci. 2025 Feb 5. doi: 10.1021/acschemneuro.5c00014.
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