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Chemical Structure : JPC-141
Catalog No.: PC-22085Not For Human Use, Lab Use Only.
JPC-141 is a potent, selective vesicular monoamine transporter-2 (VMAT2) inhibitor, potently inhibits [3H]dopamine uptake by VMAT2 in striatal vesicles with Ki of 52 nM.
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JPC-141 is a potent, selective vesicular monoamine transporter-2 (VMAT2) inhibitor, potently inhibits [3H]dopamine uptake by VMAT2 in striatal vesicles with Ki of 52 nM.
JPC-141 displays 50 to 250-fold greater selectivity for VMAT2 over dopamine, norepinephrine and serotonin plasmalemma transporters.
JPC-141 is 57-fold more selective for inhibiting VMAT2 over [3H]dofetilide binding to hERG channels expressed by HEK293.
JPC-141 prevents the METH-induced reduction in striatal dopamine content in rats.
JPC-141 decreases METH-stimulated locomotor activity in METH-sensitized rats at doses of does not alter locomotor activity in the saline control group.
JPC-141 specifically decreased iv METH self-administration at doses that had no effect on food-maintained responding.
| M.Wt | 324.47 | |
| Formula | C21H28N2O | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Chandler CM, et al. Biochem Pharmacol. 2024 Apr 3:116189.
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