Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
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GR103691 is a dopamine D3 receptor antagonist (Ki = 0.32 nM).1 It is selective for dopamine D3 receptors over dopamine D1, D2, and D4 receptors (Kis = 398.11, 39.81, and 81 nM, respectively) and over the serotonin (5-HT) receptor subtype 5-HT1A, α1-adrenergic receptors, and M1 muscarinic receptors (Kis = 3.16, 12.59, and >1,000 nM, respectively).1,2 GR103691 inhibits increases in locomotor activity induced by infusion of the GABAA and GABAC receptor agonist muscimol (Item No. 13667) into the rat ventral tegmental area (VTA; ED50 = 0.3 mg/kg) but not infusion into the substantia nigra zona reticulata (SNr; ED50 = >10 mg/kg).1 It increases the time rats spend in the light area of the light-dark exploration test and the open areas of the elevated plus maze without affecting locomotor activity, indicating anxiolytic-like behavior, when injected into the basolateral amygdala (BLA) at a dose of 5 pmol/animal.3
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1. A novel series of arylpiperazines with high affinity and selectivity for the dopamine D3 receptor. Bioor. Med. Chem. Lett. 5(3), 219-222 (1995).
2. A comparative in vitro and in vivo pharmacological characterization of the novel dopamine D3 receptor antagonists (+)-
3. Dopamine D3-