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PD 168568 is a dopamine D4 receptor antagonist (Ki = 8.8 nM).1 It is selective for dopamine D4 over D2 receptors (Ki = 1,842 nM). PD 168568 (3 mg/kg) reverses amphetamine-induced hyperlocomotion in rats. It also inhibits the growth of glioblastoma neural stem cells when used at concentrations of 25 and 50 µM.2
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1. Isoindolinone enantiomers having affinity for the dopamine D4 receptor. Bioorg. Med. Chem. Lett. 8(12), 1499-1502 (1998).
2. Inhibition of dopamine receptor D4 impedes autophagic flux, proliferation, and survival of glioblastoma stem cells. Cancer Cell 29(6), 859-873 (2016).