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Cat. No. Product Name Information
PC-63187

Brilaroxazine

Dopamine/5-HT modulator

RP-5063 (Brilaroxazine) is a multimodal dopamine and serotonin modulator with partial agonist activity at DA D2, D3, D4, 5-HT1A, and 5-HT2ARs, and antagonist activity at 5-HT2B, 5-HT6 and 5-HT7Rs.
PC-63113

A-68930 hydrochloride

D1DR agonist

A-68930 is a potent, specific, orally bioavailable agonist of the D1 dopamine receptor (D1DR) with EC50 of 2.5 nM.
PC-62128

ML398

D4R inhibitor

ML398 (CID72737723) is a potent, selective, highly brain penetrant dopamine 4 (D4R) receptor antagonist with IC50/Ki of 130 nM/60 nM.
PC-61749

Alizapride hydrochloride

D2R antagonist

Alizapride (MS 5080) is a dopamine D2 antagonist with prokinetic and antiemetic effects used in the treatment of nausea and vomiting..
PC-61748

Alizapride

D2R antagonist

Alizapride (MS 5080) is a dopamine D2 antagonist with prokinetic and antiemetic effects used in the treatment of nausea and vomiting.
PC-61553

JNJ-37822681

D2R antagonist

JNJ-37822681 is a potent, specific and fast-dissociating dopamine D2 antagonist with Ki of 158 nM.
PC-61108

PF-4363467

PF-4363467 (PF 04363467) is a novel highly potent, brain penetrant dopamine D3/D2 receptor antagonist with Ki of 1.3/692 nM respectively, with high selectivity for D3R versus other biogenic amine receptors.
PC-60744

GSK598809 hydrochloride

GSK598809 hydrochloride is a potent, selective, CNS penetrant and orally bioavailable dopamine D3 receptor antagonist with pKi of 8.9.
PC-60743

GSK598809

GSK598809 (GSK-598809) is a potent, selective, CNS penetrant and orally bioavailable dopamine D3 receptor antagonist with pKi of 8.9.
PC-60735

DETQ

Dopamine D1 modulator

DETQ is a novel potent, selective, allosteric and orally active dopamine D1 receptor potentiator with Kb of 26 nM.
PC-60665

SKF 83566 hydrobromide

Dopamine D1 inhibitor

SKF 83566 hydrobromide is a potent, selective dopamine D1 receptor antagonist with Ki of 0.56 nM.
PC-60614

A-412997 dihydrochloride

D4R agonist

A-412997 is a potent, selective dopamine D4 receptor agonist with Ki of 12.1 and 7.9 nM for rat and human D4 receptors, respectively.

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