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Cat. No. Product Name Information
PC-22235

Raclopride

Dopamine D2/D3 antagonist

Raclopride (FLA 870) is a potent, selective dopamine D2/D3 receptor antagonist, binds to D2 and D3 receptors with Ki of 1.8 nM and 3.5 nM, respectively.
PC-22227

A-77636 hydrochloride

Dopamine D1 agonist

A-77636 hydrochloride is a potent, selective, orally active and long acting dopamine D1 receptor agonist with Ki of 39.8 nM.
PC-22147

SCH23390 hydrochloride

Dopamine Receptor antagonist

SCH23390 hydrochloride is a potent and selective dopamine D1-like receptor antagonist with Kis of 0.2 nM and 0.3 nM for the D1 and D5 receptor, respectively.
PC-21488

NGD-94-1

D4R inhibitor

NGD-94-1 is a highly potent, selective dopamine D4 receptor antagonist with Ki of 3.6 nM.
PC-21487

Nemonapride

D2R antagonist

Nemonapride (YM-09151-2) is a highly potent, selective dopamine D2 receptor antagonist with Ki of 0.06 nM.
PC-21106

L-745870

D4R inhibitor

L-745870 (L-745,870) is is a potent, selective, brain-penetrant and orally active dopamine D4 receptor (D4R) antagonist with Ki of 0.43 nM.
PC-21105

CAB-01-019

D4R inhibitor

CAB-01-019 is potent, selective dopamine D4 receptor (D4R) full antagonist with binding Ki of 2.2 nM, >500-fold selectivity over D2R and D3R.
PC-20978

ZINC621433144

D4 agonist

ZINC621433144 is a Gi-biased, high-affinity full agonist of dopamine D4 receptor with Ki of 4.3 nM and cAMP EC50 of 0.18 nM.
PC-20865

GR-103691

D3 receptor antagonist

GR-103691 is a potent, selective dopamine D3 receptor antagonist with binding Ki of 0.4 nM, >100-fold selectivity over D1 and D4 receptors.
PC-20864

CJB 090

D3 receptor agonist

CJB 090 (CJB090) is a selective partial agonist of dopamine D3 receptor with binding Ki of 0.6 nM, CJB 090 is 97-fold selective for D3 receptors over D2.
PC-20863

NGB-2904

D3 receptor antagonist

NGB-2904 is a potent, highly selective dopamine D3 receptor antagonist with Ki of 2.0 nM for hD3, 56-fold selectivity over hD2.
PC-20862

PG01037

D3 receptor antagonist

PG01037 is a potent selective dopamine D3 receptor antagonist with binding Ki of 0.7 nM, displays 133- and 540-fold selectivity over D2 and D4 receptors, respectively.

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