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Cat. No. Product Name Information
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.
PC-60216

PF-592379

D3R agonist

PF-592379 is a potent, selective, orally active agonist of dopamine D3 receptor with EC50 of 21 nM.
PC-70062

ABT-724 trihydrochloride

Dopamine D4 agonist

ABT-724 trihydrochloride is a potent, selective dopamine D4 receptor agonist that activates human dopamine D4 receptors with EC50 of 12.4 nM, with no effect on dopamine D1, D2, D3, or D5 receptors.
PC-70061

ABT-724

Dopamine D4 agonist

ABT-724 is a potent, selective dopamine D4 receptor agonist that activates human dopamine D4 receptors with EC50 of 12.4 nM, with no effect on dopamine D1, D2, D3, or D5 receptors.
PC-70058

PD128907 hydrochloride

D3R agonist

PD128907 hydrochloride is a potent, selective and orally active agonist of dopamine D3 receptor (D3R) with Ki of 20 nM.
PC-70057

PF-219061

D3R agonist

PF-219061 (PF 219061, PF219061) is a potent, selective agonist of dopamine D3 receptor with EC50 of 8 nM.
PC-43961

Clozapine

Clozapine is an atypical antipsychotic agent that binds to 5-HT and dopamine receptor, is also potent at the α2-adrenoceptor with Ki of 51 nM.
PC-42584

SKF-82958 hydrobromide

Dopamine D1 agonist, ERα agonist

SKF-82958 hydrobromide is a potent, full dopamine D1 agonist, produces characteristic anorectic effects, hyperactivity and self-administration in animals.
PC-42583

SKF 82958

Dopamine D1 agonist, ERα agonist

SKF 82958 is a potent, full dopamine D1 agonist, produces characteristic anorectic effects, hyperactivity and self-administration in animals.
PC-45204

Metoclopramide

D2R antagonist

Metoclopramide is apotent dopamine D2 receptor antagonist with Ki of 28 nM.
PC-42716

SB-277011

D3R antagonist

SB-277011 (SB277011A) is a potent and selective dopamine D3 receptor antagonist with pKi of 8.0.
PC-25355

D-583

D2/D3 agonist

D-583 is a potent hybrid D2/D3 agonist and iron (II)-specific chelator with EC50 of 3.14 nM (Emax=63%) and 0.62 nM (Emax=68%) for D2 and D3 receptors respectively, exhibits anti-ferroptotic activity.

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