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Dopamine Receptor
Dopamine Receptor Isoform Specific Products
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Dopamine Receptor Related Products (1092)
Related Products (1092)
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Antibodies (7)
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Related Compound Screening Libraries (1)
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Dopamine Receptor Isoform Comparison
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Thiethylperazine-d3
0 ImagesCat. No.: HY-B1794SThiethylperazine-d3 is the deuterium labeled Thiethylperazinee (HY-B1794). Thiethylperazine, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine is also a selective ABCC1activator that reduces amyloid-β (Aβ) load in mice. Thiethylperazine has anti-emetic, antipsychotic and antimicrobial effects. -
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Raclopride-d5 hydrochloride
0 ImagesRaclopride-d5 hydrochloride is the deuterium labeled Raclopride. Raclopride is a dopamine D2/D3 receptor antagonist, which binds to D2 and D3 receptors with dissociation constants (Kis) of 1.8 nM and 3.5 nM, respectively, but has a very low affinity for D1 and D4 receptors with Kis of 18000 nM and 2400 nM, respectively. -
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SKF-80723
0 ImagesCat. No.: HY-137254CAS No.: 71636-62-9SKF-80723 is a D1 receptor agonist and can be used for study of Parkinson's disease. -
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Pentiapine (Standard)
0 ImagesCat. No.: HY-100143RCAS No.: 81382-51-6Synonyms: CGS 10746 (Standard)Pentiapine (Standard) is the analytical standard of Pentiapine (HY-100143). This product is intended for research and analytical applications. Pentiapine (CGS 10746) is a dopamine release inhibitor without binding to synaptic dopamine receptor sites. -
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Foscarbidopa (Standard)
0 ImagesCat. No.: HY-109131RCAS No.: 1907685-81-7Synonyms: ABBV-951 (Standard); Carbidopa 4′-monophosphate (Standard)Foscarbidopa (Standard) is the analytical standard of Foscarbidopa (HY-109131). This product is intended for research and analytical applications. Foscarbidopa (ABBV-951; Carbidopa 4′-monophosphate) is a proagent of Carbidopa, acts as a dopamine receptor agonist. -
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Lumateperone (Standard)
0 ImagesSynonyms: ITI-007 (Standard)Lumateperone (Standard) is the analytical standard of Lumateperone. This product is intended for research and analytical applications. Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator. Lumateperone has anticancer activity and can also be used for the study of schizophrenia and bipolar depression. -
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Aplindore fumarate
0 ImagesCat. No.: HY-129507CAS No.: 189681-71-8Synonyms: DAB-452 fumarateAplindore fumarate (DAB-452 fumarate) is a dopamine D2 receptor partial agonist. Aplindore fumarate could be used in studies of Parkinson's disease and schizophrenia. -
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7-Hydroxy-PIPAT
0 ImagesCat. No.: HY-129890CAS No.: 159559-71-47-Hydroxy-PIPAT (compound 2) is a D3R agonist. 7-Hydroxy-PIPAT is a high affinity to D3 dopamine receptor with Ki value of 0.99 nM. -
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L 646462
0 ImagesCat. No.: HY-118209CAS No.: 89149-85-9L-646462 is an antagonist of dopamine and 5-HT, with selectivity for the peripheral system (the central/peripheral activity ratio of L-646462 is 143). L-646462 can be used in research related to nausea, vomiting, and associated neurological disorders. -
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Itopride-d6
0 ImagesCat. No.: HY-B0732ASCAS No.: 1346746-82-4Synonyms: HSR803-d6 free baseItopride-d6 (HSR803-d6 (free base)) is deuterium labeled Itopride. Itopride (HSR803 free base) is a potent and orally active dopamine-2 antagonist and an acetylcholine esterase (AChE) inhibitor. Itopride enhances gastric motility through both antidopaminergic and anti-acetylcholinesterasic actions, can be used as a gastrointestinal prokinetic agent. Itopride can be used for researching gastro-esophageal reflux disease (GERD). -
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Hydrastine (Standard)
0 ImagesSynonyms: (-)-β-Hydrastine (Standard); (1R,9S)-β-Hydrastine (Standard)Hydrastine (Standard) is the analytical standard of Hydrastine (HY-B0927). This product is intended for research and analytical applications. Hydrastine ((-)-β-Hydrastine; (1R,9S)-β-Hydrastine) is a selective competitive inhibitor of tyrosine hydroxylase (TH), inhibiting dopamine biosynthesis (IC50=20.7 μM, PC12 cells). Hydrastine also inhibits the organic cation transporter OCT1 (IC50=6.6 μM). Hydrastine may cause neuronal toxicity through mitochondrial dysfunction rather than oxidative stress damage, and can aggravate cell apoptosis when combined with L-DOPA. Hydrastine can be used to study Parkinson's disease-related dopaminergic neuronal damage. -
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Metoclopramide dihydrochloride hydrate
0 ImagesMetoclopramide dihydrochloride hydrate is a potent antagonist of 5-HT3 and dopamine D2 receptor, with IC50s of 308 nM and 483 nM, respectively. Metoclopramide dihydrochloride hydrate can be used for the research of nausea and vomiting, gastro-oesophageal reflux, and gastroparesis. -
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Fenoldopam mesylate (Standard)
0 ImagesSynonyms: Fenoldopam methanesulfonate (Standard); SKF-82526 mesylate (Standard)Fenoldopam mesylate (Standard) is the analytical standard of Fenoldopam mesylate (HY-B0735A). This product is intended for research and analytical applications. Fenoldopam (SKF-82526) mesylate is a selective dopamine D1 receptor agonist. Fenoldopam mesylate binds to rat D1B dopamine receptors (Kd = 11 nM) and human D1A receptors (Kd = 17 nM) in COS-7 cell membranes expressing the cloned receptors. Fenoldopam mesylate modulates dopamine receptor expression, induces vasorelaxation in vascular tissues, reverses glomerular hyperfiltration in rat models, increases intracellular cAMP levels, promotes DARPP-32 phosphorylation in small cell lung cancer (SCLC) cells, inhibits cytokine secretion, and downregulates T cell activation markers in activated human T cells. Fenoldopam mesylate can be used for research on hypertension, acute kidney injury, psoriasis, and small cell lung cancer. -
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Ziprasidone (Standard)
0 ImagesSynonyms: CP-88059 (Standard)Ziprasidone (Standard) is the analytical standard of Ziprasidone. This product is intended for research and analytical applications. Ziprasidone (CP-88059), an orally active antipsychotic agent, is a combined 5-HT and dopamine receptor antagonist. Ziprasidone mesylate trihydrate has affinities for Rat D2 (Ki=4.8 nM), 5-HT2A (Ki=0.42 nM) and 5-HT1A (Ki=3.4 nM). -
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Fananserin (Standard)
0 ImagesCat. No.: HY-103104RCAS No.: 127625-29-0Synonyms: RP 62203 (Standard)Fananserin (Standard) is the analytical standard of Fananserin (HY-103104). This product is intended for research and analytical applications. Fananserin (RP 62203) is an orally bioavailable, potent and selective 5-hydroxytryptamine2 (5-HT2) receptor antagonist, with a Ki of 0.37 nM for the rat 5-HT2A receptor. Fananserin also is a selective dopamine D4 receptor antagonist, with a Ki of 2.93 nM for the human dopamine D4 receptor. -
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(±) Anabasine (Standard)
0 Images(±) Anabasine (Standard) is the analytical standard of (±) Anabasine (HY-W052144). This product is intended for research and analytical applications. (±) Anabasine is the racemic form of Anabasine (HY-B1532). (±) Anabasine stimulates the release of [3H]-Dopamine from mouse striatal synaptosomes. (±) Anabasine inhibits the high-affinity binding of [3H]-S-(-)-Nicotine to the striatal membrane. Anabasine is an agonist of α7nAChR and possesses anti-inflammatory and insecticidal activities. -
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S3608
0 ImagesCat. No.: HY-123440CAS No.: 57359-17-8S3608 is an atypical dopamine agonist. S3608 dose dependently increase locomotor activity (LA) in rats. -
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ST-836
0 ImagesCat. No.: HY-15238CAS No.: 1148156-63-1ST-836 is a dopamine receptor ligand; Antiparkinsonian agent. -
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Sonepiprazole mesylate
0 ImagesCat. No.: HY-123676CAS No.: 170858-34-1Synonyms: PNU-101387G mesylate; U-101387G mesylateSonepiprazole mesylate is a selective D4 dopamine antagonist with Kis of 3.6, 10.1, 5147, and 7430 nM for rD4-Dopamine, hD4.2-Dopamine, rD2-Dopamine, and Histamine-H1 receptors, respectively. -
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A31472
0 ImagesCat. No.: HY-119076CAS No.: 69319-52-4A31472 is a dopamine D-2 receptors antagonist that is promising for research of antipsychotic agents. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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