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Dopamine Receptor
Dopamine Receptor Isoform Specific Products
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Dopamine Receptor Ligands
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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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BRL 34778
0 ImagesCat. No.: HY-106820CAS No.: 86580-77-0BRL 34778 is a potent, selective and orally active dopamine D2 receptor antagonist with a Ki of 2.14 nM. BRL 34778 exhibits antipsychotic activity with low activity for extrapyramidal effects and sedation. BRL 34778 can be used for the research of neurological disease, such as schizophrenia. -
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Isoremoxipride
0 ImagesCat. No.: HY-W647997CAS No.: 107188-74-9Isoremoxipride is a dopamine antagonist. Isoremoxipride is a 3-methoxy isomer that exhibits affinities for the dopamine D2 receptor. -
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D4R antagonist-1
0 ImagesCat. No.: HY-145905CAS No.: 2846077-19-6D4R antagonist-1 is a potent and selective D4R antagonist with an IC50 of 6.87 µM. D4R antagonist-1 has the potential for the research of Parkinson’s disease. -
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Bromperidol decanoate (Standard)
0 ImagesCat. No.: HY-118551RCAS No.: 75067-66-2Synonyms: R46541 (Standard)Bromperidol decanoate (Standard) is the analytical standard of Bromperidol decanoate. This product is intended for research and analytical applications. Bromperidol decanoate (R46541) is a compound used for the inhibition of schizophrenia and has certain clinical inhibitory activity. -
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AJ-76
0 ImagesCat. No.: HY-111283CAS No.: 85379-09-5Synonyms: (+)-AJ 76; (1S,2R)-AJ 76AJ-76 ((+)-AJ 76; (1S,2R)-AJ 76) is a dopamine autoreceptor antagonist. AJ-76 can increase the synthesis and turnover of dopamine in the rat brain, while having little effect on the synthesis and turnover of serotonin (5-HT) and norepinephrine. AJ-76 can also antagonize the sedative effects of low-dose apomorphine and has a weak antagonistic effect on postsynaptic dopamine receptor. -
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(±)-Butaclamol
0 ImagesCat. No.: HY-165622CAS No.: 36504-93-5Synonyms: AY-23,028 free base; dl-Butaclamol(±)-Butaclamol is a antipsychotic agent and act as a D2 receptor antagonist. -
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Tefludazine
0 ImagesCat. No.: HY-184802CAS No.: 80273-79-6Tefludazine is an orally active antagonist of dopamine D2 receptor with an IC50 of 8.8 nM and 5-HT2 receptor with an IC50 of 8.6 nM. Tefludazine moderately inhibits the uptake of dopamine, norepinephrine and serotonin in rat brain synaptosomes, with IC50 values of 520 nM, 660 nM and 7000 nM, respectively. Tefludazine exhibits long-acting antipsychotic activity, lacks anticholinergic activity, shows Clozapine (HY-14539)-like effects at low doses and Haloperidol (HY-14538)-like effects at high doses. Tefludazine can be used for the research of psychotic disorders. -
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Thioridazine (Standard)
0 ImagesThioridazine (Standard) is the analytical standard of Thioridazine. This product is intended for research and analytical applications. Thioridazine, an antagonist of the dopamine receptor D2 family proteins, exhibits potent anti-psychotic and anti-anxiety activities. Thioridazine is also a potent inhibitor of PI3K-Akt-mTOR signaling pathways with anti-angiogenic effect. Thioridazine shows antiproliferative and apoptosis induction effects in various types of cancer cells, with specificity on targeting cancer stem cells (CSCs). -
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CI-943
0 ImagesCat. No.: HY-100161CAS No.: 89239-35-0Synonyms: (±)-CI-943CI-943 is a potential antipsychotic agent. -
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Metoclopramide (Standard)
0 ImagesMetoclopramide (Standard) is the analytical standard of Metoclopramide. This product is intended for research and analytical applications. Metoclopramide is a potent antagonist of 5-HT3 and dopamine D2 receptor, with IC50s of 308 nM and 483 nM, respectively. Metoclopramide can be used for the research of nausea and vomiting, gastro-oesophageal reflux, and gastroparesis. -
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Dopamine D3 receptor ligand-6
0 ImagesCat. No.: HY-174307CAS No.: 687634-09-9Dopamine D3 receptor ligand-6 (Compound 196476) is a selective dopamine D3 receptor (D3) antagonist. Dopamine D3 receptor ligand-6 is promising for research of substance use disorders (such as opioid and psychostimulant addiction). -
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Milsaperidone
0 ImagesCat. No.: HY-G0003ACAS No.: 501373-88-2Synonyms: (S)-Hydroxy Iloperidone; VHX-896Milsaperidone ((S)-Hydroxy Iloperidone; VHX-896) is an orally active serotonin 5-HT2A and dopamine D2 receptor antagonist. Milsaperidone ((S)-Hydroxy Iloperidone) is the active metabolite of the antipsychotic agent Iloperidone (HY-17410). Milsaperidone can be used in studies related to mental disorders such as depression. -
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S33084
0 ImagesCat. No.: HY-114618CAS No.: 273203-30-8S33084 is a dopamine D(3)-receptor antagonist with the pKi values of 8.72, 8.62 and 6.82 of cloned rat dopamine D3 receptor, native rat dopamine D3 and D2 receptor. -
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(±)-Butaclamol hydrochloride
0 ImagesCat. No.: HY-B1573ACAS No.: 36504-94-6Synonyms: AY-23,028; dl-Butaclamol hydrochloride(±)-Butaclamol hydrochloride (AY-23,028) is the antagonist for adrenergic receptor and dopamine receptor. (±)-Butaclamol hydrochloride antagonizes amphetamine or Apomorphine (HY-12723)-induced stereotyped behaviors and emesis, inhibits discriminative avoidance behavior, and induces catalepsy in rats models. -
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Pridopidine hydrochloride
0 ImagesCat. No.: HY-111210CAS No.: 882737-42-0Synonyms: ACR16 hydrochloride; ASP2314 hydrochloride; FR310826 hydrochloridePridopidine (ACR16) hydrochloride, a dopamine (DA) stabilizer, acts as a low affinity dopamine D2 receptor (D2R) antagonist. Pridopidine exerts high affinity towards sigma 1 receptor (S1R) with Ki between 70 and 80 nM, which is ~100-fold higher than its affinity toward D2R. -
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Zotepine (Standard)
0 ImagesZotepine (Standard) is the analytical standard of Zotepine. This product is intended for research and analytical applications. Zotepine, an antipsychotic agent, is a potent antagonist of 5-HT2A, 5-HT2C, Histamine H1, α1-adrenergic and Dopamine D2 receptors, with Kds of 2.6 nM, 3.2 nM, 3.3 nM, 7.3 nM and 8 nM, respectively. Zotepine exhibits antidepressive and anxiolytic effects in vivo. -
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SKF-83566 (Standard)
0 ImagesCat. No.: HY-103430ARCAS No.: 99295-33-7SKF-83566 (Standard) is the analytical standard of SKF-83566 (HY-103430A). This product is intended for research and analytical applications. SKF-83566 is an orally active, blood-brain barrier-permeable D1/D5 dopamine receptor antagonist with a Ki value of approximately 0.4-0.56 nM. SKF-83566 modulates locomotor behavior and spatial memory by blocking D1 receptors and inhibits glioblastoma progression by targeting the DRD1/c-Myc/UHRF1 pathway. SKF-83566 acts as an inhibitor of the dopamine transporter (DAT) and adenylyl cyclase 2 (AC2). SKF-83566 competitively binds to DAT to inhibit dopamine reuptake and non-competitively inhibits AC2 activity, thereby reducing cAMP accumulation. SKF-83566 is used in research areas such as dopaminergic system mechanisms, learning and memory, targeted intervention for glioblastoma, AC2 pathophysiology, antiparasitic drug screening, and synaptic plasticity (the "gating effect"). -
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Quetiapine-d8 fumarate
0 ImagesCat. No.: HY-B0031S2CAS No.: 1185247-12-4Quetiapine-d8 (fumarate) is the deuterium labeled Quetiapine. Quetiapine is a 5-HT receptors agonist with a pEC50 of 4.77 for human 5-HT1A receptor. Quetiapine is a dopamine receptor antagonist with a pIC50 of 6.33 for human D2 receptor. Quetiapine has moderate to high affinity for the human D2, HT1A, 5-HT2A, 5-HT2C receptor with pKis of 7.25, 5.74, 7.54, 5.55. Antidepressant and anxiolytic effects. -
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Thiethylperazine dimaleate (Standard)
0 ImagesThiethylperazine (dimaleate) (Standard) is the analytical standard of Thiethylperazine (dimaleate). This product is intended for research and analytical applications. Thiethylperazine dimaleate, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine dimaleate is also a selective ABCC1activator that reduces amyloid-β (Aβ) load in mice. Thiethylperazine dimaleate has anti-emetic, antipsychotic and antimicrobial effects. -
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Azaperone (Standard)
0 ImagesAzaperone (R-1929) (Standard) is the analytical standard of Azaperone (HY-B1470). This product is intended for research and analytical applications. Azaperone is an antagonist of dopamine D2 receptor (Dopamine D2 Receptor) and α-adrenergic receptor (AR). Azaperone reduces vasomotor tone, mean arterial pressure, hematocrit, hemoglobin concentration, and etorphine-induced duration; induces transient tachycardia followed by bradycardia, splenic uptake of red blood cells, and sedation; alters animal behaviors; and produces sedation with distinct onset and duration in foals. Azaperone is used for sedation and tranquilization in various animals to reduce stress and aggressive behaviors, and serves as a preanesthetic agent. -
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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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