Dopamine Receptor
- [1]. Martel JC, et al. Dopamine Receptor Subtypes, Physiology and Pharmacology: New Ligands and Concepts in Schizophrenia. Front Pharmacol. 2020 Jul 14;11:1003. [Content Brief]
- [2]. Beaulieu JM, et al. The physiology, signaling, and pharmacology of dopamine receptors. Pharmacol Rev. 2011 Mar;63(1):182-217. [Content Brief]
- [3]. Beaulieu JM, et al. Dopamine receptors - IUPHAR Review 13. Br J Pharmacol. 2015 Jan;172(1):1-23. [Content Brief]
- [4]. Rashid AJ, et al. D1-D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of Gq/11 in the striatum. Proc Natl Acad Sci U S A. 2007 Jan 9;104(2):654-9. [Content Brief]
- [5]. Hasbi A, et al. Calcium signaling cascade links dopamine D1-D2 receptor heteromer to striatal BDNF production and neuronal growth. Proc Natl Acad Sci U S A. 2009 Dec 15;106(50):21377-82. [Content Brief]
- [6]. Demchyshyn LL, et al. Dopamine D5 receptor agonist high affinity and constitutive activity profile conferred by carboxyl-terminal tail sequence. J Biol Chem. 2000 Aug 4;275(31):23446-55. [Content Brief]
- [7]. Tumova K, et al. Role of the fourth intracellular loop of D1-like dopaminergic receptors in conferring subtype-specific signaling properties. FEBS Lett. 2004 Oct 22;576(3):461-7. [Content Brief]
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Dopamine Receptor Inhibitors
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Dopamine Receptor Agonists
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Dopamine Receptor Antagonists
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Dopamine Receptor MDM2 Inhibitor
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Dopamine Receptor Controls
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Dopamine Receptor Ligands
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Dopamine Receptor Related Products (537)
Related Products (537)
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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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- Clothixamide
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Org-10490
0 ImagesCat. No.: HY-U00077CAS No.: 83507-02-2Org-10490 is an antagonist of dopamine D1 receptor and dopamine D2 receptor, used for the treatment for psychiatric disease. -
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Lensiprazine
0 ImagesCat. No.: HY-14793CAS No.: 327026-93-7Lensiprazine is a potent dopamine D2 receptor (D2R) antagonist that acts as a serotonin reuptake inhibitor. Lensiprazine can be used to study bipolar disorder and schizophrenia. -
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NMI 8739 (Standard)
0 ImagesCat. No.: HY-101540RCAS No.: 129024-87-9 -
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Haloperidol decanoate (Standard)
0 ImagesCat. No.: HY-107969RCAS No.: 74050-97-8Haloperidol decanoate (Standard) is the analytical standard of Haloperidol decanoate. This product is intended for research and analytical applications. Haloperidol decanoate is a depot preparation of haloperidol, a commonly used butyrophenone derivative with antipsychotic activity. Haloperidol decanoate can increase the striatal D2 receptor in rat. Haloperidol decanoate can improve conditions of psychoses (mainly schizophrenia). Haloperidol decanoate can lead to increased accumulation of the dopamine metabolites homo-vanillic acid. Haloperidol decanoate can reduce intestinal transport, increase gastric emptying and reduce acid output in rat model. -
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Fluphenazine-d6 hydrochloride
0 ImagesCat. No.: HY-119980BSFluphenazine-d6 (hydrochloride) is deuterium labeled Fluphenazine (hydrochloride). Fluphenazine hydrochloride is a potent, orally active phenothiazine-based dopamine receptor antagonist. Fluphenazine hydrochloride blocks neuronal voltage-gated sodium channels. Fluphenazine hydrochloride acts primarily through antagonism of postsynaptic dopamine-2 receptors in mesolimbic, nigrostriatal, and tuberoinfundibular neural pathways. Fluphenazine hydrochloride can antagonize Methylphenidate-induced stereotyped gnawing and inhibit climbing behaviour in mice. Fluphenazine hydrochloride can be used for researching psychosis and painful peripheral neuropathy associated with diabetes and has potential to inhibit SARS-CoV-2. -
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- SRI-45949
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Savoxepin mesylate
0 ImagesCat. No.: HY-119385CAS No.: 79262-47-8Savoxepin mesylate is a D2 dopamine receptor (D2 Dopamine Receptor) antagonist with antipsychotic activity. Savoxepin mesylate selectively blocks dopamine D2 receptors in the hippocampus while having no significant effect on D2 receptors in the striatum. This selective blockade helps reduce the risk of extrapyramidal side effects (EPS). -
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Olanzapine ketolactam
0 ImagesCat. No.: HY-Z4466CAS No.: 1017241-34-7Olanzapine ketolactam (compound 1) is the impurity of Olanzapine (HY-14541). Olanzapine is a selective, orally active monoaminergic antagonist. -
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UNC9994 hydrochloride (Standard)
0 ImagesCat. No.: HY-111385RCAS No.: 2108826-33-9UNC9994 hydrochloride (Standard) is the analytical standard of UNC9994 (hydrochloride) (HY-111385). This product is intended for research and analytical applications. UNC9994 hydrochloride is a functionally selective, β-arrestin–biased dopamine D2 receptor (D2R) agonist that selectively activates β-arrestin recruitment and signaling. UNC9994 hydrochloride shows a binding affinity with a Ki of 79 nM for D2R. UNC9994 hydrochloride is also an antagonist of Gi-regulated cAMP production and partial agonist for D2R/β-arrestin-2 interactions. UNC9994 hydrochloride shows antipsychotic-like activity. -
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Milenperone
0 ImagesCat. No.: HY-121898CAS No.: 59831-64-0Milenperone (R 34009) is a dopamine atagonist. Milenperone can be used in the study for neurological disease. -
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Talipexole dihydrochloride (Standard)
0 ImagesSynonyms: B-HT 920 dihydrochloride (Standard)Talipexole (dihydrochloride) (Standard) is the analytical standard of Talipexole (dihydrochloride). This product is intended for research and analytical applications. Talipexole dihydrochloride (B-HT 920 dihydrochloride) is a dopamine D2 receptor agonist, α2-adrenoceptor agonist and 5-HT3 receptor antagonist, which displays antiParkinsonian activity. -
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Propionylpromazine (Standard)
0 ImagesCat. No.: HY-111480RCAS No.: 3568-24-9Propionylpromazine (Standard) is the analytical standard of Propionylpromazine (HY-111480). This product is intended for research and analytical applications. Propionylpromazine is a dopamine receptor DRD2 antagonist. Propionylpromazine also is an effective tranquillizer. Propionylpromazine can be used in veterinary studies. -
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4-EEC hydrochloride
0 ImagesCat. No.: HY-158552CAS No.: 2446466-62-04-EEC hydrochloride is a synthetic stimulant substance. 4-EEC hydrochloride is a releasing agent for norepinephrine-dopamine. -
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Thiethylperazine (Standard)
0 ImagesThiethylperazine (Standard) is the analytical standard of Thiethylperazine. This product is intended for research and analytical applications. 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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Paliperidone palmitate (Standard)
0 ImagesSynonyms: 9-Hydroxyrisperidone palmitate (Standard)Paliperidone palmitate (Standard) is the analytical standard of Paliperidone palmitate. This product is intended for research and analytical applications. Paliperidone palmitate is an orally effective competitive antagonist of dopamine D2 receptors and 5-hydroxytryptamine 2A (5-HT2A) receptors that can cross the blood-brain barrier. Paliperidone palmitate competitively inhibits the effects of dopamine and 5-hydroxytryptamine by binding to dopamine D2 receptors and 5-HT2A receptors, regulating the balance of the neurotransmitter system and thus exerting antipsychotic activity. Paliperidone palmitate is mainly used in the research field of schizophrenia. -
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