15 Results for "

dopaminergic D2 receptor

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "dopaminergic D2 receptor" in MCE Product Catalog:

12
12 Publications Verification
Cat. No.: HY-103414
CAS No.: 84225-95-6
Purity:  99.83%
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Raclopride is a dopamine D2/D3 receptor antagonist with potential antipsychotic effects. Raclopride binds to D2 and D3 receptors with Kis of 1.8 nM and 3.5 nM, respectively .
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1 Cited Publications
Cat. No.: HY-B1225
CAS No.: 53-60-1
Synonyms: Romtiazin hydrochloride; Ampazine hydrochloride; Berophen hydrochloride
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Promazine (Romtiazin) hydrochloride is an antipsychotic and a dopamine receptor D2 antagonist. Promazine hydrochloride inhibits dopaminergic neurotransmission .
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Cat. No.: HY-100658
CAS No.: 839712-25-3
Purity:  99.79%
Research Areas:  

Neurological Disease

Didesmethyl cariprazine is an orally active, BBB-permeable metabolite of Cariprazine (HY-14763). Didesmethyl cariprazine is a partial agonist at the D2 and D3 receptors, full agonist at the 5-HT1A receptor, and antagonist at the human 5-HT2B receptor (Ki: 1.41 nM (human D2L), 0.056 nM (human D3), 1.7 nM (human 5-HT1A), 0.52 nM (human 5-HT2B)). Didesmethyl cariprazine dose-dependently inhibits the spontaneous activity of rat midbrain dopaminergic neurons .
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Cat. No.: HY-108976
CAS No.: 98185-20-7
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Raclopride tartrate is a selective dopamine D2/D3 receptor antagonist with potential antipsychotic effects. Raclopride tartrate binds to D2 and D3 receptors with Kis of 1.8 nM and 3.5 nM, respectively .
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Cat. No.: HY-B1225A
CAS No.: 58-40-2
Synonyms: Romtiazin; Ampazine; Berophen
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Promazine (Romtiazin) is an antipsychotic and a dopamine receptor D2 antagonist. Promazine inhibits dopaminergic neurotransmission .
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Cat. No.: HY-105903
CAS No.: 78541-97-6
Synonyms: Ro 22-​1319
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Piquindone (Ro 22-1319) is a potent antipsychotic agent. Piquindone binds to a D2 dopaminergic receptor subtype in a sodium-dependent manner. Piquindone can be used in the research of schizophrenia .
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Cat. No.: HY-B1225R
CAS No.: 53-60-1
Synonyms: Romtiazin hydrochloride (Standard); Ampazine hydrochloride (Standard); Berophen hydrochloride (Standard)
Promazine (hydrochloride) (Standard) is the analytical standard of Promazine (hydrochloride). This product is intended for research and analytical applications. Promazine (Romtiazin) hydrochloride is an antipsychotic and a dopamine receptor D2 antagonist. Promazine hydrochloride inhibits dopaminergic neurotransmission .
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Cat. No.: HY-B1225S
CAS No.: 1246819-33-9
Synonyms: Romtiazin-d6 hydrochloride; Ampazine-d6 hydrochloride
Promazine-d6 (hydrochloride) (Romtiazin-d6 (hydrochloride)) is deuterium labeled Promazine (hydrochloride). Promazine (Romtiazin) hydrochloride is an antipsychotic and a dopamine receptor D2 antagonist. Promazine hydrochloride inhibits dopaminergic neurotransmission .
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Cat. No.: HY-19225A
CAS No.: 155773-59-4
Synonyms: KA-672; Anseculin
Ensaculin free base (KA-672) is a NMDA antagonist and have high affinities to serotonergic 5-HT1A and 5-HT7 receptors, adrenergic α1, and dopaminergic D2 and D3 receptors. Ensaculin free base is a memory-enhancing agent. Ensaculin free base has the potential as an antidementia agent acting on various transmitter systems .
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Cat. No.: HY-103414R
CAS No.: 84225-95-6
Raclopride (Standard) is the analytical standard of Raclopride. This product is intended for research and analytical applications. Raclopride is a dopamine D2/D3 receptor antagonist with potential antipsychotic effects. Raclopride binds to D2 and D3 receptors with Kis of 1.8 nM and 3.5 nM, respectively .
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Cat. No.: HY-184573
CAS No.: 90471-34-4
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Dopamine D2 receptor modulator-1 is a positive allosteric modulator of hD2R. Dopamine D2 receptor modulator-1 enhances the potency of Dopamine (HY-B0451) on hD2R without intrinsic agonist activity. Dopamine D2 receptor modulator-1 protects dopaminergic differentiated cells from neurotoxic damage. Dopamine D2 receptor modulator-1 exhibits neuroprotective activity. Dopamine D2 receptor modulator-1 can be used in the research of Parkinson's disease .
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Cat. No.: HY-115418
CAS No.: 112892-81-6
Synonyms: U-68553B
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Alentemol hydrobromide (U-66444B) is a blood-brain barrier-permeable dopamine receptor D1, D2, D3, and D4 agonist. Alentemol hydrobromide inhibits dopamine release, reduces dopamine synthesis, regulates dopamine metabolism, suppresses the impulse activity of dopaminergic neurons, and decreases the impulse frequency of dopaminergic neurons in the substantia nigra pars compacta and ventral tegmental area. Alentemol hydrobromide is applicable to research related to schizophrenia .
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Cat. No.: HY-124524
CAS No.: 112891-97-1
Synonyms: U-66444B free base
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Alentemol (U-66444B (free base)) is a blood-brain barrier-permeable dopamine receptor D1, D2, D3, and D4 agonist. Alentemol inhibits dopamine release, reduces dopamine synthesis, regulates dopamine metabolism, suppresses the impulse activity of dopaminergic neurons, and decreases the impulse frequency of dopaminergic neurons in the substantia nigra pars compacta and ventral tegmental area. Alentemol is applicable to research related to schizophrenia .
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Cat. No.: HY-100658S
CAS No.: 1308279-08-4
Didesmethyl cariprazine-d8 is the deuterium labeled Didesmethyl cariprazine (HY-100658). Didesmethyl cariprazine is an orally active, BBB-permeable metabolite of Cariprazine (HY-14763). Didesmethyl cariprazine is a partial agonist at the D2 and D3 receptors, full agonist at the 5-HT1A receptor, and antagonist at the human 5-HT2B receptor (Ki: 1.41 nM (human D2L), 0.056 nM (human D3), 1.7 nM (human 5-HT1A), 0.52 nM (human 5-HT2B)). Didesmethyl cariprazine dose-dependently inhibits the spontaneous activity of rat midbrain dopaminergic neurons.
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Cat. No.: HY-100658R
CAS No.: 839712-25-3
Didesmethyl cariprazine (Standard) is the analytical standard of Didesmethyl cariprazine (HY-100658). This product is intended for research and analytical applications. Didesmethyl cariprazine is an orally active, BBB-permeable metabolite of Cariprazine (HY-14763). Didesmethyl cariprazine is a partial agonist at the D2 and D3 receptors, full agonist at the 5-HT1A receptor, and antagonist at the human 5-HT2B receptor (Ki: 1.41 nM (human D2L), 0.056 nM (human D3), 1.7 nM (human 5-HT1A), 0.52 nM (human 5-HT2B)). Didesmethyl cariprazine dose-dependently inhibits the spontaneous activity of rat midbrain dopaminergic neurons .
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