17 Results for "

schizophrenic

" in MedChemExpress (MCE) Product Catalog:
Products (17)

17 Results for "schizophrenic" in MCE Product Catalog:

Cat. No.: HY-B0731A
CAS No.: 150915-41-6
Synonyms: SM-9018 free base
Research Areas:  

Neurological Disease

Perospirone (SM-9018 free base) is an orally active antagonist of 5-HT2A receptor (Ki=0.6 nM) and dopamine D2 receptor (Ki=1.4 nM), and also a partial agonist of 5-HT1A receptor (Ki=2.9 nM). Perospirone is an atypical antipsychotic agent and has the potential for schizophrenic disease research .
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Cat. No.: HY-B0731
CAS No.: 129273-38-7
Synonyms: SM-9018
Research Areas:  

Neurological Disease

Perospirone hydrochloride (SM-9018) is an orally active antagonist of 5-HT2A receptor (Ki of 0.6 nM) and dopamine D2 receptor (Ki of 1.4 nM). Perospirone hydrochloride is also a partial agonist of 5-HT1A receptor (Ki of 2.9 nM). Perospirone hydrochloride is an atypical antipsychotic agent and has the potential for schizophrenic disease research .
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Cat. No.: HY-106100A
CAS No.: 108050-82-4
Purity:  99.53%
Synonyms: EMD 38362
Roxindole hydrochloride (EMD 38362), an indot-alkyl-pipenidine, is a potent agonist at dopamine autoreceptors, with an affinity for the D2-like subtype in the low nanomolar range. Roxindole can be used for the research of positive and negative schizophrenic symptoms. Roxindole is a 5-HT1A agonist and 5-HT uptake inhibitor with high affinity for 5-HT1A (IC50=0.9 nM). Antipsychotic and antidepressant activities .
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Cat. No.: HY-148337
CAS No.: 66317-22-4
Target:  

Peptides

Research Areas:  

Others

Thr-Val-Leu is a central nervous system tripeptide and reduces Thr-Val-Leu content in schizophrenic brain tissue .
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Cat. No.: HY-116746
CAS No.: 53179-12-7
Purity:  99.63%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Clopimozide is an orally active antischizophrenic agent that inhibits [ 3H]nitrendipine binding with IC50 value of 17 nM. Clopimozide is a calcium channel antagonist. Clopimozide can be used for the research of negative and positive schizophrenic symptoms .
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Cat. No.: HY-A0211
CAS No.: 2622-30-2
Target:  

Others

Research Areas:  

Neurological Disease

Carphenazine is a phenothiazine antipsychotic agent. Carphenazine can be used for researching chronic schizophrenic psychoses .
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Cat. No.: HY-122128
CAS No.: 5388-85-2
Synonyms: LY-51641
Target:  

Monoamine Oxidase

Research Areas:  

Neurological Disease

Lilly 51641 (LY-51641) is a selective and orally active Type A monoamine oxidase inhibitor. Lilly 51641 has the potential for the research of depressed and schizophrenic .
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Cat. No.: HY-121813
CAS No.: 75859-04-0
Synonyms: BW 234U
Target:  

Dopamine Transporter

Research Areas:  

Neurological Disease

Rimcazole (BW 234U) is a potent antipsychotic agent. Rimcazole also is a competitive antagonist of sigma sites. Rimcazole can be used for the research of acute schizophrenic diseases .
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Cat. No.: HY-132494S
CAS No.: 1246815-57-5
Perazine-d8 is a deuterated form of Perazine. Perazine is a potent and orally active antidepressant agent. Perazine has the potential for the research of acute schizophrenics .
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Cat. No.: HY-106100
CAS No.: 112192-04-8
Synonyms: EMD 49980
Roxindole (EMD 49980), an indot-alkyl-pipenidine, is a potent agonist at dopamine autoreceptors, with an affinity for the D2-like subtype in the low nanomolar range. Roxindole can be used for the research of positive and negative schizophrenic symptoms. Roxindole is a 5-HT1A agonist and 5-HT uptake inhibitor. Antipsychotic and antidepressant activities .
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Cat. No.: HY-106100AR
CAS No.: 108050-82-4
Synonyms: EMD 38362 (Standard)
Roxindole (hydrochloride) (Standard) is the analytical standard of Roxindole (hydrochloride). This product is intended for research and analytical applications. Roxindole hydrochloride (EMD 38362), an indot-alkyl-pipenidine, is a potent agonist at dopamine autoreceptors, with an affinity for the D2-like subtype in the low nanomolar range. Roxindole can be used for the research of positive and negative schizophrenic symptoms. Roxindole is a 5-HT1A agonist and 5-HT uptake inhibitor with high affinity for 5-HT1A (IC50=0.9 nM). Antipsychotic and antidepressant activities .
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Cat. No.: HY-B0731R
CAS No.: 129273-38-7
Synonyms: SM-9018 (Standard)
Perospirone (hydrochloride) (Standard) is the analytical standard of Perospirone (hydrochloride). This product is intended for research and analytical applications. Perospirone hydrochloride (SM-9018) is an orally active antagonist of 5-HT2A receptor (Ki of 0.6 nM) and dopamine D2 receptor (Ki of 1.4 nM). Perospirone hydrochloride is also a partial agonist of 5-HT1A receptor (Ki of 2.9 nM). Perospirone hydrochloride is an atypical antipsychotic agent and has the potential for schizophrenic disease research .
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Cat. No.: HY-A0211A
CAS No.: 2975-34-0
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Carphenazine dimaleate is a Phenothiazine (HY-Y0055) class antipsychotic active molecule. Carphenazine can be used in research on chronic schizophrenia .
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Cat. No.: HY-E70149
Synonyms: ST6GAL2
ST6 Gal Sialyltransferase 2 (EC:2.4.3.1, ST6GAL2) catalyzes the transfer of sialic acid from CMP to an oligosaccharide substrate. ST6 Gal Sialyltransferase 2 plays an important role in schizophrenic research .
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Cat. No.: HY-157958
CAS No.: 3030040-34-4
Target:  

nAChR

Research Areas:  

Neurological Disease

α7 nAChR modulator-3 (Compound 6p) is a α7 nAChR positive allosteric Modulator with a IC50 value of 1.3 μM. α7 nAChR Modulator-3 can be used to inhibit auditory gating defects in a mouse schizophrenic model .
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Cat. No.: HY-B0731AS
Synonyms: SM-9018-d8 free base
Perospirone-d8 (SM-9018-d8 (free base)) is deuterium labeled Perospirone. Perospirone (SM-9018 free base) is an orally active antagonist of 5-HT2A receptor (Ki=0.6 nM) and dopamine D2 receptor (Ki=1.4 nM), and also a partial agonist of 5-HT1A receptor (Ki=2.9 nM). Perospirone is an atypical antipsychotic agent and has the potential for schizophrenic disease research .
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Cat. No.: HY-118477
CAS No.: 173294-84-3
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Dehydrosertindole is a blood-brain barrier-permeable, orally active inhibitor of the dopamine D2 receptor. Dehydrosertindole occupies striatal dopamine D2 receptors to mediate receptor regulation. Dehydrosertindole is the active metabolite of Sertindole (HY-14543), which distributes rapidly in guinea pig myocardium and inhibits conditioned avoidance responses in rats. Dehydrosertindole can be used in research related to schizophrenia .
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