37 Results for "

Neuroleptic

" in MedChemExpress (MCE) Product Catalog:
Products (37)

37 Results for "Neuroleptic" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-121276
CAS No.: 2062-84-2
Purity:  ≥98.0%
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

Benperidol is a relatively old antipsychotic agent. Benperidol is a butyrophenone antipsychotic, with the highest neuroleptic potency in terms of D2 receptor blockade .
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Cat. No.: HY-B1904
CAS No.: 5002-47-1
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

Fluphenazine decanoate is a CNS-penetrant dopamine D2 receptor inhibitor, is a long-acting phenothiazine neuroleptic. Fluphenazine can be used for schizophrenia research .
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Cat. No.: HY-B1196
CAS No.: 51012-33-0
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

Tiapride hydrochloride is a selective and orally active D2 and D3 dopamine receptors antagonist with IC50 values of 110-320 nM and 180 nM, respectively. Tiapride hydrochloride shows anti-dyskinetic activity and anxiolytic activity. Tiapride hydrochloride is a neuroleptic agent .
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Cat. No.: HY-14264
CAS No.: 3546-03-0
Purity:  99.42%
Target:  

5-HT Receptor

연구분야:  

Neurological Disease

Cyamemazine is a neuroleptic agent that contains the phenothiazine chromophore. Cyamemazine is often used as an anxiolytic. Cyamemazine is a potent 5-HT3 (Ki of 12 nM), 5-HT2A (Ki = 1.5 nM) and 5-HT2C (Ki of 75 nM) receptors antagonist with antipsychotic activity .
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Cat. No.: HY-103415
CAS No.: 75272-39-8
Purity:  99.9%
Synonyms: YM-09151-2; Emonapride
연구분야:  

Neurological Disease

Nemonapride is a highly potent dopamine D2 receptor antagonist with a Ki of 0.06 nM. Nemonapride also activates 5-HT1A receptor with an IC50 of 34 nM. Nemonapride is an antipsychotic that readily passes through the blood brain barrier and exhibits potent neuroleptic effects in animals .
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Cat. No.: HY-W103105
CAS No.: 53786-28-0
Target:  

GABA Receptor

연구분야:  

Neurological Disease

R 29676 is a neuroleptic agent and inhibits sodium-dependent GABA binding (GABA uptake) .
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Cat. No.: HY-A0163D
CAS No.: 53772-84-2
Synonyms: (E)-Clopenthixol
연구분야:  

Infection

trans-Clopenthixol ((E)-Clopenthixol) is an antibiotic, without neuroleptic effect. trans-Clopenthixol can be used to inhibit Pseudomonas aeruginosa and Plasmodium falciparum in vitro .
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Cat. No.: HY-W436270
CAS No.: 632-47-3
Bulbocapnine hydrochloride, an aporphine alkaloid, is a dopamine receptor inhibitor. Bulbocapnine hydrochloride inhibits dopamine synthesis. Bulbocapnine hydrochloride also has neuroleptic-like, anticonvulsant and antinociceptive effects .
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Cat. No.: HY-136280
CAS No.: 139225-22-2
Purity:  99.43%
Synonyms: EMD 57445
Target:  

Sigma Receptor

연구분야:  

Neurological Disease

Panamesine (EMD 57445) is a sigma receptor ligand, which has a high affinity (IC50 6 nM) and selectivity for sigma binding sites. Panamesine is a potential atypical neuroleptic agent .
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Cat. No.: HY-116780A
CAS No.: 1225-65-6
Target:  

Cytochrome P450

연구분야:  

Neurological Disease

Prothipendyl hydrochloride is a tricyclic azaphenothiazine neuroleptic agent. Prothipendyl hydrochloride is a substrate of the CYP isozymes CYP1A2, CYP2D6, CYP2C19 and CYP3A4. Prothipendyl hydrochloride has sedating and psychomotorically damping effects. Prothipendyl hydrochloride can be used for psychomotoric agitation, sleep disorder and anxiety research .
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Cat. No.: HY-B1904A
CAS No.: 2376-65-0
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

Fluphenazine decanoate dihydrochloride is a CNS-penetrant dopamine D2 receptor inhibitor, is a long-acting phenothiazine neuroleptic. Fluphenazine can be used for schizophrenia research .
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Cat. No.: HY-B1196A
CAS No.: 51012-32-9
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

Tiapride is a selective and orally active D2 and D3 dopamine receptors antagonist with IC50 values of 110-320 nM and 180 nM, respectively. Tiapride shows anti-dyskinetic activity and anxiolytic activity. Tiapride is a neuroleptic agent .
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Cat. No.: HY-136281
CAS No.: 135135-87-4
Purity:  98.82%
Target:  

Sigma Receptor

연구분야:  

Neurological Disease

DuP 734 is a sigma receptor antagonist. DuP 734 is a selective and potent sigma and 5-HT2 receptor ligand with weak affinity for D2 receptors. DuP 734 may have antipsychotic activity without the liability of motor side effects typical of neuroleptics .
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Cat. No.: HY-U00006
CAS No.: 62030-88-0
연구분야:  

Neurological Disease

Duoperone is a neuroleptic agent and also a antiemetic agent in animal models.
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Cat. No.: HY-B1755
CAS No.: 94-12-2
Synonyms: Propyl 4-aminobenzoate
연구분야:  

Neurological Disease

Risocaine, also known as Propyl 4-aminobenzoate, with potential neuroleptic properties .
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Cat. No.: HY-A0163C
CAS No.: 58045-22-0
Synonyms: (E)-Clopenthixol dihydrochloride
연구분야:  

Infection

trans-Clopenthixol ((E)-Clopenthixol) dihydrochloride is an antibiotic agent, without neuroleptic effect. trans-Clopenthixol dihydrochloride can be used to inhibit Pseudomonas aeruginosa and Plasmodium falciparum in vitro .
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Cat. No.: HY-105545C
CAS No.: 21888-96-0
Synonyms: (+)-Benzetimide hydrochloride; (S)-(+)-Dexetimide hydrochloride; Dexbenzetimide hydrochloride
Target:  

mAChR

연구분야:  

Neurological Disease

Dexetimide hydrochloride ((+)-Benzetimide hydrochloride) is an antimuscarinic drug with the activity of suppressing neuroleptic-induced Parkinson's syndrome. Dexetimide hydrochloride is used to improve the symptoms of movement disorders caused by the use of neuroleptics. Dexetimide hydrochloride, as the (-)-enantiomer of (-)-Benzetimide, shows the ability to selectively inhibit cholinergic receptors .
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Cat. No.: HY-122979
CAS No.: 55528-07-9
Synonyms: (+)-AY-23,028; d-Butaclamol hydrochloride
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

(+)-Butaclamol hydrochloride is a neuroleptic agent with dopamine receptor-blocking activity. (+)-Butaclamol hydrochloride is (+)- enantiomer of butaclamol .
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Cat. No.: HY-160997
CAS No.: 68556-59-2
Synonyms: GRI 1665
Target:  

Dopamine Receptor

연구분야:  

Neurological Disease

Prosulpride (GRI 1665), a neuroleptics, can block selectively dopaminergic receptor .
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Cat. No.: HY-W103105R
CAS No.: 53786-28-0
R 29676 is a neuroleptic agent and inhibits sodium-dependent GABA binding (GABA uptake) .
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