52-86-8
52-86-8
Chemical Structure
Haloperidol
- CAS No.: 52-86-8
- Formula:C21H23ClFNO2
- Molecular Weight:375.86
IUPAC Name: 4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)-1-(4-fluorophenyl)butan-1-one
InChIKey: LNEPOXFFQSENCJ-UHFFFAOYSA-N
SMILES: ClC(C=C1)=CC=C1C2(O)CCN(CCCC(C3=CC=C(F)C=C3)=O)CC2
Biological Activity: Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic agent. Haloperidol can be used in the study of schizophrenia, tics in Tourette syndrome, mania in bipolar disorder, delirium, agitation, acute psychosis, and hallucinations from alcohol withdrawal.
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Haloperidol | 99.69% | Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic agent. Haloperidol can be used in the study of schizophrenia, tics in Tourette syndrome, mania in bipolar disorder, delirium, agitation, acute psychosis, and hallucinations from alcohol withdrawal. | ||||||||||||||||||||
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Haloperidol (Standard) | 99.84% | Haloperidol (Standard) is the analytical standard of Haloperidol. This product is intended for research and analytical applications. Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. | ||||||||||||||||||||
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Haloperidol solution | Haloperidol solution is mainly composed of Haloperidol (HY-14538). Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic agent. Haloperidol can be used in the study of schizophrenia, tics in Tourette syndrome, mania in bipolar disorder, delirium, agitation, acute psychosis, and hallucinations from alcohol withdrawal. | |||||||||||||||||||||
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Haloperidol-d4 | Haloperidol-d4 is deuterium labeled haloperidol, and the latter is a potent dopamine D2 receptor antagonist. | |||||||||||||||||||||
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Haloperidol-d4 N-Oxide | Haloperidol-d4 N-Oxide is the deuterium labeled Haloperidol. Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. | |||||||||||||||||||||
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Haloperidol-13C6 | Haloperidol-13C6 is the 13C6 labeled Haloperidol. Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. | |||||||||||||||||||||
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Haloperidol-d4-1 | 98.0% | Haloperidol-d4-1 is deuterium labeled haloperidol, and the latter is a potent dopamine D2 receptor antagonist. | ||||||||||||||||||||
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Deschlorohaloperidol | 99.91% | Deschlorohaloperidol (compound 8h) is an analogue of Haloperidol (HY-14538). Haloperidol is a dopamine D2 receptor (D2R) antagonist for schizophrenia. | ||||||||||||||||||||
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Moperone hydrochloride | Moperone hydrochloride is a dopamine D2-receptor antagonist, exhibiting therapeutic efficacy in the management of psychiatric disorders. | |||||||||||||||||||||
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Haloperidol hydrochloride | 99.56% | Haloperidol hydrochloride is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic agent. Haloperidol hydrochloride can be used in the study of schizophrenia, tics in Tourette syndrome, mania in bipolar disorder, delirium, agitation, acute psychosis, and hallucinations from alcohol withdrawal. | ||||||||||||||||||||
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Haloperidol lactate | 99.29% | Haloperidol lactate is a potent antipsychotic agent. Haloperidol lactate can be used in acute and chronic schizophrenia and gilles de la tourette's syndrome. Haloperidol lactate has the potential for the research of psychotic disorders. | ||||||||||||||||||||
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Haloperidol impurity 6 | Haloperidol impurity 6 (Haloperidol hydrobromide) is an impurity of Haloperidol. | |||||||||||||||||||||
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Bromperidol | 99.83% | Bromperidol (R-11333) possesses antipsychotic activity, with a high affinity for central dopamine receptors D2. Bromperidol can kill Mycobacteria in a synergistic manner with Spectinomycin. | ||||||||||||||||||||
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Bromperidol hydrochloride | 99.67% | Bromperidol (R-11333) hydrochloride possesses antipsychotic activity, with a high affinity for central dopamine receptors D2. Bromperidol hydrochloride can kill Mycobacteria in a synergistic manner with Spectinomycin. | ||||||||||||||||||||
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Moperone | 99.5% | Moperone (R 1658) is an antagonist for D2 dopamine receptor and D3 dopamine receptor, with IC50 of 1.0 nM and 1.0 nM. | ||||||||||||||||||||
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Haloperidol impurity 2 | Haloperidol impurity 2 is an impurity of Haloperidol. | |||||||||||||||||||||
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Haloperidol impurity 4 | Haloperidol impurity 4 (Haloperidol impurity E) is an impurity of Haloperidol. | |||||||||||||||||||||
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