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  3. Levomepromazine hydrochloride

Levomepromazine hydrochloride  (Synonyms: Methotrimeprazine hydrochloride)

Cat. No.: HY-B1693A
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Levomepromazine (Methotrimeprazine) hydrochloride is an orally active antipsychotic compound and Ca2+ release inducer. Levomepromazine inhibits SERCA pump and induces an increase in cytoplasmic Ca2+ levels. Levomepromazine hydrochloride has antagonistic effects on a variety of neurotransmitter receptors, including dopamine, cholinergic, serotonin, and histamine receptors. Levomepromazine hydrochloride can induce adaptive ER stress and autophagy. In addition, Levomepromazine hydrochloride has antiviral, anti-inflammatory, neuroprotective and analgesic, sedative and anti-injurious activities. Levomepromazine hydrochloride can be used in the study psychiatric disorders and relieving nausea and vomiting.

For research use only. We do not sell to patients.

Levomepromazine hydrochloride

Levomepromazine hydrochloride Chemical Structure

CAS No. : 1236-99-3

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Description

Levomepromazine (Methotrimeprazine) hydrochloride is an orally active antipsychotic compound and Ca2+ release inducer. Levomepromazine inhibits SERCA pump and induces an increase in cytoplasmic Ca2+ levels. Levomepromazine hydrochloride has antagonistic effects on a variety of neurotransmitter receptors, including dopamine, cholinergic, serotonin, and histamine receptors. Levomepromazine hydrochloride can induce adaptive ER stress and autophagy. In addition, Levomepromazine hydrochloride has antiviral, anti-inflammatory, neuroprotective and analgesic, sedative and anti-injurious activities. Levomepromazine hydrochloride can be used in the study psychiatric disorders and relieving nausea and vomiting[1][2][3][4].

In Vitro

Levomepromazine (10 μM; 24 h) hydrochloride reduces Japanese encephalitis virus (JEV)-induced Neuro2a cell death, reduces JEV RNA levels and viral titers, and significantly inhibits JEV protein translation/replication complex formation and ROS production[1].
Levomepromazine (10 μM; 24 h) hydrochloride decreases the inflammatory response of microglia by inducing autophagy[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: Japanese encephalitis virus treated Neuro2a
Concentration: 10 μM
Incubation Time: 24 h
Result: Reduced the level of JEV RNA.
In Vivo

Levomepromazine (2 mg/kg; oral gavage; 15 days) hydrochloride has antiviral and anti-inflammatory activity in a mouse model infected with Japanese encephalitis virus[1].
Levomepromazine (5-20 mg/kg; intraperitoneal injection; single dose) hydrochloride has analgesic, sedative and anti-injurious effects in mice[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Japanese encephalitis virus-S3 infected C57BL/6 mouse[1]
Dosage: 2 mg/kg
Administration: Oral gavage (i.g.); 15 days
Result: Delayed virus invasion into the brain, and significantly lower viremia.
Showed complete protection of the barrier.
Reduced levels of multiple pro-inflammatory cytokines and interferon in the brains of infected mice.
Clinical Trial
Molecular Weight

364.93

Formula

C19H25ClN2OS

CAS No.
SMILES

CN(C)C[C@@H](C)CN1C2=CC(OC)=CC=C2SC3=CC=CC=C31.Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Levomepromazine hydrochloride
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