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Clozapine

Cat. No. M3417

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Clozapine Structure
Synonym:

HF 1854

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
100mg USD 50  USD50 In stock
500mg USD 90  USD90 In stock
1g USD 140  USD140 In stock
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Quality Control & Documentation
Biological Activity

Clozapine (Clozaril) is a potent 5-HT1C receptor antagonist with an IC50 of 110 nM for 5-HT-stimulated phosphoinositide hydrolysis. It is an antipsychotic medication used in the treatment of schizophrenia, and is also used off-label in the treatment of bipolar disorder. Clozapine is classified as an atypical antipsychotic compound because its profile of binding to serotonergic as well as dopamine receptors; its effects on various dopamine mediated behaviors also differ from those exhibited by more typical antipsychotics.

Product Citations
Customer Product Validations & Biological Datas
Source Mol Metab (2017). Figure 2. Clozapine
Method Immunohistochemistry
Cell Lines whole brain
Concentrations 0.3 mg/kg
Incubation Time 0.5 h
Results We found in Figure 2 that hM3Dq-mCherry (in red) was expressed in the brainstem NTS-DMV, and upon ip injection of clozapine-N-oxide (CNO, 0.3 mg/kg), hM3Dq-mediated activation of Gcgþ neurons induced an abundant expression of the early response gene c-Fos (in green, C) in the brainstem NTS-DMV and AP compared to that in A, suggesting activation of Gcgþ neurons-mediated neural circuitry.
Protocol (for reference only)
Cell Experiment
Cell lines A549 and H1299 human NSCLC cells
Preparation method Residual CFSE was then removed by washing twice with phosphate-buffered saline (PBS), followed by cell growth in culture medium with or without 50 μM clozapine for 72 h. For cell cycle analysis, cells were fixed in 70% ethanol and stained with a PI/Triton X-100 DNA-staining solution (20 μg/mL PI, 0.1% Triton X-100, and 0.2 mg/mL RNase A in PBS) at room temperature for 30 min.
Concentrations 50 μM
Incubation time 72 h
Animal Experiment
Animal models specific pathogen–free Sprague-Dawley rats
Formulation water
Dosages 10, 30, and 100 mg/kg
Administration oral gavage
Chemical Information
Molecular Weight 326.82
Formula C18H19ClN4
CAS Number 5786-21-0
Solubility (25°C) DMSO 45 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Hou ML, et al. J Pharmacol Exp Ther. The Drug-Drug Effects of Rhein on the Pharmacokinetics and Pharmacodynamics of Clozapine in Rat Brain Extracellular Fluid by In Vivo Microdialysis.

[2] Yin YC, et al. Cell Physiol Biochem. Clozapine induces autophagic cell death in non-small cell lung cancer cells.

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Keywords: Clozapine, HF 1854 supplier, 5-HT Receptor, inhibitors, activators

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