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Blonanserin

Catalog No. T1180Cas No. 132810-10-7
Alias AD-5423

Blonanserin (AD-5423) is an atypical antipsychotic approved in Japan in January, 2008. Relative to many other antipsychotics, blonanserin has an improved tolerability profile, lacking side effects such as extrapyramidal symptoms, excessive sedation, or hypotension.

Blonanserin

Blonanserin

Purity: 100%
Catalog No. T1180Alias AD-5423Cas No. 132810-10-7
Blonanserin (AD-5423) is an atypical antipsychotic approved in Japan in January, 2008. Relative to many other antipsychotics, blonanserin has an improved tolerability profile, lacking side effects such as extrapyramidal symptoms, excessive sedation, or hypotension.
Pack SizePriceAvailabilityQuantity
5 mg$31In Stock
10 mg$48In Stock
25 mg$85In Stock
50 mg$126In Stock
100 mg$175In Stock
200 mg$315In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
Blonanserin (AD-5423) is an atypical antipsychotic approved in Japan in January, 2008. Relative to many other antipsychotics, blonanserin has an improved tolerability profile, lacking side effects such as extrapyramidal symptoms, excessive sedation, or hypotension.
Targets&IC50
5-HT2:3.98 nM(Ki), D2 receptor:14.8 nM(Ki)
In vitro
In tests of atypical antipsychotics (risperidone, olanzapine, and aripiprazole), Blonanserin showed the most potent binding affinity for human D3 receptors.Blonanserin transiently increased neuronal firing in the nucleus of the pallidum and ventral tegmental area, but not in the nucleus medius dorsalis or the medial dorsal nucleus of the thalamus, whereas risperidone increased firing in the nucleus ventral tegmental area and in the nucleus medius dorsalis but not in the nucleus dorsalis. in the medial dorsal nucleus of the rat thalamus. Blonanserin consistently increased additional extracellular levels of norepinephrine and dopamine but not serotonin, GABA, or glutamate, whereas risperidone consistently increased levels of norepinephrine, dopamine, and serotonin but not GABA or glutamate.Blonanserin increased the efflux of cortical DA and its metabolites, homovanillic acid and 3,4-dihydroxy Phenylacetic acid.
In vivo
In tests of atypical antipsychotics (risperidone, olanzapine, and aripiprazole), Blonanserin showed the most potent binding affinity for human D3 receptors.Blonanserin transiently increased neuronal firing in the nucleus of the pallidum and ventral tegmental area, but not in the nucleus medius dorsalis or the medial dorsal nucleus of the thalamus, whereas risperidone increased firing in the nucleus ventral tegmental area and in the nucleus medius dorsalis but not in the nucleus dorsalis. in the medial dorsal nucleus of the rat thalamus. Blonanserin consistently increased additional extracellular levels of norepinephrine and dopamine but not serotonin, GABA, or glutamate, whereas risperidone consistently increased levels of norepinephrine, dopamine, and serotonin but not GABA or glutamate.Blonanserin increased the efflux of cortical DA and its metabolites, homovanillic acid and 3,4-dihydroxy Phenylacetic acid.
AliasAD-5423
Chemical Properties
Molecular Weight367.5
FormulaC23H30FN3
Cas No.132810-10-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 14.29 mg/mL (38.88 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7211 mL13.6054 mL27.2109 mL136.0544 mL
5 mM0.5442 mL2.7211 mL5.4422 mL27.2109 mL
10 mM0.2721 mL1.3605 mL2.7211 mL13.6054 mL
20 mM0.1361 mL0.6803 mL1.3605 mL6.8027 mL

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