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Pruvanserin hydrochloride
🥰Excellent
Catalog No. T22762Cas No. 443144-27-2
Alias LY2422347 hydrochloride, LY 2422347 hydrochloride, EMD281014 hydrochloride, EMD 281014 hydrochloride
Pruvanserin hydrochloride (EMD 281014 HCl) is an inverse and selective 5-HT2A receptor antagonist with IC₅₀ values of 0.35 nM and 1 nM for human and rat 5-HT2A receptors, respectively. Pruvanserin hydrochloride inhibits GTP-gamma-S accumulation and alleviates tactile allodynia in diabetic rats, making it suitable for studies on Parkinson's disease, insomnia, and schizophrenia.
Pruvanserin hydrochloride
🥰Excellent
Purity: 99.6%
Catalog No. T22762Alias LY2422347 hydrochloride, LY 2422347 hydrochloride, EMD281014 hydrochloride, EMD 281014 hydrochlorideCas No. 443144-27-2
Pruvanserin hydrochloride (EMD 281014 HCl) is an inverse and selective 5-HT2A receptor antagonist with IC₅₀ values of 0.35 nM and 1 nM for human and rat 5-HT2A receptors, respectively. Pruvanserin hydrochloride inhibits GTP-gamma-S accumulation and alleviates tactile allodynia in diabetic rats, making it suitable for studies on Parkinson's disease, insomnia, and schizophrenia.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 10 mg | $823 | In Stock | |
| 50 mg | $3,390 | In Stock |
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Purity:99.6%
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Product Introduction
Bioactivity
Chemical Properties
| Description | Pruvanserin hydrochloride (EMD 281014 HCl) is an inverse and selective 5-HT2A receptor antagonist with IC₅₀ values of 0.35 nM and 1 nM for human and rat 5-HT2A receptors, respectively. Pruvanserin hydrochloride inhibits GTP-gamma-S accumulation and alleviates tactile allodynia in diabetic rats, making it suitable for studies on Parkinson's disease, insomnia, and schizophrenia. |
| Targets&IC50 | 5-HT2A Receptor (human):0.35 nM, 5-HT2A Receptor (rat):1 nM |
| Synonyms | LY2422347 hydrochloride, LY 2422347 hydrochloride, EMD281014 hydrochloride, EMD 281014 hydrochloride |
| Molecular Weight | 412.89 |
| Formula | C22H22ClFN4O |
| Cas No. | 443144-27-2 |
| Smiles | Cl.N#CC1=CNC2=C1C=CC=C2C(=O)N3CCN(CCC4=CC=C(F)C=C4)CC3 |
| Relative Density. | no data available |
| Color | White |
| Appearance | Solid |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | Ethanol: < 8 mg/mL, Sonication is recommended. DMSO: < 32 mg/mL, Sonication is recommended. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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