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S 32212 hydrochloride
🥰Excellent
Catalog No. T23292Cas No. 847871-78-7
Alias S32212 hydrochloride
S 32212 hydrochloride is a high-affinity inverse agonist at the 5-HT2C receptor (pKi = 8.18) and an antagonist at the α2-adrenergic receptor (Ki = 5.8 nM), potentiating norepinephrine with antidepressant and anxiolytic effects.
S 32212 hydrochloride
🥰Excellent
Purity: 99.77%
Catalog No. T23292Alias S32212 hydrochlorideCas No. 847871-78-7
S 32212 hydrochloride is a high-affinity inverse agonist at the 5-HT2C receptor (pKi = 8.18) and an antagonist at the α2-adrenergic receptor (Ki = 5.8 nM), potentiating norepinephrine with antidepressant and anxiolytic effects.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $98 | In Stock | |
| 5 mg | $343 | In Stock | |
| 10 mg | $512 | In Stock |
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Purity:99.77%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | S 32212 hydrochloride is a high-affinity inverse agonist at the 5-HT2C receptor (pKi = 8.18) and an antagonist at the α2-adrenergic receptor (Ki = 5.8 nM), potentiating norepinephrine with antidepressant and anxiolytic effects. |
| Alias | S32212 hydrochloride |
| Molecular Weight | 452.98 |
| Formula | C25H29ClN4O2 |
| Cas No. | 847871-78-7 |
| Smiles | Cl.O=C(NC1=CC=C(OC)C(=C1)N2CCN(C)CC2)N3C=4C=CC=5C=CC=CC5C4CC3 |
| Relative Density. | no data available |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| Solubility Information | H2O: 80 mg/mL (176.61 mM), Sonication is recommended. DMSO: 80 mg/mL (176.61 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
H2O/DMSO
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(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 μLddH2O 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 μLddH2O 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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