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5-HT6R antagonist 3 (compound 15) is an effective and selective 5-HT6R antagonist capable of crossing the blood-brain barrier. It exhibits Ki values of 14 nM for 5-HT6, 3533 nM for 5-HT1A, 35 nM for 5-HT2A, and 1449 nM for 5-HT7. This compound demonstrates anxiolytic-like effects and possesses neuroprotective and cognitive-enhancing properties, indicating potential for Alzheimer's disease research.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | 5-HT6R antagonist 3 (compound 15) is an effective and selective 5-HT6R antagonist capable of crossing the blood-brain barrier. It exhibits Ki values of 14 nM for 5-HT6, 3533 nM for 5-HT1A, 35 nM for 5-HT2A, and 1449 nM for 5-HT7. This compound demonstrates anxiolytic-like effects and possesses neuroprotective and cognitive-enhancing properties, indicating potential for Alzheimer's disease research. |
| Targets&IC50 | 5-HT2A receptor:35 nM (Ki), 5-HT1A receptor:3533 nM (Ki), 5-HT7 Receptor:1449 nM (Ki), 5-HT6 receptor:14 nM (Ki) |
| Formula | C21H26N6Se |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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