1-(3-(5-Fluoro-1H-indol-2-yl)phenyl)-N-(2-(4-isopropylpiperazin-1-yl)ethyl)piperidin-4-amine
≥98% (HPLC)
- Product Code: 109869
CAS:
1883351-01-6
| Molecular Weight: | 463.63 g./mol | Molecular Formula: | C₂₈H₃₈FN₅ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 647.6 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily explored in the field of medicinal chemistry, particularly in the development of novel therapeutic agents. Its structure suggests potential activity as a modulator of specific biological targets, such as receptors or enzymes involved in neurological or psychiatric disorders. Researchers are investigating its efficacy in treating conditions like depression, anxiety, or schizophrenia due to its interaction with serotonin receptors, given the indole moiety and piperazine substituents. Additionally, its fluorine atom may enhance metabolic stability and bioavailability, making it a promising candidate for drug development. Preclinical studies focus on optimizing its pharmacokinetic and pharmacodynamic properties to improve therapeutic outcomes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿13,716.00 |
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1-(3-(5-Fluoro-1H-indol-2-yl)phenyl)-N-(2-(4-isopropylpiperazin-1-yl)ethyl)piperidin-4-amine
This compound is primarily explored in the field of medicinal chemistry, particularly in the development of novel therapeutic agents. Its structure suggests potential activity as a modulator of specific biological targets, such as receptors or enzymes involved in neurological or psychiatric disorders. Researchers are investigating its efficacy in treating conditions like depression, anxiety, or schizophrenia due to its interaction with serotonin receptors, given the indole moiety and piperazine substituents. Additionally, its fluorine atom may enhance metabolic stability and bioavailability, making it a promising candidate for drug development. Preclinical studies focus on optimizing its pharmacokinetic and pharmacodynamic properties to improve therapeutic outcomes.
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