1-(1-(3,3-Dimethylbutanoyl)piperidin-4-yl)-3-(4-(trifluoromethyl)phenyl)urea

95%

Reagent Code: #39093
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CAS Number 1020266-54-9

science Other reagents with same CAS 1020266-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 385.42 g/mol
Formula C₁₉H₂₆F₃N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It acts as a potent inhibitor targeting specific enzymes or receptors involved in various disease pathways. Its structure, featuring a trifluoromethylphenyl group, enhances its binding affinity and selectivity, making it valuable in the design of therapeutic agents. Researchers explore its potential in treating conditions such as cancer, inflammation, or neurological disorders, where modulation of specific biological targets is critical. Additionally, its piperidine and urea moieties contribute to its stability and bioavailability, which are essential for effective drug candidates. Ongoing studies focus on optimizing its pharmacological properties for clinical applications.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿41,940.00

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1-(1-(3,3-Dimethylbutanoyl)piperidin-4-yl)-3-(4-(trifluoromethyl)phenyl)urea
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It acts as a potent inhibitor targeting specific enzymes or receptors involved in various disease pathways. Its structure, featuring a trifluoromethylphenyl group, enhances its binding affinity and selectivity, making it valuable in the design of therapeutic agents. Researchers explore its potential in treating conditions such as cancer, inflammation, or neurological disorders, where modulation of specific biolo

This compound is primarily utilized in the field of medicinal chemistry and drug development. It acts as a potent inhibitor targeting specific enzymes or receptors involved in various disease pathways. Its structure, featuring a trifluoromethylphenyl group, enhances its binding affinity and selectivity, making it valuable in the design of therapeutic agents. Researchers explore its potential in treating conditions such as cancer, inflammation, or neurological disorders, where modulation of specific biological targets is critical. Additionally, its piperidine and urea moieties contribute to its stability and bioavailability, which are essential for effective drug candidates. Ongoing studies focus on optimizing its pharmacological properties for clinical applications.

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