3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(2S)-2-pyrrolidinylMethyl]aMino]-3-Cyclobutene-1,2-dione
98%
- Product Code: 70638
CAS:
1356935-80-2
| Molecular Weight: | 407.3103192 g./mol | Molecular Formula: | C₁₇H₁₅F₆N₃O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 406.5±55.0 °C | |
| Density: | 1.49±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design of enzyme inhibitors. Its structure, featuring trifluoromethyl groups and a cyclobutene-dione core, makes it a valuable scaffold for targeting specific proteins or enzymes involved in disease pathways. Researchers explore its potential as a potent inhibitor for enzymes like proteases or kinases, which play critical roles in conditions such as cancer, inflammation, or infectious diseases. Additionally, the stereochemistry introduced by the (2S)-pyrrolidinylmethyl group enhances its binding affinity and selectivity, making it a promising candidate for further optimization in pharmaceutical research. Its applications also extend to chemical biology, where it can be used as a tool compound to study enzyme mechanisms or cellular processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿16,974.00 |
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3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(2S)-2-pyrrolidinylMethyl]aMino]-3-Cyclobutene-1,2-dione
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design of enzyme inhibitors. Its structure, featuring trifluoromethyl groups and a cyclobutene-dione core, makes it a valuable scaffold for targeting specific proteins or enzymes involved in disease pathways. Researchers explore its potential as a potent inhibitor for enzymes like proteases or kinases, which play critical roles in conditions such as cancer, inflammation, or infectious diseases. Additionally, the stereochemistry introduced by the (2S)-pyrrolidinylmethyl group enhances its binding affinity and selectivity, making it a promising candidate for further optimization in pharmaceutical research. Its applications also extend to chemical biology, where it can be used as a tool compound to study enzyme mechanisms or cellular processes.
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