3-[[(1S,2S)-2-(1-Piperidinyl)cyclohexyl]amino]-4-[[4-(trifluoromethyl)phenyl]amino]-3-cyclobutene-1,2-dione

≥95%,99%e.e.

Reagent Code: #70610
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CAS Number 1312991-08-4

science Other reagents with same CAS 1312991-08-4

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scatter_plot Molecular Information
Weight 421.5 g/mol
Formula C₂₂H₂₆F₃N₃O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is utilized in medicinal chemistry for its potential as a kinase inhibitor, particularly in targeting specific enzymes involved in cellular signaling pathways. Its structure allows it to interact with ATP-binding sites of kinases, making it a candidate for the development of therapeutic agents against diseases like cancer, where aberrant kinase activity is often observed. Researchers explore its efficacy in preclinical studies to assess its ability to modulate kinase activity and inhibit tumor growth. Additionally, its trifluoromethyl group enhances its metabolic stability and binding affinity, which is advantageous in drug design. Further studies focus on optimizing its pharmacokinetic properties and evaluating its safety profile for potential clinical applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,225.00

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3-[[(1S,2S)-2-(1-Piperidinyl)cyclohexyl]amino]-4-[[4-(trifluoromethyl)phenyl]amino]-3-cyclobutene-1,2-dione
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This compound is utilized in medicinal chemistry for its potential as a kinase inhibitor, particularly in targeting specific enzymes involved in cellular signaling pathways. Its structure allows it to interact with ATP-binding sites of kinases, making it a candidate for the development of therapeutic agents against diseases like cancer, where aberrant kinase activity is often observed. Researchers explore its efficacy in preclinical studies to assess its ability to modulate kinase activity and inhibit tu

This compound is utilized in medicinal chemistry for its potential as a kinase inhibitor, particularly in targeting specific enzymes involved in cellular signaling pathways. Its structure allows it to interact with ATP-binding sites of kinases, making it a candidate for the development of therapeutic agents against diseases like cancer, where aberrant kinase activity is often observed. Researchers explore its efficacy in preclinical studies to assess its ability to modulate kinase activity and inhibit tumor growth. Additionally, its trifluoromethyl group enhances its metabolic stability and binding affinity, which is advantageous in drug design. Further studies focus on optimizing its pharmacokinetic properties and evaluating its safety profile for potential clinical applications.

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