(2-(2,6-Dioxopiperidin-3-yl)-3-oxoisoindolin-5-yl)methyl (2-fluoro-5-(trifluoromethoxy)phenyl)carbamate

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Reagent Code: #167598
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CAS Number 2803881-11-8

science Other reagents with same CAS 2803881-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 495.38 g/mol
Formula C₂₂H₁₇F₄N₃O₆
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in pharmaceutical research and development, this compound functions as a PROTAC (Proteolysis Targeting Chimera) linker or intermediate. It enables targeted protein degradation by bridging an E3 ubiquitin ligase ligand to a protein-binding moiety, facilitating the ubiquitination and subsequent degradation of disease-related proteins. Its structure supports enhanced selectivity and cellular permeability, making it valuable in oncology and inflammatory disease research. Commonly employed in the design of degraders for transcription factors and kinases, it contributes to the development of therapies with improved efficacy and reduced off-target effects.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿11,860.00
inventory 10mg
10-20 days ฿20,330.00
inventory 25mg
10-20 days ฿38,580.00

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(2-(2,6-Dioxopiperidin-3-yl)-3-oxoisoindolin-5-yl)methyl (2-fluoro-5-(trifluoromethoxy)phenyl)carbamate
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Used primarily in pharmaceutical research and development, this compound functions as a PROTAC (Proteolysis Targeting Chimera) linker or intermediate. It enables targeted protein degradation by bridging an E3 ubiquitin ligase ligand to a protein-binding moiety, facilitating the ubiquitination and subsequent degradation of disease-related proteins. Its structure supports enhanced selectivity and cellular permeability, making it valuable in oncology and inflammatory disease research. Commonly employed in t

Used primarily in pharmaceutical research and development, this compound functions as a PROTAC (Proteolysis Targeting Chimera) linker or intermediate. It enables targeted protein degradation by bridging an E3 ubiquitin ligase ligand to a protein-binding moiety, facilitating the ubiquitination and subsequent degradation of disease-related proteins. Its structure supports enhanced selectivity and cellular permeability, making it valuable in oncology and inflammatory disease research. Commonly employed in the design of degraders for transcription factors and kinases, it contributes to the development of therapies with improved efficacy and reduced off-target effects.

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