T1817

GNF-2 is a highly selective non-ATP competitive inhibitor of Bcr-Abl.

m-PEG24-Mal is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands necessary for PROTAC molecule formation, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.

m-PEG24-NH2 is a PEG-based PROTAC linker that can be utilized in the synthesis of PROTACs (PROteolysis TArgeting Chimeras).

m-PEG24-SH is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG25-acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG25-Hydrazide is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

m-PEG25-NHS ester is a PEG-based linker for PROTACs that connects two essential ligands for the formation of PROTAC molecules, enabling selective protein degradation via the ubiquitin-proteasome system within cells.

m-PEG25-Propargyl, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG3-amido-C3-triethoxysilane is a polyethylene glycol (PEG)-based linker frequently used in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

m-PEG3-Hydrazide, a PEG-based linker for PROTACs, joins two essential ligands necessary for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG3-Mal is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.