T1553

Chlorpheniramine maleate (NCI-C55265) is a histamine H1 antagonist used in allergic reactions, hay fever, rhinitis, urticaria, and asthma.

Hydroxy-PEG6-Boc, a PEG-based PROTAC linker, is utilized in PROTAC synthesis [1].

Hydroxy-PEG7-Boc, a PEG-based PROTAC linker, is utilized in PROTAC synthesis [1].

Hydroxy-PEG4-CH2-Boc is a PEG-based linker used in PROTACs, facilitating the conjugation of two critical ligands necessary for PROTAC molecule formation. This linker enables selective protein degradation by exploiting the ubiquitin-proteasome system within cells.

Hydroxy-PEG4-CH2COOH 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.

Hydroxy-PEG4-methylamine is a polyethylene glycol (PEG) derivative commonly employed as a linker in the synthesis of PROteolysis TArgeting Chimeras (PROTACs)[1].

Hydroxy-PEG4-O-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Hydroxy-PEG5-C2-methyl ester, a polyethylene glycol (PEG) derived linker compound, is utilized in PROTAC (PROteolysis TArgeting Chimeras) synthesis[1].

Hydroxy-PEG6-acid is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

Hydroxy-PEG6-CH2-Boc is a PEG-based linker used in PROTACs to connect two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Hydroxy-PEG8-Boc, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.