T1471

Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a thiophene derivative and selective neurotransmitter uptake inhibitor for serotonin and noradrenaline (SNRI). It is an antidepressant agent and anxiolytic, also used for treating pain in patients with diabetes mellitus and fibromyalgia.

Boc-Aminooxy-PEG2-CH2COOH is a PEGylated PROTAC linker used for synthesizing PROTACs [1].

Boc-Aminooxy-PEG2 is a PEG-based linker for PROTACs, facilitating the formation of PROTAC molecules by joining two essential ligands and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Boc-Aminooxy-PEG3-acid, a PEG-based linker for PROTACs, connects two essential ligands critical for forming PROTAC molecules, thus facilitating selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

Boc-Aminooxy-PEG3-azide is a polyethylene glycol (PEG) derived PROTAC linker, engineered specifically for PROTAC synthesis[1].

Boc-Aminooxy-PEG3-bromide, a polyethylene glycol (PEG)-based PROTAC linker, is utilized in the synthesis of PROTACs, which are molecules designed for targeted protein degradation [1].

Boc-Aminooxy-PEG3-C2-NH2, a polyethylene glycol (PEG) derived linker, is utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Boc-Aminooxy-PEG3-thiol, a polyethylene glycol (PEG)-based PROTAC linker, is used in the synthesis of PROTACs[1].

Boc-Aminooxy-PEG4-azide, a polyethylene glycol (PEG) derived linker, has potential applications in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Boc-Aminooxy-PEG4-CH2CO2H is a polyethylene glycol (PEG) derivative that functions as a PROTAC linker for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Boc-Aminooxy-PEG4-NH2, a PEG-based linker for PROTACs, facilitates the formation of PROTAC molecules by joining two essential ligands and enables selective protein degradation via the ubiquitin-proteasome system within cells.