aminooxy peg2 azide

Aminooxy-PEG2-azide, a PEG-based PROTAC linker, is utilized for the synthesis of PROTACs[1] and serves as a non-cleavable 2-unit PEG ADC linker in the synthesis of antibody-drug conjugates (ADCs)[2].

t-Boc-Aminooxy-PEG2-azide is a polyethylene glycol (PEG) derived linker compound used for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Aminooxy-PEG3-azide is an ADC linker belonging to the class of PEGs, as well as three-unit PEGs, which can be used for the synthesis of antibody-coupled reactive molecules (ADCs).

Pomalidomide 4'-PEG2-azide is a synthetic E3 ligase ligand-linker conjugate, comprising a Pomalidomide-based cereblon ligand and a linker.

2-(Azido-PEG2-amido)-13-propandiol is a Polyethylene glycol (PEG)-based PROTAC linker used for synthesizing PROTACs[1].

Boc-Aminooxy-PEG1-azide is a polyethylene glycol (PEG) derived linker compound engineered for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

(S,R,S)-AHPC-(C3-PEG)2-C6-Cl is a small molecule HaloPROTAC incorporating the (S,R,S)-AHPC-based VHL ligand and a 2-unit PEG linker, capable of inducing degradation of GFP-HaloTag7 in cell-based assays [1].

Boc-Aminooxy-PEG2-bromide is a bifunctional, cleavable polyethylene glycol (PEG) linker used specifically in the synthesis of antibody-drug conjugates (ADCs) [1].

Azide-PEG-amine (MW 3500) is a polyethylene glycol (PEG) linker compound, designed for the synthesis of proteolysis targeting chimeric molecules (PROTACs)[1].

Aminooxy-PEG-OH (MW 2000) is a PEG-based PROTAC linker utilized in the synthesis of PROTACs[1].

N-(Boc-PEG2)-N-bis(PEG3-azide) is a polyethylene glycol (PEG)-derived linker utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Azide-PEG-azide (MW 20000) is a polyethylene glycol (PEG)-based linker compound used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].

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

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

Pomalidomide-PEG2-azide is a synthetic conjugate consisting of a cereblon ligand derived from Pomalidomide and a 2-unit PEG linker, designed for use in PROTAC technology as a ligand-linker conjugate of E3 ligase.

Azide-PEG-azide (MW 5000) is a polyethylene glycol (PEG)-based linker component employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

DBCO-(PEG2-Val-Cit-PAB)2 is a dual-cleavable linker used in antibody-drug conjugates (ADCs).

Aminooxy-PEG2-alcohol is a non-cleavable PEG linker comprising two units, used in the synthesis of antibody-drug conjugates (ADCs) [1] and as a PEG-based PROTAC linker for the synthesis of PROTACs [2].

TAMRA-Azide-PEG-biotin is a PEG-based linker for PROTACs, joining two essential ligands. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

Biotin-PEG2-azide, a PEG-based PROTAC linker, can be used in the synthesis of PROTACs.

Azide-PEG-azide (MW 10000) is a polyethylene glycol (PEG)-based linker essential for PROTACs synthesis and assembly[1].

Azide-PEG-amine (MW 5000) is a polyethylene glycol (PEG)-derived linker compound with azide functionality, primarily utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

m-PEG-azide (MW 20000) is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands necessary for forming PROTAC molecules, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthesized E3 ligase ligand-linker, incorporating a cereblon ligand based on Thalidomide and a 3-unit PEG linker, specifically designed for PROTAC technology applications.

Azide-PEG-azide (MW 2000) is a polyethylene glycol (PEG)-based linker used for synthesizing proteolysis-targeting chimeras (PROTACs)[1].

Aminooxy-PEG1-azide is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Azide-PEG-alcohol, a polyethylene glycol (PEG)-based PROTAC linker with a molecular weight of 2000, functions as a versatile option for the synthesis of PROTACs[1].

Bromo-PEG2-C2-azide is a non-cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].

Boc-Aminooxy-PEG2-C2-amine is a polyethylene glycol (PEG)-based linker molecule designed for use in the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

t-Boc-Aminooxy-PEG5-azide is a polyethylene glycol (PEG) derivative functioning as a linker for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

1,1,1-Trifluoroethyl-PEG2-azide is a polyethylene glycol-based azide linker compound used in synthesizing proteolysis-targeting chimeras (PROTACs)[1].

Aminooxy-PEG5-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1].

Boc-NH-PEG2-propargyl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

Bis-aminooxy-PEG2, a PEG-based linker for PROTACs, joins two essential ligands, crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

(2-Pyridyldithio)-PEG2-Boc is a polyethylene glycol-based PROTAC linker used in the synthesis of PROTACs [1].

Azide-PEG-amine (MW 2000) is a Polyethylene Glycol (PEG)-derived linker compound used in the synthesis of Proteolysis Targeting Chimeras (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.

Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthetic conjugate that combines a Thalidomide-based cereblon ligand and a linker, commonly utilized in PROTAC technology. This compound serves as a connector between the target protein and the E3 ligase, facilitating targeted protein degradation.

Azido-PEG2-azide, a PEG-based PROTAC linker, is utilized in PROTAC synthesis.

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

N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl) is a polyethylene glycol (PEG) derivative designed as a linker for PROTAC synthesis [1].

UV Cleavable Biotin-PEG2-Azide, a PEG-based PROTAC linker, enables the synthesis of PROTACs[1].

DSPE-PEG-2-Aminoethyl-alpha-mannopyranoside (MW 2000) is a polyethylene glycol (PEG) derived linker used in the synthesis of proteolysis targeting chimeras (PROTACs) [1].

Boc-N-Amido-PEG2-C2-azide is a polyethylene glycol (PEG)-based linker used in the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

Benzyl-PEG2-azide, a PEG-based PROTAC linker, is utilized in the synthesis of PROTACs.

Fluorescein-thiourea-PEG2-azide is a PEG-derived linker commonly used in the synthesis of PROTACs[1].

Pyrene-PEG2-azide is a PEG-based linker for PROTACs, connecting two essential ligands necessary for PROTAC molecule formation and facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Aminooxy-PEG4-azide, a PEG-based linker for PROTACs, connects two essential ligands critical for forming PROTAC molecules, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.