azido peg1 azide

Azido-PEG1-azide, a PEG-based PROTAC linker, is utilized in the synthesis of PROTACs (Proteolysis Targeting Chimeras).

Azido-PEG9-azide is a PEG-based PROTAC linker suitable for use in PROTAC synthesis.

Bromo-PEG1-C2-azide, a PEG-based PROTAC linker, is utilized in the synthesis of PROTACs.

Azido-PEG4-azide is a PEG-based PROTAC linker used for synthesizing PROTACs.

Azido-PEG3-azide is a PEG-based PROTAC linker utilized in PROTAC synthesis.

Azido-PEG11-azide is a PEG-based PROTAC linker used in PROTAC synthesis.

Azido-PEG5-azide, a PEG-based PROTAC linker, is used in PROTAC synthesis.

Azido-PEG1-CH2CO2H, a PROTAC linker characterized by an alkyl ether combination, can be utilized to synthesize PROTAC BRD4 Degrader-1[1].

Azido-PEG1-Val-Cit-OH is a cleavable, one-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1].

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

Azido-PEG1-CH2CO2-NHS is an alkyl ether-based linker utilized in the synthesis of PROTACs [1].

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

Azido-PEG3-S-PEG3-azide is a polyethylene glycol (PEG)-derived linker engineered for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Azido-PEG1-NHS ester is a PEG-based linker for PROTACs, enabling the formation of PROTAC molecules by joining two essential ligands and facilitating selective protein degradation through the ubiquitin-proteasome system within cells.

Azido-PEG1-amine is a PROTAC linker belonging to the PEG class, which can be used to synthesize PROTAC molecules.

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

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

Azido-PEG1-Boc, a PEG-based linker for PROTACs, connects two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

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.

Azido-PEG15-azide is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules, thereby enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

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].

Azido-PEG6-azide, a PEG-based PROTAC linker, is used in the synthesis of PROTACs [1].

Azido-PEG1-PFP ester, a PEG-based linker for PROTACs, connects two essential ligands critical for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azido-PEG1-C2-methylamine is a PEG-conjugated linker utilized in the synthesis of 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.

Azido-PEG3-SS-PEG3-azide, a polyethylene glycol (PEG) based linker, is commonly used in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Azido-PEG1, a PEG-based PROTAC linker, can be utilized in the synthesis of PROTACs.

Azido-PEG1-methyl ester is an alkyl ether-based linker used in the synthesis of PROTACs (1).

Azido-PEG1-C2-acid is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules, thereby enabling selective protein degradation via the ubiquitin-proteasome system [within cells].

m-PEG-azide (MW 10000), a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Azido-PEG7-azide, a PEG-based linker for PROTACs, joins two essential ligands, which are crucial for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

NH-bis(C2-PEG1-azide) is a PEG-based linker for PROTACs that joins two essential ligands, enabling selective protein degradation through the ubiquitin-proteasome system within cells.

m-PEG-azide (MW 2000) is a PEG-based linker used in PROTACs to join two essential ligands, facilitating the selective degradation of target proteins through the ubiquitin-proteasome system within cells.

m-PEG-azide (MW 5000) is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands to enable selective protein degradation via the ubiquitin-proteasome system in cells.

N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) is a polyethylene glycol (PEG)-based PROTAC linker used in the synthesis of PROTACs[1].

1-Isothiocyanato-PEG3-azide is a PEG-based PROTAC linker used for PROTAC synthesis [1].

Thalidomide 4'-ether-PEG1-azide, a Thalidomide-based cereblon ligand, facilitates the recruitment of CRBN protein. This compound is capable of being linked to a protein ligand via a linker to construct PROTACs [1].

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

Lenalidomide-PEG1-azide is an E3 ligase ligand-linker conjugate that incorporates the cereblon ligand based on Lenalidomide and a linker. It is designed for use in the development of PROTAC BRD4 Degrader-2[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].

Pomalidomide-PEG1-azide is an E3 ligase ligand-linker conjugate that combines the cereblon ligand based on Pomalidomide with a linker. This compound is instrumental in designing PROTAC BRD4 Degrader-1[1].

N-Boc-N-bis(C2-PEG1-azide) is an alkyl ether-based PROTAC linker suitable for synthesizing 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].

Azido-PEG8-azide is a PEG-based linker used in PROTACs that joins two essential ligands, facilitating 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.