azido-peg-1-azide

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

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

Azido-PEG4-CH2-Boc, a four-unit cleavable polyethylene glycol (PEG) linker compound, is used in the synthesis of antibody-drug conjugates (ADCs) [1] and PROTACs [2]. Characterized by its azide functional group and PEG backbone, it facilitates drug-antibody conjugation in ADCs and enables PROTAC synthesis using PEG and alkyl/ether moieties.

m-PEG4-azide, also referred to as 13-Azido-2,5,8,11-tetraoxatridecane, functions as a PEG-based PROTAC linker suitable for PROTACs synthesis[1].

N-(Azido-PEG3)-N-Boc-PEG4-acid is a PEG-based PROTAC linker with a terminal azide group, primarily used in PROTAC synthesis [1].

N-(Azido-PEG4)-N-Boc-PEG4-NHS ester is a PEG-based PROTAC linker with a terminal azide group, commonly used in the synthesis of 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-PEG3-S-PEG4-propargyl is a polyethylene glycol (PEG)-based linker containing azide and propargyl groups, designed specifically for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Azido-PEG3-SS-NHS is a three-unit polyethylene glycol (PEG) linker with an azide group, a cleavable disulfide bond, and an N-hydroxysuccinimide ester, primarily used in the synthesis of antibody-drug conjugates (ADCs) [1].

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

N-Methyl-N'-(azido-PEG2-C5)-Cy5 is a polyethylene glycol (PEG)-based linker with an azide functionality, primarily used in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Bocaminooxyacetamide-PEG2-Azido, a cleavable two-unit PEG ADC linker used in synthesizing antibody-drug conjugates (ADCs) [1], is a click chemistry reagent. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups.

Azido-PEG1-Val-Cit-PABC-PNP, a 1 unit PEG ADC linker, is utilized in the development of antibody-drug conjugates (ADCs) [1]. This compound serves as a click chemistry reagent featuring an Azide group, facilitating copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules bearing Alkyne groups. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.