Azido-PEG6-Br is a heterobifunctional polyethylene glycol linker designed for modular PROTAC and targeted protein degradation workflows. Structurally, it comprises a six-unit PEG chain that provides aqueous solubility and conformational flexibility, terminated by an azide group for orthogonal bioorthogonal conjugation and a terminal bromide handle suitable for nucleophilic substitution or further functionalization. In PROTAC construction, this linker enables researchers to connect two chemically distinct components—typically a ligand for an E3 ligase and a ligand for the target protein—while the PEG spacer helps reduce steric interference and can improve effective reach and productive ternary complex formation. The azide moiety supports efficient click-type coupling strategies, allowing late-stage assembly under mild conditions. As a result, Azido-PEG6-Br is valuable for generating PROTAC analog libraries, optimizing linker length and attachment geometry, and facilitating systematic structure–activity relationship studies in targeted degradation research.
Structure of 2062663-64-1
* For research and manufacturing use only. Not for human or clinical use.
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Azido-PEG6-Br is a bifunctional polyethylene glycol-based linker designed for modular PROTAC assembly, enabling efficient conjugation between a ligand bearing a bromide-reactive handle and an azide-bearing partner. Its PEG character supports favorable solubility and conformational flexibility, which can improve productive ternary complex formation in targeted protein degradation workflows. The points below describe the molecule’s structure and practical reactivity considerations for constructing PROTACs in a research setting.
Structure: Azido-PEG6-Br contains an azide functional group and a terminal bromide separated by a polyethylene glycol chain. The structure features ether linkages within the PEG backbone and carbon–nitrogen bonds in the azide, providing a flexible, polar, and chemically stable linker suitable for bioconjugation.
Reactivity: The azide group is commonly used in copper-catalyzed azide–alkyne cycloaddition or related click chemistries, while the bromide can serve as an electrophile for nucleophilic substitution with amines or other nucleophiles to form C–N or related linkages. Typical PROTAC linker coupling strategies employ inert or controlled atmospheres, appropriate polar solvents, and catalysts such as copper(I) for click reactions, with reaction conditions optimized to preserve sensitive ligands.
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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