m-PEG7-azide is a meta-functionalized, methoxy-terminated polyethylene glycol linker bearing an azide group, providing a hydrophilic, flexible chain of approximately seven ethylene glycol units for conjugation chemistry. The PEG segment improves aqueous solubility and reduces nonspecific interactions, while the terminal azide enables bioorthogonal coupling reactions such as copper-free click chemistry with strained alkynes or other azide-reactive partners. In PROTAC and targeted protein degradation workflows, this linker is used to spatially separate a ligand-binding “warhead” from a second module (e.g., an E3 ligase binder), tuning effective reach, relative orientation, and linker length to promote formation of the ternary complex required for ubiquitination and subsequent degradation. Its modular handle supports systematic structure–activity relationship studies, allowing researchers to rapidly generate and compare conjugates with controlled physicochemical properties and cell-compatible assembly strategies.
Structure of 208987-04-6
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m-PEG7-azide is a polyethylene glycol (PEG)-based azide linker designed for modular assembly of PROTACs and other targeted conjugates. Its PEG spacer provides conformational flexibility and improved solubility, while the terminal azide enables efficient bioorthogonal coupling to complementary handles. This combination supports reliable linker installation and subsequent formation of well-defined ternary-recruiting architectures. The structure and reactivity of this linker are described in detail below.
Structure: The linker comprises a PEG chain terminating in an azide functional group, featuring ether linkages along the polyether backbone and a terminal N3 moiety. The flexible, hydrophilic PEG segment promotes favorable dispersion in aqueous media and helps reduce steric constraints during conjugation and target engagement.
Reactivity: The azide is well suited for copper-free or copper-catalyzed azide–alkyne cycloaddition with an appropriate alkyne partner to form a stable triazole linkage. Typical conjugation workflows use compatible polar solvents and mild conditions to preserve sensitive ligands, with reaction progress monitored by standard analytical methods. The mechanism relies on selective cycloaddition between the azide and terminal alkyne under bioorthogonal conditions.
* 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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