t-Boc-N-amido-PEG7-azide is a protected, azide-functional polyethylene glycol (PEG) linker designed for modular PROTAC synthesis. Structurally, it incorporates a Boc-protected amide terminus and a PEG7 chain that provides hydrophilicity and conformational flexibility, terminating in an azide group suitable for bioorthogonal conjugation. In PROTAC architectures, such linkers help tune the spatial relationship between the target-binding ligand and the E3 ligase-recruiting moiety, often improving productive ternary complex formation by reducing steric clashes and enabling favorable linker dynamics. The azide handle supports copper-free “click” reactions (e.g., with cyclooctyne/DBCO partners) to install the linker onto complementary components under mild conditions, while the amide functionality enables controlled coupling strategies during synthesis. This reagent is valuable for researchers optimizing linker length, attachment chemistry, and solubility to enhance targeted protein degradation performance in vitro.
Structure of 206265-96-5
* For research and manufacturing use only. Not for human or clinical use.
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t-Boc-N-amido-PEG7-azide is a polyethylene glycol (PEG)-based linker bearing an azide handle and a protected amide functionality, designed to facilitate modular assembly of PROTACs. Its flexible PEG chain can improve solubility and conformational adaptability between the target-binding ligand and the E3 ligase-recruiting moiety. The azide group enables reliable chemoselective conjugation strategies commonly used in targeted protein degradation workflows. The
Structure: The molecule contains a PEG oligomer backbone with an azide substituent and a Boc-protected amide, providing a flexible, hydrophilic linker domain. It features carbamate and amide linkages, along with ether linkages typical of PEG, which together support stable, non-volatile handling and controlled functional-group exposure.
Reactivity: The azide enables copper(I)-catalyzed azide–alkyne cycloaddition or related azide-compatible coupling routes to install the linker between PROTAC fragments under mild conditions. The Boc group can be removed using standard acidolysis to reveal the amide for subsequent coupling chemistries, such as amide bond formation. Solvent systems that maintain PEG solubility and preserve azide integrity are typically selected, with catalysts and bases chosen to minimize side reactions.
* 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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